Treatment patterns and outcomes in early-stage ALK-rearranged non-small cell lung cancer

医学 杜瓦卢马布 阶段(地层学) 内科学 肺癌 肿瘤科 外科 癌症 无容量 免疫疗法 生物 古生物学
作者
Sabine Schmid,Miguel Hernández García,Siu Mee Cheng,L. Zhan,Simren Chotai,Karmugi Balaratnam,Khaleeq Khan,Devalben Patel,M. Catherine Brown,Robin Sachdeva,Wei Xu,Frances A. Shepherd,Adrian G. Sacher,Natasha B. Leighl,Penelope Ann Bradbury,Patrick M. Moriarty,M. Sara Kuruvilla,Geoffrey Liu
出处
期刊:Lung Cancer [Elsevier]
卷期号:166: 58-62 被引量:7
标识
DOI:10.1016/j.lungcan.2022.01.020
摘要

We evaluated the baseline demographics, treatment patterns, and outcomes of patients with ALK-rearranged early stage (Stage I-III) non-small cell lung cancer (NSCLC). We also evaluated the efficacy and toxicity of durvalumab consolidation treatment in patients with ALK-rearranged unresectable stage III disease.Retrospective chart-review analysis of all patients with histologically confirmed stage I-III reflexively tested ALK-rearranged NSCLC managed with curative intent at two Canadian Centers.Of 48 patients, 19 (40%) were stage I, 5 (10%) were stage II and 24 (50%) were stage-III. Median progression-free survival (PFS) was 27.6 months overall (95%CI: 20.5-51.4) and 144.4 months in stage-I, 27.6 months in stage-II and 14.9 months in stage III patients. Of 20 patients with unresectable stage-III disease treated with chemoradiation (9 also received durvalumab consolidation), 18/90% have relapsed. Median PFS was 10.9 months (95%CI:5.9-22.5). A non-significant trend toward improved PFS was seen in patients receiving additional durvalumab compared to patients treated with chemoradiation alone (median PFS, 12.5 vs 5.9 months, p = 0.16). Toxicity-related treatment modifications on subsequent first ALK-TKI at time of metastatic disease were needed in three (33%) patients who had received chemoradiation alone and two (29%) patients with consolidation durvalumab; no relevant pulmonary or hepato-toxicity was observed overall.Treatment strategies and PFS of patients with Stage I-III ALK-rearranged NSCLC are similar to patients without molecular driver alterations. Durvalumab consolidation treatment appears generally safe in patients with unresectable stage III ALK-rearranged disease; however, the degree of benefit of such an approach remains unclear.
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