Cobo Manuel, Rodríguez-Abreu Delvys, Pérez Parente Diego, Ruiz Gracia Pedro, González Jorge G
Hospital Regional Universitario de Málaga General, Malága, Spain.
Complejo Hospitalario Universitario Insular Materno-Infantil de Gran Canaria, Universidad de Las Palmas de Gran Canaria, Las Palmas, Spain.
Oncol Ther. 2021 Jun;9(1):41-53. doi: 10.1007/s40487-021-00139-3. Epub 2021 Feb 13.
Atezolizumab is a monoclonal antibody targeting the programmed death ligand 1 (PD-L1) that was approved in 2017 in the USA and Europe for the second-line treatment of advanced or metastatic non-small cell lung cancer (NSCLC). This review article describes the practical clinical issues associated with atezolizumab treatment in NSCLC using a combination of four illustrative cases and a narrative literature review. The first two cases highlight the importance of tumor mutational status when making treatment decisions. A 62-year-old man with epidermal growth factor receptor (EGFR)-mutated, PD-L1-positive, stage IV lung adenocarcinoma received treatment with second-line atezolizumab + bevacizumab, carboplatin, and paclitaxel (BCP) after first-line osimertinib. In the second case, a 63-year-old man with stage IVb lung adenocarcinoma with anaplastic lymphoma kinase (ALK) translocation received sixth-line treatment with atezolizumab + BCP. The two final cases both had extensive metastases. A 55-year-old woman with EGFR-mutated lung adenocarcinoma received second-line treatment with atezolizumab + BCP after development of multiple metastases, followed by atezolizumab + bevacizumab until last follow-up. A 42-year-old man with PD-L1-positive pulmonary adenocarcinoma (negative for EGFR mutations) developed liver and brain metastases after several lines of therapy. He underwent holocranial radiation and received atezolizumab + BCP, which resulted in a decrease in all measurable and evaluable tumoral lesions. These illustrative cases indicate that the type and number of mutations may influence treatment response to atezolizumab, and that atezolizumab may provide clinical benefit in patients with high disease burden.
阿替利珠单抗是一种靶向程序性死亡配体1(PD-L1)的单克隆抗体,于2017年在美国和欧洲获批用于晚期或转移性非小细胞肺癌(NSCLC)的二线治疗。本文通过四个典型病例及文献综述,阐述了NSCLC患者接受阿替利珠单抗治疗时的实际临床问题。前两个病例强调了治疗决策时肿瘤突变状态的重要性。一名62岁的男性,表皮生长因子受体(EGFR)突变、PD-L1阳性、IV期肺腺癌患者,一线使用奥希替尼治疗后,接受二线阿替利珠单抗联合贝伐单抗、卡铂和紫杉醇(BCP)治疗。在第二个病例中,一名63岁的男性,IVb期肺腺癌伴间变性淋巴瘤激酶(ALK)易位,接受了阿替利珠单抗联合BCP的六线治疗。最后两个病例均有广泛转移。一名55岁的女性,EGFR突变的肺腺癌患者,在出现多处转移后接受二线阿替利珠单抗联合BCP治疗,随后接受阿替利珠单抗联合贝伐单抗治疗直至最后一次随访。一名42岁的男性,PD-L1阳性肺腺癌(EGFR突变阴性),在经过多线治疗后出现肝转移和脑转移。他接受了全脑放疗并接受阿替利珠单抗联合BCP治疗,所有可测量和可评估的肿瘤病灶均缩小。这些典型病例表明,突变的类型和数量可能影响对阿替利珠单抗的治疗反应,并且阿替利珠单抗可能为疾病负担高的患者带来临床获益。