Does Immediate Breast Reconstruction Lead to a Delay in Adjuvant Chemotherapy for Breast Cancer? A Meta-Analysis and Systematic Review

被引:6
|
作者
Cook, Patrick [1 ]
Yin, Grace [2 ]
Ayeni, Femi E. [3 ]
Eslick, Guy D. [4 ]
Edirimanne, Senarath [3 ,5 ]
机构
[1] Univ Sydney, Nepean Clin Sch, Dept Surg, Camperdown, NSW, Australia
[2] Univ New South Wales, St George & Sutherland Clin Sch, Dept Surg, Sydney, NSW, Australia
[3] Univ Sydney, Nepean Inst Acad Surg, Nepean Clin Sch, Camperdown, NSW, Australia
[4] Univ Newcastle, Hunter Med Res Inst, NHMRC Ctr Res Excellence Digest Hlth, Dept Epidemiol, New Lambton Hts, NSW, Australia
[5] Dept Surg, Nepean Hosp Clin Bldg,Level 3,POB 63, Penrith, NSW 2750, Australia
关键词
Adjuvant; Breast neoplasm; Chemotherapy; Complication; QUALITY-OF-LIFE; NEOADJUVANT CHEMOTHERAPY; MASTECTOMY; IMPACT; INITIATION; DELIVERY; TIME; COMPLICATIONS; OUTCOMES; TRENDS;
D O I
10.1016/j.clbc.2023.03.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Concerns currently exist that for women with breast cancer, undergoing immediate breast reconstruction may delay adjuvant chemotherapy, therefore worsening oncologic outcomes. The authors performed a system-atic review and meta-analyses of the existing published data. Results revealed an increased mean time to chemotherapy of 3.50 days from 40.38 days postsurgery to 43.56 days. Although there is a delay in timing of adjuvant chemotherapy, this is unlikely to be of clinical significance, as it is within the accepted 90 days window of safety. Timely delivery of adjuvant chemotherapy is crucial. With an increasing frequency of immediate breast reconstruc-tions (IBR) following mastectomy (MAS), concerns have arisen regarding its complication rates and effects on time to chemotherapy. The aim was to conduct a systematic review and meta-analysis to determine if there is a prolonged time to chemotherapy (TTC) after IBR and MAS. Electronic databases, reference lists and relevant articles were searched systematically. Eligibility criteria included women receiving adjuvant chemotherapy who underwent either MAS only or MAS and IBR. Random-effects models were used in the analysis. A total of 29 studies were included in qualitative analysis, comprising of 156,000 patients (IBR: 57,159; MAS: 98,841). But 23 studies had sufficient data to be included in the meta-analysis. Sixteen papers concluded there was no difference in TTC compared to MAS. There was a difference of 3.50 days between TTC in IBR versus MAS (95% CI [0.42, 6.57], P value = .0256; IBR = 43.56 days, MAS = 40.38 days). The rate of patients being delayed past 90 days was not significantly higher in IBR (OR = 1.34, 95% CI [0.76, 2.38], P = .310). IBR patients were more likely to have complications compared to the MAS group (OR = 2.04, 95% CI [1.04-4.01], P < .01). We concluded that there is a statistically significant longer time to chemotherapy following IBR of 3.50 days, yet there is no difference in delays past 90 days. Therefore, the longer TTC in IBR is unlikely to be of any clinical significance.
引用
收藏
页码:e285 / e295
页数:11
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