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CHAPTER 1 Introduction to Oncoplastic Breast Surgery
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History of Oncoplasty
In an eort to reduce the incidence of local recurrence and maintain natural breast contour, the concept of oncoplastic surgery was introduced.
29,30
Oncoplastic surgery diers from standard BCT in that the margin and volume of excision is typically greater than that of lumpectomy or quadrantec­tomy. With BCT, an excision margin of 1–2 mm is usu­ally sucient; whereas with oncoplastic surgery, excision margins typically range from 1–2 cm and resection volumes typically range from 100–200 cm3. e resultant deformity is usually reconstructed immediately using volume replace­ment or displacement techniques; however, a staged imme­diate reconstruction can also be considered. Reconstructive options include adjacent tissue rearrangement, reduction mammaplasty, or distant aps. When symmetry is desired, contralateral procedures can be performed immediately at the time of partial breast reconstruction or on a delayed basis and include reduction mammaplasty, mastopexy, or augmentation. Breast conservation using oncoplastic tech­niques has resulted in survival and local recurrence rates that are essentially equal to that of MRM.
31,32
e purpose of this introductory chapter is to review the history of these oncoplastic procedures and several of the landmark studies as well as highlight some of the sur­geons that have made signicant contributions to onco­plastic surgery. As oncoplastic surgery gains acceptance and popularity, an optimal and systematic approach to management is becoming increasingly necessary. is introductory chapter will review many of the relevant vignettes of oncoplastic surgery, and the subsequent chap­ters will expand upon many of the principles, concepts, and techniques. 
Safety and Efficacy of Oncoplastic Surgery
e indications and patient selection criteria for oncoplastic surgery is now well appreciated and accepted. Oncoplastic surgeons should be aware of all aspects related to the indi­cations, techniques, and recovery for women considering partial mastectomy. Safety in oncoplastic surgery requires an appreciation of tumor biology and an understanding of what constitutes an appropriate margin. e process begins by obtaining a diagnosis that can be accomplished using various techniques that include ne-needle aspiration, core needle biopsy, and excisional biopsy. e next step is the excision. e importance of obtaining a clear margin becomes evident when one considers that the relative risk of developing a recurrence is 15-fold higher in patients in whom the surgical margin was not clear of tumor. positive margin can be related to the size of the primary tumor (T3 > T2 > T1) and to histological subtype (lobu­lar > ductal).33 Preoperative identication of these women with inltrating lobular carcinoma who may be at higher risk of a positive surgical margin can be sometimes made via mammography based on the presence of architectural distortion.
35
33,34
A
It is known that larger tumors have an increased likeli­hood of a positive margin; therefore, obtaining wider mar­gins may decrease the likelihood of a positive margin. Kaur etal demonstrated that, as resection margins increase, the incidence of a positive margin is reduced, especially when comparing oncoplastic resection to standard quadrantec­tomy.36 Mean resection volume in this study was 200 cm3 following oncoplastic resection and 117 cm3 following quadrantectomy. Giacalone etal have demonstrated that, following oncoplastic resection, glandular removal was increased, histological margins were wider, and the need for re-excision was decreased.37 In addition, there was a trend toward fewer mastectomies following oncoplastic resection (2/42, 4.8%) compared with standard lumpectomy (12/57,
21.1%). Additional studies and supportive data will be reviewed in upcoming chapters. 
Immediate Reconstruction of the Partial Mastectomy Deformity
e techniques currently used for the reconstruction of the partial mastectomy defect are based on two dierent concepts: volume displacement and volume replacement. Volume displacement procedures include local tissue rear­rangement, reduction mammaplasty, and mastopexy. Vol­ume replacement procedures include local and remote aps from various regions of the body. ese techniques are usu­ally applied independently; however, new strategies can uti­lize them simultaneously.
e indications for volume displacement and replace­ment are dierent and, various algorithms have been devised to assist with the decision-making process.
38-40
In general, women with smaller breasts with minimal ptosis were found to be better candidates for volume replacement procedures (e.g., local ap, latissimus dorsi, and lateral thoracic ap), whereas, in women with larger and more ptotic breasts, volume displacement procedures (e.g., adjacent tissue rear­rangement, reduction mammaplasty, and mastopexy) are usually performed. e simultaneous use of replacement and displacement has recently been described for women with small to moderate breast volume in which parenchy­mal rearrangement is combined with the use of a small
41-43
device.
e history of these techniques as they relate to
oncoplastic surgery will be further reviewed. 
Volume Displacement with Reduction Mammaplasty
Reduction mammaplasty as an oncoplastic modality has been performed since the early 1980s.44 Over the years, this has become the principal method by which oncoplas­tic reconstruction has been performed. reported on their 14-year experience in 101 women who were selected for oncoplastic resection because a standard lumpectomy would have resulted in a signicant contour
45,46
Clough et al
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abnormality.45 e primary technique utilized was an inverted “T” with nipple–areolar complex based on a supe­rior pedicle. A contralateral reduction mammaplasty for symmetry was performed immediately in 83% of women and secondarily in 17% of women. Mean tumor excision weight was 222 grams. e 5-year local recurrence rate was
9.4%, the overall survival rate was 95.7%, and the metas­tasis-free survival rate was 82.8%. Cosmetic outcome was satisfactory in 82% of women. It was demonstrated that cosmetic outcome tended to deteriorate when radiotherapy was delivered preoperatively compared with postoperatively.
Spear et al have reported on their 6-year multidisci­plinary experience combining wide excision of tumor with immediate bilateral reduction mammaplasty.47 All women had mammary hypertrophy with a mean exci­sion volume of 1085 grams per breast. Follow-up ranged from 1–6 years with a mean of 24 months. Complications included fat necrosis (n = 3), nipple hypopigmentation (n = 2), hematoma, and complex scar. Patient satisfaction was scored on a visual analog scale that ranged from 1–4 with a mean score of 3.3. A panel of independent observ­ers also graded the outcomes and scored the pre-radiation outcome as a 2.9 and the post-radiation outcome as 3.03. No woman developed a local recurrence, although one woman died of metastatic disease. e principal con­clusions from this study were that partial mastectomy followed by oncoplastic and contralateral reduction mam­maplasty was oncologically safe and avoided the asymme­try that was typically observed following BCT alone or following total mastectomy with immediate total breast reconstruction.
Losken etal have reported on their 10-year experience utilizing reduction mammaplasty in the setting of onco­plastic surgery.
39,48
A total of 20 women were included in this review. Mean tumor size was 1.5 mm, and the mean weight of the tumor specimen was 288 grams. e excised surgical margins were negative in 80%. e most common reduction technique was a superomedial or inferior pedicle. Postoperative abnormal mammograms were noted in eight women (40%), all of whom under­went additional biopsy. No woman was noted to have a recurrence with a mean follow-up of 23 months. Breast aesthetics and patient satisfaction were acceptable in all women.
ese studies and others have demonstrated the utility of reduction mammaplasty in the setting of oncoplastic sur­gery. It is important to note that no two oncoplastic reduc­tion procedures are the same and that oncoplastic reductions are dierent from standard breast reductions. Parenchymal displacement may take the form of a ap of vascularized parenchyma or as parenchymal rotation advancement. If there is doubt about obtaining a clear margin at the time of the primary excision, a staged immediate reconstruction can be performed following margin conrmation. Figs. 1.1–1.2 illustrate a patient before and after oncoplastic reduction mammaplasty. 
Fig. 1.1 Preoperative marking of a woman with mammary hypertro-
phy and left breast cancer in preparation for left oncoplasty and right reduction mammaplasty.
Fig. 1.2 Postoperative image at 1 year following left breast radiation
therapy demonstrating good volume, contour, and symmetry.
Volume Displacement with Adjacent Tissue Rearrangement
Adjacent tissue rearrangement is the most common method by which the partial mastectomy defect is reconstructed. ese techniques rarely require a two-team approach, as the ablative surgeon is usually able to use these techniques and close these defects. Adjacent tissue rearrangement is indi­cated when the partial deformity extends to the chest wall and there is sucient adjacent tissue to close the defect and maintain a natural contour. Volume displacement is per­formed but without the need to create parenchymal aps. Volume replacement is usually not necessary because there is sucient local tissue. e primary goal of adjacent tis­sue rearrangement is to avoid the contour deformity that is sometimes seen with traditional breast conservation. With this method of oncoplastic reconstruction, the excision is
usually extended to the chest wall, and the adjacent paren-
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chyma is undermined and mobilized to permit the closure of small or large deformities without creating a contour abnormality.
Specic parenchymal rearrangement procedures include batwing mastopexy, radial segment quadrantectomy, donut mastopexy, and reduction mastopexy. Veronesi etal intro­duced the concept of segmental parenchymal wide exci­sion including the overlying skin.49 is allowed for the quadrantectomy approach that was instrumental in estab­lishing the feasibility of BCT. ese operations were gener­ally performed using a radial approach for tumors that were laterally based. An alternative to the radial approach was the periareolar approach initially described by Amanti etal.50 is permitted excisions that resulted in less conspicuous scars. With the introduction of the periareolar subcutane­ous quadrantectomy, also known as the periareolar donut mastopexy, incisions could be created circumferentially around the nipple–areolar complex and remain relatively inconspicuous. Anderson et al. introduced various concepts that include skin incisions using a parallelogram pattern and batwing mastopexy.44 ese parallelogram incisions allowed for wider excision margins while maintaining the natural contour of the breast. e batwing mastopexy is an exten­sion of this concept and is used primarily for centrally situ­ated tumors near the nipple–areolar complex. Clough et al introduced the technique of reduction mastopexy lumpec­tomy.45 is technique has been especially useful for tumors situated near the lower pole of the breast. Standard lumpec­tomy of these tumors would often result in an inferiorly displaced nipple–areolar complex. 
Volume Replacement with Local and Remote Flaps
Local and remote aps for volume replacement are most useful for defects in which volume displacement procedures would not be adequate due to small breast volume or due to extensive resection. e selection of a local or remote ap will depend upon the abilities of the reconstructive surgeon and the location of the defect. Flaps can be musculocutane­ous and perforator-based and can be transferred on a vas­cularized pedicle or as a free tissue transfer. Many of these options will be reviewed in the subsequent chapters. What is provided in this chapter is a brief overview of the techniques and their origins.
e most common ap for immediate reconstruction following partial mastectomy has been the latissimus dorsi musculocutaneous ap. deformities of the superior, lateral, and inferior aspects of the breasts. ere are several methods by which the latissimus dorsi ap can be harvested. e traditional technique involves making a posterolateral thoracic inci­sion, whereas more modern techniques utilize an endo-
53,56
scope.
With the endoscopic technique, the muscle is
accessed through the breast and axillary incision without
51-56
is ap is indicated for
CHAPTER 1 Introduction to Oncoplastic Breast Surgery
Fig. 1.3 A lower pole defect is demonstrated following partial mas-
tectomy.
the need to incise or excise remote skin. Kat etal have reviewed their 3-year experience in 30 women who had oncoplastic surgery using the latissimus dorsi musculocu­taneous ap.52 Flap survival was 100%, and all patients were pleased with aesthetic outcomes. Losken etal have reviewed their 5-year experience using the latissimus dorsi muscle ap harvested endoscopically in 39 women.53 Donor site morbidities occurred in 12 women (31%) and included a seroma in 7 women as well as skin necrosis, lymphedema, dehiscence, hypertrophic scarring, and a persistent sinus tract.
Harvesting the latissimus dorsi as a mini-ap is advan­tageous because the size of the ap can be tailored to t the size of the defect.
54,55
e LD mini-ap is generally harvested through an extended anterolateral breast inci­sion that is used for the resection as well. Rainsbury has demonstrated that this ap extends the role of BCT and oncoplastic surgery; enables reconstruction for a deformity involving 20–30% of the breast; can be used for central, upper inner, and upper outer quadrant tumors; and can be performed immediately or on a delayed basis.55 Gendy etal have used the latissimus dorsi mini-ap for oncoplasty in 89 women and compared outcomes with immediate breast reconstruction following total skin-sparing mastec­tomy.54 Findings were favorable for the oncoplastic tech­niques with regard to postoperative complications (8% vs 14%), further surgical interventions (12% vs 79%), nip­ple sensory loss (2% vs 98%), restricted activities (54% vs 73%), and cosmetic outcome (visual analog score: 83.5 vs 72). Figs. 1.3–1.6 illustrate a patient following partial breast reconstruction with a latissimus dorsi musculocu­taneous ap.
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Fig. 1.4 A latissimus dorsi musculocutaneous flap is harvested in
preparation for delayed reconstruction.
Perforator aps for partial breast reconstruction include the thoracodorsal artery perforator (TDAP) ap, the lateral thoracic ap, and the intercostal perforator ap.
57-60
e TDAP is an adipocutaneous ap in which the latissimus dorsi muscle is totally spared. e vascularity of the ap is derived from the perforating branches of the thoracodorsal artery and vein. e lateral thoracic ap is a fasciocutaneous ap that is perfused via the lateral thoracic, axillary, or tho­racodorsal artery and vein. e intercostal perforator ap is perfused via a perforating intercostal artery and vein that is based along the inferior aspect of the anterior axillary line. ese aps are usually transferred on a vascularized pedicle but may be transferred as a free tissue transfer as well.
Clinical experience with these aps has been encourag­ing. Levine et al have provided an algorithm for perfora­tor ap utilization.57 e rst choice is the TDAP ap, followed by the lateral thoracic ap, and nally the inter­costal perforator ap. e decision is based on the quality of the vessels during the operative procedure. Munhoz etal have used the lateral thoracic ap in 34 women for partial breast reconstruction.59 Complications included partial ap necrosis in three (8.8%), fat necrosis in two (5.8%), and infection in one (2.9%). Donor-site complications included a seroma in ve women (14.7%) and wound dehiscence in three (8.8%). Patient satisfaction was achieved in 88% of women with a mean follow-up period of 23 months. 
Fig. 1.5 The latissimus dorsi flap is inset into the defect.
Fig. 1.6 Postoperative follow-up demonstrating restoration of vol-
ume, contour, and symmetry.
Combining Volume Displacement and Replacement
A relatively recent innovation in the oncoplastic armamen­tarium is to combine volume displacement and replacement simultaneously. women with smaller breasts who desire oncoplasty but seek an alternative to the classical volume replacement techniques described. Alternatives to the use of mini-aps or perforator aps can include the use of devices, namely implants, but also resorbable materials that are available as three-dimensional constructs that have been used for radiation imaging.
e biplanar oncoplasty was initially described by Nahabedian et al. and Miraliakbari et al, and incorporates the use of breast implants or tissue expanders placed under the pectoralis major muscle as well as parenchymal rear­rangement that occurs above the pectoralis major mus­cle, hence, the name biplanar oncoplasty. prosthetic devices such as breast implants in the setting of oncoplasty and radiation therapy has historically resulted in higher complication rates such as capsular contracture, pre­mature removal, and decreased patient satisfaction. How­ever, the increased use of prosthetic devices coupled with the use of acellular dermal matrices in the setting of radia­tion therapy has reduced the incidence of capsular contrac­ture and made the biplanar technique more feasible. Barnea etal will discuss this operation in greater detail in one of the later chapters. Figs. 1.7–1.10 illustrate a patient following simultaneous volume displacement and replacement using a prosthetic device.
41-43
is technique is primarily indicated in
41-42
e use of
Fig. 1.7 Preoperative image of a patient with multifocal breast cancer
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scheduled for partial mastectomy.
CHAPTER 1 Introduction to Oncoplastic Breast Surgery
Fig. 1.9 One-week follow-up in which the defect was reconstructed
with a biplanar technique consisting of tissue rearrangement and placement of a 180mL subpectoral silicone gel implant.
7
Fig. 1.8 The 201-gram specimen is excised.
A second option that incorporates volume displacement and replacement simultaneously utilizes an entirely dierent prosthetic device called BioZorb®.
61,62
is is an implant­able, resorbable, three-dimensional coil that is used to mark the site of tumor extirpation for radiation therapy localiza­tion. Its other benet is that it can behave like a ller mate­rial to act as a volume replacement device. e dierence between this approach and the biplanar approach is that the volume replacement and displacement occur above the pec­toralis major muscle. Following insertion of the BioZorb® device at the base of the partial mastectomy defect, paren­chymal rearrangement occurs to cover the device followed by skin closure. Contour and volume abnormalities can be minimized. Nahabedian will review this technique in a sub­sequent chapter. 
Conclusion
is introductory chapter was prepared to review the his­tory of oncoplastic surgery and to provide a framework for
Fig. 1.10 One-year follow-up demonstrating good volume, contour,
and symmetry.
the remaining chapters. All of the principles, concepts, and specic techniques will be discussed in greater detail in the forthcoming chapters.
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54. Gendy RK, Able JA, Rainsbury RM. Impact of skin sparing mas­tectomy with immediate reconstruction and breast sparing recon­struction with miniaps on the outcomes of oncoplastic breast surgery. Br J Surg. 2003;90:433–439.
55. Rainsbury RM. Breast sparing reconstruction with latissimus dorsi miniaps. EJSO. 2002;28:891–895.
56. Monticciolo DL, Ross D, Bostwick 3rd J, etal. Autologous breast reconstruction with endoscopic latissimus dorsi musculosubcuta­neous aps in patients choosing breast-conserving therapy: mam­mographic appearance. Am J Roentgenol. 1996;167:385–389.
57. Levine JL, Soueid NE, Allen RJ. Algorithm for autologous breast reconstruction for partial mastectomy defects. Plast Reconstr Surg. 2005;116:762–767.
58. Holmstrom H, Lossing C. e lateral thoracodorsal ap in breast reconstruction. Plast Reconstr Surg. 1986;577:933.
59. Munhoz A, Montag E, Arruda EG, et al. e role of the lat­eral thoracodorsal fasciocutaneous ap in immediate con­servative breast surgery reconstruction. Plast Reconstr Surg. 2006;116:1699–1710.
60. Angrigiani C, Grilli D, Siebert J. Latissimus dorsi musculocuta­neous ap without muscle. Plast Reconstr Surg. 1995;96:1608–
1614.
61. Harms S, Lebovic G, Kaufman CS, Cross M. Mammographic imaging after partial breast reconstruction: impact of a bioab­sorbable breast implant. J Clin Oncol. 2015;33(28):111.
62. Wiens N, Torp L, Wol B, et al. Eect of BioZorb® surgical marker placement on post-operative radiation boost target vol­ume. Int J Radiat Oncol. 2018;7:175–179.
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Safety of Oncoplastic Breast Reconstruction
PETER W. THOMPSON AND GRANT W. CARLSON
Introduction
Historically, early stage breast cancer has been treated with either mastectomy or breast conservation therapy (local tumor excision with adjuvant radiation therapy). Clinico­pathologic characteristics such as tumor size and extent of breast involvement determine patient suitability for one approach or the other. Landmark prospective studies have shown that these two approaches have equivalent disease­free and overall survival.
Total mastectomy can be a cosmetically deforming and psychologically taxing procedure. Breast reconstruction fol­lowing mastectomy involves use of prosthetic techniques or harvesting autologous tissue from distant sites to recreate a breast mound. Breast conservation is therefore appealing in its potential to preserve the native breast mound; however, an acceptable cosmetic result is not guaranteed. Up to 40% of patients who undergo breast conservation have had an unacceptable cosmetic result.
Oncoplastic techniques utilize plastic surgical methods of volume displacement and replacement to achieve the pri­mary goal of negative surgical margins as well as the sec­ondary goal of optimal aesthetic result and breast symmetry. Oncoplastic breast conservation has become an increasingly common technique compared with traditional breast con­servation over the last 10 years by facilitating reconstruc­tion after larger volume resections.3 Oncoplastic surgery has greatly expanded the group of patients who may be can­didates for breast conservation, and studies using validated questionnaires have demonstrated excellent levels of patient satisfaction.4 Concerns regarding the oncologic safety of these techniques have increased, mirroring their rising popularity. Safety data pertaining to oncoplastic breast sur­gery are limited by a lack of prospective data and long-term follow-up.
When discussing reconstructive options with pati ents, oncologic risks and benets should be reviewed. With
1
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oncoplastic procedures, appropriate patient counseling re­quires attention to several important clinical questions:
• Do oncoplastic techniques aect the rate of positive margins in breast conservation, and how should positive margins be managed?
• Do oncoplastic techniques aect the rate of local recur­rence, disease-free survival, and overall survival?
• Does oncoplastic surgery result in a higher incidence of complications?
• Does oncoplastic surgery aect the delivery of radiation or future surveillance of breast cancer? In this chapter, the available data to answer these impor-
tant questions will be reviewed. 
Margins in Oncoplastic Surgery
e three goals of breast conservation therapy (BCT) are to remove the primary tumor, decrease breast tumor recur­rence, and optimize cosmesis. Positive margins have been clearly shown to be a risk factor for local recurrence, but until recently there was no consensus as to what constitutes a “negative” margin. Based on a meta-analysis of 33 stud­ies reporting on more than 32,000 patients, the Society for Surgical Oncology and American Society of Radiation Oncology released a joint guideline dening a negative margin as “no ink on tumor.”5 ere was no evidence that obtaining a wider margin, such as a threshold of >2 mm or >5 mm, resulted in a lower rate of local recurrence. is recommendation is important when considering an onco­plastic breast conservation procedure, which is often oered to patients with larger tumors who might not be good can­didates for standard breast conservation. In a meta-analysis of more than 8500 patients published in 2014, Losken etal compared the outcomes of patients who had undergone standard breast conservation with patients who had under­gone immediate breast reconstruction using oncoplastic techniques. ey found that, despite overall signicantly
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CHAPTER 2 Safety of Oncoplastic Breast Reconstruction
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larger tumor size and lumpectomy specimen weight in the oncoplastic group, the overall positive margin rate was sig­nicantly lower in the oncoplastic group compared with the standard breast conservation group (12% vs 21%).6 An acceptably low positive margin rate following oncoplastic breast conservation has been conrmed in multiple stud­ies, ranging from 0–21% according to a recent systematic review published by Piper etal.
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One concern voiced by critics about oncoplastic breast conservation techniques, which utilize volume displace­ment and parenchymal rearrangement to ll the empty space created by tumor excision, is that the architecture and orientation of the lumpectomy cavity becomes dis­torted. is has the potential to make identication and re-excision of previous surgical margins more dicult, and in these cases completion mastectomy may be necessary to achieve negative surgical margins. Data from Piper etal suggest that the overall rates of re-excision and comple­tion mastectomy in patients undergoing oncoplastic breast conservation are acceptably low (3.5% and 3.7%, respec­tively).7 Despite larger tumor size in patients undergoing oncoplastic breast conservation, available data comparing re-excision and completion mastectomy rates between patients undergoing oncoplastic and standard breast con­servation suggest that re-excision of positive margins is less frequently required in the oncoplastic group, whereas completion mastectomy is required at similar rates between the two groups.
6,8,9
Piper etal suggest placement of clips in the cardinal directions of the lumpectomy cavity to both facilitate re­excision in the setting of positive margins and to assist with targeting of the radiation boost. e authors make the argument that, because local tumor recurrence usu­ally occurs in the previous lumpectomy site, marking with clips also allows a second re-excision of breast tissue rather than completion mastectomy in the setting of local recurrence.
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A good understanding of factors predictive of margin positivity is necessary to properly counsel patients consider­ing breast conservation versus total mastectomy, as a nd­ing of positive margins after breast conservation will often necessitate additional surgery. In a retrospective review by Clough etal of 272 patients undergoing oncoplastic BCT, the only factor predictive of margin positivity after multi­variate analysis was invasive lobular tumor histology.10 A retrospective review by Amabile etal looking at 129 patients undergoing oncoplastic breast surgery further identied obesity, tumor multifocality, and the presence of microcal­cications on mammogram as predictive of the need for re-excision.
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In summary, oncoplastic breast conservation techniques can be oered to patients with acceptable rates of margin positivity compared with standard breast conservation; however, proper patient selection is essential, as margin positivity is one of the primary factors predictive of local recurrence. 
Local Recurrence, Distant Recurrence, Disease-Free Survival, and Overall Survival Following Oncoplastic Breast Conservation
e primary determinant of the safety and applicability of any oncologic procedure is its eect on recurrence and survival. As mentioned previously, the ecacy of BCT as a treatment for early stage breast cancer has been established by landmark studies demonstrating equivalent disease-free and overall survival compared with mastectomy.1 As onco­plastic modications of standard breast conservation tech­niques have only become a mainstream treatment option in the last 10–15 years, long-term follow-up data evaluating safety and ecacy are less readily available. De La Cruz etal performed a systematic review of 55 articles pertaining to oncoplastic outcomes including 6011 patients with a mean follow-up of 50.5 months. Most patients included in this analysis had early-stage breast cancers with invasive ductal histology. e authors analyzed recurrence and survival out­comes for three dierent follow-up intervals. Among 871 patients with the longest follow-up (at least 5 years), the rates of overall survival, disease-free survival, local recur­rence, and distant recurrence were 93.4%, 85.4%, 6%, and
11.9%, respectively.12 e authors noted that these rates compare favorably with rates of local recurrence and overall survival after standard breast conservation, suggesting that long-term outcome is more dependent on patient factors and tumor biology than on surgical technique. Given the equivalent recurrence and survival outcomes with onco­plastic techniques, these procedures may be safely oered to most women who might also be candidates for standard breast conservation; the potential benet of improved cos­mesis with oncoplastic surgery does not appear to compro­mise cancer recurrence and survival. 
Complications Following Oncoplastic Breast Reconstruction
Preoperative counseling of patients considering oncoplas­tic breast reconstruction must also include a discussion of complications. Overall safety of the oncoplastic approach can be considered in comparison to standard breast con­servation, in comparison to bilateral breast reduction, or in comparison to total mastectomy with reconstruction. All of these analyses have been performed with a nding of favor­able complication proles for oncoplastic reconstruction. e overall complication rate of oncoplastic reconstruction ranges from 14–16% in systematic review and meta-anal­ysis of the literature. vary depending on publication but include delayed wound healing, fat necrosis, infection, nipple necrosis, seroma, and hematoma; these complications vary in incidence from <1–4%.
7,12
Complications requiring operative intervention
make up on average around 3% of all complications.
6,12
e most common complications
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SECTION I Oncoplastic Breast Surgery – Getting Started
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Compared with standard breast conservation with lum p ­ectomy, oncoplastic techniques may have a comparable or slightly lower rate of complications. In a National Surgical Quality Improvement Program (NSQIP) database analy­sis of nearly 76,000 patients undergoing BCT, the overall 30-day rate of complications in patients undergoing onco­plastic breast surgery was 1.7% compared with 1.9% in patients undergoing standard breast conservation.14 In their meta-analysis of oncoplastic breast reconstruction with an average follow-up of 37 months, Losken etal found that the overall rate of complications was 15.5% in the oncoplastic group compared with 25.9% in the standard breast con­servation group, albeit with a shorter follow-up period in the oncoplastic group.6 Lower rates of seroma in oncoplas­tic reconstructions compared with standard breast conserva­tion may be attributable to lling of the lumpectomy cavity by displacement and rearrangement of the remaining breast parenchyma in a way that obliterates the dead space.
3
Oncoplastic reconstruction also appears to have a lower rate of complications compared with total mastectomy and reconstruction. In their retrospective cohort study includ­ing more than 9800 patients with breast cancer, Carter etal found that patients undergoing oncoplastic reconstruction had a lower rate of hematoma, infection, and wound heal­ing complications compared with patients who underwent total mastectomy and reconstruction.3 Losken etal demon­strated that, in a population of breast cancer patients with macromastia, patients who underwent total mastectomy with reconstruction by either implant-based or autologous methods had nearly twice the overall rate of complications compared with patients who underwent oncoplastic recon­struction (22% vs 43%).15 is dierence is at least par­tially attributable to risks associated with implants as well as donor-site complications, although in women with very large breasts, the potential for seroma, hematoma, infection, and contour deformities are greater when a reconstruction must ll a larger mastectomy cavity.
e oncoplastic reconstruction approach often involves a contralateral mastopexy or reduction for symmetry on the non-cancer breast. In this instance, the nal result is aesthetically similar to a bilateral reduction mammaplasty performed for symptomatic macromastia. In a prospective evaluation of patients undergoing bilateral breast reduction either with or without breast cancer, the overall rate of com­plications was similar (18.8% for oncoplastic group, 18.3% for breast reduction group). Seroma was the most common complication in both groups at around 5–6%. Interestingly, approximately 50% of the complications in the oncoplastic group occurred in the non-cancer breast.16 From this, the authors conclude that oncoplastic reconstruction with con­tralateral reduction has a safety prole similar to a standard bilateral breast reduction.
Surgical complications immediately following oncoplastic breast reconstruction can negatively aect oncologic outcome by delaying the administration of adjuvant therapies. Data directly analyzing timing of adjuvant therapies following
oncoplastic reconstruction are limited; most of the available evidence, although lacking in detail, supports the claim that complications following oncoplastic reconstruction have min­imal eect on timing of delivery of adjuvant therapy.
6,13,16
In contrast, one retrospective institutional review published by Hillberg etal examined outcomes of 150 patients undergoing oncoplastic breast reconstruction performed by a single sur­geon; the authors reported that 8.2% of patients experienced a delay in receiving adjuvant radiation due to a complication. ese results may be aected by a higher than expected over­all complication rate in this series (37.5%).17 Similarly, evi­dence that oncoplastic reconstruction delays administration of adjuvant chemotherapy is lacking. A retrospective review of 169 breast cancer patients performed by Khan etal dem­onstrated no dierence in time to initiation of adjuvant che­motherapy whether standard breast conservation, oncoplastic breast conservation, mastectomy alone, or mastectomy with immediate reconstruction was performed.
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Appropriate patient selection for oncoplastic reconstruc­tion includes identication of patients at increased risk for postoperative complications. In their NSQIP database analysis, Cil etal identied several factors that were inde­pendently associated with an increased risk of postopera­tive complication in the 30-day period.14 ese included obesity, smoking, American Academy of Anesthesiologists (ASA) category 3 or 4, diabetes, bleeding disorder, chronic obstructive pulmonary disease (COPD), and a longer oper­ative time. Of these, the presence of a bleeding disorder had the highest association with postoperative complications (odds ratio 1.8). Multiple other studies have identied ele­vated body mass index (BMI) as a risk factor for postopera­tive complications.
16
In summary, patients who undergo oncoplastic recon­struction have a favorable complication prole compared with patients undergoing standard breast conservation or other methods of reconstruction. Oncoplastic techniques do not appear to negatively aect timing of radiation deliv­ery. Appropriate technique and patient selection are crucial to minimize postoperative morbidity. 
Cancer Surveillance Following Oncoplastic Reconstruction
Oncoplastic breast conservation techniques by denition preserve the majority of the breast parenchyma; therefore, ongoing mammographic surveillance of the remaining breast tissue is crucially important to detect cancer recur­rence. Critics of oncoplastic reconstruction have voiced concerns that distortion of parenchymal architecture and more extensive postsurgical changes compared with stan­dard breast conservation may negatively aect the early detection of local tumor recurrence. Oncoplastic breast reconstruction combines time-tested techniques of stan­dard breast conservation and breast reduction. e mam­mographic changes following these procedures are well
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