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SECTION III Oncoplastic Breast Surgery – Outcomes
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Fig. 17.2 Superficial nipple necrosis is a risk following periareolar
incisions.
Fig. 17.3 Full thickness necrosis of the nipple–areolar complex is an
uncommon complication but can occur with wide undermining and devascularization.
Fig. 17.5 Cellulitis following oncoplastic surgery.
Fig. 17.6 Hematoma extending beyond the breast borders is noted
following oncoplastic reduction mammaplasty.
Fig. 17.4 Fat necrosis following oncoplastic reduction mammaplasty
is demonstrated on this computed tomography scan.
Postoperative antibiotics are considered in some patients dependent upon native risk factors. Hematoma occurrence is rare and usually preventable with good hemostasis follow­ing the ablative and reconstructive portions of the opera­tion. Postoperative hematoma will usually require operative evacuation, especially if the bleeding is active and associated with severe swelling. A preoperative coagulation prole and avoidance of aspirin products is recommended.
When assessing aesthetic outcomes and patient satisfac­tion, oncoplastic reduction techniques have been shown to carry a signicant positive eect, thus again outweighing the risk of complications in the majority of patients. Validated patient satisfaction surveys administered to patients follow­ing these procedures have shown signicant improvements in postoperative patient assessment (relative to preoperative) with emotional health and acceptance of the patient’s own body after surgery. Furthermore, comprehensive patient
CHAPTER 17 Complications of Oncoplastic Breast Surgery
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TABLE
Complication Rates Seen with Oncoplastic Breast Reduction, Based on Timing of the Procedure Relative
1 7.1
to Tumor Excision
Timing and Outcomes for Oncoplastic Reconstruction
Delayed
Overall Immediate
Patients 160 117 18 25
Complications 28.1% 20.5% 33.3% 60% 0.001
Infection 5% 3.4% 0 16% 0.019
Fat necrosis 1.9% 0.9% 0 8% 0.047
Mean satisfaction 69.8% 72.8% 68% 61.8% NS
Mean aesthetic outcome 62.5% 63.9% 54.6% 58.8% NS
Ergo FM, Losken A et.al. The use of reduction mammaplasty with BCT: an analysis of timing and outcomes. Plast Reconstr Surg 2015; 135:963e. NS, not significant.
immediate Delayed P-value
satisfaction surveys have not illustrated a decrease in post­operative self-assessment of any factors related to the breasts by patients, including physical appearance, emotional well­being, condence, and sexuality.
ere is also been a clear benet from the standpoint of complication reduction to performing immediate oncoplas­tic reduction at the time of partial mastectomy. Large series have shown that patients undergoing immediate oncoplastic reduction for reconstruction exhibit an approximately 20% overall complication rate. When the oncoplastic reduction is delayed, oftentimes until after adjuvant radiation treat­ment has been completed, the complication rate rises to the 60% range (Table 17.1).8 e largest dierences seen in specic complications when comparing immediate versus delayed oncoplastic reduction are seen with infection rates (3% vs 16%), fat necrosis (0.9% vs 8%), and asymmetry of the breasts (8.5% vs 24%).8 us, experience indicates that there is a signicant benet to proceeding with immediate oncoplastic reduction from the standpoint of complication/ morbidity reduction.
When reduction mammaplasty is requested follow-
Fig. 17.7 Preoperative image of a woman with mammary hypertrophy
and previous right breast conservation treatment.
ing breast conservation, there are two schools of thought. e rst is that reduction mammaplasty should be avoided because the complication rate is so high, and a mastectomy should thus be considered. e other is that it is accept­able to proceed with a reduction mammaplasty; however, there are several tenants that must be considered. e rst is patient selection. If the skin is severely damaged and brotic, reduction should be avoided; however, if the skin is relatively soft, then reduction can be considered. Under­mining should be kept to a minimum to maintain adequate perfusion. Wedge excision of the parenchyma using a sharp scalpel rather than electrocautery is advised. Free nipple graft should be considered. Although, this will not guaran-
elevation. Figs. 17.9–17.14 illustrate a patient following oncoplastic reduction mammaplasty complicated by a posi­tive margin on nal pathology.
It is important to remember that re-operations on a pre­viously radiated breast are more prone to adverse events. It is also important to recognize that patients undergoing delayed oncoplastic reduction routinely report lower patient satisfaction rates on validated surveys, compared with those undergoing immediate oncoplastic reconstruction, with regard to all categories of well-being. Blinded surgeon assessment of outcomes illustrates similar improved subjec­tive assessment for immediate reconstruction outcomes. 
tee a complication-free operation, the complications can be reduced. Figs. 17.7 and 17.8 illustrate a patient with severe
Local/Regional Flaps
mammary hypertrophy following right breast conservation therapy. Following the reduction mammaplasty, distortion of the inferolateral aspect of the breast was noted with arm
If there is insucient tissue for local tissue rearrangement due to defect size or location, local or regional aps provide
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Fig. 17.8 Postoperative image following reduction mammaplasty in a
previously radiated breast. The degree of soft tissue fibrosis is evident with arm elevation.
Fig. 17.11 The left excision/partial mastectomy has been performed
demonstrating a significant contour defect.
Fig. 17.9 Preoperative image of a woman with left breast cancer
scheduled for oncoplastic reduction mammaplasty.
Fig. 17.10 The preoperative marking before oncoplastic reduction
mammaplasty.
Fig. 17.12 The oncoplastic reduction is complete but the margin is
positive on the left.
Fig. 17.13 Following completion mastectomy and tissue expander
reconstruction.
Fig. 17.14 Following exchange to a permanent implant and nipple–
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areolar reconstruction at 2-year follow-up.
viable options for reconstruction. Local aps from the sub­axillary region are useful for moderate defects in the smaller breast. More lateral defects may be reconstructed with a transposition or rotational ap, moving skin and subcu­taneous fat that is lateral to the breast, into defects in the outer quadrants. e latissimus dorsi ap provides sucient volume to correct almost any partial mastectomy defect, is technically simple, and has relatively low morbidity. Because of the dierent skin color and texture with this ap, it is bet­ter to replace an entire aesthetic unit during latissimus dorsi reconstruction. However, this ap can still be performed if no skin is missing by transferring the muscle and subcuta­neous tissue alone. Another common rotational ap option for oncoplastic reconstruction is the thoracodorsal artery perforator (TDAP) ap.
e average reported complication rate for oncoplastic ap reconstruction is in the 14% range.9 Some series have reported higher rates with volume replacement and tissue rotation, but the highest subset of complications in these series tend to be related to ap donor site morbidity and potential ap loss. With the oncoplastic latissimus ap, overall reported complication rates are in the 35% range. However, the majority (70%) of these complications relate to ap donor site morbidity. Of these, seroma (20% range) is the most commonly encountered complication.
ere are several techniques that are useful for the pre­vention and management of seroma following latissimus dorsi ap reconstruction. e use of closed suction drains is useful to remove excess uid and also to maintain a nega­tive pressure environment. Quilting sutures are also recom­mended to decrease the potential dead space within the harvest space. ese sutures can minimize shear forces that tend to promote the lack of adherence.
e management of seroma is usually achieved by obser­vation with occasional aspiration. Aspiration can be per­formed using a large bore needle and 60-mL syringe. A closed suction drain can also be placed if the seroma is recurrent. e use of talc or other adhesiogenic materials can also be
CHAPTER 17 Complications of Oncoplastic Breast Surgery
considered to create soft tissue adhesion and brosis. Surgi­cal exploration and scarication of the seroma cavity is a last resort and considered for refractory cases. 
Oncologic Outcomes
Recurrence
With oncoplastic reconstruction, concern exists that local tissue rearrangement may aect local recurrences and the ability to detect them. However, numerous studies have demonstrated that oncoplastic techniques have low local recurrence rates when compared with breast conserving therapy alone. Rietjens et al found that local recurrence rates were low over long-term follow-up, with a 3% rate at 5 years and no recurrences seen in those tumors smaller than 2 cm.10 is is replicated in other large series, which reported ranges of 1.5–2.5% local recurrence rates when evaluating series of women undergoing bilateral reduction mammaplasty.
In a prospective cohort study of patients with locally advanced breast cancer undergoing oncoplastic surgery, Bogusevicius etal reported a local/regional recurrence rate of 10% at 86 months.11 However, these patients had larger tumors and longer follow-up than the previously mentioned studies. Additionally, excision of multifocal tumors within the same quadrant has been shown to be oncologically safe with the wide margins that can be taken with oncoplastic procedures.
e one likely benet of oncoplastic reduction speci­cally, and all oncoplastic reconstruction methods, is that the reconstructive procedures allow for larger oncologic resec­tions with wider margins. us, this likely results in a lower recurrence rate compared with oncologic resection alone. Most large cohort series assessing oncoplastic reduction mammaplasty patients report local recurrence rates in the 8% range at 10 years, and an overall long-term survival rate in the 83% range. Although the link between larger resec­tion margins and lower recurrence rates in the breast has never been clearly established, there is a likely positive rela­tionship. is accounts for the consistent ndings in most reports of 5-year recurrences of 3.4% range for lumpectomy in all patients relative to 2% range reported for oncoplastic patients. 
Positive Margins
Although oncoplastic techniques allow for wider resections, the tissue rearrangement performed in reconstruction may complicate management of positive margins. Positive mar­gins have been reported in wide ranges, between 2.7–22%, and have been associated with higher stage, positive nodes, positive lymphovascular invasion, use of neoadjuvant che­motherapy, larger initial T stage, positive estrogen receptor, and younger age. Many oncoplastic techniques utilize der­moglandular aps, which transposes tissue from one area of the breast to another.7 If a second surgical stage is needed
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TABLE
for presence of disease at the edges of the specimen, this can become challenging due to the displacement of the glandu­lar tissue from the previous surgery, thereby making further excision very dicult.
these patients undergo completion mastectomy. Addition­ally, because most mammaplasty techniques rely on a uni­pedicle or bipedicle technique, subsequent need for surgery risks pedicle compromise, thereby restricting future thera-
Reported Rates of Positive Margins and Need for Follow-up Completion Mastectomy from Multiple Series
17.2
when Performing Tumor Excision with Immediate Oncoplastic Breast Surgery
Resection Margin Involvement and Reoperation Rates Following Oncoplastic Reconstruction
Author Year OBCS # OBCS + margin OBCS re-excision Mastectomy conversion
Crown 2015 387 18% 18% 15%
Mansell 2015 119 13.4% 1.6% 11.9%
DeLorenzi 2016 454 2.9% 0 15.4%
Chauhan 2016 33 0 0 0
Carter 2016 1177 4.8% NR NR
OBCS, Oncoplastic breast conservation surgery. Carter SA, etal. Ann Surg Oncol 2016; 23(10):3190–3198; Chauhan, etal. Indian J Surg Oncol 2016; 7(4):413–419; DeLorenzi Eur J Surg Oncol 2016; 42(1):71–77; Mansell J, etal. Breast 2017; 32:179–185; Crown A, etal. Ann Surg Oncol 2015; 22:3363–3368.
rates have ranged from 5–15% (Table 17.2). ese low rates have been demonstrated despite including patients with tumors greater than 4 cm preoperatively.
When assessing oncoplastic reduction techniques spe-
Although re-excision is possible in such cases, more often
cically, multivariate regression models have found certain tumor characteristics to be predictive of need for comple­tion mastectomy. ese include estrogen receptor (ER)­positive status, BMI over 30, and specimen weights greater than 1000 grams at time of resection. 
peutic options.
Intraoperative frozen section has been evaluated as a
Delay of Adjuvant Therapy
means to combat positive margins with oncoplastic recon­struction as well. When frozen section has been assessed as a diagnostic technique to evaluate margins in patients under­going latissimus dorsi mini-aps with partial mastectomy, approximately 30% of patients had positive frozen sections. ese sections illustrated a sensitivity of 83% and accuracy of 96% when compared with paran sections. Overall, local recurrence rate ranges around 0.9% with a median follow-up of more than 40 months when frozen section is used at time of oncoplastic reconstruction.
Caruso etal evaluated the utility of intraoperative frozen section in patients undergoing therapeutic mammaplasty. ey found that 8/52 patients (3 false positives, 5 true posi­tives) had positive frozen sections with a sensitivity of 83% and accuracy of 94%. Based on their ndings, they advo­cated for intraoperative assessment of margins as a means of improving local control in a single stage, thereby reducing the need for secondary re-excisions or mastectomies (none in their study).12 Figs. 17.9–17.14 illustrate a patient fol­lowing oncoplastic reduction mammaplasty who had a posi­tive margin who then underwent a completion mastectomy and reconstruction. 
When assessing complications related to oncoplastic recon­struction, the nal factor that must be considered is delay of adjuvant oncologic treatment due to postoperative mor­bidity. Hillberg etal assessed a large series of patients under­going immediate oncoplastic reconstruction at the time of partial mastectomy.13 is series included patients under­going both oncoplastic reduction mammaplasty, as well as local/regional rotational aps for volume replacement and defect reconstruction.
e overall complication rate reported was 37.5% with 10% of patients requiring antibiotic treatment and 6.6% requiring a corrective operation. Of all the complications experienced, approximately 80% occurred before planned adjuvant radiation treatment. As a result, 8.2% of all patients in this series experienced a delay in the planned start of radiation therapy. us, although overall compli­cation rates in these can be high, approximately 10% of patients experiencing a complication will undergo a delay in adjuvant treatment. ose patient characteristics that pre­dict complications leading to adjuvant treatment delay are greater patient age, greater patient BMI, and larger lumpec­tomy resection weights. 
Need for Completion Mastectomy
Conclusion
Although large long-term follow-up studies are lacking for oncoplastic breast surgery, published studies have described low rates of need for completion mastectomy. Reported
Oncoplastic breast reconstruction can be performed through a number of techniques, all of which serve to minimize
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aesthetic deformities and improve patient satisfaction fol­lowing breast conservation. Although these techniques are powerful in their ability to improve overall outcomes, the complication rates must be taken into account when coun­seling patients. In general, the addition of an oncoplastic technique will increase the complication rate, relative to oncologic resection alone, due to the larger amount of sur­gery. However, in the majority of cases, this risk is justied given the vastly improved appearance and patient satisfac­tion encountered with the reconstructed conserved breast. Surgeons must always consider performing these procedures in the immediate setting, as a delay of the oncoplastic recon­struction, oftentimes after adjuvant radiation therapy, will signicantly increase associated complication rates.
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;347:1233–1241.
2. Losken A, Dugal CS, Styblo TM, Carlson GW. A meta-analysis comparing breast conservation therapy alone to the oncoplastic technique. Ann Plast Surg. 2014;72:145–149.
3. Piper M, Peled AW, Sbitany H. Oncoplastic breast surgery: cur­rent strategies. Gland Surg. 2015;4(2):154–163.
4. Warren Peled A, Sbitany H, Foster RD, Esserman LJ. Onco­plastic mammoplasty as a strategy for reducing reconstructive complications associated with postmastectomy radiation therapy. Breast J. 2014;20:302–307.
5. Chang EI, Warren Peled A, Foster RD, etal. Evaluating the fea­sibility of extended partial mastectomy and immediate reduction mammoplasty reconstruction as an alternative to mastectomy. Ann Surg. 2012;255:1151–1157.
6. Kronowitz SJ, Feledy JA, Hunt KK, etal. Determining the opti­mal approach to breast reconstruction after partial mastectomy. Plast Reconstr Surg. 2006;117:1–11.
7. 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.
8. Egro FM, Pinell-White X, Hart AM, Losken A. e use of reduc­tion mammaplasty with breast conservation therapy: an analysis of timing and outcomes. Plast Reconstr Surg. 2015;135(6):963e–971e.
9. Losken A, Hart AM, Chatterjee A. Updated evidence on the oncoplastic approach to breast conservation therapy. Plast Recon- str Surg. 2017;140:14S–22S. 5S Advances in Breast Reconstruc­tion.
10. Rietjens M, Urban CA, Rey PC, et al. Long-term oncological results of breast conservative treatment with oncoplastic surgery. Breast. 2007;16(4):387–395.
11. Bogusevicius A, Cepuliene D, Sepetauskiene E. e integrated evaluation of the results of oncoplastic surgery for locally advanced breast cancer. Breast J. 2014;20(1):53–60.
12. Caruso F, Ferrara M, Castiglione G, etal. erapeutic mamma­plasties: full local control of breast cancer in one surgical stage with frozen section. Eur J Surg Oncol. 2011;37(10):871–875.
13. Hillberg NS, Meesters-Caberg MAJ, Beugels J, Winkens B, Viss­ers YLJ, van Mulken TJM. Delay of adjuvant radiotherapy due to postoperative complications after oncoplastic breast conserving surgery. Breast. 2018;39:110–116.
18
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Local Recurrence and Reconstructive Options Following Oncoplastic Breast Surgery
RACHEL ROLPH AND JIAN FARHADI
e management of recurrent breast cancer is a multidis­ciplinary challenge. Clinical and radiological follow-up of patients following breast cancer treatment aims to detect early locoregional and distant metastasis. Local breast recur­rence represents the reappearance of cancer and can occur at or near the site of excision following breast-conserving surgery (BCS) or in the soft tissues of the anterior chest wall or skin ap following mastectomy. In the case of oncoplastic surgery, the majority of local recurrence appears at the ini­tial site where the resection was performed.
e clinical presentation of a patient with a local recur­rence may vary and includes a new lump or rmness within the operated breast, nipple inversion or discharge, as well as skin changes, for example, erythema, rash, rm nodules, oedema, tethering, or thickening of scar tissue (Figs. 18.1 and
18.2). Dierential diagnoses include postoperative brosis,
fat necrosis, suture granulomas, benign breast disease, and post-radiotherapy skin changes. Persistent edema and ery­thematous skin overlying the operated breast should raise the suspicion of inammatory recurrent breast cancer and war­rants punch biopsy; however, this can be dicult to dieren­tiate from mastitis and post-radiotherapy skin changes. Even rarer is cutaneous metastasis “en cuirasse” located on thoracic and abdominal walls characterized by inltrated, hard, and sclerodermiform plaques.
Mammography is the mainstay of surveillance imaging following BCS detecting 8–50% of ipsilateral recurrences, whereas ultrasound and magnetic resonance imaging remain supplementary surveillance modalities.2 Mammographic appearances of ipsilateral recurrence include new nondys­trophic microcalcications, a new mass compared with baseline mammogram, increased architectural distortion or opacity, and an increase in skin thickening after posttreat­ment changes have subsided.3 Not all local recurrences will be associated with mammographic change, and a normal mammogram does not exclude local recurrence. Stereotactic
1
and core biopsies histologically conrm the diagnosis of local recurrence.
Local recurrence rates following surgery vary widely in the literature due to dierences in patient cohort selection, extent of surgery, and use of adjuvant therapies. e inci­dence of local recurrence after BCS and radiotherapy ranges from 10–22% at 10 years and, after mastectomy, ranges from 5–15% at 10 years. is 3–4 years for BCS and 2–3 years for mastectomy.3 Breast recurrence is a predictor of distant metastasis and decreased survival. A meta-analysis by the Early Breast Cancer Trial­ists’ Collaborative Group demonstrated a negative eect of a local recurrence on survival.7 In 5–15% of cases, local recur­rence is associated with concomitant regional and distant metastasis; therefore, computed tomography and positron emission tomography staging is considered for all patients with conrmed local recurrence.
Fig. 18.1 Local recurrence following right breast oncoplasty demon-
strating ulcerated nodules along the medial perimeter of the breast.
4-6
e median time to recurrence
6,8
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CHAPTER 18 Local Recurrence and Reconstructive Options Following Oncoplastic Breast Surgery
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Fig. 18.2 Local recurrence following right mastectomy demonstrating
nodularity in the subcutaneous tissues around the mastectomy scar.
e a etiology of local recurrence remains unclear; however, theories include incomplete excision of the primary tumor, unrecognized multifocal disease, entrapment of tumor cells within obstructive lymphatics, and local implantation of sys­temic circulating cells.9 In the context of local recurrence alone, excision surgery and adjuvant therapies have curative intent. For patients presenting with local recurrence and distant metas­tasis, a multidisciplinary approach will be required to assess the need for palliative resection of the local recurrence as an adjunct to systemic treatment.
Determinants of Local Recurrence
e importance of negative margins in BCS cannot be over­stated, and positive margins are a risk factor for increased local recurrence. Positive margins according to the joint guidelines of the American Society of Breast Surgeons/ Society of Surgical Oncology/American Society of Radia­tion Oncology constitute “ink on tumor” for invasive breast cancer and less than 2 mm margins for ductal carcinoma in situ.10 Current UK guidelines from the Association of Breast Surgery consensus dene positive margins as 1 mm for both invasive and ductal carcinoma in situ.11 A systematic review on oncologic reporting in BCS highlighted variation in the frequency of margin involvement (0–36%) and local recur­rence rates of 0–10.8%.12 Positive margins (ink on invasive or ductal carcinoma in situ) are associated with a twofold increase in the risk of ipsilateral recurrence compared with negative margins.13 More widely clear margins than no ink on tumor do not signicantly decrease the rate of recurrence compared with no ink on tumor even in high-risk groups with unfavorable biology.13 Local recurrence is inuenced more by tumor biology and therapy than surgical margin.14 Young age at diagnosis (less than 40 years) is a signicant
risk factor for local recurrence at 5 years with a relative risk of 2.21 (95% CI 1.62–3.02).
15,16
Body mass index gain fol­lowing BCS is also signicantly associated with higher rates of recurrence.
17
Pan etal performed a meta-analysis of the results of 88 trials involving 62,923 women with estrogen receptor (ER)-positive breast cancer who were disease-free after 5 years of scheduled endocrine therapy.18 e risk of disease recurrence, both locally and distant, was strongly correlated with the original TMN clas­sication (tumour, node, metastasis) status and tumor grade. During the study period from 5–20 years, the absolute risk of local recurrence with T1N0 ER positive breast cancer or a con­tralateral breast cancer were low grade 17%, moderate grade 22%, and high grade 26%. Tumor grade and size are signicant predictors of recurrence after adjustment to other variables.
19,20
Breast tumors can be divided into subtypes based on molecular proling, particularly those diering in prolifera­tion.21 Measurement of the level of activation of the prolif­eration pathway is via Ki-67 expression. Ki-67 is a nuclear protein associated with cellular proliferation. Immuno-stain­ing can assess the percentage of breast cancer cells expressing Ki67 (<14%; >14%). Molecular subtypes of breast cancer include luminal A (ER-positive or progesterone receptor [PR]-positive and Ki-67 < 14%); luminal B (ER- or PR-pos­itive and Ki-67 14%); luminal human epidermal growth factor receptor 2 (HER2) (ER- or PR-positive and HER2­positive); HER2-enriched (ER-negative, PR-negative, and HER2-positive); and basal-like (ER-, PR-, and HER2­negative, triple negative). Luminal B, HER2 positive, and triple negative subtypes all show signicant increased risk for both local recurrence and distant recurrence following BCS.22 Five-year local recurrence rates following BCS and radiotherapy for each subtype have been reported: 0.8% for luminal A, 2.3% for luminal B, 1.1% for luminal HER2,
10.8% for HER2-enriched, and 6.7% for triple-negative disease.23 Similarly, after mastectomy, patients with luminal A tumors had the lowest rates of local recurrence, 8% at 10 years.24 Gene expression proling by microarray analysis is being used to identify gene expression proles that can pre­dict local recurrence. Although still being rened, researchers have been able to identify subgroups of patients at increased risk of developing local recurrence following BCS.
25,26
Indications and Techniques for Second Oncoplastic Breast Surgery
e standard treatment recommended for ipsilateral recur­rence following BCS is salvage mastectomy with radiotherapy to the chest wall if not already administered previously.27 e management plan following salvage surgery is formulated in a multidisciplinary approach to determine the benets of radio­therapy, endocrine, and chemotherapy on a case-by-case basis with the aim to reduce secondary recurrence and distant metas­tasis. e adjuvant treatment strategy will take into account the biology of the original tumor, time to recurrence, patient TN status, age, previous adjuvant treatments, and comorbidities.
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Patients presenting with ipsilateral recurrence in the tumor bed may decline salvage mastectomy and seek alterna­tive treatment options. For this small subgroup of patients, repeat breast-conserving surgery (rBCS) with or without additional radiotherapy may be considered. Patients with inammatory breast cancer, small volume breasts, multi­centric or multifocal recurrence, skin involvement, or poor tumor biology (e.g., high grade, triple negative, HER2-pos­itive) are not candidates for this approach. Patient choice would be the main determining factor to consider a second conservative surgery and is not to be oered routinely. e evidence base supporting rBCS is limited and therefore can­not currently be recommended over mastectomy.28 Small unifocal recurrence in a large volume breast, a long interval to recurrence, and amenable tumor location would be fac­tors enabling rBCS to be technically feasible. Cosmesis in the re-operated breast may be compromised in rBCS due to reduced pliability of the breast parenchyma, signicant volume disparity between breasts, and post-radiotherapy changes to the skin envelope. ere are no published level 1 studies comparing salvage mastectomy versus rBCS ± radiotherapy for patients with ipsilateral breast recurrence. Low incidence of recurrence and heterogeneity of the recur­rence population, for example, timing to recurrence, tumor staging and biology, means recruitment, and design of a large-scale study comparing the two treatments, proves dif­cult. Two phase II prospective trials investigating the use of partial breast re-irradiation following rBCS are in progress (https://clinicaltrials.gov).
e use of secondary repeat breast conservation surgery for local recurrence was rst described by Kurtz etal in a retrospective analysis of 52 patients.29 Wide local excision alone was performed for stage I–II breast cancer patients for small, slow-growing, ipsilateral recurrence. ey reported no signicant dierences between mastectomy and rBCS for 10-year overall survival (54% and 64%, respectively). A higher rate of secondary recurrence was however observed in the rBCS without re-irradiation (38% vs 25%). Since then, the majority of published studies on this topic are small retrospective, non-randomized cohort studies.28 ey are subject to selection bias and poor study quality. Patients receiving rBCS are more often to have better prognostic characteristics compared with those treated with mastec­tomy (e.g., size, multifocality, aggressive tumor biology). A recent retrospective cohort study by Kolben etal has reported data supporting the use of rBCS in selected patients.30 Of 170 patients, 34.1% of women underwent secondary BCS, whereas 65.9% were treated by salvage mastectomy. Five­year ipsilateral recurrence-free rate after secondary BCS was
77.6% (Standard Deviation (SD) ± 6.1%) and 75.0% (SD ± 4.5%) for patients after mastectomy. Five-year disease­free survival was 57.3% (SD ± 8.2%), and 61.9% (SD ±
5.5%); 5-year overall survival was 84.7% (SD ± 5.8%), and
72.6% (SD ± 5.1%), respectively. Ishitobi etal reported a 20% local recurrence rate following rBCS alone.31 Survival rates following rBCS compared with salvage mastectomy are conicting. Alpert etal reported a 64.5% survival rate
at 10 years with no signicant dierence between salvage mastectomy and rBCS observed in 271 patients undergo­ing rBCS or mastectomy for recurrence (55% vs 45%).32 Yoshida et al reported no signicant dierence in overall survival between the two surgical approaches after adjust­ment for clinical and tumor characteristics.33 In contrast, Chen etal observed signicantly better survival rates at 5 years following salvage mastectomy when compared with rBCS (78% vs 67%, p = 0.003).
34
Kurtz et al reported risk factors associated with second­ary recurrence following rBCS alone.35 rough multivariate analysis, the group reported that the disease-free interval to recurrence and resection margins signicantly inuence local control following rBCS. Five-year local control was 92% for recurrences occurring after 5 years versus 49% for shorter inter­vals, and 73% for negative margins versus 36% for positive or indeterminate margins. e authors concluded that wide exci­sion represents an alternative to mastectomy in salvage treat­ment for selected patients with mobile tumors, 2 cm or smaller in diameter, and no signs of rapid growth.35 Prior adjuvant sys­temic therapy, skin or muscle inltration, and lymphovascular inltration in the breast recurrence are additional risk factors for shorter disease-free survival following rBCS.
30
Re-irradiation following rBCS is an emerging concept in the treatment of recurrence, although it remains in an experi­mental phase. Repeat irradiation to the resected breast cavity following rBCS is a technique applied to reduce secondary local recurrences rst reported in the 1990s.36 Ishitobi etal reported 5-year second recurrence survival rates are improved with post-rBCS radiotherapy; radiotherapy after initial sur­gery, radiotherapy after salvage surgery, and no radiotherapy were 78.0%, 93.5%, and 52.7%, respectively.31 ere is no consensus regarding the optimal treatment for patients who have previously had BCS with irradiation. e normal tis­sue tolerance does not permit a second full-dose course of radiotherapy to the entire breast after a second BCS. Re­irradiation to the entire breast is poorly tolerated due to poor cosmetic outcome and high toxicity rates.37 New modes of delivering focal radiotherapy to the breast have raised the pos­sibility of localized radiation therapy for women post-rBCS. Accelerated partial breast irradiation (APBI) is proposed as an alternative to whole breast re-irradiation. APBI limits irra­diation to the target area post-wide local excision plus 1–2 cm margin of tissue in a shorter time period while delivering equivalent doses to whole breast irradiation.37 A number of techniques are reported including multicatheter interstitial brachytherapy (IB), balloon catheter brachytherapy, intraop­erative radiation therapy (IORT), and external beam irradia­tion (EBI). A recent Cochrane review summarizing evidence for partial breast irradiation (PBI) and APBI for treatment of primary breast cancer versus whole breast radiotherapy highlighted the limitations of the data currently available in this eld. e authors reported cosmetic outcomes and late eects were worse with PBI/APBI, but less skin toxicity was noted.38 Local recurrence was increased with PBI/APBI (the dierence was small) with no evidence of detriment in other oncologic outcomes.
38
CHAPTER 18 Local Recurrence and Reconstructive Options Following Oncoplastic Breast Surgery
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153
Studies applying this technology to recurrent breast cancer treatment following rBCS are limited to small case series, varying follow-up durations, and subject to selec­tion bias. e majority of studies report results for rBCS with brachytherapy for patients with small T0-2 recurrent lesions, no metastasis, and negative resection margins with late onset of recurrence (mean 70 months).39 Authors report EBI with 45 Gy (1.8 Gy per fraction) to rBCS is gener­ally well tolerated with low acute and late skin toxicities and good local disease control.40 e prognostic factors for favorable overall survival rates were younger age (p = 0.045), lower T category (p = 0.019), and N0 category (p = 0.005).
Hannoun-Levi etal have reported promising results for 217 women treated with multicatheter brachytherapy fol­lowing rBCS.41 Secondary local recurrence rates were 5.6% (1.5–9.5) at 5 years and 7.2% (2.1–12.1) at 10 years. Over­all survival rates for 5 and 10 years were 88.7% (83.1–94.8) and 76.4% (66.9–87.3%), respectively, and report compa­rable results to salvage mastectomy. Similar overall survival and disease-free survival rates have been reported in other small case series.
42,43
Grade 1–2 toxicities are observed in the majority of patients (skin atrophy, pigmentation, tel­angiectasia, slight induration, and loss of subcutaneous
42,44
fat).
Approximately 11% of women experience grade 3 or 4 toxicities (marked skin atrophy, gross telangiectasia, ulceration, severe brosis, eld contracture, necrosis).
42,44
e most common side eect reported from IB is cutane­ous and subcutaneous brosis (up to 60%) as a function of dose and volume, which may considerably aect overall cos­metic outcome following secondary oncoplastic surgery due to parenchymal tethering.
39,45,46
Factors aecting cosmesis include the distance of the catheter or balloon from the skin, the type of device used, the volume of residual breast tissue after rBCS, and degree of initial breast asymmetry.47 Com­plications related to device include persistent breast pain, a chronic abscess in the sinus tract of the balloon catheter, and infections of the catheter tract requiring mastectomy and antibiotics, respectively.48 Proponents of the technique report stable cosmetic scores (from excellent to good) and patient satisfaction in 60–80% of patients; however, most studies did not use standardized evaluation schemes.
39,45,48
In 2007, Kraus-Tiefenbacher etal reported on the use of IORT following rBCS.49 Fifteen patients were treated after previous EB radiotherapy after ipsilateral breast recurrence. At median follow-up, short, acute toxicity 26 months after IORT was reported as mild with no grade 3–4 toxicities in the group. Further high quality research is required to sup­port rBCS with or without re-irradiation in routine clinical practice. 
BCS and radiotherapy, and data are limited to observational studies. Decisions regarding reconstruction in this cohort should be made within a multidisciplinary team with a tailored individual approach. Options regarding the tim­ing and types of reconstruction vary considerably among surgeons, particularly in this context.
50,51
Authors empha­size the need for careful detailed assessment and discussion with patients regarding their risk factors, disease extent, reconstructive options, and personal preferences. Figs.
18.3 and 18.4 illustrate a patient diagnosed with left breast
cancer managed with oncoplasty who early on developed a recurrence managed with mastectomy and device-based reconstruction.
e majority of patients will have received radiotherapy following their initial BCS. Histological analysis of the eects of radiotherapy to breast tissue reveals considerable architectural tissue change: epidermal hyperplasia, atro­phy of dermal appendages, high density of dermal collagen bers, and unidirectional alignment of dermal collagen bers.52 In the context of prosthetic breast reconstruction, these changes are strongly associated with complications including diculty in expanding irradiated skin, grade 3 and 4 Baker capsular contracture (relative risk 3.75), and expander/implant extrusion following prosthetic recon­struction. prosthetic reconstruction in the irradiated breast is associ-
52-54
e presence of acellular dermal matrix with
ated with an increased complications rate with a 2.3-fold greater chance of reoperation.
55
Systematic reviews on radiotherapy in the context of post-mastectomy reconstruction report prosthetic recon­struction is associated with an increased reconstructive failure rate and overall complication rate when compared with autologous reconstruction.
56-59
Despite this, the fre­quency of immediate prosthetic-based reconstruction in the setting of radiation therapy is increasing.60 e detrimental eect of radiotherapy persists regardless of two-stage versus one-stage prosthetic reconstruction and the timing of the
Reconstructive Options Following Salvage Mastectomy for Recurrence
Despite international guidelines recommending salvage mastectomy following recurrence, there are no level 1 stud­ies to guide surgeons’ choice for reconstruction following
Fig. 18.3 The patient developed a local recurrence following previ-
ous breast conserving surgery and was scheduled for left skin-sparing mastectomy and tissue expander reconstruction.
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