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广泛期小细胞肺癌(ES-SCLC)患者一线化疗联合免疫治疗后的二线治疗结果:一项大型法国多中心研究。

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.

机构信息

Nantes Université, Centre Hospitalier Universitaire Nantes, Medical oncology, F-44000 Nantes, France; Nantes Université, Inserm UMR 1307, CNRS UMR 6075, Université d'Angers, CRCI2NA Nantes, France.

Service de pneumologie et oncologie thoracique, CHU d'Ambroise-Paré, Boulogne-Billancourt, France.

出版信息

Lung Cancer. 2024 Aug;194:107887. doi: 10.1016/j.lungcan.2024.107887. Epub 2024 Jul 8.

Abstract

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.

摘要

简介

化疗联合免疫治疗(CT-IO)是广泛期小细胞肺癌(ES-SCLC)患者的标准治疗方法。本研究评估了 CT-IO 后的二线(2L)治疗效果。

方法

纳入了来自 10 个中心的所有接受一线 CT-IO 后二线治疗的患者。他们被分为 3 组:铂类药物、鲁比卡丁或其他药物(拓扑替康、CAV、紫杉烷类)。我们根据治疗和铂类无间隔期(PFI)<或≥90 天评估总生存期(OS)和二线无进展生存期(2L-PFS)。

结果

在 82 例患者中,中位年龄为 67.0 岁,29.3%的患者表现状态≥2,36.6%的患者有脑转移,69.5%的患者被认为是“铂类敏感”,30.5%的患者是“铂类耐药”(PFI≥或<90 天)。作为二线治疗,37/82 例(45.1%)患者接受了铂类双联治疗,21/82 例(25.6%)患者接受了鲁比卡丁治疗,24/82 例(29.3%)患者接受了其他药物治疗。PFI≥90 天的患者主要接受铂类药物再挑战治疗(34/57,59.6%)。中位随访 18.5 个月时,铂类耐药/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)(对数秩检验,p=0.017)。铂类耐药/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)。铂类药物再挑战/鲁比卡丁/其他药物治疗患者的中位 OS 分别为 8.1(95%CI,6.3-12.9)/4.9(95%CI,3.7-6.8)/5.1 个月(95%CI,2.5-7.8)(p=0.017)。铂类药物再挑战/鲁比卡丁/其他药物治疗患者的中位 2L-PFS 分别为 4.6(95%CI,3.9-7.2)/2.7(95%CI,1.6-3.9)/2.2 个月(95%CI,1.5-4.1)(p=0.025)。

讨论

尽管在我们的真实世界人群中具有特别不利的特征,但一线 CT-IO 后铂类药物再挑战显示出有希望的结果。IO 后使用鲁比卡丁的疗效与其他无铂类药物方案一样低。

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