Bryant Mary K, Ward Christine, Gaber Charles E, Strassle Paula D, Ollila David W, Laks Shachar
Department of Surgery, University of North Carolina, Chapel Hill, North Carolina.
Department of Surgery, Stony Brook University Hospital, Stony Brook, New York.
J Surg Oncol. 2020 Sep;122(4):653-659. doi: 10.1002/jso.26048. Epub 2020 Jun 20.
Merkel cell carcinoma (MCC) is a rare and aggressive form of skin cancer. It is an immunogenic tumor as evident by its association with Polyomavirus, immunotherapy response, and increased prevalence in the immunosuppressed population.
We sought to evaluate the impact of known clinicopathological determinants and immunosuppression on the risk of recurrence and mortality of MCC patients.
A retrospective, observational cohort study of patients diagnosed and/or treated with MCC at two tertiary academic institutions. We compared clinicopathological determinants, treatment modalities, and immunosuppression status on clinical outcomes of recurrence, disease-specific survival, and overall survival.
We evaluated 90 patients within our study and 34% had a cancer recurrence during follow-up. Patients with recurrence were significantly more likely to be immunosuppressed (32% vs 5%; P = .001). Estimated 5-year recurrence was 43%, and immunosuppressed patients were significantly more likely to recur (Hazard ratio [HR] 3.67 [1.80-7.51]; P < .0001). Immunosuppressed patients had significantly elevated cancer-specific mortality (HR 6.11[1.61-23.26]; P = .008).
Retrospective review with a prolonged observation period and changing treatment modalities.
Immunocompromised patients had a threefold increased incidence of 5-year mortality and over twofold increased incidence of any recurrence as non-immunocompromised patients. Patients' immunosuppressive status should be considered when making decisions regarding treatment, surveillance, and prognostication.
默克尔细胞癌(MCC)是一种罕见且侵袭性强的皮肤癌形式。它是一种免疫原性肿瘤,这从其与多瘤病毒的关联、免疫治疗反应以及在免疫抑制人群中患病率增加可以明显看出。
我们试图评估已知的临床病理决定因素和免疫抑制对MCC患者复发和死亡风险的影响。
对在两家三级学术机构诊断和/或治疗的MCC患者进行一项回顾性观察队列研究。我们比较了临床病理决定因素、治疗方式和免疫抑制状态对复发、疾病特异性生存和总生存等临床结局的影响。
我们研究中评估了90例患者,34%在随访期间出现癌症复发。复发患者免疫抑制的可能性显著更高(32%对5%;P = 0.001)。估计5年复发率为43%,免疫抑制患者复发的可能性显著更高(风险比[HR] 3.67[1.80 - 7.51];P < 0.0001)。免疫抑制患者的癌症特异性死亡率显著升高(HR 6.11[1.61 - 23.26];P = 0.008)。
回顾性研究,观察期较长且治疗方式不断变化。
免疫功能低下患者的5年死亡率发生率比非免疫功能低下患者增加了两倍,任何复发的发生率增加了一倍多。在做出治疗、监测和预后决策时,应考虑患者的免疫抑制状态。