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A prognostic model for platinum‐doublet as second‐line chemotherapy in advanced non‐small‐cell lung cancer patients

机译:晚期非小细胞肺癌患者二线铂类药物作为二线化疗的预后模型

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摘要

Poor prognosis of advanced non‐small‐cell lung cancer (NSCLC) patients and the promising therapeutic effect of platinum urge the oncologists to evaluate the role of platinum doublet as second‐line chemotherapy and establish the definition of platinum sensitivity in NSCLC. We retrospectively analyzed 364 advanced NSCLC patients who received platinum‐doublet regimens as second‐line chemotherapy after platinum‐based first‐line treatment. Patients were divided into four groups by their time‐to‐progression (TTP) after first‐line chemotherapy: 0–3, 4–6, 7–12, and >12‐month group, respectively. Treatment efficacy of patients' overall survival (OS), progression‐free survival (PFS), and response rate (RR), as well as treatment‐related toxicity, were compared among the four groups. A prognosis score system and a nomogram were established by Cox proportional hazard model, and validated by concordance index (c‐index). Median OS was 14.0, 16.0, 20.0, 25.0 months for patients in the 0–3, 4–6, 7–12, >12‐month group, respectively. Age ≤60 years (P = 0.002), female (P = 0.019), and TTP>12 months (P = 0.003) were independent prognostic factors. Prognostic score was calculated by adding 1 point each for any of the above three indicators, with a c‐index of 0.590 (95% confidential interval [CI], 0.552–0.627). Median OS were equal to 25.0, 16.0, and 11.0 months for best (2–3 points), intermediate (1 point) and worst (0 point) category, respectively (P < 0.0001). A nomogram that integrated patient's age, gender, and TTP for OS has a c‐index of 0.623 (95% CI, 0.603–0.643). Female, younger than 60 years, and TTP greater than 12 months may indicate prolonged survival after platinum‐doublet second‐line chemotherapy in advanced NSCLCpatients.
机译:晚期非小细胞肺癌(NSCLC)患者的预后较差,铂的治疗效果令人鼓舞,这促使肿瘤科医生评估铂双线药物作为二线化疗的作用,并确立了NSCLC中铂敏感性的定义。我们回顾性分析了364名在铂类一线治疗后接受铂类双联疗法作为二线化疗的晚期NSCLC患者。根据一线化疗后的进展时间(TTP)将患者分为四组:分别为0–3、4–6、7–12和> 12个月组。比较了四组患者的总生存期(OS),无进展生存期(PFS)和缓解率(RR)以及治疗相关的毒性。通过Cox比例风险模型建立预后评分系统和列线图,并通过一致性指数(c-index)进行验证。 0-3、4-6、7-12,> 12个月组患者的OS中位数分别为14.0、16.0、20.0、25.0月。年龄≤60岁(P = 0.002),女性(P = 0.019)和TTP> 12个月(P = 0.003)是独立的预后因素。通过为上述三个指标中的任何一个加1分,计算出预后评分,c指数为0.590(95%机密区间[CI],0.552–0.627)。最佳类别(2-3点),中级(1点)和最差(0点)类别的中值OS分别等于25.0、16.0和11.0个月(P <0.0001)。结合患者的年龄,性别和OS的TTP的列线图的c指数为0.623(95%CI,0.603-0.643)。女性,年龄小于60岁且TTP大于12个月的患者可能表明晚期NSCLC患者接受铂类双线二线化疗后生存期延长。

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