Durable complete response to pembrolizumab in microsatellite stable colorectal cancer.

Marzieh Gomar, Masoumeh Najafi, Mahdi Aghili, Salvatore Cozzi, Amin Jahanbakhshi
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Abstract

Introduction: Immunotherapy by checkpoint inhibitors, i.e., anti-programmed death-1(PD-1) or anti-programmed death-ligand 1 (PD-L1) antibodies, has gained more attention managing solid tumors. Pembrolizumab (an anti-PD-1 antibody) in metastatic colorectal cancer (CRC) was approved in 2017 by the US FDA.

Reason for the report: Pembrolizumab is not effective in microsatellite stable, mismatch-repair-proficient (MSS-pMMR) molecular phenotype, which comprises most CRC patients. In this report, we present the first case of metastatic CRC with a dramatic and durable response to pembrolizumab despite being of MSS-pMMR phenotype. A 34-year-old woman, presented seven years ago with T3N2bM0 colon cancer and an appendix carcinoid tumor. The last relapse with bilateral pulmonary metastases was refractory to all treatments. Although it seemed unresponsive to immunotherapy because of MSS molecular phenotype, due to the high expression level of PD-L1 (85%), we started treatment with pembrolizumab 200 mg every three weeks and continued for the overall 19 courses. Surprisingly, a rapid and complete response was observed that last until now, i.e., 17 months after discontinuation of pembrolizumab.

Outcome: Despite non-promising results in the current clinical trials, MSS-pMMR colorectal cancer patients' deprivation from immunotherapy seems not to be reasonable. There are ongoing clinical trials on checkpoint inhibitors either alone or in combination with other drugs. However, immunostaining for PD-L1 should be considered as a possible response predictor. Immunotherapy either by cell-based approaches or by checkpoint inhibitors may revolutionize cancer treatment Pembrolizumab has been approved by the FDA in 2017 for colorectal cancer. However, MSS-pMMR molecular phenotype which comprises the majority of CRC patients, has not shown a good response to checkpoint inhibitors. We present a MSS-pMMR case with complete and durable response to pembrolizumab We suggest immunostaining for PD-L1 as a possible response predictor to checkpoint inhibitors.

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微卫星稳定型结直肠癌患者对 pembrolizumab 的持久完全应答。
导言:检查点抑制剂(即抗程序性死亡-1(PD-1)或抗程序性死亡配体1(PD-L1)抗体)的免疫疗法在实体瘤的治疗中受到越来越多的关注。Pembrolizumab(一种抗PD-1抗体)治疗转移性结直肠癌(CRC)于2017年获得美国FDA批准:Pembrolizumab对微卫星稳定、错配修复功能良好(MSS-pMMR)分子表型无效,而大多数CRC患者都是这种表型。在本报告中,我们介绍了第一例尽管属于 MSS-pMMR 表型,但对 pembrolizumab 有显著和持久应答的转移性 CRC 患者。一位 34 岁的女性患者,七年前患 T3N2bM0 结肠癌和阑尾类癌。最近一次复发伴有双侧肺转移,对所有治疗方法均呈难治性。虽然由于 MSS 分子表型,患者似乎对免疫疗法没有反应,但由于 PD-L1 的高表达水平(85%),我们开始使用 pembrolizumab 200 毫克,每三周一次,持续治疗了 19 个疗程。令人惊讶的是,我们观察到了快速的完全应答,这种应答一直持续到现在,即停用 pembrolizumab 17 个月后:尽管目前的临床试验结果并不乐观,但MSS-pMMR结直肠癌患者被剥夺免疫疗法似乎并不合理。目前正在进行检查点抑制剂单独使用或与其他药物联合使用的临床试验。不过,PD-L1 的免疫染色应被视为一种可能的反应预测指标。以细胞为基础的免疫疗法或检查点抑制剂可能会彻底改变癌症治疗方法 Pembrolizumab 已于 2017 年获得 FDA 批准用于治疗结直肠癌。然而,占大多数 CRC 患者的 MSS-pMMR 分子表型对检查点抑制剂的反应并不理想。我们建议将 PD-L1 免疫染色作为检查点抑制剂的可能反应预测指标。
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