[局部晚期癌症新辅助放化疗后延长等待时间对肿瘤消退的影响]。

K Zheng, L Jin, F Shen, X H Gao, X M Zhu, G Y Yu, L Q Hao, Z Lou, H Wang, E D Yu, C G Bai, W Zhang
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引用次数: 0

摘要

目的:探讨延长等待时间对局部晚期癌症(LARC)患者新辅助放化疗(nCRT)后肿瘤消退的影响。方法:收集2012年1月至2021年12月在海军医科大学第一附属医院完成nCRT治疗的728例LARC患者的临床病理数据进行回顾性分析。主要研究终点是持续完全反应(SCR)。共有498名男性和230名女性,年龄(M(IQR))为58(15)岁(范围:22至89岁)。采用Logistic回归模型探讨等待时间是否是影响SCR的独立因素。曲线拟合用于表示SCR的累积发生率与等待时间之间的关系。将患者分为常规等待时间组(4至n=581)和延长等待时间组,12吨=147)。根据情况,使用t检验、Wilcoxon秩和检验或χ2检验对两组之间的肿瘤消退、器官保存和手术条件进行比较。对数秩检验用于阐明两组之间的生存差异。结果:所有患者的SCR发生率为21.6%(157/728)。等待时间是SCR的独立影响因素,每增加一天,OR值为1.010(95%CI:1.001~1.020,P=0.031)。SCR的累积发生率随着等待时间的延长而逐渐增加,其中第10周增加最快。延长等待时间组的SCR发生率更高(27.9%(41/147)vs.20.0%(116/581),χ2=3.901,P=0.048),随访期器官保存率也更高(21.1%(31/147)vs.10.7%(62/581),χ0=10.510,P=0.001),常规和延长等待时间组的3年总生存率分别为95.6%和92.2%,局部复发/无再生生存率无统计学差异,两组患者的无病生存率和总生存率(χ2=1.878,P=0.171;χ2=0.078,P=0.780;χ2=1.265,P=0.261)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The impact of extended waiting time on tumor regression after neoadjuvant chemoradiotherapy for locally advanced rectal cancer].

Objective: To investigate the influence of extending the waiting time on tumor regression after neoadjuvant chemoradiology (nCRT) in patients with locally advanced rectal cancer (LARC). Methods: Clinicopathological data from 728 LARC patients who completed nCRT treatment at the First Affiliated Hospital, Naval Medical University from January 2012 to December 2021 were collected for retrospective analysis. The primary research endpoint was the sustained complete response (SCR). There were 498 males and 230 females, with an age (M(IQR)) of 58 (15) years (range: 22 to 89 years). Logistic regression models were used to explore whether waiting time was an independent factor affecting SCR. Curve fitting was used to represent the relationship between the cumulative occurrence rate of SCR and the waiting time. The patients were divided into a conventional waiting time group (4 to <12 weeks, n=581) and an extended waiting time group (12 to<20 weeks, n=147). Comparisons regarding tumor regression, organ preservation, and surgical conditions between the two groups were made using the t test, Wilcoxon rank sum test, or χ2 test as appropriate. The Log-rank test was used to elucidate the survival discrepancies between the two groups. Results: The SCR rate of all patients was 21.6% (157/728). The waiting time was an independent influencing factor for SCR, with each additional day corresponding to an OR value of 1.010 (95%CI: 1.001 to 1.020, P=0.031). The cumulative rate of SCR occurrence gradually increased with the extension of waiting time, with the fastest increase between the 10th week. The SCR rate in the extended waiting time group was higher (27.9%(41/147) vs. 20.0%(116/581), χ2=3.901, P=0.048), and the organ preservation rate during the follow-up period was higher (21.1%(31/147) vs. 10.7%(62/581), χ2=10.510, P=0.001). The 3-year local recurrence/regrowth-free survival rates were 94.0% and 91.1%, the 3-year disease-free survival rates were 76.6% and 75.4%, and the 3-year overall survival rates were 95.6% and 92.2% for the conventional and extended waiting time groups, respectively, with no statistical differences in local recurrence/regrowth-free survival, disease-free survival and overall survival between the two groups (χ2=1.878, P=0.171; χ2=0.078, P=0.780; χ2=1.265, P=0.261). Conclusions: An extended waiting time is conducive to tumor regression, and extending the waiting time to 12 to <20 weeks after nCRT can improve the SCR rate and organ preservation rate, without increasing the difficulty of surgery or altering the oncological outcomes of patients.

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