Neoadjuvant and Adjuvant Systemic Therapy for Early-Stage Non-small-Cell Lung Cancer

被引:20
|
作者
Isaacs, James [1 ]
Stinchcombe, Thomas E. [1 ]
机构
[1] Duke Univ, Duke Canc Inst, Div Med Oncol, Med Ctr, DUMC 3841, Durham, NC 27710 USA
关键词
PATHOLOGICAL COMPLETE RESPONSE; OPEN-LABEL; PREOPERATIVE CHEMOTHERAPY; SINGLE-ARM; MULTICENTER; SURVIVAL; IMMUNOTHERAPY; ATEZOLIZUMAB; BEVACIZUMAB; GEFITINIB;
D O I
10.1007/s40265-022-01721-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Approximately a third of patients with non-small-cell lung cancer (NSCLC) present with surgically resectable disease. Patients who undergo surgical resection are at a high risk of relapse, and neoadjuvant and adjuvant chemotherapy improves disease-free survival (DFS) and overall survival (OS). The outcomes with neoadjuvant and adjuvant chemotherapy are similar, and both are used in clinical practice. Recent trials investigated the role of immunotherapy and targeted therapy in patients with early-stage disease. A phase III trial of adjuvant atezolizumab compared with standard of care (SOC) in patients with resected stage II or III disease and PD-L1 expression of 1% or greater, and a second trial of adjuvant pembrolizumab compared with placebo in patients with stage IB-III (regardless of tumor proportion score PD-L1 expression), both demonstrated an improvement in DFS. In the neoadjuvant setting, results of a phase III trial of chemotherapy and nivolumab compared with chemotherapy alone revealed an improvement in pathological complete response rate and event-free survival in patients with stage IB-IIIA disease. Finally, for epidermal growth factor receptor (EGFR) mutant NSCLC, a phase III trial of osimertinib compared with SOC revealed an improvement in DFS. The results of these and ongoing trials illustrate the integration of immunotherapy and targeted therapies into the treatment paradigm of patients with surgically resected NSCLC and have led to FDA and EMA approvals in selected populations. Neoadjuvant trials have investigated novel endpoints such as major and complete pathological response, which have the potential to serve as surrogate endpoints for future trials.
引用
收藏
页码:855 / 863
页数:9
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