Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_732_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
30.08.2026
Размер:
51 Мб
Скачать
SECTION III Oncoplastic Breast Surgery – Outcomes
https://t.me/medicina_free
174
been found to reduce the eects of acute dermatitis.
102
Grade 1 or 2 CTCAE dermatitis may be treated with petroleum­based emollients. More severe cases may be managed with silver sulfadiazine cream. Breast pain is commonly reported in about 20–30% of women, although it may not be associ­ated with radiation.
103
Patients and physicians tend to rate breast cosmesis
after BCT good to excellent in 75–80%.
104
Fat necrosis
is present in 1–4% of patients undergoing BCT, although
TABLE
Onset and Dose Threshold of Acute Radiation
20.6
Dermatitis
Reaction Type Onset Dose Threshold (Gy)
Erythema 7–10 days 6
Dry desquamation 3–4 weeks 20
Moist desquamation 4+ weeks 30
Ulceration 5+ weeks >40
99
it is up to 10–30% in women undergoing IORT. Moder­ate to severe breast brosis is more common in patients who receive increased radiation in WBI through a boost (30.4% vs 15.0%) and manifests weeks to years following treatment. A radiation boost often increases the incidence of breast brosis (5.2% vs 1.8%).68 Animal studies seem to indicate that fat grafting improves the quality of irradi­ated skin, with histological evidence of repair in a treated
105
group.
Khouri etal described using external expansion of the radiated breast to expand the parenchymal space and improve the vascularity before performing autologous fat grafting.
105a
is will allow for placement of higher fat volumes when compared with patients who underwent BCT on average 7 years after treatment.
106
Further study needs to be done on autologous fat grafting therapeutics in the setting of BCT. 
Summary
e demonstration of safety and ecacy following RT in the management of breast cancer has revolutionized treat­ment options and made breast conservation and onco­plastic therapy possible. Recent advancement in APBI techniques has been designed with the expressed purpose to limit the amount of radiation exposure to normal tis­sues. Renement of technique may provide improved cosmesis and decrease radiation impact to normal tissue; trials are currently underway, and patient recruitment is progressing. Future studies should rene the criteria for BCT as certain subgroups seem to benet more than oth­ers. In addition, patient-reported outcome measures, such as the BreastQ, should be routinely utilized to quantify the eect on quality of life and psychosocial well-being among dierent treatment types. e role of plastic sur­gery is becoming increasing appreciated as we bridge the gap between treatment of disease and treatment of the patient as a whole.
Fig. . The acute toxicity of radiation at two weeks demonstrating
dermatitis and desquamation.
TABLE
Common Terminology Criteria for Adverse Events (CTCAE) by the National Cancer Institute Classication
20.7
of Acute Dermatitis (v5.0)
Stage 1 Stage 2 Stage 3 Stage 4 Stage 5
Faint erythema, dry
desquamation
100
Moderate to brisk erythema,
patch moist desquama­tion confined to skin folds and creases, moderate edema
Moist desquamation in areas
other than skin folds and creases, bleeding induced by minor trauma or abra­sion
Life-threatening conse-
quences, skin necrosis or ulceration of full thickness dermis, spontaneous bleed­ing from involved site, skin graft indicated
Death
CHAPTER 20 Radiation Therapy Considerations and Oncoplastic Breast Surgery
https://t.me/medicina_free
175
References
1. Fisher B, Anderson S, Bryant J, etal. Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation for the treatment of invasive breast cancer. N Engl J Med. 2002;347(16):1233–1241.
2. Veronesi U, Cascinelli N, Mariani L, etal. Twenty-year follow­up of a randomized study comparing breast-conserving surgery with radical mastectomy for early breast cancer. N Engl J Med. 2002;347(16):1227–1232.
3. Litiere S, Werutsky G, Fentiman IS, et al. Breast conserving therapy versus mastectomy for stage I-II breast cancer: 20 year follow-up of the EORTC 10801 phase 3 randomised trial. Lan- cet Oncol. 2012;13(4):412–419.
4. Arriagada R, Le MG, Rochard F, Contesso G. Conservative treatment versus mastectomy in early breast cancer: patterns of failure with 15 years of follow-up data. Institut Gustave-Roussy Breast Cancer Group. J Clin Oncol. 1996;14(5):1558–1564.
5. Blichert-Toft M, Nielsen M, During M, et al. Long-term results of breast conserving surgery vs. mastectomy for early stage invasive breast cancer: 20-year follow-up of the Danish randomized DBCG-82TM protocol. Acta Oncol. 2008;47(4):672–681.
6. Simone NL, Dan T, Shih J, etal. Twenty-ve year results of the national cancer institute randomized breast conservation trial. Breast Cancer Res Treat. 2012;132(1):197–203.
7. Early Breast Cancer Trialists’ Collaborative G, Darby S, McGale P, etal. Eect of radiotherapy after breast-conserving surgery on 10-year recurrence and 15-year breast cancer death: meta­analysis of individual patient data for 10,801 women in 17 ran­domised trials. Lancet. 2011;378(9804):1707–1716.
8. Vinh-Hung V, Verschraegen C. Breast-conserving surgery with or without radiotherapy: pooled-analysis for risks of ipsilat­eral breast tumor recurrence and mortality. J Natl Cancer Inst. 2004;96(2):115–121.
9. Singh NK, Singh AM. Oncoplastic breast surgery and the eects of radiation therapy. In: Nahabedian MY, ed. Oncoplastic surgery of the breast. New York, NY: Elsevier; 2009:137–148.
10. Connell PP, Hellman S. Advances in radiotherapy and implica­tions for the next century: a historical perspective. Cancer Res. 2009;69(2):383–392.
11. Zeman EM. e biological basis of radiation oncology. In: Gunderson L, Tepper J, eds. Clinical radiation oncology. 4th ed. New York NY: Elsevier; 2016:2–40.
12. Hall EJ, Cox JD. Physical and biologic basis of radiation therapy. In: Cox JD, Ang KK, eds. Radiation oncology - ratio- nale, technique, results. 9th ed. New York, NY: Elsevier; 2010: 3–49.
13. Evans S, Young M, Higgins S, Moran MS. Biological basis of radiotherapy of the breast. In: Bland K, Copeland E, Klim­berg VS, Gradishar W, eds. e breast: comprehensive manage- ment of benign and malignant diseases. New York, NY: Elsevier; 2018:663–671.
14. Fisher B, Brown A, Mamounas E, etal. Eect of preoperative chemotherapy on local-regional disease in women with operable breast cancer: ndings from National Surgical Adjuvant Breast and Bowel Project B-18. J Clin Oncol. 1997;15(7):2483–2493.
15. Fisher B, Bryant J, Wolmark N, etal. Eect of preoperative chemotherapy on the outcome of women with operable breast cancer. J Clin Oncol. 1998;16(8):2672–2685.
16. Mittendorf EA, Buchholz TA, Tucker SL, etal. Impact of che­motherapy sequencing on local-regional failure risk in breast cancer patients undergoing breast-conserving therapy. Ann Surg. 2013;257(2):173–179.
17. Shin HC, Han W, Moon HG, etal. Breast-conserving surgery after tumor downstaging by neoadjuvant chemotherapy is onco­logically safe for stage III breast cancer patients. Ann Surg Oncol. 2013;20(8):2582–2589.
18. Kurtz JM, Jacquemier J, Amalric R, et al. Breast-conserv-
ing therapy for macroscopically multiple cancers. Ann Surg. 1990;212(1):38–44.
19. Yerushalmi R, Tyldesley S, Woods R, Kennecke HF, Speers C, Gelmon KA. Is breast-conserving therapy a safe option for patients with tumor multicentricity and multifocality? Ann Oncol. 2012;23(4):876–881.
20. Kiebert GM, de Haes JC, van de Velde CJ. e impact of breast-conserving treatment and mastectomy on the quality of life of early-stage breast cancer patients: a review. J Clin Oncol. 1991;9(6):1059–1070.
21. Engel J, Kerr J, Schlesinger-Raab A, Sauer H, Holzel D. Qual­ity of life following breast-conserving therapy or mastectomy: results of a 5-year prospective study. Breast J. 2004;10(3):223–
231.
22. Howes BH, Watson DI, Xu C, Fosh B, Canepa M, Dean NR. Quality of life following total mastectomy with and without reconstruction versus breast-conserving surgery for breast can­cer: a case-controlled cohort study. J Plast Reconstr Aesthet Surg. 2016;69(9):1184–1191.
23. Dahlback C, Ullmark JH, Rehn M, Ringberg A, Manjer J. Aes­thetic result after breast-conserving therapy is associated with quality of life several years after treatment. Swedish women evaluated with BCCT.core and BREAST-Q. Breast Cancer Res Treat. 2017;164(3):679–687.
24. Chand ND, Browne V, Paramanathan N, Peiris LJ, Laws SA, Rainsbury RM. Patient-reported outcomes are better after oncoplastic breast conservation than after mastectomy and autologous reconstruction. Plast Reconstr Surg Glob Open. 2017;5(7):e1419.
25. Veiga DF, Veiga-Filho J, Ribeiro LM, etal. Quality-of-life and self-esteem outcomes after oncoplastic breast-conserving sur­gery. Plast Reconstr Surg. 2010;125(3):811–817.
26. Houssami N, Macaskill P, Marinovich ML, Morrow M. e association of surgical margins and local recurrence in women with early-stage invasive breast cancer treated with breast-conserving therapy: a meta-analysis. Ann Surg Oncol. 2014;21(3):717–730.
27. Moran MS, Schnitt SJ, Giuliano AE, etal. Society of Surgical Oncology-American Society for Radiation Oncology consensus guideline on margins for breast-conserving surgery with whole­breast irradiation in stages I and II invasive breast cancer. Int J Radiat Oncol Biol Phys. 2014;88(3):553–564.
28. Park CC, Mitsumori M, Nixon A, etal. Outcome at 8 years after breast-conserving surgery and radiation therapy for inva­sive breast cancer: inuence of margin status and systemic ther­apy on local recurrence. J Clin Oncol. 2000;18(8):1668–1675.
29. Freedman G. Breast conserving therapy for invasive breast cancers. In: Bland K, Copeland E, Klimberg VS, Gradishar W, eds. e breast: comprehensive management of benign and malig- nant diseases. New York, NY: Elsevier; 2018:693–705.
30. Toesca A, Gentilini O, Peccatori F, Azim Jr HA, Amant F. Locoregional treatment of breast cancer during pregnancy. Gynecol Surg. 2014;11(4):279–284.
31. Dilaveri CA, Sandhu NP, Neal L, etal. Medical factors inu­encing decision making regarding radiation therapy for breast cancer. Int J Womens Health. 2014;6:945–954.
32. Lin A, Abu-Isa E, Grith KA, Ben-Josef E. Toxicity of radio­therapy in patients with collagen vascular disease. Cancer. 2008;113(3):648–653.
33. Nahabedian MY. Discussion: an oncoplastic breast aug­mentation technique for immediate partial breast recon­struction following breast conservation. Plast Reconstr Surg. 2017;139(2):358e–359e.
34. Cochrane RA, Valasiadou P, Wilson AR, Al-Ghazal SK, Mac­millan RD. Cosmesis and satisfaction after breast-conserving surgery correlates with the percentage of breast volume excised. Br J Surg. 2003;90(12):1505–1509.
SECTION III Oncoplastic Breast Surgery – Outcomes
https://t.me/medicina_free
176
35. Losken A, Hart AM, Chatterjee A. Updated evidence on the onco-
plastic approach to breast conservation therapy. Plast Reconstr Surg. 2017;140:14S–22S (5S Advances in Breast Reconstruction).
36. Nahabedian MY, Patel KM, Kaminsky AJ, Cocilovo C, Mira­liakbari R. Biplanar oncoplastic surgery: a novel approach to breast conservation for small and medium sized breasts. Plast Reconstr Surg. 2013;132(5):1081–1084.
37. Sosin M, Devulapalli C, Fehring C, etal. Breast cancer follow­ing augmentation mammaplasty: a case-control study. Plast Reconstr Surg. 2018;141(4):833–840.
38. Gray RJ, Forstner-Barthell AW, Pockaj BA, Schild SE, Halyard MY. Breast-conserving therapy and sentinel lymph node biopsy are feasible in cancer patients with previous implant breast aug­mentation. Am J Surg. 2004;188(2):122–125.
39. Handel N, Lewinsky B, Jensen JA, Silverstein MJ. Breast con­servation therapy after augmentation mammaplasty: is it appro­priate? Plast Reconstr Surg. 1996;98(7):1216–1224.
40. Karanas YL, Leong DS, Da Lio A, etal. Surgical treatment of breast cancer in previously augmented patients. Plast Reconstr Surg. 2003;111(3):1078–1083; discussion 1084–1076.
41. Taghian A, Jeong JH, Mamounas E, etal. Patterns of locore­gional failure in patients with operable breast cancer treated by mastectomy and adjuvant chemotherapy with or without tamoxifen and without radiotherapy: results from ve National Surgical Adjuvant Breast and Bowel Project randomized clinical trials. J Clin Oncol. 2004;22(21):4247–4254.
42. de Bock GH, van der Hage JA, Putter H, Bonnema J, Bartelink H, van de Velde CJ. Isolated loco-regional recurrence of breast cancer is more common in young patients and following breast conserving therapy: long-term results of European Organisation for Research and Treatment of Cancer studies. Eur J Cancer. 2006;42(3):351–356.
43. Anders CK, Hsu DS, Broadwater G, etal. Young age at diagno­sis correlates with worse prognosis and denes a subset of breast cancers with shared patterns of gene expression. J Clin Oncol. 2008;26(20):3324–3330.
44. Lagendijk M, van Maaren MC, Saadatmand S, etal. Breast con­serving therapy and mastectomy revisited: breast cancer-specic survival and the inuence of prognostic factors in 129,692 patients. Int J Cancer. 2018;142(1):165–175.
45. Fisher B, Anderson S, Redmond CK, Wolmark N, Wickerham DL, Cronin WM. Reanalysis and results after 12 years of follow­up in a randomized clinical trial comparing total mastectomy with lumpectomy with or without irradiation in the treatment of breast cancer. N Engl J Med. 1995;333(22):1456–1461.
46. Hetelekidis S, Schnitt SJ, Silver B, et al. e signicance of extracapsular extension of axillary lymph node metasta­ses in early-stage breast cancer. Int J Radiat Oncol Biol Phys. 2000;46(1):31–34.
47. Healey EA, Osteen RT, Schnitt SJ, etal. Can the clinical and mammographic ndings at presentation predict the presence of an extensive intraductal component in early stage breast cancer? Int J Radiat Oncol Biol Phys. 1989;17(6):1217–1221.
48. Fajdic J, Djurovic D, Gotovac N, Hrgovic Z. Criteria and procedures for breast conserving surgery. Acta Inform Med. 2013;21(1):16–19.
49. Morrow M, Strom EA, Bassett LW, etal. Standard for breast conservation therapy in the management of invasive breast car­cinoma. CA Cancer J Clin. 2002;52(5):277–300.
50. Gray JR, McCormick B, Cox L, Yahalom J. Primary breast irra­diation in large-breasted or heavy women: analysis of cosmetic outcome. Int J Radiat Oncol Biol Phys. 1991;21(2):347–354.
51. Moody AM, Mayles WP, Bliss JM, etal. e inuence of breast size on late radiation eects and association with radiotherapy dose inhomogeneity. Radiother Oncol. 1994;33(2):106–112.
52. Johansen J, Overgaard J, Rose C, etal. Cosmetic outcome and breast morbidity in breast-conserving treatment–results from the Danish DBCG-82TM national randomized trial in breast cancer. Acta Oncol. 2002;41(4):369–380.
53. Iwuchukwu OC, Harvey JR, Dordea M, Critchley AC, Drew PJ. e role of oncoplastic therapeutic mammoplasty in breast cancer surgery–a review. Surg Oncol. 2012;21(2):133–141.
54. Clarke M, Collins R, Darby S, etal. Eects of radiotherapy and of dierences in the extent of surgery for early breast cancer on local recurrence and 15-year survival: an overview of the ran­domised trials. Lancet. 2005;366(9503):2087–2106.
55. Nixon AJ, Recht A, Neuberg D, et al. e relation between the surgery-radiotherapy interval and treatment outcome in patients treated with breast-conserving surgery and radiation therapy without systemic therapy. Int J Radiat Oncol Biol Phys. 1994;30(1):17–21.
56. Punglia RS, Saito AM, Neville BA, Earle CC, Weeks JC. Impact of interval from breast conserving surgery to radiotherapy on local recurrence in older women with breast cancer: retrospec­tive cohort analysis. BMJ. 2010;340:c845.
57. Huang J, Barbera L, Brouwers M, Browman G, Mackillop WJ. Does delay in starting treatment aect the outcomes of radiotherapy? A systematic review. J Clin Oncol. 2003;21(3): 555–563.
58. Chen Z, King W, Pearcey R, Kerba M, Mackillop WJ. e relationship between waiting time for radiotherapy and clinical outcomes: a systematic review of the literature. Radiother Oncol. 2008;87(1):3–16.
59. Hershman DL, Wang X, McBride R, Jacobson JS, Grann VR, Neugut AI. Delay in initiating adjuvant radiotherapy follow­ing breast conservation surgery and its impact on survival. Int J Radiat Oncol Biol Phys. 2006;65(5):1353–1360.
60. Hickey BE, Francis DP, Lehman M. Sequencing of chemother­apy and radiotherapy for early breast cancer. Cochrane Database Syst Rev. 2013;(4):CD005212.
61. Fisher CM, Rabinovitch R. Frontiers in radiotherapy for early-stage invasive breast cancer. J Clin Oncol. 2014;32(26):2894–2901.
62. Buchholz TA. Radiotherapy and survival in breast cancer. Lan- cet. 2011;378(9804):1680–1682.
63. Whelan TJ, Pignol JP, Levine MN, etal. Long-term results of hypofractionated radiation therapy for breast cancer. N Engl J Med. 2010;362(6):513–520.
64. Haviland JS, Owen JR, Dewar JA, et al. e UK Standardi­sation of Breast Radiotherapy (START) trials of radiotherapy hypofractionation for treatment of early breast cancer: 10-year follow-up results of two randomised controlled trials. Lancet Oncol. 2013;14(11):1086–1094.
65. Yarnold J, Ashton A, Bliss J, etal. Fractionation sensitivity and dose response of late adverse eects in the breast after radiother­apy for early breast cancer: long-term results of a randomised trial. Radiother Oncol. 2005;75(1):9–17.
66. Owen JR, Ashton A, Bliss JM, etal. Eect of radiotherapy frac­tion size on tumour control in patients with early-stage breast cancer after local tumour excision: long-term results of a ran­domised trial. Lancet Oncol. 2006;7(6):467–471.
67. Smith BD, Bellon JR, Blitzblau R, etal. Radiation therapy for the whole breast: executive summary of an American Society for Radiation Oncology (ASTRO) evidence-based guideline. Pract Radiat Oncol. 2018.
68. Bartelink H, Maingon P, Poortmans P, etal. Whole-breast irra­diation with or without a boost for patients treated with breast­conserving surgery for early breast cancer: 20-year follow-up of a randomised phase 3 trial. Lancet Oncol. 2015;16(1):47–56.
69. Shah C, Harris EE, Holmes D, Vicini FA. Partial breast irra­diation: accelerated and intraoperative. In: Bland K, Copeland E, Klimberg VS, Gradishar W, eds. e breast: comprehensive management of benign and malignant diseases. New York, NY: Elsevier; 2018:706–715.
70. Fraass BA, Eisbruch A, Feng M. Intensity modulated and image guided radiation therapy. In: Tepper JE, Gunderson LL, eds. Clinical radiation oncology. 4th ed. New York, NY: Elsevier; 2016:294–323.
CHAPTER 20 Radiation Therapy Considerations and Oncoplastic Breast Surgery
https://t.me/medicina_free
177
71. Taylor A, Powell ME. Intensity-modulated radiotherapy–what
is it? Cancer Imaging. 2004;4(2):68–73.
72. Berrang TS, Olivotto I, Kim DH, etal. ree-year outcomes of a Canadian multicenter study of accelerated partial breast irra­diation using conformal radiation therapy. Int J Radiat Oncol Biol Phys. 2011;81(5):1220–1227.
73. Shaitelman SF, Khan AJ, Woodward WA, etal. Shortened radi­ation therapy schedules for early-stage breast cancer: a review of hypofractionated whole-breast irradiation and accelerated par­tial breast irradiation. Breast J. 2014;20(2):131–146.
74. Baglan KL, Sharpe MB, Jaray D, et al. Accelerated partial breast irradiation using 3D conformal radiation therapy (3D­CRT). Int J Radiat Oncol Biol Phys. 2003;55(2):302–311.
75. Rodriguez N, Sanz X, Dengra J, etal. Five-year outcomes, cos­mesis, and toxicity with 3-dimensional conformal external beam radiation therapy to deliver accelerated partial breast irradiation. Int J Radiat Oncol Biol Phys. 2013;87(5):1051–1057.
76. Pashtan IM, Recht A, Ancukiewicz M, et al. External beam accelerated partial-breast irradiation using 32 gy in 8 twice-daily fractions: 5-year results of a prospective study. Int J Radiat Oncol Biol Phys. 2012;84(3):e271–e277.
77. Vicini FA, Chen P, Wallace M, etal. Interim cosmetic results and toxicity using 3D conformal external beam radiotherapy to deliver accelerated partial breast irradiation in patients with early-stage breast cancer treated with breast-conserving therapy. Int J Radiat Oncol Biol Phys. 2007;69(4):1124–1130.
78. Olivotto IA, Whelan TJ, Parpia S, etal. Interim cosmetic and tox­icity results from RAPID: a randomized trial of accelerated par­tial breast irradiation using three-dimensional conformal external beam radiation therapy. J Clin Oncol. 2013;31(32):4038–4045.
79. Hepel JT, Tokita M, MacAusland SG, et al. Toxicity of three­dimensional conformal radiotherapy for accelerated partial breast irradiation. Int J Radiat Oncol Biol Phys. 2009;75(5):1290–1296.
80. Leonard KL, Hepel JT, Hiatt JR, Dipetrillo TA, Price LL, Wazer DE. e eect of dose-volume parameters and interfrac­tion interval on cosmetic outcome and toxicity after 3-dimen­sional conformal accelerated partial breast irradiation. Int J Radiat Oncol Biol Phys. 2013;85(3):623–629.
81. Chafe S, Moughan J, McCormick B, et al. Late toxicity and patient self-assessment of breast appearance/satisfaction on RTOG 0319: a phase 2 trial of 3-dimensional conformal radia­tion therapy-accelerated partial breast irradiation following lumpectomy for stages I and II breast cancer. Int J Radiat Oncol Biol Phys. 2013;86(5):854–859.
82. Correa C, Harris EE, Leonardi MC, et al. Accelerated par­tial breast irradiation: executive summary for the update of an ASTRO evidence-based consensus statement. Pract Radiat Oncol. 2017;7(2):73–79.
83. Livi L, Buonamici FB, Simontacchi G, etal. Accelerated par­tial breast irradiation with IMRT: new technical approach and interim analysis of acute toxicity in a phase III randomized clini­cal trial. Int J Radiat Oncol Biol Phys. 2010;77(2):509–515.
84. Lewin AA, Derhagopian R, Saigal K, et al. Accelerated partial breast irradiation is safe and eective using intensity-modulated radiation therapy in selected early-stage breast cancer. Int J Radiat Oncol Biol Phys. 2012;82(5):2104–2110.
85. Lei RY, Leonard CE, Howell KT, etal. Four-year clinical update from a prospective trial of accelerated partial breast intensity­modulated radiotherapy (APBIMRT). Breast Cancer Res Treat. 2013;140(1):119–133.
86. Donovan E, Bleakley N, Denholm E, et al. Randomised trial of standard 2D radiotherapy (RT) versus intensity modulated radiotherapy (IMRT) in patients prescribed breast radiotherapy. Radiother Oncol. 2007;82(3):254–264.
87. Mukesh MB, Barnett GC, Wilkinson JS, et al. Randomized controlled trial of intensity-modulated radiotherapy for early breast cancer: 5-year results conrm superior overall cosmesis. J Clin Oncol. 2013;31(36):4488–4495.
88. Jagsi R, Ben-David MA, Moran JM, etal. Unacceptable cosme­sis in a protocol investigating intensity-modulated radiotherapy with active breathing control for accelerated partial-breast irra­diation. Int J Radiat Oncol Biol Phys. 2010;76(1):71–78.
89. Liss AL, Ben-David MA, Jagsi R, et al. Decline of cosmetic outcomes following accelerated partial breast irradiation using intensity modulated radiation therapy: results of a single-insti­tution prospective clinical trial. Int J Radiat Oncol Biol Phys. 2014;89(1):96–102.
90. Coles CE, Grin CL, Kirby AM, et al. Partial-breast radio­therapy after breast conservation surgery for patients with early breast cancer (UK IMPORT LOW trial): 5-year results from a multicentre, randomised, controlled, phase 3, non-inferiority trial. Lancet. 2017;390(10099):1048–1060.
91. Veronesi U, Orecchia R, Maisonneuve P, etal. Intraoperative radiotherapy versus external radiotherapy for early breast can­cer (ELIOT): a randomised controlled equivalence trial. Lancet Oncol. 2013;14(13):1269–1277.
92. Vaidya JS, Wenz F, Bulsara M, et al. Risk-adapted targeted intraoperative radiotherapy versus whole-breast radiotherapy for breast cancer: 5-year results for local control and over­all survival from the TARGIT-A randomised trial. Lancet. 2014;383(9917):603–613.
93. Hepel J, Wazer DE. A awed study should not dene a new standard of care. Int J Radiat Oncol Biol Phys. 2015;91(2): 255–257.
94. Freedman G. Radiation complications and their management. In: Bland K, Copeland E, Klimberg VS, Gradishar W, eds. e
breast: comprehensive management of benign and malignant dis­eases. New York, NY: Elsevier; 2018:716–725.
95. Darby SC, McGale P, Taylor CW, Peto R. Long-term mortal­ity from heart disease and lung cancer after radiotherapy for early breast cancer: prospective cohort study of about 300,000 women in US SEER cancer registries. Lancet Oncol. 2005;6(8): 557–565.
96. Noal S, Levy C, Hardouin A, etal. One-year longitudinal study of fatigue, cognitive functions, and quality of life after adjuvant radiotherapy for breast cancer. Int J Radiat Oncol Biol Phys. 2011;81(3):795–803.
97. Geinitz H, Zimmermann FB, Stoll P, et al. Fatigue, serum cytokine levels, and blood cell counts during radiotherapy of patients with breast cancer. Int J Radiat Oncol Biol Phys. 2001;51(3):691–698.
98. Bower JE, Ganz PA, Desmond KA, etal. Fatigue in long-term breast carcinoma survivors: a longitudinal investigation. Cancer. 2006;106(4):751–758.
99. Kole AJ, Kole L, Moran MS. Acute radiation dermatitis in breast cancer patients: challenges and solutions. Breast Cancer (Dove Med Press). 2017;9:313–323.
100. Institute NC. Common Terminology Criteria for Adverse Events (CTCAE). 2017. https://ctep.cancer.gov/protocoldevelopment
/electronic_applications/docs/CTCAE_v5_Quick_Reference_8 .5x11.pdf. Accessed April 19, 2018.
101. Freedman GM, Li T, Nicolaou N, Chen Y, Ma CC, Anderson PR. Breast intensity-modulated radiation therapy reduces time spent with acute dermatitis for women of all breast sizes during radiation. Int J Radiat Oncol Biol Phys. 2009;74(3):689–694.
102. Bostrom A, Lindman H, Swartling C, Berne B, Bergh J. Potent corticosteroid cream (mometasone furoate) signicantly reduces acute radiation dermatitis: results from a double-blind, random­ized study. Radiother Oncol. 2001;59(3):257–265.
103. Rayan G, Dawson LA, Bezjak A, etal. Prospective comparison of breast pain in patients participating in a randomized trial of breast-conserving surgery and tamoxifen with or without radio­therapy. Int J Radiat Oncol Biol Phys. 2003;55(1):154–161.
104. Frassica DA, Bajaj GK, Tsangaris TN. Treatment of compli­cations after breast-conservation therapy. Oncology (Williston Park). 2003;17(8):1118–1128; discussion 1131–1116, 1141.
SECTION III Oncoplastic Breast Surgery – Outcomes
https://t.me/medicina_free
178
105. Garza RM, Paik KJ, Chung MT, etal. Studies in fat graft­ing: Part III. Fat grafting irradiated tissue--improved skin quality and decreased fat graft retention. Plast Reconstr Surg. 2014;134(2):249–257.
105a. Khouri RK, Rigotti G, Khouri RK Jr, etal. Tissue-engineered
breast reconstruction with Brava-assisted fat grafting: a 7-year,
488-patient, multicenter experience. Plast Reconstr Surg. 2015; 135(3):643–58.
106. Mirzabeigi MN, Lanni M, Chang CS, et al. Treating breast conservation therapy defects with brava and fat grafting: technique, outcomes, and safety prole. Plast Reconstr Surg. 2017;140(3):372e–381e.
21
https://t.me/medicina_free
Patient Satisfaction and Outcomes Following Oncoplastic Breast Surgery
TAMMY JU, CHRISTINE TEAL, AND BRIDGET A. OPPONG
Introduction
Breast Conservation
Increased compliance with breast cancer screening guide­lines, as well as advancements in imaging technology, have led to earlier detection of breast cancer. Currently, the majority of breast cancers are diagnosed at earlier clinical stages. is should eliminate the need for mastectomy in a majority of cases as multiple randomized studies with extensive follow-up have established that breast conserva­tion therapy (BCT) confers equivalent local control and survival as mastectomy, including the National Surgical Adjuvant Breast and Bowel Project (NSABP) B-06 study.1 e oncologic safety of BCT, considered when the tumor size-to-breast size ratio is favorable in selected patients, has been well established. However, there continues to be an increasing trend toward mastectomy. Recent studies show persistently high mastectomy rates, even when women are candidates for lumpectomy.2 Despite the extensive data showing no survival advantage with mastectomy, this has not dissuaded women from choosing mastectomy for both treatment and prophylaxis.
e topic of contralateral prophylactic mastectomy has added to the decision-making process fueling the increase in mastectomy rates in patients with unilateral breast cancer.2 Hypotheses explaining why women opt for more extensive surgery include fear and perceived risk in the contralateral breast, optimal reconstruction outcomes, increase in genetic testing and determination of risk prole, as well as the use of breast magnetic resonance imaging (MRI) that can detect smaller cancers. ere are record numbers of prophy­lactic mastectomies being performed in the United States. Data show that mastectomy rates have increased in recent years with high rates of risk-reducing surgery for high-risk patients and those already diagnosed with breast cancer.3 Although there are general guidelines providing indications for both bilateral prophylactic mastectomy and contralat­eral prophylactic mastectomy, when it should be advised remains controversial. e factors associated with this
phenomenon are unclear and likely involve a complex inter­play of patient and physician factors. As more women opt for this type of surgical management in the high-risk and cancer management settings, the question arises as to what benchmark should surgeons utilize to advise their patients?
When deliberating over cancer treatment options, one concern patients often voice is the potential asymmetry after breast conservation surgery that can result in the removal of a signicant fraction of total breast volume. In addi­tion, breast asymmetry is compounded by the overall size reduction that occurs after whole breast irradiation. Whole breast radiotherapy after BCT can reduce the risk of local recurrence as much as threefold compared with surgery alone1 and, therefore, is a necessary component of breast conservation. Many patients after an initial satisfactory cosmetic result following breast conservation will develop a progressive asymmetry over time, prompting the need for additional surgery. is is usually a contralateral reduction mammaplasty (Fig. 21.1). erefore, symmetrization proce­dures done at the time of lumpectomy can be an important addition to BCT with the benet of optimizing long-term cosmetic results and perhaps even discouraging unnecessary mastectomies. As a consequence of the advancements in oncoplastic surgery, especially among the west coast surgi­cal oncology pioneers, oncoplastic procedures are becoming more accepted and utilized. 
Outcomes after Oncoplastic Surgery
Patient Outcomes
As oncoplastic techniques increase in popularity and utiliza­tion, evidence-based analyses of surgical outcomes will be important to support further adoption. Although there is not an overabundance of literature on oncoplastic breast sur­gical techniques, in recent years multiple studies have been published. In the largest comprehensive literature review to date on oncoplastic breast-conserving surgery (BCS), data were extracted from 55 studies that collectively evaluated
179
SECTION III Oncoplastic Breast Surgery – Outcomes
Left Breast Reduction for symmetry years after right breast
https://t.me/medicina_free
180
lumpectomy and radiation
Fig. 21.1 Delayed contralateral reduction for asymmetry years after right lumpectomy and whole breast irradiation.
6011 patients.4 Wise pattern mastopexy was the most com­monly utilized oncoplastic technique, performed in 35.4% of patients, followed by the round block (14.8%) and latis­simus dorsi volume replacement (9.5%) techniques. is systematic review by Cruz etal is one of the few studies to have short-term and long-term outcomes. Long-term data revealed oncoplastic surgery to have high rates of overall and disease-free survival and low local recurrence thereby con­rming the oncologic safety of this procedure in patients with T1–T2 invasive breast cancers.
Of the short-term outcomes, margin status is one of the most important measures of success, and 11 studies reported specic margins for 1455 patients. Among these patients, 143 (9.8%) were classied as having positive mar­gins, of which 113 (7.8%) had tumor on ink. Other short­term data reported included postoperative complications, including liponecrosis, skin necrosis, hematoma, seroma, delayed wound healing, nipple necrosis, and/or infection, which occurred in 14.3% of patients. Specically, compli­cation rates from oncoplastic BCS in this study, includ­ing liponecrosis (3.3%), skin necrosis (0.5%), hematoma (2.5%), seroma (1.0%), delayed wound healing (2.2%), nipple necrosis (0.4%), and/or infection (1.9%), closely reected those found in a previous study that further dem­onstrated no statistically signicant dierence in the inci­dence of these issues among women undergoing oncoplastic and non-oncoplastic lumpectomies. However, Tenofsky et al found a higher incidence of non-healing wounds in the oncoplastic group compared with the non-oncoplastic group (8.6 vs 1.2%; p = 0.042).5 It is important to note that this did not prolong time to radiation within the oncoplas­tic group. erefore, oncoplastic reconstruction at the time of BCS does not appear to signicantly increase the risk of postoperative complications that would delay initiation of adjuvant therapy. 
Cosmetic Outcomes and Patient Satisfaction
In the systematic review by Cruz etal, 25 studies also evalu­ated cosmetic outcomes in 1962 patients. e vast majority reported positive results with oncoplastic surgery achieving excellent, good, fair, or poor outcomes in 55.2%, 31.0%,
9.4%, and 4.4% of patients, respectively.4 When it comes to the literature, however, there are limited studies investigat­ing patient-reported satisfaction and outcomes after onco­plastic surgery. Furthermore, it has been shown that there is a lack of consistent and validated measures by which these patient outcomes are reported.6 e majority of the studies are from Europe or South America and do not include the U.S. population. In addition, within these studies, hetero­geneity exists in the denition of oncoplastic or breast con­servation surgery along with their comparison group (if one is included). Overall, recent studies show positive patient­reported satisfaction with aesthetic results,7 breast appear­ance,8 improvement in functional return to work/activity9 and overall satisfaction gery compared with standard lumpectomy/mastectomy.
e majority of this data is collected from questionnaires in the postoperative period to assess patient-reported sat­isfaction and outcomes. For example, a study in the UK by Chand et al compared therapeutic mammoplasty (onco­plastic breast conservation surgery [OBCS]) to a latissimus dorsi miniap and gave patients the BreastQ questionnaire to assess satisfaction.8 Patients who underwent OBCS felt their breasts had a more natural feel, were better in terms of size, less likely to report neck pain, and reported higher overall satisfaction. Interestingly, this was one of the few studies that asked about emotional/sexual well-being and found that there was no dierence between groups, suggest­ing anxiety about a cancer diagnosis and treatment inu­ences emotional well-being more than the type of surgery performed.
8
6,8
after undergoing oncoplastic sur-
CHAPTER 21 Patient Satisfaction and Outcomes Following Oncoplastic Breast Surgery
https://t.me/medicina_free
181
Some studies cite specic patient populations that OBCS may have the most benet in, such as patients with macro­mastia.9 Kelsall etal performed a study from the UK compar­ing OBCS to mastectomy with immediate reconstruction. When unmatched, body image scale, breast appearance, and return to work/function were better in the OBCS group. However, when matched to case controls, women with larger breasts reported better body image scores and self­rated breast appearance, which was not seen in women with smaller breasts. Even when patients required postoperative radiation, patients in the OBCS cohort reported better body image scores compared with those with mastectomy/ immediate reconstruction.9 Somewhat contradictory to this, a study in 2017 by Ojala etal compared aesthetic and functional outcomes 3 years after surgery and found that, overall, patients in the conventional group had better self­reported aesthetic outcomes than the oncoplastic resection group10 using two types of questionnaires. Of note, they found larger tumors and tumor multifocality were predictors of poor aesthetic outcomes. However, this cohort study was limited by only a small percentage undergoing oncoplastic surgery (n = 86: 23%) compared with conventional surgery (n = 293: 77%). Nonetheless, conventional resection may be better for certain patients. Another study in 2015 out of Brazil by Santos etal actually examined aesthetic outcomes of oncoplastic versus lumpectomy patients evaluated by a software system, specialists, and patients. Although the soft­ware and specialists reported signicantly better aesthetic outcomes in the oncoplastic group, patients did not.
11
ere is currently a large prospective trial occurring in the Netherlands comparing women who undergo BCS to evaluate cosmetic outcome, patient satisfaction, and qual­ity of life based on the lumpectomy technique; however, it has not been completed.12 is will be one of a limited number of prospective trials investigating the utilization and outcomes of oncoplastic techniques compared with standard lumpectomy. Further, the investigators have a goal to use the data to create a clinical decision model to guide the use of oncoplastic techniques in the future (Table 21.1). 
Current Practices
Surgical management discussions for newly diagnosed breast cancer have moved beyond just the standard lumpectomy or mastectomy. Oncoplastic techniques are now frequently added with the benet of increasing cos­mesis while permitting the breast surgeon to also excise a larger specimen, likely reducing the risk of margin positiv­ity. Adding this oncoplastic option can be done in a pri­mary, immediate, or delayed fashion. Most commonly, the oncoplastic portion is performed in conjunction with the initial lumpectomy. Although some breast or general sur­geons may utilize these techniques themselves, the major­ity, in our area, work in conjunction with plastic surgeons who perform tissue rearrangements in the ipsilateral breast with contralateral symmetrization. Our plastic surgeons
commonly do reductions and/or mastopexies as their most common procedures, which is similar to approaches reported in the literature.
Delayed or Two-Stage Oncoplastic Surgery
A decision the surgical oncologist faces when contemplat­ing adding oncoplastic techniques is timing (i.e., whether to perform the lumpectomy and plastic surgery component in the same operation or separate the two in a delayed fash­ion). A major factor is the breast surgeon’s condence in the ability to extirpate the tumor and obtain clear margins. Specic cases at risk for positive margins typically include patients who do not have a discrete or focal tumor, or who have discordance in the extent of disease estimations based on conicting mammographic, ultrasound, or breast MRI measurements. is subset also tends to include those with DCIS or an extensive intraductal component and inva­sive lobular histology. If based on the measures discussed, there is a higher than average risk of inadequate margin and consequently a need for possible re-excision, consid­eration should be given to delaying the plastic surgery component when utilizing an oncoplastic approach. is allows another attempt to attain clear margins, instead of committing the patient to mastectomy due to the dicul­ties of re-excisions after rearrangement of the breast tissues. Although re-excision in general may be less accurate due to postoperative changes, it is much more complicated by the tissue rearrangements performed during reductions or mastopexy. For patients in whom there is such a concern, delaying the plastic surgery portion of the case is the opti­mal decision.
Included in this category are those who have undergone neoadjuvant chemotherapy. Although there is geographic and institutional variation, neoadjuvant chemotherapy is used in approximately one-quarter of new diagnoses. With data demonstrating improvement in long-term outcome with this approach in certain subgroups, such as HER-2 positive subtypes, more patients will be oered neoadjuvant chemotherapy. Another strategy is the use of neoadjuvant chemotherapy to downstage the axilla in the hopes of avoiding axillary lymph node dissections that have the inherent risk of chronic lymphedema. Posttreat­ment breast MRI is the most common modality utilized to assess treatment response and residual disease. e post­chemotherapy imaging compared with pretreatment base­line can guide surgical decision making; however, MRI can often give an inaccurate estimation of the extent of dis­ease. erefore, a delayed approach is frequently helpful in this population to conserve the breast and/or avoid mas­tectomy. Once margins are evaluated and conrmed free of tumor, the patient can have their oncoplastic procedure with the plastic surgeon 1–2 weeks later. Furthermore, for women with moderate to severe mammary hypertrophy, oncoplastic techniques will allow the breast surgeon to remove a larger segment of the breast that will reduce risk of a positive margin (Fig. 21.2). 
SECTION III Oncoplastic Breast Surgery – Outcomes
https://t.me/medicina_free
182
TABLE
Summary of Recent Studies for Patient-Reported Outcomes after Oncoplastic Breast Surgery
21.1
Sample
Author Year
Santos etal [10] 2015 Brazil Multicenter 122 - BCCT Software
Rezai etal [6] 2015 Germany Single-center cohort 558 - customized satisfac-
Ojala etal [9] 2017 Finland Single-center 379 - BCTOS
Chand etal [7] 2017 UK Single-center 150 -BreastQ question-
Kelsall etal [8] 2017 UK Single-center case
Catsman etal
[11]
2018 Netherlands Prospective single-
Country Type of Study
matched cohort study
center cohort study
Size
567 -BIS
TBD -expert panel
Satisfaction Tool Used Results
- aesthetic specialists
- custom question­naire
tion questionnaire
- custom question­naire
naire
-Q-score
-custom question­naire
-BCCT
-BreastQ and other questionnaires
- BCCT/software and specialists reported improved aesthetic out­come with oncoplastics
- patients reported no dif­ference
- 78% of patients with BCS reported aesthetic outcomes as “good” or “very good”
- conventional resec­tion may be better in selected patients
- 89% of women rated oncoplastic BCS better than mastectomy
- more natural breast with higher overall satisfac­tion compared with latissimus flap
-Unmatched cases favored oncoplastic BCS over mastectomy with IBR regarding BIS, appearance, and function
- Case matched showed women with larger breasts had better appearance scores, function, and return to work
- TBD
BCCT, core software; BCS, breast-conserving surgery; BCTOS, Breast Cancer Treatment Outcome Scale Questionnaire; BIS, body image scale; BreastQ, validated patient reported outcomes questionnaire following breast reconstruction; IBR, ; Q-score, software generating scores for breast appearance, physical, emotional, and sexual well-being; TBD, To be determined.
Intraoperative Margin Assessment
During breast conservation surgery, margin assessment in real time would be ideal. is can potentially save the patient from having to undergo additional procedures, such as re-excision or mastectomy. e economic and qual­ity of life benets to the patient when additional surgery is avoided cannot be overstated. As a consequence, there has been sustained interest in dierent techniques that can assess margins intraoperatively. Especially when an onco­plastic breast surgery is planned, it would be even more ben­ecial to have denitive surgery in one operation. Dierent intraoperative margin techniques have been trialed includ­ing frozen section analysis, touch prep, and a variety of new
devices including Dune. None of these have been widely adopted given the limited data available and concerns about histological accuracy. For example, during frozen section analysis, the generally fatty breast tissue is dicult to x for reliable analysis. At our institutions, therefore, it is not generally performed. 
Re-excision after Oncoplastic Breast Surgery
A potential device that can aid in re-excision if needed after oncoplastic BCS is the BioZorb device. In 2013, the BioZorb tissue marker was introduced as an implant­able device that, when sutured into a lumpectomy cavity,
CHAPTER 21 Patient Satisfaction and Outcomes Following Oncoplastic Breast Surgery
Right Oncoplastic Breast Reconstruction
MainMenu
MainMenu
https://t.me/medicina_free
Left Breast Reduction
183
A
Right Oncoplastic Breast Reconstruction Left Breast Reduction
B
Fig. 21.2 (A and B) Immediate oncoplastic breast conservation surgery (OCBS) following neoadjuvant
chemotherapy. Right oncoplastic breast reduction and left breast reduction. (Photos courtesy Drs. Eliza­beth Feldman and Samir Rao.)
allows for postoperative, three-dimensional visualization of the tumor removal site boundaries. Initial reports indi­cate that the bio-absorbable marker was readily identi­ed on postoperative clinical imaging and that placement reduced planned treatment/radiation BOOST volumes by approximately 30–40%. e device’s trellis-type frame­work has also been shown to improve oncoplastic breast reconstruction outcomes.13 is marker is sutured into the lumpectomy bed providing a palpable guide in the imme­diate postoperative period. In the event that a re-excision is indicated based on nal pathology, the device can provide guidance to accurately locate the lumpectomy cavity even after extensive tissue rearrangements. Consequently, the surgeon can again attempt breast conservation, sparing the patient an unwanted mastectomy. e device also replaces the standard clips placed at the borders of the lumpectomy cavity. 
Conclusion
In summary, oncoplastic breast surgery has increased in popularity but is still relatively new. erefore, the data on the patient experience is overall limited, but the cur­rent studies denitely show promise. Utilization of onco­plastic techniques has increased patient satisfaction after breast conservation in comparison to women who undergo standard lumpectomy practices. erefore, it is important that oncoplastic options are discussed at the time of initial consultation so that they may optimally be performed at the same time as lumpectomy to minimize delaying adju­vant treatment. Another crucial consideration is the oer­ing of this approach before radiation therapy because the patient’s options are limited after radiation has been com­pleted. Patients who have an oncoplastic approach have improved cosmesis and are generally more satised with