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新辅助或辅助化疗治疗 cT2-4N0-1 期非小细胞肺癌的结果:倾向评分匹配分析。

Outcomes after neoadjuvant or adjuvant chemotherapy for cT2-4N0-1 non-small cell lung cancer: A propensity-matched analysis.

机构信息

Thoracic Surgery Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.

出版信息

J Thorac Cardiovasc Surg. 2019 Feb;157(2):743-753.e3. doi: 10.1016/j.jtcvs.2018.09.098. Epub 2018 Oct 10.

Abstract

OBJECTIVE

Comparative survival between neoadjuvant chemotherapy and adjuvant chemotherapy for patients with cT2-4N0-1M0 non-small cell lung cancer has not been extensively studied.

METHODS

Patients with cT2-4N0-1M0 non-small cell lung cancer who received platinum-based chemotherapy were retrospectively identified. Exclusion criteria included stage IV disease, induction radiotherapy, and targeted therapy. The primary end point was disease-free survival. Secondary end points were overall survival, chemotherapy tolerance, and ability of Response Evaluation Criteria In Solid Tumors response to predict survival. Survival was estimated using the Kaplan-Meier method, compared using the log-rank test and Cox proportional hazards models, and stratified using matched pairs after propensity score matching.

RESULTS

In total, 330 patients met the inclusion criteria (n = 92/group after propensity-score matching; median follow-up, 42 months). Five-year disease-free survival was 49% (95% confidence interval, 39-61) for neoadjuvant chemotherapy versus 48% (95% confidence interval, 38-61) for adjuvant chemotherapy (P = .70). On multivariable analysis, disease-free survival was not associated with neoadjuvant chemotherapy or adjuvant chemotherapy (hazard ratio, 1.1; 95% confidence interval, 0.64-1.90; P = .737), nor was overall survival (hazard ratio, 1.21; 95% confidence interval, 0.63-2.30; P = .572). The neoadjuvant chemotherapy group was more likely to receive full doses and cycles of chemotherapy (P = .014/0.005) and had fewer grade 3 or greater toxicities (P = .001). Response Evaluation Criteria In Solid Tumors response to neoadjuvant chemotherapy was associated with disease-free survival (P = .035); 15% of patients receiving neoadjuvant chemotherapy (14/92) had a major pathologic response.

CONCLUSIONS

Timing of chemotherapy, before or after surgery, is not associated with an improvement in overall or disease-free survival among patients with cT2-4N0-1M0 non-small cell lung cancer who undergo complete surgical resection.

摘要

目的

新辅助化疗与辅助化疗在 cT2-4N0-1M0 期非小细胞肺癌患者中的生存比较尚未得到广泛研究。

方法

回顾性分析接受铂类化疗的 cT2-4N0-1M0 期非小细胞肺癌患者。排除标准包括 IV 期疾病、诱导放疗和靶向治疗。主要终点是无病生存。次要终点是总生存、化疗耐受性和实体瘤反应评价标准的反应能力预测生存。采用 Kaplan-Meier 法估计生存,对数秩检验和 Cox 比例风险模型比较,倾向性评分匹配后分层匹配对。

结果

共 330 例患者符合纳入标准(n=92/组,经倾向性评分匹配后;中位随访时间为 42 个月)。新辅助化疗组 5 年无病生存率为 49%(95%置信区间,39-61),辅助化疗组为 48%(95%置信区间,38-61)(P=0.70)。多变量分析显示,无病生存率与新辅助化疗或辅助化疗无关(风险比,1.1;95%置信区间,0.64-1.90;P=0.737),总生存率也无关(风险比,1.21;95%置信区间,0.63-2.30;P=0.572)。新辅助化疗组更有可能接受全剂量和全周期化疗(P=0.014/0.005),且毒性反应 3 级或以上的发生率较低(P=0.001)。新辅助化疗的实体瘤反应评价标准与无病生存率相关(P=0.035);新辅助化疗组 15%(14/92)的患者有主要病理缓解。

结论

在完全手术切除的 cT2-4N0-1M0 期非小细胞肺癌患者中,化疗时机(手术前或手术后)与总生存或无病生存的改善无关。

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