医学
卡铂
化疗
内科学
肿瘤科
卵巢癌
养生
置信区间
揭穿
紫杉烷
化疗方案
药敏试验
多西紫杉醇
临床研究阶段
无进展生存期
癌症
乳腺癌
顺铂
作者
Benoît You,Patrick Robelin,Michel Tod,Christophe Louvet,Jean‐Pierre Lotz,Sophie Abadie‐Lacourtoisie,Michel Fabbro,Christophe Desauw,Nathalie Bonichon-Lamichhane,Jean‐Emmanuel Kurtz,Philippe Follana,Marianne Leheurteur,Francesco Del Piano,Gwénaël Ferron,Gaëtan De Rauglaudre,Isabelle Ray‐Coquard,Pierre Combe,Annick Chevalier-Place,Florence Joly,Alexandra Léary,Éric Pujade-Lauraine,Gilles Freyer,Olivier Colomban
标识
DOI:10.1158/1078-0432.ccr-20-0054
摘要
Abstract Purpose: In patients with ovarian cancer receiving neoadjuvant chemotherapy, the first-line treatment success will depend on both the tumor-primary chemosensitivity and the completeness of interval debulking surgery (IDS). The modeled CA-125 ELIMination rate constant K (KELIM), calculated with the CA-125 longitudinal kinetics during the first 100 chemotherapy days, is a validated early marker of tumor chemosensitivity. The objective was to investigate the role of the chemosensitivity relative to the success of first-line medical–surgical treatment. Experimental Design: The CA-125 concentrations were prospectively measured in the randomized phase II trial CHIVA (NCT01583322, carboplatin–paclitaxel regimen ± nintedanib, and IDS, n = 188 patients). The KELIM predictive value regarding the tumor response rate, likelihood of complete IDS, risk of subsequent platinum-resistant relapse (PtRR), progression-free survival (PFS), and overall survival (OS) was assessed using univariate and multivariate tests. Results: The data from 134 patients were analyzed. KELIM was an independent and major predictor of subsequent PtRR risk, and of survivals. The final logistic regression model, including KELIM [OR = 0.13; 95% confidence interval (CI), 0.03–0.49] and complete IDS (no vs. yes, OR = 0.30; 95% CI, 0.11–0.76) highlights the preponderant role of chemosensitivity on the success of the first-line treatment. In patients with highly chemosensitive diseases, the patient prognosis was driven more by the chemotherapy-induced antitumor effects than by the surgery. Conclusions: The tumor-primary chemosensitivity, assessed by the modeled CA-125 KELIM calculated during neoadjuvant chemotherapy (http://www.biomarker-kinetics.org/CA-125-neo), may be a major parameter to consider for decision-making regarding IDS attempt, and selecting patients for treatments meant to reverse the primary chemoresistance. See related commentary by May and Oza, p. 4432