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Locally advanced breast cancer patients should be cautious about the immediate breast reconstruction after mastectomy: a pooling analysis of safety and efficacy

Abstract

Background

The purpose of this study was to compare safety and efficacy outcomes between immediate breast reconstruction (IBR) and mastectomy alone in locally advanced breast cancer patients.

Methods

We conducted a comprehensive literature search of PUBMED, EMBASE, and Cochrane databases. The primary outcomes evaluated were overall survival, disease-free survival, and local recurrence. The secondary outcome was the incidence of surgical complications. All data were analyzed using Review Manager 5.3.

Results

Sixteen studies, involving 15,364 participants were included in this meta-analysis. Pooled data demonstrated that patients underwent IBR were more likely to experience surgical complications than those underwent mastectomy alone (HR: 3.96, 95%CI [1.07,14.67], p = 0.04). No significant difference was found in overall survival (HR: 0.94, 95%CI [0.73,1.20], p = 0.62), disease-free survival (HR: 1.03, 95%CI [0.83,1.27], p = 0.81), or breast cancer specific survival (HR: 0.93, 95%CI [0.71,1.21], p = 0.57) between IBR group and Non-IBR group.

Conclusions

Our study demonstrates that IBR after mastectomy does not affect the overall survival and disease-free survival of locally advanced breast cancer patients. However, IBR brings with it a nonnegligible higher risk of complications and needs to be fully evaluated and carefully decided.

Introduction

Breast cancer is the most common cancer and the second leading cause of cancer death, and the incidence rates have risen in most recent years by 0.5% annually [1]. Mastectomy is a common and effective treatment for breast cancer patients, while mastectomy not only leads to various physical discomfort, including loss of sensation, impaired body image, and sexual function but also impairs mental health [2, 3]. Research has shown that immediate breast reconstruction (IBR) after mastectomy can restore body image and preserve femininity [4], breast cancer survivors underwent IBR generally report better quality of life in psychosocial, sexual, and physical well-being domains [5, 6], especially in younger women. In addition, immediate autologous reconstruction could preserve the natural skin envelope and relatively reducing scar formation, reduce the adhesion of the skin paddle to the chest wall with improved cosmesis [7, 8]. IBR after breast cancer mastectomy is on the rise because of its positive impact on patient’s quality of life over the past 10 years [9,10,11], while it is generally limited to patients with low-risk diseases, with significantly lower use for higher tumor stages (p < 0.0001), despite these potential benefits [12].

Locally advanced breast cancer (LABC) refers to a large category of breast cancer with extensive lesion invasion or regional lymph node metastasis, without distant metastasis, including clinical stage IIB to IIIC. Modest improvement in survival or QoL (Quality of Life) was achieved in recent years underscoring the unmet need in LABC patients [13]. The surgical complexity and high-risk oncological characteristics make IBR a huge challenge for LABC patients. In addition, comprehensive treatment including neoadjuvant chemoradiotherapy and post-mastectomy radiotherapy is becoming the new normal for LABC patients [14,15,16], therefore, the technical feasibility of IBR has to be taken into consideration.

To date, it is gradually accepted that LABC is no longer contraindicated for breast reconstruction. There are different views on whether IBR should be performed. Some retrospective studies report IBR has a survival advantage over mastectomy for possible antitumorigenic effect of implants [16], and neither increases the risk of local recurrence (LR) nor delays adjuvant therapy [17]. But there’s also report of IBR associating with a worse outcome of local control [18]. Additionally, a risk assessment nomogram has been developed to broaden the application of IBR in LABC patients, allowing surgeons to recommend IBR through preoperative evaluation. Identified risk factors include older age, unmarried status, and more advanced stage [19]. However, this study focused solely on oncological outcomes, and many surgeons are also concerned about the potential increased risk of complications associated with IBR in LABC patients. Therefore, we performed a meta-analysis comparing overall survival, disease-free survival, local recurrence, and surgical complications in LABC patients who underwent IBR after mastectomy and mastectomy alone.

Methods and materials

This meta-analysis was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) standards [20], and the protocol was registered in the PROSPERO database (CRD42024501216).

Data sources

Two independent reviewers conducted searched of the PubMed, Embase, and Cochrane Library databases from inception to December 2023 for relevant English articles. Reviewers manually evaluated full texts of studies based on the prespecified inclusion criteria and exclusion criteria, and all references were managed in an Endnote database (Version 19.0). Any discrepancies were resolved by discussion and got consensus with a third reviewer.

Study selection

Studies were eligible for the meta-analysis if they fulfilled the inclusion criteria: (1) retrospective or prospective cohort studies; (2) comparison between IBR (IBR-group) with mastectomy alone (Non-IBR group) in LABC female patients; (3) report at least one of the outcome indicators. Studies were excluded if they were: (1) conference abstract, letters, editorials opinions, meta-analysis, or reviews. (2) single-arm cohort studies. Two studies [21, 22] both used SEER database but included different population and were both included in our analysis.

Risk of bias (quality) assessment

Reviewers assessed the quality of included studies using the Newcastle-Ottawa Scale (NOS). More than six stars were considered to be of high quality. Two reviewers independently assessed the quality of all included studies by selection, comparability and exposure. Discrepancies were re-examined by a third reviewer, and a consensus was reached by discussion.

Data extraction

Reviewers (CY.Z., JY.L.) independently extracted data from included studies into tables including study region, publication year, Enrollment time span, study design, participant characteristics, surgical characteristics, oncology outcomes, and surgical complications. Additional reviewer (YY.Q.) reviewed data for accuracy. Oncology outcomes includes overall survival (OS), disease-free survival (DFS), breast cancer specific survival (BCSS), and local recurrence (LR). Local recurrence was defined as any recurrence in the ipsilateral mastectomy site. Surgical complications were classified as major complications and minor complications, of which major complications were defined as complications requiring reoperation or other nonconservative subsequent treatment. Reconstruction methods are categorized into autologous and alloplastic reconstruction. Autologous reconstruction utilizes the patient’s own tissue, whereas alloplastic reconstruction predominantly employs various types of implants. All data were extracted directly from publications, and contacting authors for additional information was not necessary. and contacting authors for additional information was not necessary.

Data synthesis

A pooled data synthesis was performed by the Review Manager (RevMan Version 5.4.). For observation-event outcomes (including positive margins, LR, and surgical complications), odds ratios (OR) and 95% CIs of events for IBR to Non-IBR were retrieved or calculated. For time-to-event outcomes (including OS, DFS, BCSS), hazard ratios (HR) were pooled according to the inverse of variance method. If the survival curves of OS, DFS, and BCSS were reported in the literature, the survival data were extracted using Engauge Digitizer version 4.1 software and then calculated using the Excel attachment calculations spreadsheet provided by Tierney et al [23].

Statistically significant heterogeneity was defined as a P value less than 0.1 or an I² statistic greater than 50%. In the absence of heterogeneity, pooled estimates of ORs or HRs with their 95% CIs were calculated using the Mantel-Haenszel method. In the presence of heterogeneity, the Der Simonian and Laird random effects method were used to pool primary study estimates. All significance testing was two-sided, and results were considered statistically significant if P < 0.05. Funnel plots were presented as an assessment tool for publication bias.

Results

A total of 16 retrospective studies involving 15,364 participants (4135 patients underwent IBR, 11,229 patients underwent mastectomy alone) met inclusion criteria and provided survival or surgical complication outcomes for the meta-analysis (Fig. 1) [22, 24,25,26,27,28,29,30,31,32,33,34,35,36,37,38]. Studies were mostly conducted in North America, with additional studies in Asia and Europe (Table 1). Ten articles were published in the last five years contributing to good applicability.

Fig. 1
figure 1

Flowchart of study selection process

Table 1 Basic characteristics and the quality evaluation of the studies included

Pooled information was shown in Table 2. The median age of the IBR group was significantly younger than Non-IBR group (Mean difference = -7.78, 95%CI [-9.95, -5.61], p < 0.0001). Patients in Non-IBR group were likely to have more advanced clinical tumor stages than those in IBR group (p < 0.001). Tripe negative breast cancer patients were more common in Non-IBR group (OR = 0.77, 95%CI [0.64,0.92], p = 0.005). There were no significant differences between the two groups in histology grade (OR = 0.99, 95%CI [0.77,1.28], p = 0.94) (Table 2, Supplementary Figure S1).

Table 2 Characteristics of studies included in the meta-analysis

Oncological outcomes

Overall survival was reported in 9 studies, pooled HR data demonstrated that patients underwent IBR were associated with better overall survival than those in Non-IBR group, but the difference was not significant (HR: 0.95, 95%CI [0.86,1.06], p = 0.36). Similarly, there’s no significant difference in DFS (HR: 1.01, 95%CI [0.82,1.26], p = 0.91) and BCSS (HR: 0.93, 95%CI [0.71,1.21], p = 0.57) between IBR group and Non-IBR group. None of the included studies showed a statistically significant difference in DFS between study groups. The pooled OR for LR was 1.12 (95% CI: [0.79, 1.59], p = 0.53) as shown in Fig. 2d. there were no significant differences in the frequency of LR in patients treated with IBR compared with those who underwent mastectomy alone. Taqi et al. reported a relatively higher local recurrence (1.9% vs. 0%; RR: 6.90, 95% CI: [0.33,142.40]) with a relatively more advanced tumor stage in IBR group.

Fig. 2
figure 2

Forest plot of survival information included in the study. (a) OS; (b) BCSS; (c) DFS; (d) LR

Surgical process

As expected, axillary lymph node dissection (ALND) was less common in patients underwent IBR because of the earlier N stage. Interestingly, the concern of a higher positive margin rate due to additional surgical process in IBR group was not found (HR: 1.79, 95%CI [0.87,3.69], p = 0.11) (Fig. 3).

Fig. 3
figure 3

Forest plot of positive margin rate

Surgical complications

It is noteworthy that patients in IBR group had a significantly higher surgical complication risk than patients underwent mastectomy alone (HR: 3.96, 95%CI [1.07,14.67], p = 0.04), mainly due to a significantly higher major complication rate (HR: 5.14, 95%CI [1.69,15.61], p = 0.004). In terms of minor complications, the rates of the two groups were comparable (HR: 3.22, 95%CI [0.47,22.00], = 0.23) (Fig. 4).

Fig. 4
figure 4

Forest plot of postoperative complication included in the study. (a) Total complication; (b) Major complication; (c) Minor complication

Survival outcomes in PSM studies

We also conducted an analysis comprised of 3 matched cohort studies separately, where patients who had undergone IBR were matched to patients of similar age and tumor stage undergoing mastectomy without IBR (Supplementary, Table S1). There were a total of 2432 pairs. There were no significant differences between the two groups in histology grade (OR = 0.99, 95%CI [0.89,1.11] p = 0.89). After matching, the OS and BCSS of the IBR group and the Non-IBR group were almost identical (OS: HR 0.99, 95%CI [0.89,1.10], p = 0.87; BCSS: HR 0.99, 95%CI [00.82,1.21], p = 0.95) (Fig. 5).

Fig. 5
figure 5

Survival of studies using PSM. (a) OS; (b) BCSS

Publication bias

An assessment of publication bias indicated no small study effects for OS, BCSS, LR, and surgical complications.

Discussion

Prior studies reported a satisfactory oncological safety of IBR in all-stage populations [38], while our meta-analysis was the first to concentrate on LABC patients and to demonstrate the oncological outcomes based on a relatively large sample size, to reveal the surgical complication risks.

Compared with mastectomy alone, IBR was significantly associated with higher total surgical complication and major complication risks in this meta-analysis. Of 8 studies reporting complication rates, Tomita et al. was the only one to describe a significantly lower complication rate in the IBR group [35]. In effect, in this single-center retrospective study, only seroma was reported more frequently in patients without breast reconstruction, other complications still dominate in IBR group, which may be the implications of reporting bias.

Major complication usually brings more hospital stays, which will increase the duration of adjuvant therapy and affect patient therapeutic experiences [35]. Common complications of IBR include surgical site infection, flap necrosis, and seroma. The possible reason is that the operation technique of IBR is more complicated with longer operation times. Surgeons are also concerned that post-surgical complications could delay the timely administration of therapies. However, two articles that examined the interval until adjuvant therapy administration reported that the differences in timing were statistically nonsignificant, even when complications occurred more frequently following reconstruction [24, 35].

IBR could be broadly divided into autologous reconstruction and alloplastic reconstruction, latissimus dorsi flap and transverse rectus abdominus myo-cutaneous are commonly used in autologous reconstruction, and alloplastic reconstruction mainly contains various implants.

For alloplastic reconstruction, implantation materials pose a greater risk of infection, and expander or recurrent infections leading to expander or implant loss can impede further therapy.

This is particularly problematic for delayed reconstruction, where infections cause inflammation and scarring, delaying subsequent surgeries. Furthermore, inflammation and capsule formation caused by expanders in delayed-reconstruction make preparing the flap recipient site technically more challenging [39]. Autologous reconstruction, while involving larger wound surfaces and a higher risk of wound infection, generally results in complications that are easier to manage. Unlike alloplastic reconstruction, the most common complications of autologous reconstruction, such as delayed wound healing or infection, do not typically lead to severe consequences like failure of reconstruction [40].

Additionally, postoperative radiotherapy, often required for LABC patients, carries risks of poor wound healing. A recent systematic review comparing complications between immediate reconstruction and reconstruction after radiotherapy in patients undergoing autologous reconstruction found similar rates of flap loss, infection, fat necrosis, and wound healing complications [41], despite capsular contracture after IBR impact some aesthetic outcomes [42].

Autologous reconstruction is considered the gold standard for breast reconstruction, and is preferred in post-radiation patients [43, 44]. A retrospective cohort study highlighted the potential advantages of autologous reconstruction over alloplastic reconstruction, demonstrating a significantly lower reconstruction failure rate. However, no differences were observed in major complications or tumor outcomes between the two methods [45].While a prospective study showed that patients undergoing autologous reconstruction had better psychosocial well-being, despite the higher incidence of severe complications compared to alloplastic reconstruction [46]. Our further analysis of the effect of reconstruction methods on complications shows that autologous reconstruction had no advantage over alloplastic reconstruction in reducing surgical complications (OR: 0.80, 95%CI: [0.22,2.93], p = 0.73).

In terms of oncologic outcome, the present meta-analysis indicated that patients underwent IBR and patients underwent mastectomy alone were comparable in terms of overall survival and disease-free survival. Figure 2 shows that a few studies trended towards a worse OS outcome in IBR group, of which Di lenone A et al. reported a worse but non-statistically significant overall survival (HR:1.92, 95%CI: [0.69, 5.34], p = NS) [35], because of the relatively balanced T stage compared to other studies. The effect of IBR in LABC patients on survival has been investigated with controversial results in recent years. Sang et al. retrospectively compared 104 patients received IBR with 1715 patients underwent conventional mastectomy in a neoadjuvant chemotherapy cohort and found no statistical difference between groups related to DFS (HR: 0.72, p = 0.37) and LR (OR:2.83, p = 0.30) [37]. A single unit cohort study also demonstrated IBR may not compromise oncological and cosmetic outcomes with a low loco-regional recurrence (3.5%) or distant metastasis rate (3.2%) 1/28 after a median 61 months follow-up [17]. Conversely, several studies suggest that IBR should be carefully evaluated preoperatively. Di lenone A et al. reported a slightly worse overall survival (HR: 1.92, p = 0.21) comparing an oncoplastic surgery [34]. In terms of surgical process, there was no difference in positive margin rate (Fig. 4), suggesting that IBR, while aesthetic, did not affect the local-regional control of the surgery, which is consistent with local recurrence outcome.

With the limitations inherent in retrospective reviews and cosmetic procedures, enrolled patients were inevitably younger and had earlier stages [47], these imbalances in demographic factors and tumor characteristics may result in potential selection bias. However, survival outcomes were still comparable in the analysis comprising 3 matched cohort studies, while we assumed that the negative effects of IBR on survival need to be further assessed.

To conclude, although IBR in LABC patients does not prominently affect the oncology outcome of the patients, it brings an inevitably greater risk of complications and affects the follow-up treatment of the patients. Considering the long-term prognosis of the patients, we do not recommend IBR in LABC patients. Therefore, we suggest complication risks and ambiguous oncologic outcomes must be disclosed to patients during the initial consultation and surgeons should not encourage patients to sway IBR over conventional mastectomy arbitrarily in the future.

Our review has several limitations. Firstly, some demographic and tumor characteristics of patients were imbalanced, which may result in selection bias and selective reporting bias, these confounders constitute our evidence base and may limit interpretations. Secondly, there was little information about surgery available in primary articles, and the influence of surgery-related factors on outcome variables could not be further elaborated. We couldn’t determine whether it was a technical problem with the surgeon or the procedure itself that made the difference in complication risk. Thirdly, some HRs of survival measures were manually extracted from survival curves, resulting in inconsistent data sources. Fourthly, we failed to conduct the analysis of patient satisfaction because of the inconsistency and imprecision of different scales. In addition, the heterogeneity with respect to the type of mastectomy and reconstruction techniques may be a source of study bias, which is hard to generalize.

Conclusion

Our updated meta-analysis is the first to evaluate oncologic outcomes and surgical complications in LABC patients underwent IBR compared to mastectomy. The review illustrates that patients underwent IBR has comparable overall survival, disease-free survival, and breast cancer specific survival to patients underwent mastectomy. Nevertheless, considering the significantly higher complication rates, IBR should be cautiously conducted. Further prospective, randomized studies with long-term follow-up are required to evaluate the survival outcomes of LABC patients underwent IBR.

Data availability

No datasets were generated or analysed during the current study.

References

  1. Giaquinto AN, Sung H, Miller KD, Kramer JL, Newman LA, Minihan A, Jemal A, Siegel RL. Breast Cancer statistics, 2022. Cancer J Clin. 2022;72:524–41.

    Article  Google Scholar 

  2. Fanakidou I, Zyga S, Alikari V, Tsironi M, Stathoulis J, Theofilou P. Mental health, loneliness, and illness perception outcomes in quality of life among young breast cancer patients after mastectomy: the role of breast reconstruction. Qual Life Res. 2017;27:539–43.

    Article  PubMed  Google Scholar 

  3. Archangelo SCV, Sabino M, Veiga DF, Garcia EB, Ferreira LM. Sexuality, depression and body image after breast reconstruction. Clinics 2019, 74.

  4. Cordeiro PG. Breast Reconstruction after surgery for breast Cancer. N Engl J Med. 2008;359:1590–601.

    Article  CAS  PubMed  Google Scholar 

  5. Victoria M, Marie B, Dominique R, Caroline A, Marc-Karim BD, Julien M, Sophie L, Anne-Déborah B. Breast reconstruction and quality of life five years after cancer diagnosis: VICAN French National cohort. Breast Cancer Res Treat. 2022;194:449–61.

    Article  PubMed  Google Scholar 

  6. van Bommel ACM, de Ligt KM, Schreuder K, Maduro JH, Van Dalen T, Peeters MTFDV, Mureau MAM, Siesling S. The added value of immediate breast reconstruction to health-related quality of life of breast cancer patients. Eur J Surg Oncol. 2020;46:1848–53.

    Article  PubMed  Google Scholar 

  7. Qureshi AA, Odom EB, Parikh RP, Myckatyn TM, Tenenbaum MM. Patient-reported outcomes of aesthetics and satisfaction in Immediate breast Reconstruction after Nipple-Sparing Mastectomy with implants and Fat Grafting. Aesthetic Surg J. 2017;37:999–1008.

    Article  Google Scholar 

  8. Harcourt DM, Rumsey NJ, Ambler NR, Cawthorn SJ, Reid CD, Maddox PR, Kenealy JM, Rainsbury RM, Umpleby HC. The Psychological Effect of Mastectomy with or without breast Reconstruction: a prospective, Multicenter Study. Plast Reconstr Surg. 2003;111:1060–8.

    Article  PubMed  Google Scholar 

  9. Fancellu A, Sanna V, Cottu P, Feo CF, Scanu AM, Farina G, Bulla A, Spanu A, Paliogiannis P, Porcu A. Mastectomy patterns, but not rates, are changing in the treatment of early breast cancer. Experience of a single European institution on 2315 consecutive patients. Breast. 2018;39:1–7.

    Article  PubMed  Google Scholar 

  10. Dayaratna N, Nguyen CL, Spillane A, Mak C, Warrier SK, Dusseldorp JR. Trends and variations in post-mastectomy breast reconstruction rates in Australia over 10 years. ANZ J Surg. 2023;93:242–50.

    Article  PubMed  Google Scholar 

  11. Jagsi R, Jiang J, Momoh AO, Alderman A, Giordano SH, Buchholz TA, Kronowitz SJ, Smith BD. Trends and Variation in Use of breast Reconstruction in patients with breast Cancer undergoing mastectomy in the United States. J Clin Oncol. 2014;32:919–26.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Lang JE, Summers DE, Cui H, Carey JN, Viscusi RK, Hurst CA, Waer AL, Ley MLB, Sener SF, Vijayasekaran A. Trends in post-mastectomy reconstruction: a SEER database analysis. J Surg Oncol. 2013;108:163–8.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Aebi S, Karlsson P, Wapnir IL. Locally advanced breast cancer. Breast. 2022;62:S58–62.

    Article  PubMed  Google Scholar 

  14. Kong X, Song J, Gao P, Gao R, Zhang L, Fang Y, Wang Y, Gao J, Wang J. Revolutionizing the battle against locally advanced breast cancer: a comprehensive insight into neoadjuvant radiotherapy. Med Res Rev. 2023;44:606–31.

    Article  PubMed  Google Scholar 

  15. Sousa C, Cruz M, Neto A, Pereira K, Peixoto M, Bastos J, Henriques M, Roda D, Marques R, Miranda C et al. Neoadjuvant radiotherapy in the approach of locally advanced breast cancer. ESMO Open 2020, 5.

  16. Fischer-Valuck BW, Michalski JM, Mitra N, Christodouleas JP, DeWees TA, Kim E, Smith ZL, Andriole GL, Arora V, Bullock A, et al. Effectiveness of postoperative radiotherapy after radical cystectomy for locally advanced bladder cancer. Cancer Med. 2019;8:3698–709.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Clement Z, Egbeare D, Kollias J, Gill G, Whitfield R, Bingham J, Bochner M. Safety and efficacy of immediate autologous breast reconstruction after mastectomy in patients undergoing neoadjuvant chemoradiotherapy for locally advanced breast cancer. Breast Dis. 2022;41:267–72.

    Article  PubMed  Google Scholar 

  18. Aurilio G, Bagnardi V, Graffeo R, Nolè F, Petit JY, Locatelli M, Martella S, Iera M, Rey P, Curigliano G, et al. Does immediate breast reconstruction after mastectomy and neoadjuvant chemotherapy influence the outcome of patients with non-endocrine responsive breast cancer? Anticancer Res. 2014;34:6677–83.

    PubMed  Google Scholar 

  19. Pan J, Peng L, Xia C, Wang A, Tong X, Chen X, Zhang J, Xu X. Survival nomogram for patients with locally advanced breast Cancer undergoing Immediate breast Reconstruction: a SEER Population-based study. Clin Breast Cancer. 2023;23:e219–29.

    Article  PubMed  Google Scholar 

  20. Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, Shamseer L, Tetzlaff JM, Akl EA, Brennan SE et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021.

  21. Wang M, Chen H, Wu K, Ding A, Zhang P, Zhang M. Post-mastectomy immediate breast reconstruction is oncologically safe in well-selected T4 locally advanced breast cancer: a large population-based study and matched case–control analysis. Breast Cancer Res Treat. 2019;176:337–47.

    Article  PubMed  Google Scholar 

  22. Wu SG, Zhang WW, Sun JY, Lin Q, He ZY. Comparison of survival outcomes of locally advanced breast cancer patients receiving postmastectomy radiotherapy with and without immediate breast reconstruction: a population-based analysis. Cancer Manage Res. 2018;10:1993–2002.

    Article  CAS  Google Scholar 

  23. Practical. methods for incorporating summary time-to-event data into meta-analysis.

  24. Newman LA, Kuerer HM, Hunt KK, Ames FC, Ross MI, Theriault R, Fry N, Kroll SS, Robb GL, Singletary SE. Feasibility of immediate breast reconstruction for locally advanced breast cancer. Ann Surg Oncol. 1999;6:671–5.

    Article  CAS  PubMed  Google Scholar 

  25. Rey P, Martinelli G, Petit JY, Youssef O, De Lorenzi F, Rietjens M, Garusi C, Giraldo A. Immediate breast reconstruction and high-dose chemotherapy. Ann Plast Surg. 2005;55:250–4.

    Article  CAS  PubMed  Google Scholar 

  26. Lim W, Ko BS, Kim HJ, Lee JW, Eom JS, Son BH, Lee TJ, Ahn SH. Oncological safety of skin sparing mastectomy followed by immediate reconstruction for locally advanced breast cancer. J Surg Oncol. 2010;102:39–42.

    Article  PubMed  Google Scholar 

  27. Prabhu R, Godette K, Carlson G, Losken A, Gabram S, Fasola C, O’Regan R, Zelnak A, Torres M. The impact of skin-sparing mastectomy with immediate reconstruction in patients with stage III breast cancer treated with neoadjuvant chemotherapy and postmastectomy radiation. Int J Radiat Oncol Biol Phys. 2012;82:e587–593.

    Article  PubMed  Google Scholar 

  28. Hsieh TY, Lin YN, Lin SD, Lai CS, Chang KP, Lee SS, Huang SH, Hou MF, Chen FM, Ou-Yang F. Immediate transverse rectus abdominis musculocutaneous flap reconstruction is associated with improved cancer-specific survival in locally advanced breast cancer. Ann Plast Surg. 2014;73(Suppl 1):S31–36.

    Article  CAS  PubMed  Google Scholar 

  29. Da Costa Vieira RA, Ribeiro LM, Carrara GFA, Abrahão-Machado LF, Kerr LM, Nazário ACP. Effectiveness and safety of Implant-based breast Reconstruction in locally advanced breast carcinoma: a matched case-control study. Breast Care. 2019;14:200–9.

    Article  Google Scholar 

  30. Yoon WS, Rim CH, Yang DS, Lee JA, Son GS, Chang YW, Woo SU, Kim DW, Dhong ES. Long-term outcomes of immediate autologous breast reconstruction after definite adjuvant therapy in intermediate and locally advanced breast cancer. Ann Transl Med. 2019;7:743.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Stein MJ, Karir A, Arnaout A, Roberts A, Cordeiro E, Zhang T, Zhang J. Quality-of-life and Surgical outcomes for breast Cancer patients treated with therapeutic reduction Mammoplasty Versus Mastectomy with Immediate Reconstruction. Ann Surg Oncol. 2020;27:4502–12.

    Article  PubMed  Google Scholar 

  32. Dudley CM, Wiener AA, Stankowski-Drengler TJ, Schumacher JR, Francescatti AB, Poore SO, Greenberg CC, Neuman HB. Rates of Ipsilateral Local-regional recurrence in high-risk patients undergoing Immediate Post-mastectomy Reconstruction (AFT-01). Clin Breast Cancer. 2021;21:433–9.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Taqi K, Pao JS, Chen L, Ma C, Zhang M, McKevitt E, Bazzarelli A, Dingee C, Warburton R. Immediate breast reconstruction in locally advanced breast cancer: is it safe? Breast Cancer Res Treat. 2021;190:175–82.

    Article  PubMed  Google Scholar 

  34. Di Leone A, Franco A, Terribile DA, Magno S, Fabi A, Sanchez AM, D’Archi S, Scardina L, Natale M, Mason EJ et al. Level II oncoplastic surgery as an alternative option to Mastectomy with Immediate breast Reconstruction in the Neoadjuvant setting: a multidisciplinary single Center experience. Cancers (Basel) 2022, 14.

  35. Tomita S, Matsunaga N, Fujita Y, de Kerckhove M, Fujii M, Honda Y, Tokisawa H, Aruga T, Terao Y. Safety evaluation of immediate breast reconstruction for locally advanced breast cancer in Japanese patients. J Plast Reconstr Aesthet Surg. 2022;75:2526–34.

    Article  PubMed  Google Scholar 

  36. Wu ZY, Han HH, Kim HJ, Chung IY, Kim J, Lee SB, Son BH, Eom JS, Kim SB, Ahn JH, et al. A propensity score-matched analysis of long-term oncologic outcomes after nipple-sparing Versus Conventional Mastectomy for locally advanced breast Cancer. Ann Surg. 2022;276:386–90.

    Article  PubMed  Google Scholar 

  37. Sang Y, Chen J, Yang B, Hao S, Huang X, Liu G, Shao Z, Wu J. Surgical options of the breast and clinical outcomes in breast cancer patients after neoadjuvant chemotherapy: a single-center retrospective study. Cancer Res 2023, 83.

  38. Zhang P, Li CZ, Wu CT, Jiao GM, Yan F, Zhu HC, Zhang XP. Comparison of immediate breast reconstruction after mastectomy and mastectomy alone for breast cancer: a meta-analysis. Eur J Surg Oncol (EJSO). 2017;43:285–93.

    Article  CAS  PubMed  Google Scholar 

  39. Bitoiu B, Schlagintweit S, Zhang Z, Bovill E, Isaac K, Macadam S. Conversion from Alloplastic to Autologous breast Reconstruction: what are the inciting factors? Plast Surg (Oakv). 2024;32:213–9.

    Article  PubMed  Google Scholar 

  40. Meresse T, Chaput B, Grolleau JL, Gangloff D. Complication des lambeaux en reconstruction mammaire. Ann De Chirurgie Plast Esthétique. 2019;64:594–619.

    Article  CAS  Google Scholar 

  41. Kelley BP, Ahmed R, Kidwell KM, Kozlow JH, Chung KC, Momoh AO. A systematic review of morbidity associated with autologous breast reconstruction before and after exposure to radiotherapy: are current practices ideal? Ann Surg Oncol. 2014;21:1732–8.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Spear SL, Ducic I, Low M, Cuoco F. The effect of radiation on pedicled TRAM flap breast reconstruction: outcomes and implications. Plast Reconstr Surg. 2005;115:84–95.

    Article  CAS  PubMed  Google Scholar 

  43. Recommendations of the AGO Breast Committee. (2022) Diagnosis and treatment of patients with early and advanced breast Cancer wa-oda.

  44. (2021) NCCN Clinical Practice Guidelines in Oncology BC, Version 2.2021—March 12, 2021, NCCN.org).

  45. Tanos G, Prousskaia E, Chow W, Angelaki A, Cirwan C, Hamed H, Farhadi J. Locally advanced breast Cancer. Plast Reconstr Surg - Global Open 2016, 4.

  46. Sadok N, Krabbe-Timmerman IS, Buisman NH, van Aalst VC, de Bock GH, Werker PMN. Short-term quality of life after Autologous compared with alloplastic breast Reconstruction: a prospective study. Plast Reconstr Surg. 2023;152:S55–68.

    Article  Google Scholar 

  47. Reddy KG, Strassle PD, McGuire KP. Role of Age, Tumor Grade, and Radiation Therapy on Immediate Postmastectomy breast Reconstruction. Clin Breast Cancer. 2018;18:313–9.

    Article  PubMed  Google Scholar 

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Acknowledgements

We are grateful to all authors who worked for the current study.

Funding

This work was supported by the Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences (CAMS) Initiative for Innovative Medicine (Grant No. 2021-I2M-1-022) and the National High Level Hospital Clinical Research Funding (No. 2022-PUMCH-B-003).

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Cheng-Yu Zeng: Formal analysis, Resources, Software, Writing - original draft Yan-Yu Qiu: Data curation, Methodology, Resources, Writing - original draft Jia-Yi Li: Resources, Software Jian-Hao Huang: Data curation, Software Xue-Song Bai: Data curation, Resources Xian-Lin Han: Formal analysis, Funding acquisition, Supervision, Writing - review & editing Xiao-Dong He: Formal analysis, Funding acquisition, Methodology, Supervision, Writing - review & editing All authors reviewed the manuscript.

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Correspondence to Xian-Lin Han or Xiao-Dong He.

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Zeng, CY., Qiu, YY., Li, JY. et al. Locally advanced breast cancer patients should be cautious about the immediate breast reconstruction after mastectomy: a pooling analysis of safety and efficacy. World J Surg Onc 22, 165 (2024). https://doi.org/10.1186/s12957-024-03444-z

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