Extreme Oncoplastic Surgery for Multifocal/Multicentric and Locally Advanced Breast Cancer

Koppiker, Chaitanyanand B.; Noor, Aijaz Ul; Dixit, Santosh; Busheri, Laleh; Sharan, Gautam; Dhar, Upendra; Allampati, Hari Kiran; Nare, Smeeta

doi:https://doi.org/10.1155/2019/4262589

International Journal of Breast Cancer

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Abstract Introduction Methods Results Discussion Conclusion Data Availability Ethical Approval Consent Conflicts of Interest Acknowledgments Supplementary Materials References Copyright Related Articles

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Volume 2019 | Article ID 4262589 | https://doi.org/10.1155/2019/4262589

Extreme Oncoplastic Surgery for Multifocal/Multicentric and Locally Advanced Breast Cancer

Chaitanyanand B. Koppiker,¹Aijaz Ul Noor,¹Santosh Dixit,¹Laleh Busheri,¹Gautam Sharan,²Upendra Dhar,¹Hari Kiran Allampati,³and Smeeta Nare¹

Academic Editor: Vladimir F. Semiglazov

Received28 Oct 2018

Accepted27 Dec 2018

Published20 Feb 2019

Abstract

Introduction. Breast conserving surgery (BCS) followed by radiation therapy (RT) has become the preferred alternative to mastectomy for patients with early stage breast cancer (BC). Randomized trials have confirmed equivalent locoregional control and overall survival for BCS and mastectomy. Extreme Oncoplasty (EO) extends the indications of BCS for patients who would otherwise require mastectomy, ensuring better aesthetic outcomes and oncological safety. Methods. BC patients with multifocal/multicentric (MF/MC) tumors, extensive DCIS, or large tumor >50mm underwent EO at our breast unit. Therapeutic reduction mammaplasty (TRM) with wise pattern preoperative markings and dual pedicle technique involving parenchymal rearrangement was used for oncoplastic reconstructions in majority of the cases followed by RT. Patient reported outcome measures (PROMs) were assessed using the validated Breast-Q questionnaire. Results. Of the 39 patients in the study, 36 had unilateral and 3 had bilateral BC. Mean age was 47.2 years. Median tumor size was 75mm. 17 (43.6%) patients received NACT; none achieved a complete clinical response. 28 (71.8%) patients were administered to adjuvant chemotherapy. 33(84.6%) patients received RT to the breast with a median dose of 50Gy in 28 fractions and a boost dose of 10Gy in 5 fractions to the tumor bed. No major complications or local recurrences were observed. Excellent Breast-Q scores were observed in patients undergoing EO after 12 months of follow-up. Conclusion. EO followed by RT results in acceptable local-regional control, low rate of complications, and high patient satisfaction. In selected patients, EO could provide a safe alternative for breast conservation surgery instead of mastectomy.

1. Introduction

Breast conservation therapy (BCT) which includes breast conservation surgery (BCS) and adjuvant radiation therapy (RT) is a standard protocol to achieve high local control with acceptable aesthetic outcomes [1–3]. Multiple prospective randomized trials [4], some with a follow-up of 20 years, have established equivalent survival rates between mastectomy and breast conservation surgery (BCS) with negative margins. Recent studies from various countries including India indicate that women treated with BCT have a significant survival advantage when compared to mastectomy [5–7].

At present, breast surgeons are attempting to extend the scope of breast conservation so as to include scenarios which are otherwise contraindicated for BCS particularly in multicentric (MC) or multifocal (MF) tumors. Clinical management of MF/MC breast tumors is a challenge since the choice of optimal surgical approach is controversial. Previously, mastectomy was considered as the standard choice [8–10]. However, significant local recurrence rates (2.5% to ~40%) have limited the utility of mastectomy in such scenarios [11–15].

In contrast, breast cancer (BC) patients with large T2 and T3 tumors (size range: 40-120mm) who underwent BCT were shown to have acceptable cosmesis without compromising locoregional control or survival [16]. In the last decade, oncoplastic breast surgery (OBS) has emerged as an integrated approach to achieve optimal oncological outcomes and cosmesis. This approach allows tumor excision with wider margins during BCS without compromising the aesthetic outcome [17]. In addition, OBS has shown comparable oncological efficacy with conventional BCS in achieving adequate surgical margins and recurrence rates [18–21].

In recent years, the technique of “Extreme Oncoplasty” (EO) has emerged as a promising option in selective patients with adequate breasts (cup size ≥ C) where in BCS is possible inspite of large volume resections [22]. Indeed, EO could be used to conserve breasts in scenarios for which mastectomy would be have been the treatment of choice offered by most surgeons. These situations include (a) tumor size >50 mm, (b) MF and MC tumors, (c) extensive ductal carcinoma in situ (DCIS), (d) extensive intraductal component > 50 mm, (d) previously irradiated breast with a new or recurrent cancer within the same breast, (e) a locally advanced breast carcinoma with limited or partial imaging response to neoadjuvant chemotherapy (NACT), and (f) patient with excision biopsy with inappropriate scar [22, 23]. Thus, EO provides an alternative to mastectomy, extends the scope of breast conservation, provides better clinical outcomes, and improves quality of life (QoL) [22].

There are very few reports in the literature which describe the application of the EO technique in BC management. Therefore, the aim of this study is to analyze the clinical, postsurgical, and patient satisfaction outcomes in an EO study cohort at our breast unit. In this report, we describe our experience in a series of 39 BC patients who underwent EO using wise pattern/vertical scar therapeutic reduction mammaplasty (TRM) technique.

2. Material and Methods

2.1. Surgical Technique

Our EO surgery technique encompasses excision of large volume of the breast dictated by the extent of tumor. This is facilitated by the technique of Therapeutic Reduction Mammoplasty (TRM) which is performed either by a wise pattern and/or vertical scar skin pattern. In some patients, the central wedge excision with immediate nipple reconstruction (wise pattern) and in few patients nipple areolar grafting was performed. In exceptional cases, lateral mammaplasty techniques were used.

The surgery begins by marking out the wise pattern. The next step is to localize the tumor and excise it with wide margins by going through one of the limbs of the wise pattern. This localization is performed either preoperatively by stereotactic guide-wire placement or by placement of wire and needle on the operating table using a high resolution ultrasonography. The tumor and its quadrant are then widely excised and further imaging of the specimen is performed using specimen mammography to ensure that the tumor is excised with wide margins. After this step, the shaved margins of the cavity are further excised and sent for frozen sections. Once clarity about the tumor margins of the excision cavity is achieved, the decision is made to use one of the pedicles for carrying the nipple areolar complex (NAC) and filling in the defect by appropriate mobilization of the internal local breast flaps.

Most of the cases in our study cohort have been operated using the dual pedicle technique. NAC was carried on superior pedicle and the inferior pedicle was used to fill the defect caused by excision of the tumor.

2.2. Patient Selection

This is a single institutional study involving retrospective analysis of prospectively collected data. During the study duration, a total of 42 BC patients with large breasts having either MF/MC or large tumor (>50 mm) or previous oddly placed large scar or extensive DCIS were included. All patients were initially recommended to have a mastectomy but agreed to breast conservation after appropriate counseling by the breast oncoplastic surgeon. For the purpose of this study, large breast is defined as the one with a cup size of C or larger. Written informed consent was obtained from all patients for collection of study-relevant medical data inclusive of clinical management and routine follow-up visits. Data collection included demography, medical history, clinicopathological characteristics, details of adjuvant therapy, surgical intervention, postsurgery complications, and follow-up details.

Out of these 42 patients, 39 completed one-year postsurgery follow-up and were analyzed for surgical outcomes and patient reported outcome measures (PROMs).

2.3. Clinical Management

BC diagnosis was based upon clinical examination and radiological evaluation of breast and axilla using Full Field Digital Mammography (FFDM) with 3-D Tomosynthesis (Siemens Mammomat Inspiration™) and Ultrasonography (Siemens Acuson S2000™). Histopathological studies on Tru-Cut biopsy samples (majority of cases) or vacuum assisted biopsy (for index tumors, Encor Ultra™) samples were performed for confirming diagnosis of breast carcinoma. Similarly, ultrasonography and fine needle aspiration cytology were used for investigating axillary lymph node metastasis. Confirmed BC cases underwent EO surgery at a network hospital site. The oncologic management with chemoradiation protocols was undertaken by a multidisciplinary clinical team in accordance with the current NCCN guidelines.

2.4. Radiation Therapy

The Radiation Therapy (RT) dose planning was aimed at achieving a Biologically Effective Dose (BED) of 50 Gy for all patients. The breast along with the supraclavicular region (if indicated) was irradiated by 6 MV photon beams using Forward Plan Field-in-Field Intensity Modulated Radiation Therapy (F-P FiF IMRT). Two tangential fields along with multiple subfields were used for this treatment. CT images (5-mm thickness) were obtained at different transverse sections covering the region of interest with adequate margins to create a 3D image. Volume delineation (CTV, Contralateral breast, Lung and Heart) on CT images was performed on an Eclipse™ contouring station. Computerized treatment planning was performed on Eclipse™ treatment planning system (TPS) (Version 13.5.35). High energy linear accelerator (Elekta Synergy, Elekta Medical System™, UK) with 80 leaves Multileaf Collimator (MLCi) was used for tangential treatments to the breast field. RT plan was accepted if at least 95% of prescribed dose covers the 100% of planning target volume (PTV). Hot spot in PTV was accepted up to 110% of prescribed dose. Tumor bed boost, wherever indicated, was performed using either an electron portal or Simultaneous Integrated Boost (SIB) technique.

2.5. Study Assessments

Postsurgery outcomes were assessed by oncosurgeons. Complications such as hematoma, seroma, infection, skin necrosis, nipple necrosis, and wound dehiscence were recorded. Complications were classified as “major” when they required surgical intervention and “minor” when they were managed conservatively. We also noted the time between completion of the surgery and start of the adjuvant therapy to ascertain any delays in the adjuvant therapy.

2.6. PROMs

The Patient Reported Outcomes Measures (PROMs) were used to evaluate patient satisfaction and quality of life (QoL) after EO. To assess PROMs, a standardized Breast-Q questionnaire was utilized. The Breast-Q module was divided into multiple independent scales. Higher scores indicate greater patient satisfaction and functionality [24].

3. Results

3.1. Representative Case Study

A 40-year-old patient with E-cup breasts presented with a large diffuse lump in the left upper outer quadrant (UOQ). Mammogram revealed a MF/MC tumor that extended from 3 o’ clock position to 12 o’ clock position measuring 11.8 x 7.9 mm. Tru-Cut biopsy suggested DCIS of intermediate grade. Immunohistochemistry revealed ER (Estrogen Receptor)/PR (Progesterone Receptor) positive status. The patient was initially advised mastectomy but insisted on conserving her breast and sought a second opinion. Hence, TRM was planned. The tumor was localized with localization wires under mammography guidance. The patient was marked for wise pattern incision and excision of the whole UOQ was performed. Specimen mammography was performed to confirm complete removal of tumor. Shave margins were sent for frozen section evaluation and were reported negative. The skin over lower, medial, lateral, and superomedial quadrants was mobilized in the mastectomy plane and other quadrants were used to fill the defect. Since the dissected sentinel node was positive, further axillary dissections were performed through the same incision. 2/16 nodes were positive. Though the tumor location was close to the nipple, the nipple core and margins of the NAC were negative for DCIS on frozen sections. The breast tissue was reshaped and reconstructed. The NAC was used as a nipple-areola graft. The post-op histopathology revealed Grade II IDC with extensive DCIS and a lesion spanning 75 mm in UOQ. The patient received adjuvant RT, followed by electron boost to the tumor bed. The patient was counseled for adjuvant therapy and chose to have adjuvant endocrine therapy. The patient tolerated treatment well and is disease-free after 4 years post-diagnosis. The pre- and postsurgery images for this patient are depicted in Figure 1. The maximum and mean doses of RT received by the structures are tabulated in Supplementary Table 1.

(a)

(b)

(c)

(d)

3.2. Study Cohort Demography

Out of 42 EO cases, 39 patients with large breasts who had completed 12 months post-surgery follow-up were included in the study. 36 patients had unilateral and 3 had bilateral BCs. Tumors were found in the upper outer quadrant of the breast in 22 (56.4%) patients, lower outer quadrant in 06 (15.4%) patients, and lower inner quadrant in 06 (15.4%) patients. The mean age of patients at diagnosis was 46.3 years. Majority of these patients were at stages II or III. Most of the diagnosed BC cases were IDC and/or DCIS. 17 (43.6%) patients received NACT; none achieved a complete clinical response. In addition, adjuvant therapy was administered to 71.8% of patients. In the postoperative period, adjuvant chemotherapy and/or RT was administered to patients according to clinical indications. 32 (82.05%) patients received RT (Table 1).

Demographic distribution of study participants and their clinicopathological characteristics are summarized in Table 1. The median tumor size was 75mm. Clear margins were achieved in all the patients on frozen section as well confirmed on final histopathology analysis. The average margin achieved distance was 5mm. No local recurrence was observed (Table 2). None of the patients in our study cohort experienced any delays in their adjuvant therapies.

3.3. Postoperative Outcomes

There were no major postoperative complications (defined as requiring inpatient hospitalization or returning to the operating theatre). There were 3 cases of minor complications including 1 case of seroma and 2 cases of minor wound healing. All of them were treated conservatively in the outpatient settings (Table 3).

3.4. Radiation Therapy

Of the 39 patients included in this study, 32 patients underwent RT as clinically indicated. It was not possible to obtain RT-related data from the remaining 7 patients as they were lost to follow-up. While 22 of these 32 patients received RT to the whole breast alone, 10 received RT to the breast along with the supraclavicular region. Out of 32 patients, 18 patients had left-sided lesion and 14 patients had right-sided lesion. Forward Plan Intensity Modulated Radiation Therapy (IMRT) was used to treat 27 patients. 4 of the 5 patients who were treated using Volumetric Modulated Arc Therapy (VMAT) also received Simultaneous Integrated Boost (SIB). (Supplementary Table 2)

3.5. PROMs

PROMs data was collected from the study participants after 12 months postsurgery with the Breast-Q questionnaire. Out of 39 study participants, 29 (74.3%) responded to the questionnaire. These PROMs were used to assess patient reported satisfaction and QoL after EO. The results indicated improvement in the following four areas evaluated after surgery. The mean scores for BREAST-Q scales (±standard deviation) were Satisfaction with Breasts (78.0±16.6), Satisfaction with Outcome (85.7±13.7), Psychosocial Wellbeing (90.8 ± 11.5) and Sexual Wellbeing (75.8±11.7) (Table 4).

4. Discussion

BCT is considered a standard treatment option for selective BC patients with acceptable oncological safety, improved aesthetic outcomes, and better survival. In patients with large tumors, BCT is feasible if excision margins are free of tumor and an acceptable cosmesis can be obtained [3, 4, 16]. Results from NSABP-06 and EORTC-10801 trials have indicated that BCT is safe for patients with tumors >20mm [4, 25].

OBS allows tumor excision with wider resection margins and acceptable oncological and aesthetic outcomes [26]. This approach can achieve higher rates of negative margins with low local recurrence and better cosmesis. OBS has been shown to have a positive impact on QoL and self-esteem of patients. [27]. OBS technique namely TRM allows wide excision, reduced margin positivity, and better aesthetic outcome compared to conventional BCS [28–30]. Therefore, the indications for conventional BCS can be extended further for large tumors (>40mm), central quadrant and MF/MC tumors and extensive DCIS. Indeed, TRM is considered as a suitable option for OBS, especially, in women with large breasts on which wide resections can be performed [31, 32].

Given the increased risk of local recurrence, defining appropriate indication(s) for choosing BCS over mastectomy in patients with MC/MF tumors is important [8–10]. However, current indications are ambivalent. Local recurrence rates and overall survival after BCS did not differ in patients with unifocal or multifocal tumors [33]. In contrast, in selected MF/MC cases, BCS followed by adjuvant therapy was shown to be a safe alternative to mastectomy if negative surgical margins were achieved during surgery [14]. Furthermore, a recent study comparing oncological outcomes after mastectomy or BCS in patients with unifocal or MF/MC tumors shows significant increase in local recurrence rates after mastectomy [15]. Recently, the EO technique introduced by Silverstein et al. has demonstrated successful BCS outcomes and improvement in QoL in patients with MF/MC and large tumors (≥ 50mm). With this technique, the rate of local recurrence was comparable in patients with MF tumors that underwent either EO or conventional BCS.

In our study, we report the oncoplastic outcomes after EO in a single institutional cohort of 39 patients with large breasts (cup size ≥ C) with MC/MF or large tumors (≥50mm). While no major complications were observed after EO procedure, a low rate of minor complications (7.7%) was observed. The PROMs in these patients indicate better acceptance of the EO procedure with improvement in QoL. Breast-Q parameters such as satisfaction with breast, satisfaction with outcome, psychosocial wellbeing, and sexual wellbeing showed a positive trend after EO.

RT is an integral component of BCT and improves locoregional tumor control along with disease-free and overall survival [34–36]. However, RT increases the risk of postoperative complications such as severe capsular contracture in implant-based breast reconstructions [37–39]. Alternatively, autologous reconstruction can be a feasible option for patients that require PMRT [39]. However, this surgery type is associated with significant morbidity, complication, and longer hospital stay. Therefore, choice of optimal RT technique is critical in OBS to ensure satisfactory oncological outcomes with minimal postoperative complications.

Conventionally, a RT plan encompasses a total dose of 45-50 Gy in 25 daily fractions over 5 weeks followed by a boost of 10-16 Gy in 5-8 fractions. Nowadays, hypofractionated RT (dose >2 Gy per fraction) delivered in fewer fractions over a shorter treatment period is an alternative option [40]. In addition, a tumor bed boost delivered to selective patients by an electron beam of specific energy after whole breast irradiation (WBI) has been shown to improve local control, particularly, in patients <40 years [41]. Currently, newer RT techniques such as Simultaneous Integrated Boost (SIB) have been introduced to deliver boost dose concomitant to WBI, thereby reducing skin toxicity and fibrosis [42]. Indeed, in our study cohort, the 4 EO patients who received an SIB-IMRT did not develop any major complications. This observation indicates the feasibility of using SIB-IMRT for in patients who have undergone EO surgery.

Despite the promising results related to post-EO surgery outcomes and RT-associated complications, our study has a few limitations. This study only describes data from single breast unit with small number of patients (n = 39) with a 12-month postsurgery follow-up. To overcome these limitations, we are continually recruiting patients to increase the sample size and ensure long-term follow-up. In future, a multicentric study will be needed to avoid investigator bias.

5. Conclusion

The preliminary results of our study indicate that selective patients (with MF/MC or large tumors) who were initially considered for mastectomy can be alternatively treated using EO followed by RT (with an optional boost to tumor bed, if indicated). EO can be considered as a safe and feasible surgical option for such patients without compromising aesthetic outcomes.

Abbreviations (Arranged Alphabetically)

BC:	Breast Cancer
BCS:	Breast Conservation Surgery
BCT:	Breast Conservation Therapy
DCIS:	Ductal Carcinoma In Situ
EO:	Extreme Oncoplasty
IDC:	Intraductal Carcinoma
MF/MC:	Multifocal/Multicentric
NAC:	Nipple Areolar Complex
OBS:	Oncoplastic Breast Surgery
PROMs:	Patient Reported Outcome Measures
QoL:	Quality of Life
RT:	Radiation Therapy
SIB:	Simultaneous Integrated Boost
TRM:	Therapeutic Reduction Mammaplasty
UOQ:	Upper Outer Quadrant.

Data Availability

The figures and tables used to support the findings of this study are included within the article. The figures and tables used to support the findings of this study are included within the supplementary information file(s). The medical records and related data used to support the findings of this study are restricted by the Independent Ethics Committee (IEC) of the parent institute (Prashanti Cancer Care Mission) in order to protect the patient privacy. Data will be available from corresponding author upon request after approval of the IEC.

Ethical Approval

The study was approved by the Independent Ethics Committee.

All subjects gave their consent for the use of their personal and medical information including images in the publication of this study.

Conflicts of Interest

The authors declare no conflicts of interest.

Acknowledgments

The study authors would like to thank all participants who consented to participate in this study. We also acknowledge Bajaj Auto Ltd. for providing support to research activities at Prashanti Cancer Care Mission, Pune. We are grateful to the MAPI Research Trust for giving permission to use BREAST-Q (http://www.mapitrust.org). The contribution of Dr. Laxmi Shekhawat, Dr. Nutan Gangurde, Dr. Dhara Patel, and Dr. Devaki Kelkar is acknowledged. We also thank Prof. L. S. Shashidhara (Indian Institute of Science Education and Research, Pune) for suggestions and advice throughout the work. We would also like to thank management and staff of Ruby Hall Clinic, Pune, where all surgeries where performed.

Supplementary Materials

Supplementary Table 1: Dose Received by Different Structures (for Representative Case Study). Supplementary Table 2: RT data for EO Cohort. (Supplementary Materials)

References

M. Clarke, R. Collins, S. Darby et al., “Effects of radiotherapy and of differences in the extent of surgery for early breast cancer on local recurrence and 15-year survival: an overview of the randomized trial,” The Lancet, vol. 366, no. 9503, pp. 2087–2106, 2005.
View at: Publisher Site | Google Scholar
J. A. van Dongen, A. C. Voogd, I. S. Fentiman et al., “Long-term results of a randomized trial comparing breast-conserving therapy with mastectomy: european organization for research and treatment of cancer 10801 trial,” Journal of the National Cancer Institute, vol. 92, no. 14, pp. 1143–1150, 2000.
View at: Publisher Site | Google Scholar
U. Veronesi, N. Cascinelli, L. Mariani et al., “Twenty-year follow-up of a randomized study comparing breast-conserving surgery with radical mastectomy for early breast cancer,” The New England Journal of Medicine, vol. 347, no. 16, pp. 1227–1232, 2002.
View at: Publisher Site | Google Scholar
B. Fisher, S. Anderson, J. Bryant 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,” The New England Journal of Medicine, vol. 347, no. 16, pp. 1233–1241, 2002.
View at: Publisher Site | Google Scholar
S. Hofvind, Å. Holen, T. Aas, M. Roman, S. Sebuødegård, and L. A. Akslen, “Women treated with breast conserving surgery do better than those with mastectomy independent of detection mode, prognostic and predictive tumor characteristics,” European Journal of Surgical Oncology, vol. 41, no. 10, pp. 1417–1422, 2015.
View at: Publisher Site | Google Scholar
O. J. Hartmann-Johnsen, R. Kåresen, E. Schlichting, and J. F. Nygård, “Survival is better after breast conserving therapy than mastectomy for early stage breast cancer: a registry-based follow-up study of norwegian women primary operated between 1998 and 2008,” Annals of Surgical Oncology, vol. 22, no. 12, pp. 3836–3845, 2015.
View at: Publisher Site | Google Scholar
A. Nandakumar, G. K. Rath, A. C. Kataki et al., “Decreased survival with mastectomy vis-à-vis breast-conserving surgery in stage II and III breast cancers: a comparative treatment effectiveness study,” Journal of Global Oncology, vol. 3, no. 4, pp. 304–313, 2017.
View at: Publisher Site | Google Scholar
K. A. Leopold, A. Recht, S. J. Schnitt et al., “Results of conservative surgery and radiation therapy for multiple synchronous cancers of one breast,” International Journal of Radiation Oncology Biology Physics, vol. 16, no. 1, pp. 11–16, 1989.
View at: Publisher Site | Google Scholar
J. M. Kurtz, J. Jacquemier, R. Amalric et al., “Breast-conserving therapy for macroscopically multiple cancers,” Annals of Surgery, vol. 212, no. 1, pp. 38–44, 1990.
View at: Publisher Site | Google Scholar
L. D. Wilson, M. Beinfield, C. F. McKhann, and B. G. Haffty, “Conservative surgery and radiation in the treatment of synchronous ipsilateral breast cancers,” Cancer, vol. 72, no. 1, pp. 137–142, 1993.
View at: Publisher Site | Google Scholar
L. C. Cho, N. Senzer, and G. N. Peters, “Conservative surgery and radiation therapy for macroscopically multiple ipsilateral invasive breast cancers,” The American Journal of Surgery, vol. 183, no. 6, pp. 650–654, 2002.
View at: Publisher Site | Google Scholar
J. Kaplan, G. Giron, P. I. Tartter, I. J. Bleiweiss, A. Estabrook, and S. R. Smith, “Breast conservation in patients with multiple ipsilateral synchronous cancers,” Journal of the American College of Surgeons, vol. 197, no. 5, pp. 726–729, 2003.
View at: Publisher Site | Google Scholar
S. Okumura, M. Mitsumori, C. Yamauchi et al., “Feasibility of breast-conserving therapy for macroscopically multiple ipsilateral breast cancer,” International Journal of Radiation Oncology Biology Physics, vol. 59, no. 1, pp. 146–151, 2004.
View at: Publisher Site | Google Scholar
O. Gentilini, E. Botteri, N. Rotmensz et al., “Conservative surgery in patients with multifocal/multicentric breast cancer,” Breast Cancer Research and Treatment, vol. 113, no. 3, pp. 577–583, 2009.
View at: Publisher Site | Google Scholar
R. Woods, K. A. Gelmon, S. Tyldesley, H. F. Kennecke, C. Speers, and R. Yerushalmi, “Impact of mulitfocal/multicentric versus unifocal breast cancer on local recurrence,” Journal of Clinical Oncology, vol. 28, no. 15, pp. 514–514, 2010.
View at: Publisher Site | Google Scholar
P. Romestaing, Y. Lehingue, C. Carrie et al., “Role of a 10-Gy boost in the conservative treatment of early breast cancer: results of a randomized clinical trial in Lyon, France,” Journal of Clinical Oncology, vol. 15, no. 3, pp. 963–968, 1997.
View at: Publisher Site | Google Scholar
G. Zucca-Matthes, A. Manconi, R. A. da Costa Viera et al., “The evolution of mastectomies in the oncoplastic breast surgery era,” Gland Surgery, vol. 2, no. 2, pp. 102–106, 2013.
View at: Google Scholar
K. B. Clough, M. Soussaline, F. Campana et al., “Mammoplasty combined with irradiation: conservative treatment of cancers located in the lower quadrants,” Annales de Chirurgie Plastique Esthétique, vol. 35, no. 2, pp. 117–122, 1990.
View at: Google Scholar
I. Cothier-Savey, Y. Otmezguine, E. Calitchi et al., “Value of reduction mammoplasty in the conservative treatment of breast neoplasm. A propos of 70 cases,” Annales de Chirurgie Plastique Esthétique, vol. 41, no. 4, pp. 346–353, 1996.
View at: Google Scholar
J. Y. Petit, M. Rietjens, C. Garusi, M. Greuze, and C. Perry, “Integration of plastic surgery in the course of breast-conserving surgery for cancer to improve cosmetic results and radicality of tumor excision,” Recent Results in Cancer Research, vol. 152, pp. 202–211, 1998.
View at: Google Scholar
S. L. Spear, C. V. Pelletiere, A. J. Wolfe, T. N. Tsangaris, and M. F. Pennanen, “Experience with reduction mammaplasty combined with breast conservation therapy in the treatment of breast cancer,” Plastic and Reconstructive Surgery, vol. 111, no. 3, pp. 1102–1109, 2002.
View at: Publisher Site | Google Scholar
M. J. Silverstein, N. Savalia, S. Khan, and J. Ryan, “Extreme oncoplasty: breast conservation for patients who need mastectomy,” The Breast Journal, vol. 21, no. 1, pp. 52–59, 2015.
View at: Publisher Site | Google Scholar
K. B. Clough, J. S. Lewis, B. Couturaud, A. Fitoussi, C. Nos, and M.-C. Falcou, “Oncoplastic techniques allow extensive resections for breast-conserving therapy of breast carcinomas,” Annals of Surgery, vol. 237, no. 1, pp. 26–34, 2003.
View at: Publisher Site | Google Scholar
A. L. Pusic, A. F. Klassen, A. M. Scott, J. A. Klok, P. G. Cordeiro, and S. J. Cano, “Development of a new patient-reported outcome measure for breast surgery: the BREAST-Q,” Plastic and Reconstructive Surgery, vol. 124, no. 2, pp. 345–353, 2009.
View at: Publisher Site | Google Scholar
S. Litière, G. Werutsky, I. S. Fentiman et al., “Breast conserving therapy versus mastectomy for stage I-II breast cancer: 20 year follow-up of the EORTC 10801 phase 3 randomised trial,” The Lancet Oncology, vol. 13, no. 4, pp. 412–419, 2012.
View at: Publisher Site | Google Scholar
L. Mansfield, A. Agrawal, and R. I. Cutress, “Oncoplastic breast conserving surgery,” Gland Surgery, vol. 2, no. 3, pp. 158–162, 2013.
View at: Google Scholar
D. F. Veiga, J. Veiga-Filho, L. M. Ribeiro et al., “Quality-of-life and self-esteem outcomes after oncoplastic breast-conserving surgery,” Plastic and Reconstructive Surgery, vol. 125, no. 3, pp. 811–817, 2010.
View at: Publisher Site | Google Scholar
N. Kaur, J.-Y. Petit, M. Rietjens et al., “Comparative study of surgical margins in oncoplastic surgery and quadrantectomy in breast cancer,” Annals of Surgical Oncology, vol. 12, no. 7, pp. 539–545, 2005.
View at: Publisher Site | Google Scholar
P.-L. Giacalone, P. Roger, O. Dubon, N. El Gareh, J.-P. Daurés, and F. Laffargue, “Lumpectomy vs oncoplastic surgery for breast-conserving therapy of cancer. A prospective study about 99 patients,” Annales De Chirurgie, vol. 131, no. 4, pp. 256–261, 2006.
View at: Publisher Site | Google Scholar
P.-L. Giacalone, P. Roger, O. Dubon et al., “Comparative study of the accuracy of breast resection in oncoplastic surgery and quadrantectomy in breast cancer,” Annals of Surgical Oncology, vol. 14, no. 2, pp. 605–614, 2007.
View at: Publisher Site | Google Scholar
F. Hernanz, S. Regaño, A. Vega, and M. Gómez Fleitas, “Reduction mammaplasty: an advantageous option for breast conserving surgery in large-breasted patients,” Surgical Oncology, vol. 19, no. 4, pp. e95–e102, 2010.
View at: Publisher Site | Google Scholar
A. M. Munhoz, E. Montag, and R. Gemperli, “Current aspects of therapeutic reduction mammaplasty for immediate early breast cancer management: an update,” World Journal of Clinical Oncology, vol. 5, no. 1, pp. 1–18, 2014.
View at: Publisher Site | Google Scholar
W. Lim, E.-H. Park, S.-L. Choi et al., “Breast conserving surgery for multifocal breast cancer,” Annals of Surgery, vol. 249, no. 1, pp. 87–90, 2009.
View at: Publisher Site | Google Scholar
T. J. Whelan, J. Julian, J. Wright, A. R. Jadad, and M. L. Levine, “Does locoregional radiation therapy improve survival in breast cancer? A meta-analysis,” Journal of Clinical Oncology, vol. 18, no. 6, pp. 1220–1229, 2000.
View at: Publisher Site | Google Scholar
J. Van De Steene, G. Soete, and G. Storme, “Adjuvant radiotherapy for breast cancer significantly improves overall survival: the missing link,” Radiotherapy & Oncology, vol. 55, no. 3, pp. 263–272, 2000.
View at: Publisher Site | Google Scholar
M. Clarke, R. Collins, S. Darby et al., “Effects of radiotherapy and of differences in the extent of surgery for early breast cancer on local recurrence and 15-year survival: an overview of the randomized trials,” Lancet, vol. 366, no. 9503, pp. 2087–2106, 2005.
View at: Google Scholar
A. O. Momoh, R. Ahmed, B. P. Kelley et al., “A systematic review of complications of implant-based breast reconstruction with prereconstruction and postreconstruction radiotherapy,” Annals of Surgical Oncology, vol. 21, no. 1, pp. 118–124, 2014.
View at: Publisher Site | Google Scholar
M. B. Nava, A. E. Pennati, L. Lozza, A. Spano, M. Zambetti, and G. Catanuto, “Outcome of different timings of radiotherapy in implant-based breast reconstructions,” Plastic and Reconstructive Surgery, vol. 128, no. 2, pp. 353–359, 2011.
View at: Publisher Site | Google Scholar
S. E. Gabriel, J. E. Woods, W. M. O'Fallon, C. M. Beard, L. T. Kurland, and L. J. Melton III, “Complications leading to surgery after breast implantation,” The New England Journal of Medicine, vol. 336, no. 10, pp. 677–682, 1997.
View at: Publisher Site | Google Scholar
S. M. Bentzen, R. K. Agrawal, E. G. Aird et al., “The UK Standardisation of Breast Radiotherapy (START) trial a of radiotherapy hypofractionation for treatment of early breast cancer: a randomised trial,” The Lancet Oncology, vol. 9, no. 4, pp. 331–341, 2008.
View at: Publisher Site | Google Scholar
H. Bartelink, J. C. Horiot, P. M. Poortmans et al., “Impact of a higher radiation dose on local control and survival in breast-conserving therapy of early breast cancer: 10-year results of the randomized boost versus no boost EORTC 22881-10882 trial,” Journal of Clinical Oncology, vol. 25, no. 22, pp. 3259–3264, 2007.
View at: Publisher Site | Google Scholar
M. Guerrero, X. Allen, M. Earl et al., “Simultaneous integrated boost for breast cancer using imrt: a radiobiological and treatment planning study,” International Journal of Radiation Oncology Biology Physics, vol. 59, no. 5, pp. 1513–1522, 2004.
View at: Publisher Site | Google Scholar

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Copyright © 2019 Chaitanyanand B. Koppiker et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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