Institute of Oncology, Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel.
Pathology Department, Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel.
Lung Cancer. 2019 Dec;138:109-115. doi: 10.1016/j.lungcan.2019.09.025. Epub 2019 Oct 1.
Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related death world-wide. Immune checkpoint inhibitors (ICI) have become the most promising type of treatment in oncology in general, and significantly so in NSCLC. Limited data is available about mechanisms of primary resistance. Data is lacking about mechanisms involved in acquired resistance or mixed responses in NSCLC. We aimed to identify mechanisms of resistance by studying biopsies taken from sites of secondary progression.
We identified all cases of NSCLC that have received ICI for advanced disease in our institute. Of these cases, those that have demonstrated acquired resistance or mixed responses, and have underwent a biopsy from a progressive lesion were analyzed. Selected specimens were subjected to next-generation sequencing (NGS; Oncomine™ Solid Tumour Fusion Transcript Kit).
Out of 664 lung cancer cases, 249 were NSCLC that have received ICI. Of these, eight cases matched our search criteria. Two of them demonstrated transformation to small cell lung cancer (SCLC; 2/8, 25%). NGS verified a common origin to a matched pre-treatment NSCLC specimen and an on-treatment progressive SCLC specimen. In two cases no tumor cells were found and in the remaining four the pathology was similar to the initial biopsy. In one of the cases of SCLC transformation platinum-etoposide chemotherapy was administered, with short-term benefit only and further disease progression.
Mechanisms of acquired resistance to ICI include SCLC transformation. Repeat biopsies of progressing lesions after initial response or in cases of mixed response can shed light on mechanisms of resistance.
非小细胞肺癌(NSCLC)是全球癌症相关死亡的主要原因。免疫检查点抑制剂(ICI)已成为肿瘤学中最有前途的治疗类型,尤其是在 NSCLC 中。关于原发性耐药的机制,目前数据有限。关于 NSCLC 获得性耐药或混合反应中涉及的机制的数据缺乏。我们旨在通过研究继发进展部位的活检来确定耐药机制。
我们确定了在我们研究所接受 ICI 治疗晚期疾病的所有 NSCLC 病例。在这些病例中,对那些表现出获得性耐药或混合反应并进行进展性病变活检的病例进行了分析。选择的标本进行下一代测序(NGS;Oncomine™ 实体瘤融合转录试剂盒)。
在 664 例肺癌病例中,有 249 例为接受 ICI 的 NSCLC。其中,有 8 例符合我们的搜索标准。其中 2 例表现为小细胞肺癌(SCLC;2/8,25%)转化。NGS 证实了治疗前 NSCLC 标本和治疗中进展性 SCLC 标本的共同起源。在 2 例中未发现肿瘤细胞,在其余 4 例中,病理与初始活检相似。在 SCLC 转化的 1 例中,给予顺铂-依托泊苷化疗,仅短期获益,随后疾病进展。
ICI 获得性耐药的机制包括 SCLC 转化。在初始反应后或混合反应病例中,对进展病变进行重复活检可以揭示耐药机制。