Department of Medicine, Section of Hematology and Oncology, The University of Chicago Medicine, Chicago, IL.
Department of Radiation Oncology, The Queen's Medical Center, Honolulu, HI.
Clin Lung Cancer. 2024 Dec;25(8):e448-e452. doi: 10.1016/j.cllc.2024.08.004. Epub 2024 Aug 13.
Immunotherapy in combination with chemotherapy is first-line treatment for patients with extensive-stage small-cell lung cancer (ES-SCLC). Growing evidence suggests that radiation, specifically stereotactic body radiation therapy (SBRT), may enhance the immunogenic response as well as cytoreduce tumor burden. The primary objective of the study is to determine the progression free survival for patients with newly diagnosed ES-SCLC treated with combination multisite SBRT and chemo-immunotherapy (carboplatin, etoposide, and durvalumab).
This is a multicenter, single arm, phase 2 study. Patients with treatment-naïve, ES-SCLC will be eligible for this study. Patients will receive durvalumab 1500mg IV q3w, carboplatin AUC 5 to 6 mg/mL q3w, and etoposide 80 to 100 mg/m2 on days 1 to 3 q3w for four cycles, followed by durvalumab 1500mg IV q4w until disease progression or unacceptable toxicity. Ablative radiation will be delivered 1 to 4 extracranial sites in 3 or 5 fractions, determined by location, during cycle 2. The primary endpoint is progression-free survival, measured from day 1 of chemoimmunotherapy. Secondary endpoints include grade ≥3 toxicity by CTCAE v5.0 within three months of RT, overall survival, response rate, time to second line systemic therapy, and time to new distant progression.
Now that immunotherapy is an established part of ES-SCLC management, it is important to further optimize its use and effect. This study will investigate the progression-free survival of combined SBRT and chemo-immunotherapy in patients with ES-SCLC. In addition, the data from this study may further inform the immunogenic role of SBRT with chemo-immunotherapy, as well as identify clinical, biological, or radiomic prognostic features.
免疫疗法联合化疗是广泛期小细胞肺癌(ES-SCLC)患者的一线治疗方法。越来越多的证据表明,放疗,特别是立体定向体部放疗(SBRT),可能增强免疫原性反应,并减少肿瘤负担。本研究的主要目的是确定接受联合多部位 SBRT 和化疗免疫治疗(卡铂、依托泊苷和度伐利尤单抗)治疗的新诊断为 ES-SCLC 患者的无进展生存期。
这是一项多中心、单臂、2 期研究。未经治疗的 ES-SCLC 患者有资格参加本研究。患者将接受度伐利尤单抗 1500mg IV q3w、卡铂 AUC 5 至 6mg/ml q3w 和依托泊苷 80 至 100mg/m2,第 1 至 3 天 q3w,共 4 个周期,随后度伐利尤单抗 1500mg IV q4w,直至疾病进展或不可接受的毒性。在第 2 周期期间,根据位置,将 1 至 4 个颅外部位的消融性放疗分为 3 或 5 个剂量。主要终点是从化疗免疫治疗的第 1 天开始的无进展生存期。次要终点包括 RT 后 3 个月内按 CTCAE v5.0 分级≥3 的毒性、总生存期、反应率、二线全身治疗时间和新远处进展时间。
由于免疫疗法已成为 ES-SCLC 治疗的重要组成部分,因此,进一步优化其使用和效果非常重要。本研究将研究联合 SBRT 和化疗免疫治疗在 ES-SCLC 患者中的无进展生存期。此外,本研究的数据可能进一步阐明 SBRT 联合化疗免疫治疗的免疫原性作用,并确定临床、生物学或放射组学的预后特征。