奥拉帕尼
医学
放射治疗
阶段(地层学)
肺癌
肿瘤科
癌症
内科学
核医学
生物
生物化学
聚合酶
基因
古生物学
聚ADP核糖聚合酶
作者
Andreas Rimner,Benjamin H. Lok,Daphna Y. Gelblum,Rupesh Kotecha,Jacob Y. Shin,Quincey LaPlant,Annemarie F. Shepherd,Narek Shaverdian,Charles B. Simone,Vanessa J. Ng,Alina Ionescu,Helena A. Yu,Robert Michael Daly,Michael Offin,Ellen Yorke,Michelle S. Ginsberg,Zhigang Zhang,Abraham J. Wu,Charles M. Rudin
标识
DOI:10.1158/1078-0432.ccr-24-4342
摘要
Abstract Purpose: Patients with extensive-stage small cell lung cancer (ES-SCLC) are commonly treated with induction systemic therapy and consolidative thoracic radiation therapy (TRT). PARP inhibitors have demonstrated radiosensitization in preclinical lung cancer models. We performed an investigator-initiated, multi-institutional, single-arm, open label phase I study of concurrent olaparib with TRT. Patients and Methods: Patients without progression after induction platinum/etoposide +/- atezolizumab were treated with oral olaparib for 3 weeks and concurrent low-dose TRT (30 Gy/10 fractions) in weeks 2 and 3. Olaparib dose started at 50mg twice daily and escalated in 50mg/dose increments in cohorts of 3 patients each. Primary objectives were the safety and maximum tolerated dose (MTD) of olaparib + TRT. Secondary objectives included in-field local recurrence rate, progression-free survival (PFS), and overall survival (OS). Results: Between 10/2018 and 03/2022, 24 patients with a median age of 68 years were treated (median follow-up: 11.4 months) with platinum/etoposide and 30 Gy/10 fractions TRT; 10 patients also received atezolizumab. The MTD of olaparib with TRT was 200mg twice daily. There were 3 grade 3 (G3) dose-limiting adverse events (AEs), including pneumonitis/pneumonia, esophagitis, and abdominal pain. The most common G2-3 treatment-related AEs were esophagitis (n=12) and pneumonitis/pneumonia (n=2). There were no G4 or 5 AEs. The 12-month cumulative incidence of local recurrence was 27%, median PFS and OS were 3.6 months and 17.7 months, respectively. Conclusions: This study defined a MTD and recommended phase II dose of 200mg twice daily olaparib with concurrent low-dose TRT, and the combination appeared safe without unexpected toxicities.
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