新辅助全身化疗后有 1-3 个临床阳性淋巴结且病理结果为阴性的患者,乳房切除术后放疗是否能延长其生存期?来自汇总分析的共识?

IF 1.3 Q4 ONCOLOGY
Muna Alamoodi
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引用次数: 0

摘要

以类固醇为基础的化疗的出现彻底改变了乳腺癌的治疗。这一进步有助于改善对无法手术的肿瘤的分期反应。它还有助于使临床(cN+)阳性淋巴结(LN)病理阴性(ypN0)。cN+ 患者的标准治疗方法包括切除术后放疗(PMRT),无论新辅助化疗反应如何。然而,1-3个LN阳性患者的PMRT仍缺乏明确的指导原则。关于PMRT对1-3个LN阳性患者生存期的益处,许多回顾性研究结果尚无定论。本汇总分析试图达成共识。对PubMed数据库的检索截止到2023年10月。共检索到27篇论文,其中11篇符合纳入标准。每项研究的无局部复发生存率(LRRFS)、无疾病生存率(DFS)和总生存率(OS)均以表格形式列出,并分别设立了 PMRT 和 NO PMRT 两组。然后将结果汇总进行分析。患者总数为 8340 人,PMRT 组为 4136 人,NO PMRT 组为 4204 人。PMRT组的LRRFS、DFS和OS分别为96.9%、82.1%和87.3%,NO PMRT组分别为93.2%、79.6%和84.8%。两组的 LRRFS、DFS 或 OS 无统计学意义(分别为 p = 0.61、p = 0.61 和 p = 0.38)。PMRT似乎不会给T1-3期pN1和ypN0患者带来生存益处。这项汇总分析的结果应通过更长时间的前瞻性随访加以证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Does Post-Mastectomy Radiotherapy Confer Survival Benefits on Patients With 1-3 Clinically Positive Lymph Nodes Rendered Pathologically Negative After Neoadjuvant Systemic Chemotherapy: Consensus from A Pooled Analysis?
The advent of taxane-based chemotherapy has revolutionized breast cancer care. This advance has helped improve the response to downstaging tumors that might otherwise be inoperable. It has also helped in rendering clinically (cN+) positive lymph nodes (LNs) pathologically negative (ypN0). The standard of care for cN+ patients included post-mastectomy radiotherapy (PMRT), regardless of the response to neoadjuvant chemotherapy. However, PMRT in patients with 1-3 positive LNs still lacks definitive guidelines. Numerous retrospective results have been inconclusive about the benefit of PMRT on survival in patients with 1-3 positive LNs. This pooled analysis attempts to reach a consensus. The PubMed database was searched through October 2023. The search yielded 27 papers, of which 11 satisfied the inclusion criteria. The locoregional recurrence-free survival (LRRFS), disease-free survival (DFS), and overall survival (OS) for each study were tabulated when given, and two groups were created, the PMRT and NO PMRT, respectively. The results were then pooled for analysis. The total number of patients was 8340, 4136 in the PMRT group, and 4204 in the NO PMRT group, respectively. The LRRFS, DFS, and OS were 96.9%, 82.1%, and 87.3% for the PMRT group and 93.2%, 79.6%, and 84.8% for the NO PMRT group, respectively. There was no statistical significance in LRRFS, DFS, or OS between the two groups (p = 0.61, p = 0.61, and p = 0.38, respectively). PMRT does not seem to confer survival benefits in patients with pN1 rendered ypN0 for stages T1-3. This pooled analysis's findings should be confirmed prospectively with a longer period of follow-up.
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