广泛期小细胞肺癌(ES-SCLC)患者一线化疗加免疫疗法后的二线治疗效果:法国一项大型多中心研究

IF 4.5 2区 医学 Q1 ONCOLOGY
Elvire Pons-Tostivint , Remy Ezzedine , Thomas Goronflot , Perrine Crequit , Thierry Chatellier , Judith Raimbourg , Jaafar Bennouna , Etienne Giroux Leprieur , Marie Porte
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引用次数: 0

摘要

导言化疗联合免疫疗法(CT-IO)是治疗广泛期小细胞肺癌(ES-SCLC)患者的标准疗法。本研究评估了CT-IO后二线治疗(2L)的有效性。患者和方法纳入了来自10个中心的所有在一线CT-IO后接受2L治疗的患者。他们被分为三组:铂类、鲁比替丁或其他药物(拓扑替康、CAV、紫杉类)。我们根据治疗方法和无铂期(PFI)< 或≥90天评估了总生存期(OS)和2L无进展生存期(2L-PFS)。结果 在纳入的82例患者中,中位年龄为67.0岁,29.3%的患者无铂期≥2,36.6%的患者脑部进展,69.5%的患者被认为是 "对铂敏感",30.5%的患者被认为是 "对铂耐药"(PFI分别≥或< 90天)。作为 2L,37/82(45.1%)名患者接受了铂双联疗法,21/82(25.6%)名患者接受了鲁比替丁疗法,24/82(29.3%)名患者接受了其他疗法。PFI≥90天的患者主要接受铂类再挑战治疗(34/57,59.6%)。中位随访时间为18.5个月,铂金耐药/敏感患者的中位OS分别为5.0个月(95 %CI,1.5-7.9)/6.8个月(95 %CI,5.5-8.7)(对数秩p = 0.017)。铂耐药/敏感患者的中位2L-PFS分别为1.9个月(95 %CI,1.2-4.7)/3.9个月(95 %CI,2.9-6.0)。铂重试/鲁比替丁/其他疗法的中位OS分别为8.1个月(95 %CI,6.3-12.9)/4.9个月(95 %CI,3.7-6.8)/5.1个月(95 %CI,2.5-7.8)(P = 0.017)。中位2L-PFS分别为4.6个月(95 %CI,3.9-7.2)/2.7个月(95 %CI,1.6-3.9)/2.2个月(95 %CI,1.5-4.1),铂类再挑战/鲁比替丁/其他疗法分别为4.6个月(95 %CI,3.9-7.2)/2.7个月(95 %CI,1.6-3.9)/2.2个月(95 %CI,1.5-4.1)(p = 0.025)。IO后使用鲁比替丁的疗效与其他无铂方案一样低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Second-line treatment outcomes after first-line chemotherapy plus immunotherapy in Extensive-Stage small cell lung cancer (ES-SCLC) patients: A large French multicenter study

Introduction

Chemotherapy combined with immunotherapy (CT-IO) is the standard treatment for patients with Extensive-Stage Small Cell Lung Cancer (ES-SCLC). This study evaluates the effectiveness of second-line (2L) following CT-IO.

Patients and Methods

All patients from 10 centers who received a 2L after a first-line CT-IO were included. They were divided into 3 groups: platinum-based, lurbinectedin or others (topotecan, CAV, taxanes). We assessed overall survival (OS) and 2L progression-free survival (2L-PFS) according to treatment and platinum free-interval (PFI) < or 90 days.

Results

Among 82 patients included, median age was 67.0 years, 29.3 % had a Performans Status ≥ 2, 36.6 % had brain progression, 69.5 % were considered “platine-sensitive” and 30.5 % “platine-resistant” (PFI ≥ or < 90 days, respectively). As 2L, 37/82 patients (45.1 %) received platinum-doublet, 21/82 (25.6 %) lurbinectedin and 24/82 (29.3 %) others. Patients with a PFI ≥ 90 days received mainly platinum-based rechallenge (34/57, 59.6 %). With a median follow-up of 18.5 months, the median OS was 5.0 months (95 %CI, 1.5–7.9) / 6.8 months (95 %CI, 5.5–8.7) for platinum-resistant / sensitive, respectively (log rank p = 0.017). The median 2L-PFS was 1.9 months (95 %CI, 1.2–4.7) / 3.9 months (95 %CI, 2.9–6.0) for platinum-resistant / sensitive, respectively. Median OS was 8.1 (95 %CI, 6.3–12.9) / 4.9 (95 %CI, 3.7–6.8) / 5.1 months (95 %CI, 2.5–7.8) with platinum rechallenge / lurbinectedin / others, respectively (p = 0.017). Median 2L-PFS was 4.6 (95 %CI, 3.9–7.2) / 2.7 (95 %CI, 1.6–3.9) / 2.2 months (95 %CI, 1.5–4.1) with platinum rechallenge / lurbinectedin / others, respectively (p = 0.025).

Discussion

Platinum-based rechallenge after a first-line CT-IO showed promising results despite particularly unfavorable characteristics within our real-word population. Lurbinectedin when used after IO demonstrated as low efficacy as other platinum-free regimens.

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来源期刊
Lung Cancer
Lung Cancer 医学-呼吸系统
CiteScore
9.40
自引率
3.80%
发文量
407
审稿时长
25 days
期刊介绍: Lung Cancer is an international publication covering the clinical, translational and basic science of malignancies of the lung and chest region.Original research articles, early reports, review articles, editorials and correspondence covering the prevention, epidemiology and etiology, basic biology, pathology, clinical assessment, surgery, chemotherapy, radiotherapy, combined treatment modalities, other treatment modalities and outcomes of lung cancer are welcome.
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