Amaral Teresa, Seeber Olivia, Mersi Edgar, Sanchez Stephanie, Thomas Ioannis, Meiwes Andreas, Forschner Andrea, Leiter Ulrike, Eigentler Thomas, Keim Ulrike, Garbe Claus
Center for Dermatooncology, Department of Dermatology, Eberhard Karls University of Tuebingen, 72076 Tuebingen, Germany.
Portuguese Air Force-Health Care Direction, 1649-020 Lisbon, Portugal.
Cancers (Basel). 2020 Apr 22;12(4):1027. doi: 10.3390/cancers12041027.
Primary resistance to immunotherapy can be observed in approximately 40-65% of the stage IV melanoma patients treated with immune checkpoint inhibitors. A minority of the patients receive a second-line therapy, and the clinical benefit is small.
Stage IV melanoma patients treated with first-line PD-1-based immunotherapy between January 2015 and December 2018 were investigated. Primary resistance was defined as progressive disease (PD) at the time of the first tumor assessment after starting immunotherapy. Patients with complete response, partial response, and stable disease were classified as having disease control (DC). Overall survival (OS) and progression-free survival (PFS) were evaluated by Kaplan-Meier estimator. Univariate and multivariate logistic regression analyses were performed to determine prognostic factors associated with OS.
Three hundred and nineteen patients were included, and 40% had primary resistance to immunotherapy. The median follow-up time was 22 months. Patients with primary resistance had 1-, 2-, and 3-year OS rates of 41%, 15%, and 10%, respectively, compared to 91%, 81%, and 65% for the patients who achieved DC. The following independently significant prognostic factors for OS were identified: protein S100B level and primary tumor localization. There was a statistically significant difference for OS ( < 0.0001) but not for PFS ( = 0.230) when analyzing risk groups formed with a combination of these two variables (low-, intermediate-, and high-risk subgroups).
Melanoma patients with primary resistance to immunotherapy have a dismal prognosis. Response at the first tumor assessment after starting immunotherapy is a stronger prognostic factor for the further course of the disease than pretreatment risk factors.
在接受免疫检查点抑制剂治疗的IV期黑色素瘤患者中,约40%-65%可观察到对免疫治疗的原发性耐药。少数患者接受二线治疗,临床获益较小。
对2015年1月至2018年12月期间接受一线基于PD-1免疫治疗的IV期黑色素瘤患者进行研究。原发性耐药定义为开始免疫治疗后首次肿瘤评估时出现疾病进展(PD)。完全缓解、部分缓解和疾病稳定的患者被分类为疾病控制(DC)。采用Kaplan-Meier估计器评估总生存期(OS)和无进展生存期(PFS)。进行单因素和多因素逻辑回归分析以确定与OS相关的预后因素。
纳入319例患者,40%对免疫治疗有原发性耐药。中位随访时间为22个月。原发性耐药患者的1年、2年和3年OS率分别为41%、15%和10%,而实现DC的患者分别为91%、81%和65%。确定了以下对OS具有独立显著意义的预后因素:蛋白S100B水平和原发肿瘤部位。分析由这两个变量组合形成的风险组(低、中、高风险亚组)时,OS有统计学显著差异(<0.0001),但PFS无差异(=0.230)。
对免疫治疗有原发性耐药的黑色素瘤患者预后不佳。开始免疫治疗后首次肿瘤评估时的反应比治疗前风险因素对疾病进一步发展的预后影响更强。