Durvalumab联合同步放化疗治疗有限期小细胞肺癌患者:一项前瞻性单臂2期临床试验

IF 5.1 2区 医学 Q1 ONCOLOGY
Cancer Pub Date : 2026-03-15 DOI:10.1002/cncr.70351
Chunyang Song MMed, Xiaohan Zhao MMed, Shuguang Li MD, Xuehan Guo MMed, Xueyuan Zhang MD, Xiaobin Wang MMed, Youmei Li MD, Ke Yan MMed, Jingwei Su MD, Jinrui Xu MMed, Shuchai Zhu MD, Wenbin Shen MD
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引用次数: 0

摘要

背景:目前有限期小细胞肺癌(LS-SCLC)的标准治疗是同步放化疗(cCRT)加巩固免疫治疗,伴或不伴预防性颅脑照射(PCI)。然而,目前尚不清楚免疫治疗与放化疗同时进行是否会带来额外的益处。该临床试验旨在研究durvalumab联合放化疗治疗LS-SCLC的有效性和安全性。方法:在这项单臂2期研究中,LS-SCLC患者每3周接受3(1-4)个周期的依托泊苷、顺铂或卡铂和杜伐单抗治疗,随后进行30次每日一次的胸部放疗,总肿瘤体积为60.0 Gy,计划目标体积为54.0 Gy,并进行化学免疫治疗。在cCRT + durvalumab治疗后,患者每3周接受durvalumab巩固治疗,至少持续1年。在放化疗完成后,PCI被推荐给部分或完全缓解的患者。评估疗效和不良事件。结果:从2021年3月1日至2024年4月30日,共有51例患者入组,中位随访时间为32.0个月。1年、2年和3年无进展生存期(PFS)分别为56.9%、35.9%和28.2%,中位PFS为17.0个月。1年、2年和3年总生存率(OS)分别为88.1%、68.6%和49.6%,中位OS为32.0个月。17例(33.4%)患者出现3级或4级不良事件,其中7例与免疫相关。结论:这些结果表明,在放化疗中加入durvalumab耐受性良好,并显示出令人鼓舞的疗效,支持进一步研究符合根治性放化疗条件的LS-SCLC患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Durvalumab combined with concurrent chemoradiotherapy in patients with limited-stage small cell lung cancer: A prospective, single-arm, phase 2 clinical trial

Durvalumab combined with concurrent chemoradiotherapy in patients with limited-stage small cell lung cancer: A prospective, single-arm, phase 2 clinical trial

Background

The current standard treatment for limited-stage small cell lung cancer (LS-SCLC) is concurrent chemoradiotherapy (cCRT) plus consolidation immunotherapy, with or without prophylactic cranial irradiation (PCI). However, it remains unknown whether administering immunotherapy concurrently with chemoradiotherapy confers additional benefit. This clinical trial is designed to investigate the efficacy and safety using durvalumab with chemoradiotherapy for LS-SCLC.

Methods

In this single-arm phase 2 study, patients with LS-SCLC received three (1–4) cycles of etoposide, cisplatin, or carboplatin, and durvalumab every 3 weeks, following by thoracic radiotherapy of 60.0 Gy to the gross tumor volume and 54.0 Gy to the planning target volume in 30 once-daily fractions and chemoimmunotherapy. After cCRT plus durvalumab, patients received durvalumab consolidation therapy every 3 weeks for a minimum of 1 year. PCI was recommended to patients with partial or complete response when chemoradiotherapy completed. Efficacy and adverse events were assessed.

Results

Overall, 51 patients were enrolled from March 1, 2021, to April 30, 2024, with a median follow-up of 32.0 months. The 1-, 2-, and 3-year progression-free survival (PFS) rates were 56.9%, 35.9%, and 28.2%, respectively, and the median PFS was 17.0 months. The 1-, 2-, and 3-year overall survival (OS) rates were 88.1%, 68.6%, and 49.6%, respectively, and the median OS was 32.0 months. There were 17 (33.4%) patients with grade 3 or 4 adverse events, 7 of which were immune‑related.

Conclusions

These results suggest that the addition of durvalumab to chemoradiotherapy was well tolerated and showed encouraging efficacy, supporting further investigation in patients with LS-SCLC eligible for radical chemoradiotherapy.

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来源期刊
Cancer
Cancer 医学-肿瘤学
CiteScore
13.10
自引率
3.20%
发文量
480
审稿时长
2-3 weeks
期刊介绍: The CANCER site is a full-text, electronic implementation of CANCER, an Interdisciplinary International Journal of the American Cancer Society, and CANCER CYTOPATHOLOGY, a Journal of the American Cancer Society. CANCER publishes interdisciplinary oncologic information according to, but not limited to, the following disease sites and disciplines: blood/bone marrow; breast disease; endocrine disorders; epidemiology; gastrointestinal tract; genitourinary disease; gynecologic oncology; head and neck disease; hepatobiliary tract; integrated medicine; lung disease; medical oncology; neuro-oncology; pathology radiation oncology; translational research
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