Tomsitz Dirk, Schlaak Max, Zierold Sarah, Pesch Giulia, Schulz Thomas U, Müller Genoveva, Zecha Christine, French Lars E, Heinzerling Lucie
Department of Dermatology and Allergy, University Hospital, Ludwig Maximilian University of Munich, 80337 Munich, Germany.
Department of Dermatology, Venereology and Allergology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, 10117 Berlin, Germany.
Cancers (Basel). 2022 Jul 5;14(13):3282. doi: 10.3390/cancers14133282.
Predictive markers for immune checkpoint inhibitor (ICI) therapy are needed. Thus, baseline blood counts have been investigated as biomarkers, showing that lymphopenia at the start of therapy with (ICI) is associated with a worse outcome in metastatic melanoma. We investigated the relationship between the occurrence of lymphopenia under ICI and disease outcome. Patients with metastatic melanoma who had undergone therapy with ICI were identified in our database. Only patients with a normal lymphocyte count at baseline were included in this retrospective study. Progression-free survival (PFS) and overall survival (OS) were compared between patients in which lymphopenia occurred during ICI therapy and those who did not develop lymphopenia. In total, 116 patients were analyzed. Lymphopenia occurred in 42.2% of patients, with a mean onset after 17 weeks (range 1-180 weeks). The occurrence of lymphopenia during immunotherapy was significantly associated with a shorter PFS and OS. Patients who developed lymphopenia ( = 49) had a mean PFS of 13.3 months (range 1-67 months) compared to 16.9 months (range 1-73 months) for patients who did not develop lymphopenia ( = 67; = 0.025). Similarly, patients with lymphopenia had a significantly shorter OS of 28.1 months (range 2-70 months) compared with 36.8 months (range 4-106 months) in patients who did not develop lymphopenia ( = 0.01). Patients with metastatic melanoma who develop lymphopenia during ICI therapy have a worse prognosis with significantly shorter PFS and OS compared with patients who do not develop lymphopenia.
免疫检查点抑制剂(ICI)治疗需要预测标志物。因此,人们已经对基线血细胞计数作为生物标志物进行了研究,结果表明,ICI治疗开始时的淋巴细胞减少与转移性黑色素瘤的较差预后相关。我们研究了ICI治疗期间淋巴细胞减少的发生与疾病预后之间的关系。在我们的数据库中识别出接受过ICI治疗的转移性黑色素瘤患者。本回顾性研究仅纳入基线淋巴细胞计数正常的患者。比较了ICI治疗期间出现淋巴细胞减少的患者与未出现淋巴细胞减少的患者的无进展生存期(PFS)和总生存期(OS)。总共分析了116例患者。42.2%的患者出现淋巴细胞减少,平均发病时间为17周(范围1 - 180周)。免疫治疗期间淋巴细胞减少的发生与较短的PFS和OS显著相关。出现淋巴细胞减少的患者(n = 49)的平均PFS为13.3个月(范围1 - 67个月),而未出现淋巴细胞减少的患者(n = 67)为16.9个月(范围1 - 73个月)(P = 0.025)。同样,出现淋巴细胞减少的患者的OS明显较短,为28.1个月(范围2 - 70个月),而未出现淋巴细胞减少的患者为36.8个月(范围4 - 106个月)(P = 0.01)。与未出现淋巴细胞减少的患者相比,ICI治疗期间出现淋巴细胞减少的转移性黑色素瘤患者预后更差,PFS和OS显著缩短。