Atezolizumab in combination with bevacizumab, paclitaxel and carboplatin for the first-line treatment of patients with metastatic non-squamous non-small cell lung cancer, including patients with EGFR mutations

被引:52
作者
Reck, Martin [1 ]
Shankar, Geetha [2 ]
Lee, Anthony [2 ]
Coleman, Shelley [2 ]
McCleland, Mark [2 ]
Papadimitrakopoulou, Vassiliki A. [3 ]
Socinski, Mark A. [4 ]
Sandler, Alan [2 ]
机构
[1] German Ctr Lung Res, Airway Res Ctr North, Lung Clin Grosshansdorf, Grosshansdorf, Germany
[2] Genentech Inc, Prod Dev Oncol, San Francisco, CA 94080 USA
[3] Univ Texas MD Anderson Canc Ctr, Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[4] AdventHlth Canc Inst, Thorac Oncol Program, Orlando, FL USA
关键词
Atezolizumab; bevacizumab; ENDOTHELIAL GROWTH-FACTOR; PHASE-II TRIAL; OPEN-LABEL; VEGF EXPRESSION; RESPONSE RATES; MULTICENTER; ERLOTINIB; ADENOCARCINOMA; CHEMOTHERAPY; RESISTANCE;
D O I
10.1080/17476348.2020.1701439
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction: Cancer immunotherapy has revolutionized the treatment of patients with advanced or metastatic non-small cell lung cancer (NSCLC). However, specific patient groups (e.g. patients with activating epidermal growth factor receptor [EGFR] mutations) do not appear to derive benefit from immune checkpoint inhibitor (ICI) monotherapy. Combining ICIs, such as atezolizumab, with chemotherapy and/or targeted therapies may help to address this unmet need. Areas covered: Atezolizumab is an anti-programmed death-ligand 1 therapy for several tumor types. We review its clinical efficacy and safety in the treatment of advanced or metastatic NSCLC, with a specific focus on the combination of atezolizumab with bevacizumab, carboplatin, and paclitaxel (ABCP). Data from IMpower150 show that the ABCP regimen provided clinical benefit to patients with non-squamous NSCLC, including those with EGFR mutations. Expert opinion: Combining ICIs with chemotherapy has proven to be superior to chemotherapy alone. However, tumor resistance to ICIs will likely increase as these drugs enter earlier lines of therapy, underscoring a need for effective treatments when immunotherapy fails. Data suggest that the ABCP regimen may circumvent ICI resistance mechanisms. Continued investigation into the regimen's mechanisms, improved patient profiling/selection, and treatment personalization will drive further development/discoveries.
引用
收藏
页码:125 / 136
页数:12
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