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Real‐world outcomes of neoadjuvant chemoimmunotherapy in patients with nonsmall cell lung cancer: Predictors of surgery, pathologic complete response, and event‐free survival

化学免疫疗法 医学 新辅助治疗 肿瘤科 完全响应 肺癌 癌症 内科学 克拉斯 临床试验 突变 化疗 梅德林 细胞 总体生存率
作者
Alissa J. Cooper,Edoardo Garbo,Andrea Arfè,Michael Conroy,Narek Shaverdian,Matthew J. Bott,Teresa Gorría,Federica Pecci,Mihaela Aldea,Valsamo Anagnostou,Adam J. Schoenfeld,Daniel R. Gomez,Patrick M. Forde,Mark M. Awad,David R. Jones,Biagio Ricciuti,Jamie E. Chaft
出处
期刊:Cancer [Wiley]
卷期号:131 (18): e70081-e70081 被引量:2
标识
DOI:10.1002/cncr.70081
摘要

BACKGROUND: Trials of neoadjuvant chemoimmunotherapy (chemoIO) have changed the standard of care for resectable nonsmall cell lung cancer (NSCLC). This study characterizes the outcomes of off-trial patients who received treatment with neoadjuvant chemoIO. METHODS: The authors analyzed records of patients with stage IB-III NSCLC who received neoadjuvant chemoIO with an intent to proceed to surgical resection at three US academic institutions. Clinical, demographic, and pathologic factors were incorporated in univariable and multivariable regression models to identify associations with outcomes (resection status, pathologic complete response [pCR], and subsequent event-free survival [EFS]) after standard-of-care neoadjuvant chemoIO. RESULTS: Analyses included 115 patients, of whom 63% had stage III disease, 77% completed three cycles of chemoIO, and 78% underwent surgical resection. Ages older than 72 years versus 64 years and younger were associated with not proceeding to surgery in univariable (p = .006) and multivariable (p = .014) regression analyses. Nineteen patients (17%) had tumors with a pCR, and 34 (30%) had a major pathologic response. Positive programmed death-ligand 1 (PD-L1) expression (≥50%; vs. negative PD-L1 expression: odds ratio, 12.1; 95% confidence interval, 2.0-73.7; p = .007) and KRAS mutations (vs. wild-type KRAS: odds ratio, 3.9; 95% confidence interval, 1.07-14.4; p = .039) were associated with a higher probability of pCR in univariable analysis. The median event-free survival was not reached and did not differ among subgroups stratified by key clinical variables. CONCLUSIONS: The results from this study confirm the trial experience of high pCR rates after neoadjuvant chemoIO. This supports the use of chemoIO irrespective of KRAS mutation status, PD-L1 expression, and histology, but suggests that this approach may be less suitable for older patients.
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