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CHAPTER 2 Safety of Oncoplastic Breast Reconstruction
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documented and to a certain extent may be extrapolated to predict changes following oncoplastic reconstruction. In a small case-control study, Roberts et al compared the mammographic ndings of 87 patients who had undergone breast reduction to those of 30 patients with macromastia who did not undergo breast reduction. e authors found that mammographic ndings following breast reduction did not increase the rate of obtaining additional imaging studies or diagnostic interventions and suggested that this nding was likely generalizable to oncoplastic breast recon­struction.19 In contrast, two small series comparing post­operative cancer surveillance between patients undergoing oncoplastic reconstruction or standard breast conservation suggested a higher rate of need for additional imaging and tissue sampling in the oncoplastic group.
20,21
Although the expected mammographic changes following breast reduc­tion (oil cysts, fat necrosis, calcications) are distinct from those found in patients with breast cancer, it is possible that the increased pretest suspicion in a patient with a history of breast cancer leads to an increased request for additional imaging and biopsies. 
Conclusions
Oncoplastic reconstruction techniques hold great appeal for their ability to extend the indications for breast conserva­tion to patients with larger tumors in whom standard breast conservation would not provide acceptable cosmesis. e widespread applicability of these techniques depends on an oncologic safety prole comparable to standard BCT. Avail­able data suggest that rates of positive margins, local recur­rence, distant recurrence, disease-free survival, and overall survival following oncoplastic breast reconstruction com­pare favorably with outcomes following both breast conser­vation and mastectomy. Oncoplastic breast reconstruction can be accomplished with a reasonable complication rate, and when complications do occur there is likely a minimal impact on the timing of adjuvant therapy administration. Appropriate patient selection and preoperative discussion are essential to optimize patient decision making and sur­gical outcomes following oncoplastic breast reconstruction.
References
1. Jacobson JA, Danforth DN, Cowan KH, etal. Ten-year results of
a comparison of conservation with mastectomy in the treatment of stage I and II breast cancer. N Engl J Med. 1995;332(14):907–911.
2. Haloua MH, Krekel NM, Winters HA, etal. A systematic review
of oncoplastic breast-conserving surgery: current weaknesses and future prospects. Ann Surg. 2013;257(4):609–620.
3. Carter SA, Lyons GR, Kuerer HM, etal. Operative and onco-
logic outcomes in 9861 patients with operable breast cancer: single-institution analysis of breast conservation with oncoplastic reconstruction. Ann Surg Oncol. 2016;23(10):3190–3198.
4. Losken A, Hart AM, Broecker JS, Styblo TM, Carlson GW.
Oncoplastic breast reduction technique and outcomes: an evolu­tion over 20 years. Plast Reconstr Surg. 2017;139(4):824e–833e.
5. 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. Ann Surg Oncol. 2014;21(3):704–716.
6. Losken A, Dugal CS, Styblo TM, Carlson GW. A meta-analysis comparing breast conservation therapy alone to the oncoplastic technique. Ann Plast Surg. 2014;72(2):145–149.
7. Piper ML, Esserman LJ, Sbitany H, Peled AW. Outcomes fol­lowing oncoplastic reduction mammoplasty: a systematic review. Ann Plast Surg. 2016;76(suppl 3):S222–S226.
8. Losken A, Pinell-White X, Hart AM, et al. e oncoplastic reduction approach to breast conservation therapy: benets for margin control. Aesthet Surg J. 2014;34(8):1185–1191.
9. Wijgman DJ, Ten Wolde B, van Groesen NR, et al. Short term safety of oncoplastic breast conserving surgery for larger tumors. Eur J Surg Oncol. 2017;43(4):665–671.
10. Clough KB, Gouveia PF, Benyahi D, et al. Positive margins after oncoplastic surgery for breast cancer. Ann Surg Oncol. 2015;22(13):4247–4253.
11. Amabile MI, Mazouni C, Guimond C, etal. Factors predictive of re-excision after oncoplastic breast-conserving surgery. Anticancer Res. 2015;35(7):4229–4234.
12. De La Cruz L, Blankenship SA, Chatterjee A, et al. Out­comes after oncoplastic breast-conserving surgery in breast cancer patients: a systematic literature review. Ann Surg Oncol. 2016;23(10):3247–3258.
13. Fitoussi AD, Berry MG, Fama F, etal. Oncoplastic breast surgery for cancer: analysis of 540 consecutive cases [outcomes article]. Plast Reconstr Surg. 2010;125(2):454–462.
14. Cil TD, Cordeiro E. Complications of oncoplastic breast sur­gery involving soft tissue transfer versus breast-conserving surgery: an analysis of the NSQIP database. Ann Surg Oncol. 2016;23(10):3266–3271.
15. Losken A, Pinell XA, Eskenazi B. e benets of partial versus total breast reconstruction for women with macromastia. Plast Reconstr Surg. 2010;125(4):1051–1056.
16. Gulcelik MA, Dogan L, Camlibel M, et al. Early complica­tions of a reduction mammoplasty technique in the treatment of macromastia with or without breast cancer. Clin Breast Cancer. 2011;11(6):395–399.
17. Hillberg NS, Meesters-Caberg MAJ, Beugels J, et al. Delay of adjuvant radiotherapy due to postoperative complications after oncoplastic breast conserving surgery. Breast. 2018;39: 110–116.
18. Khan J, Barrett S, Forte C, etal. Oncoplastic breast conserva­tion does not lead to a delay in the commencement of adju­vant chemotherapy in breast cancer patients. Eur J Surg Oncol. 2013;39(8):887–891.
19. Roberts JM, Clark CJ, Campbell MJ, Paige KT. Incidence of abnormal mammograms after reduction mammoplasty: implications for oncoplastic closure. Am J Surg. 2011;201(5): 611–614.
20. Dolan R, Patel M, Weiler-Mitho E, et al. Imaging results fol­lowing oncoplastic and standard breast conserving surgery. Breast Care (Basel). 2015;10(5):325–329.
21. Losken A, Schaefer TG, Newell M, Styblo TM. e impact of partial breast reconstruction using reduction techniques on post­operative cancer surveillance. Plast Reconstr Surg. 2009;124(1): 9–17.
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Indications and Patient Selection for Oncoplastic Breast Surgery
KIRSTEN EDMISTON
Introduction
e newly diagnosed breast cancer patient and her interdis­ciplinary treatment team must address both the local control (breast) and systemic control (body) issues to minimize the risk of recurrence. From a surgical perspective, the fundamental goals are to remove the tumor with an adequate margin of nor­mal tissue while optimizing the long-term aesthetic outcomes for the patient. e technical decision then becomes whether to proceed with breast conservation therapy (lumpectomy and radiation) or a mastectomy with or without reconstruction. With the pioneering work of the National Surgical Adjuvant Breast and Bowel Project (NSABP), Umberto Veronesi, MD, and others in the 1970s, breast conservation therapy (BCT) has been well established as oncologically safe, oering similar local control rates and equivalent long-term survival rates compared with non-nipple-sparing mastectomy. sparing mastectomy (NSM) has been demonstrated to be a third alternative for patients requiring or requesting removal of the breast parenchyma while preserving the skin envelope and nipple–areolar complex (NAC). Breast-conserving lumpectomy and radiation therapy must then be evaluated as an alternative to both nipple-sparing and non-NSM with reconstruction.
e benets of breast conservation over mastectomy are well established. Clinical outcome studies with 20-year follow-up have demonstrated that breast conservation is equivalent to mastectomy in terms of overall survival.3 In addition, preservation of the natural breast confers a signi­cant psychological advantage for many women diagnosed with breast cancer. In most cases, preservation of the NAC is possible; therefore, the natural breast elements remain, and the majority of women are happy with the nal breast appearance. With the advent of oncoplastic techniques, breast conservation can be expanded to include wider mar­gins of resection and achieve local recurrence rates that are similar to mastectomy.4 As the reconstructive options have expanded, so has the prevalence of oncoplastic surgery.
ere are several dierences between traditional breast conservation and oncoplastic surgery. With traditional
1,2
More recently, nipple-
lumpectomy, the skin is opened directly over the localized lesion. e tumor is then removed, oriented, and sent for pathological evaluation. e skin is closed without attempts to close the internal cavity. For small tumors (either duc­tal carcinoma in situ [DCIS] or invasive breast cancer), this approach is adequate. Unfortunately, up to 40–45% of patients can be found to have positive margins requiring re-operation to achieve negative margins. 30% of patients undergoing lumpectomy and subsequent radiation therapy surveyed were found to be dissatised with their cosmetic outcome.7 Cosmetic defects included deformity of the overall shape of the breast, volume loss, changes in the shape and location of the nipple, and Snoopy deformities of the NAC after a transverse incision in the lower central breast. e challenge thus becomes extending the indications for lumpectomy while minimizing the risk of positive margins to optimize the cosmetic results after not only the surgical lumpectomy but also radiation therapy.
In the 1990s, Werner Audretsch, Christian Gabka, and Heinz Bohmert applied reduction mammoplasty and mas­topexy concepts to expand the number of patients who are candidates for breast conservation as “oncoplastic surgery.”8 e term oncoplastic breast surgery is a Greek-derived word that literally means “molding of tumor”; however, in its present context it refers to excision of the tumor (onco) and reconstruction and shaping of the breast (plastic). is often requires a team approach between the oncologic and reconstructive surgeon. Today, the spectrum of oncoplastic surgery includes four basic techniques including:
1. Local tissue mobilization and rearrangement
2. Reduction pattern mammoplasty
3. Skin and nipple rearrangement
4. Volume replacement
is chapter will discuss the aspects of the tumor char­acteristics, patient’s anatomy, medical comorbidities, treatment-related issues, psychosexual concerns, and pos­sible complications that aect the indications and patient selection for oncoplastic breast surgery over NSM and non-NSM. 
4-6
Historically,
14
CHAPTER 3 Indications and Patient Selection for Oncoplastic Breast Surgery
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Indications
Oncoplasty enables the breast surgery team to excise more breast tissue, widening the margin of clearance between the tumor and the normal parenchyma. In addition, natural breast appearance is more likely to be achieved, although the volume will be less. ese benets have expanded the number of patients eligible for breast conservation. Many women who are treated with oncoplastic breast conserva­tion surgery would otherwise have needed a mastectomy and/or have had a poor aesthetic result. Fundamentally,
the indications for oncoplastic breast surgery are the same as those for breast conservation surgery. Patients should be considered for BCT if they have an adequate tumor-to-breast volume ratio to establish negative margins and are candidates for radiation therapy. All
patients undergoing breast-conserving surgery (lumpec­tomy, partial segmental mastectomy, quadrantectomy, and tylectomy) should be assessed for their oncoplastic needs. e most common indications for oncoplastic breast sur­gery are tumor size (37%), poor tumor location (22%), oncocosmetic (1%), multifocality (10%), skin retraction (9%), positive margins after previous surgery (5%), and other reasons (5%).
It is also important to identify patients who are not candidates for breast conservation. Historically, absolute contraindications to BCT include (1) patients with a high probability of recurrence due to multicentric disease or the inability to obtain clear margins; (2) patients who are cur­rently pregnant; (3) those with active collagen vascular dis­ease, such as active lupus and scleroderma10; and (4) those with a history of prior breast irradiation either related to prior breast cancer or Hodgkin’s disease. Soft contrain­dications include (1) patients with a high probability of subsequent breast cancers including those with BRCA1/2 mutations, PTEN, etc.; (2) tumors that directly involve the NAC; and (3) patients with high tumor-to-breast ratios.
e increasing use of neoadjuvant chemotherapy has in c­reased the number of patients eligible for breast- conserving surgery and oncoplastic tissue rearrangement. is is, in part, predicated on the invasive tumor molecular subtype. Neoadjuvant dual HER2 blockade with trastuzumab and pertuzumab in combination with cytotoxic chemotherapy for patients with HER2+ amplication results in a high pathology complete response (pCR) (16.8–66.2%)11. Patients with ER+/HER2- cancers have lower pCR rates (7.0–16%), and those with triple negative tumors have 33–35% chances of achieving a pCR12; 40–70% overall will achieve a partial response. 
9
Patient Selection
Comprehensive preoperative evaluation is necessary to deter­mine patients appropriate for oncoplasty and the necessary type of reconstruction. e surgical team should obtain the patient’s history of any prior breast surgery, chest radiation, and infections. Risks factors for wound complications such
as diabetes mellitus, active smoking, cardiovascular condi­tions, history of Ehlers-Danlos, coagulopathies, poor nutri­tion, and obesity should be noted. Patients with a history of chronic pain, bromyalgia, and opioid dependence should also be assessed to coordinate optimal care with their pri­mary care provider.
It is also important to understand the patient’s psychosex­ual concerns and feelings about her breast. Loss of nipple– areolar and breast sensation may be important to patients undergoing breast surgery in terms of quality of life and sat­isfaction. Patients undergoing skin-sparing mastectomy and NSM can have considerable loss in skin and nipple sensa­tion. Many patients complain of loss of sexual arousal with breast or nipple stimulation after mastectomy. As such, fear of loss of nipple sensation may be an important consider­ation for oncoplastic tissue rearrangement. Very little data are currently available about the risks of nipple sensation loss after oncoplastic breast surgery and radiation. Concerns about nipple viability, postoperative nipple positioning, fears about the risk of recurrence, and risks of needing addi­tional surgery should be ascertained along with the patient’s history of anxiety. Lastly, patients’ concerns about foreign body implantation and complications, including the remote risk of implant-associated anaplastic large-cell lymphoma, should be addressed.
On physical exam, the surgeon should clinically evalu­ate the patient’s breast and chest anatomy for breast sym­metry, prior scars, bra size, and degrees of ptosis. Enlarged lymph nodes should be assessed for possible regional dis­ease. Patients who have had prior breast conservation and radiation therapy are generally not good candidates for oncoplastic surgery. Diagnostic mammogram, ultrasound, and breast magnetic resonance imaging (MRI) should be strongly considered to precisely identify the location and extent of the breast tumor. Patients undergoing neoadju­vant chemotherapy should undergo another preoperative MRI to assess the extent of the residual tumor and rule out the possibility of disease progression. is will conrm that breast conservation and oncoplastic tissue rearrangement is still possible. 
Tumor Characteristics
Invasive Breast Carcinoma
Oncoplastic surgery has been shown to have no adverse eects related to local recurrence, disease-free, or overall survival for all stages of breast cancer.
For patients with invasive lobular carcinoma, extensive microcalcications, or multifocal breast cancer, the possibil­ity or risk of positive margins is an important consideration for oncoplastic planning. 
Ductal Carcinoma In-Situ (DCIS)
e management of DCIS remains controversial to minimize overtreatment and undertreatment. Despite this, margin
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status is one of the most important determinants in local recur­rence and clinical outcomes. e Society of Surgical Oncol­ogy (SSO)/ American Society Radiation Oncology (ASRO)/ American Society of Clinical Oncology (ASCO) Consensus Guidelines on margins for DCIS, published in 2016, recom­mend at least 2-mm margins to reduce the risk of in-breast recurrence relative to narrower negative margins.13 Paren­thetically, the multidisciplinary panel also noted that clinical judgment was necessary to determine whether patients with smaller negative margin widths (≥ 1 mm) require re-excision. ey identied additional factors important to consider before additional surgery, including an assessment of residual calcications on postexcision mammogram, extent of DCIS in proximity to margin, and which margin is close (anteriorly just under the skin and posteriorly excised to the pectoral fas­cia) versus margins associated with residual breast tissue. e routine practice of obtaining negative margin widths wider than 2 mm is not supported by the evidence.
In a recent case-control study, De Lorenzi etal at the Euro­pean Institute of Oncology (IEO) compared oncoplastic breast surgery followed by radiation (44 patients) and conservative breast surgery alone followed by radiation (375 patients).14 e primary endpoints were disease-free survival (DFS) and ipsilateral breast tumor recurrence (IBTR). e tumor size was larger in the oncoplastic group. is was expected as oncoplasty can manage the resection of larger volumes of breast tissue. e average annual rates of invasive IBTR were
1.6% and 1.0% for the oncoplastic and conservative patients, respectively. e authors also found no dierence in the rates of contralateral breast cancer distant metastasis and contra­lateral breast cancer. ey observed similar rates of focally involved margins (focally ink on DCIS) in 4.5% and 3.5%, respectively, for the oncoplastic and conservative patients. Close margins (<1 mm) were observed in 22.8% and 17.9%, respectively. None of their patients underwent further surgery. ey conclude that oncoplastic breast surgery is a safe and valid treatment component for patients with DCIS.
In a recent review of DCIS, Song etal reviewed their experience at Emory Healthcare System.15 Twenty-eight patients were included in the study. erapeutic mam­moplasty was the denitive procedure in 64%. ere were 10 patients (36%) who required re-operation: 9 for posi­tive margins and 1 for residual microcalcications. Positive margin rates were independent of tumor location. All 10 patients requiring completion mastectomy or re-excision had intermediate or high-grade disease. In addition, the women requiring re-operation were younger (mean 45.6; median 43) compared with those who did not require re­operation (mean 57; median 57). e authors concluded that oncoplastic reduction techniques are appropriate for DCIS taking into account patient selection and improved conrmation of negative margins. One strategy to minimize the incidence of positive margins is to obtain a preoperative breast MRI, which is useful in determining the extent of DCIS and establishing the boundaries for resection. Intra­operative margin assessment can also reduce the risk of posi­tive margins. 
Fig. 3.1 Preoperative photograph of a patient with A cup breasts and
not a candidate for oncoplasty.
Fig. 3.2 Postoperative photograph following nipple-sparing mastec-
tomy and two-stage reconstruction at 2-year follow-up.
The Impact of the Tumor-to-Breast Size Ratio on Oncoplastic Breast Surgery
In general, women with an A or B cup breast are poor can­didates for oncoplastic tissue rearrangement or reduction. ey simply do not have enough breast tissue. In this popu­lation, small tumors can be excised with local tissue mobi­lization for adequate closure. Alternatively, the patient may be a candidate for neoadjuvant chemotherapy to shrink the tumor, allowing her to be converted from a mastectomy to breast conservation. If not, the patient may be best suited for mastectomy and immediate implant reconstruction.
Figs. 3.1 and 3.2 illustrate a patient with an A cup who
completed NSM and two-stage prosthetic reconstruction.
Patients with a C cup breast may be candidates for an oncoplastic reduction. e decisions will be based on the tumor-to-breast ratio, degree of ptosis, and sucient vol­ume to adequately rearrange the tissue. ese are usually well suited for tissue rearrangement, particularly if they
CHAPTER 3 Indications and Patient Selection for Oncoplastic Breast Surgery
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Fig. 3.3 Preoperative photograph of a woman with C cup breasts and
left breast cancer who is a good candidate for oncoplasty with tissue rearrangement.
17
Fig. 3.5 Postoperative photograph following ipsilateral oncoplastic
tissue rearrangement and contralateral reduction mammaplasty for symmetry at 2-year follow-up.
Fig. 3.4 Preoperative markings demonstrating wire localization in the
lower outer quadrant.
have signicant ptosis and can tolerate a modication of the NAC position. Lack of ptosis may be problematic due to the xed nipple–areolar position. Figs. 3.3–3.5 illustrate a patient with a C cup breast following oncoplastic tissue rearrangement.
Larger breasted women with a D or larger cup breast often have some degree of ptosis. e additional breast tis­sue and mobility of the NAC lend well to reconstruction using reduction mammoplasty techniques. Figs. 3.6 and 3.7 illustrate a woman with DD breasts following oncoplastic reduction mammaplasty.
Women who have had prior breast augmentation with implants present a special challenge. Up front, it is impor­tant to recognize that the presence of a breast implant does not have an adverse eect on the ecacy of treatment to
Fig. 3.6 Preoperative photograph and markings of a patient with DD
breasts and a left breast cancer who is a good candidate for oncoplas­tic reduction mammaplasty.
minimize the risk of recurrence. Although they often pres­ent with D cup or larger, the pre-augmentation breast is often an A or B cup with reduced breast tissue for recruit­ment. is is complicated by the fact that women with breast augmentation implants have an increased risk of developing capsular contracture and brosis slowly over time after breast radiation. is progressive contracture may begin 6–9 months after radiation completion and continue for 2–10 years. e patient may notice that the implant becomes xed, rm, and uncomfortable leading to decreased patient satisfaction. Patients with breast implants are also at increased risk for infection after radiation therapy.
Given these problems, the question remains how to
optimally treat these patients. One option for women
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Fig. 3.7 Postoperative photograph following bilateral oncoplastic
reduction mammaplasty at 2-year follow-up.
Fig. 3.9 Postoperative photograph following breast conservation
demonstrating severe capsular contracture and distortion of the left breast.
augmentation following biopsy (see Fig. 3.8) and onco­plasty with radiation (see Fig. 3.9).
It is important to recognize that it is not just the tumor size that denes the type of oncoplastic tissue reconstruction procedure but rather the interplay between the tumor size, breast size (volume and bra size), and estimated percentage of breast volume that would be removed (see Fig. 3.10). 
Fig. 3.8 Preoperative photograph of a woman status postbilateral
breast augmentation following a biopsy for left breast cancer.
with early stage disease would be a nipple-sparing or skin­sparing mastectomy and replacement with a same size or larger implant. is approach can achieve excellent cos­metic results with the potential NAC preservation, albeit often insensate. is can avoid the need for radiation. For early stage patients who decline a mastectomy, the options become either treat with the implant in place or remove the implant and plan for a tissue ap reconstruction in the future after radiation. e majority of women are reluc­tant to have the implants removed, which results in a much smaller breast volume. For these reasons, oncoplastic sur­gery is not usually recommended for women with breast implants to avoid the long-term aesthetic issues related to capsular contracture and infection. Figs. 3.8 and 3.9 illus­trate a patient with breast cancer in the setting of breast
Extent and Location of the Anticipated Breast/Skin Excision
Tumor location is a critical factor in determining the type of reconstruction and pedicle design. In a recent study of 980 patients, Rummel etal identied approximately 51% of tumors were located in the upper outer quadrant (UOQ) compared with 15.6% in the upper inner quadrant (UIQ), 14.2% in the lower outer quadrant (LOQ), 10.6% in the central breast, and 8.1% in the lower inner quadrant (LIQ).16 A thorough preoperative discussion and review of the mammogram and MRI images by both the breast surgeon and the reconstructive surgeon is essential to understand the extent and location of the planned resection and reconstructive needs. Both need to have a shared mental model. e presence of tumor within or extremely close to the skin is an indication to consider neoad­juvant chemotherapy for tumor shrinkage except for patients with ER/PR+/HER2 neu(-) tumors or DCIS. As such, the need to remove breast skin as part of a partial segmental mas­tectomy is now rare. Skin involvement of the LIQ and LOQ quadrant can frequently be excised within the boundaries of the inverted T pattern. For skin involvement of the UOQ and UIQ outside the boundaries of a traditional inverted T pat­tern, consideration can be given to rotate, split, or otherwise modify the inverted T skin pattern.
For central/NAC skin involvement, a vertically oriented elliptical incision can be made for a central resection with pres­ervation of the anterior projection and native shape. Tumors close to but not directly involving the NAC may be managed
CHAPTER 3 Indications and Patient Selection for Oncoplastic Breast Surgery
% Breast excised
Volume of breast (cm3)
38F 40F
r
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25
20
15
10
32A
5
Bra size
32D 32C 34B 36A
34C
36B
32B 34A
Volume
Replacement
Simple
Wide Local Excision
34D 36C 38B
34DD
36D 38C 40B
Therapeutic
36DD
38D 40C
Mastopexy
36E
38DD
40D
38E
40DD
Therapeutic
Reduction
Mammaplasty
40E
5
4
3
2
1
Tumour
diamete
(cm)
0
200
with a batwing resection or a central resection to assure negative margins. Radiation therapy will still be needed in this situation. Alternatively, the patient may be considered for a skin-sparing mastectomy with immediate volume reconstruction using either a tissue expander/implant or tissue transfer. is would potentially eliminate the need for radiation therapy and the potential complications of capsular contracture and brosis.
e challenge occurs when a large amount of skin needs to be resected, particularly in the UOQ or UIQ. e team will need to consider the overall breast volume and the patient’s aesthetic goals. e patient may be best served with a mas­tectomy and immediate reconstruction. A latissimus ap can be considered for a large UOQ skin defect. e potential problems with a latissimus ap in this context include skin color and texture mismatches. In addition, the latissimus ap is then no longer available for future reconstructive needs if the patient develops a recurrence after radiation therapy or needs a ap reconstruction and is not a candidate for a deep inferior epigastric perforator (DIEP) ap, transversus rectus abdominus myocutaneous (TRAM) ap, or other ap. 
Immediate versus Delayed Reconstruction
Kronowitz etal reviewed their experience with 69 patients at e University of Texas MD Anderson Cancer Center.17
300
400
500
600
700
800
900
1000
1100
1200
1300
1400
Fig. 3.10 An algorithmic chart listing oncoplastic treatment options. (From Macmillan RD, McCulley SJ.
Oncoplastic breast surgery: what, when and for whom? Curr Breast Cancer Rep 2016; 8:112–117.)
Fifty patients underwent immediate repair of partial mastec­tomy defects before external beam radiation therapy, which included local tissue rearrangement in 28%, breast reduc­tion in 66%, and aps in 6%. Nineteen patients underwent delayed reconstruction after external beam radiation therapy of which 32% had local tissue rearrangements, 42% had breast reductions, and 26% had aps. Results included a complication rate of 26% for immediate reconstruction and 42% for delayed reconstruction. Autologous aps were asso­ciated with increased complications when performed imme­diately compared with local tissue rearrangement; however, aps were associated with a lower complication rate when performed on a delayed basis. e authors concluded that the immediate repair of partial mastectomy defects with volume displacement techniques (reduction mammaplasty, tissue rearrangement) resulted in fewer complications and better aesthetic outcomes. Spear etal demonstrated that reduction mammaplasty or mastopexy performed following radiation therapy resulted in a complication rate of 28%.18 Figs. 3.11
and 3.12 illustrate a patient following breast conservation
without oncoplasty followed several years later with ipsi­lateral autologous fat grafting and contralateral reduction mammaplasty for symmetry. Figs. 3.13–3.15 illustrate a patient following breast conservation followed several years later by performing a bilateral reduction mammaplasty. 
1500
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Fig. 3.11 Preoperative photograph following right breast conservation
demonstrating a mild contour abnormality.
Fig. 3.13 Preoperative photograph of a woman with severe mammary
hypertrophy following left breast conservation therapy.
Fig. 3.12 Postoperative photograph following autologous fat grafting
of the lumpectomy defect as well as a contralateral reduction mam­maplasty for symmetry.
Impact of Intraoperative Radiation Therapy
Intraoperative radiation therapy (IORT) has become an alternative to whole breast radiation therapy. IORT delivers a single intraoperative dose of radiation to the tumor bed at the time of surgical excision. e Targeted Intraoperative Radiotherapy Versus Whole Breast Radiotherapy for Breast Cancer (TARGIT-A) demonstrated similar breast cancer mortality in patient undergoing IORT and whole breast radiation after lumpectomy (WBRT) (2.6% [1.5–4.3%] for TARGIT vs 1.9% [1.1.–3.2] for WBRT; p = 0.56). Wound­related complications were similar for both groups, but grade 3 or 4 skin complications were signicantly reduced with TARGIT (4 of 1720 vs 13 of 1731, p = 0.029).19 e main advantage of IORT is that a single dose of 20 Gy can safely be delivered directly to the tumor bed while sparing the healthy surrounding tissue.
Fig. 3.14 Postoperative anterior view following bilateral reduction mam-
maplasty demonstrating mild asymmetry and distortion of the left breast.
Fig. 3.15 Postoperative oblique view demonstrating distortion along
the inframammary region due to delayed healing at the trifurcation point.
CHAPTER 3 Indications and Patient Selection for Oncoplastic Breast Surgery
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IORT in patients undergoing oncoplastic tissue rear­rangement raises the possibility of wound-healing compli­cations. Cracco et al studied the surgical outcomes, early complication rates, and esthetic results after oncoplastic breast surgery of 83 patients undergoing IORT and 109 patients treated with WBRT with a mean follow-up time of 17 months.20 e early postoperative complication rate after IORT was 26.6%. e majority were liponecrosis (12%), seroma formation (7.4%), and infection/dehiscence (2.4%). In contrast, the early postoperative complication rate after WBRT was 14.7%. e most common complications were hematomas (7.6%), liponecrosis (1.9%), and seroma for­mation (1.9%). e complication rates after IORT were statistically higher (p < 0.0001). Despite this increase in early complications, the late cosmetic results were good in both IORT and WBRT groups (84.3% and 88%, respec­tively). ey concluded that IORT did not appear to nega­tively inuence the cosmetic outcomes after conservative breast surgery and oncoplastic reconstruction.20 Crown and Grumley analyzed their experience with oncoplasty patients undergoing either IORT or WBRT at Virginia Mason Med­ical Center.21 Minor surgical site complications occurred in 29 patients (17.9%) in the IORT group, compared with 20 patients (6.9%) in the WBRT group (p = 0.001). Obesity, smoking, diabetes, chemotherapy, advanced age, tumor size, and need for re-excision were not associated with increased rates of complications.8 Overall, oncoplastic breast surgery is a safe reasonable reconstructive option for patients under­going IORT. 
Indications for Nipple-Sparing Mastectomy
An increasing proportion of women with newly diagnosed unilateral breast cancer are choosing mastectomy (either unilateral or bilateral) for treatment with immediate breast reconstruction. Expanded genetic testing has also identied women at high risk for developing breast cancer for whom bilateral prophylactic mastectomy is recommended. NSM is generally indicated in women with small to moderate breast volume (A, B, and C cup) based on vascular perfusions fac­tors following mastectomy. Traditional indications included tumors that were less than 3 cm in diameter, greater than 2 cm from the NAC, and with clinically negative axillary lymph nodes.22 Current guidelines however suggest that NSM can be safely performed so long as margin status is appropriate.23 e topic of mastectomy versus oncoplasty will be further discussed in a separate chapter. 
Conclusion
Collaboration between the breast surgeon and plastic sur­geon is recommended to develop a shared mental model of the patient’s tumor and anatomy, treatment plan (includ­ing the need for radiation therapy), and the patient’s aes­thetic goals both in the short term as well as in the long term. Together the team must answer the questions: Is the patient a candidate for breast conservative surgery and
oncoplasty? If so, what type of oncoplastic surgery would best suit the patient’s needs and its timing? Alternatively, would the patient be best served with an NSM or non­NSM with reconstruction? As oncoplastic techniques con­tinue to evolve and expand and the evidence mounts that this technique is safe and eective with excellent surgical and aesthetic outcomes, the indications and prevalence of this technique will certainly increase.
References
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SECTION I Oncoplastic Breast Surgery – Getting Started
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19. Vaidya J, Wenz F, Bulsara M, Tobias J, Joseph D, Keshtgar 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.
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