Durvalumab plus tremelimumab in advanced or metastatic soft tissue and bone sarcomas: a single-centre phase 2 trial

医学 杜瓦卢马布 银耳霉素 肉瘤 内科学 人口 软组织肉瘤 肿瘤科 外科 临床终点 不利影响 癌症 临床试验 病理 彭布罗利珠单抗 易普利姆玛 免疫疗法 环境卫生
作者
Neeta Somaiah,Anthony P. Conley,Edwin R. Parra,Heather Lin,Behrang Amini,Luisa M. Solis Soto,Ruth Salazar,Carmélia Maria Noia Barreto,Honglei Chen,Swati Gite,Cara Haymaker,Elise F. Nassif,Chantale Bernatchez,Akash Mitra,J. Andrew Livingston,Vinod Ravi,Dejka M. Araujo,Robert S. Benjamin,Shreyaskumar Patel,Maria A. Zarzour
出处
期刊:Lancet Oncology [Elsevier BV]
卷期号:23 (9): 1156-1166 被引量:143
标识
DOI:10.1016/s1470-2045(22)00392-8
摘要

Few standard treatment options are available for patients with metastatic sarcomas. We did this trial to evaluate the efficacy, safety, and changes in the tumour microenvironment for durvalumab, an anti-PD-L1 drug, and tremelimumab, an anti-CTLA-4 drug, across multiple sarcoma subtypes.In this single-centre phase 2 trial, done at The University of Texas MD Anderson Cancer Center (Houston, TX USA), patients aged 18 years or older with advanced or metastatic sarcoma with an Eastern Cooperative Oncology Group performance status of 0 or 1 who had received at least one previous line of systemic therapy were enrolled in disease subtype-specific groups (liposarcoma, leiomyosarcoma, angiosarcoma, undifferentiated pleomorphic sarcoma, synovial sarcoma, osteosarcoma, alveolar soft-part sarcoma, chordoma, and other sarcomas). Patients received 1500 mg intravenous durvalumab and 75 mg intravenous tremelimumab for four cycles, followed by durvalumab alone every 4 weeks for up to 12 months. The primary endpoint was progression-free survival at 12 weeks in the intention-to-treat population (all patients who received at least one dose of treatment). Safety was also analysed in the intention-to-treat population. This trial is registered with ClinicalTrials.gov, NCT02815995, and is completed.Between Aug 17, 2016, and April 9, 2018, 62 patients were enrolled, of whom 57 (92%) received treatment and were included in the intention-to-treat population. With a median follow-up of 37·2 months (IQR 1·8-10·1), progression-free survival at 12 weeks was 49% (95% CI 36-61). 21 grade 3-4 treatment-related adverse events were reported, the most common of which were increased lipase (four [7%] of 57 patients), colitis (three [5%] patients), and pneumonitis (three [5%] patients). Nine (16%) patients had a treatment related serious adverse event. One patient had grade 5 pneumonitis and colitis.The combination of durvalumab and tremelimumab is an active treatment regimen for advanced or metastatic sarcoma and merits evaluation in specific subsets in future trials.AstraZeneca.
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