Rastrelli Marco, Ferrazzi Beatrice, Cavallin Francesco, Chiarion Sileni Vanna, Pigozzo Jacopo, Fabozzi Alessio, Tropea Saveria, Vecchiato Antonella, Costa Alessandra, Parisi Alessandro, Rossi Carlo Riccardo, Del Fiore Paolo, Alaibac Mauro
Surgical Oncology Unit, Veneto Institute of Oncology IOV⁻IRCCS, 35121 Padua, Italy.
Dermatology Unit and Pathology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padua, Italy.
Cancers (Basel). 2018 Sep 24;10(10):350. doi: 10.3390/cancers10100350.
Merkel Cell Carcinoma (MCC) is a rare but highly aggressive neuroendocrine neoplasm of the skin. This study aimed at describing characteristics, treatment, and prognosis of a series of consecutive cases of MCC patients, in order to contribute to the investigation of this rare malignancy and provide better patient care. This is a retrospective cohort study including all 90 patients diagnosed and/or treated for MCC between 1991 and 2018 at the Veneto Institute of Oncology in Padua (Italy). Patient and tumor characteristics, treatment, and immunohistochemical data were extracted from a prospectively collected local database. There were 68 primary (76%) and 22 non-primary (15 occult primary, three metastatic, four recurrence) tumors (24%). CK20 expression was associated with reduced overall (HR 2.92, 95% CI 1.04⁻8.16) and disease-specific (HR 4.62, 95% CI 1.31⁻16.28) survival. Immunomodulatory regimens for treatment of other comorbidities were associated with reduced disease-specific ((HR 2.15, 95% CI 1.06⁻4.36) and recurrence-free (HR 3.08, 95% CI 1.44⁻6.57) survival. Iatrogenic immunomodulation resulted as the main factor associated with impaired prognosis. Lack of CK20 expression was associated with better survival.
默克尔细胞癌(MCC)是一种罕见但侵袭性很强的皮肤神经内分泌肿瘤。本研究旨在描述一系列连续的MCC患者的特征、治疗方法及预后情况,以推动对这种罕见恶性肿瘤的研究,并为患者提供更好的治疗。这是一项回顾性队列研究,纳入了1991年至2018年期间在意大利帕多瓦的威尼托肿瘤研究所诊断和/或治疗的所有90例MCC患者。从一个前瞻性收集的本地数据库中提取患者和肿瘤特征、治疗方法及免疫组化数据。有68例原发性肿瘤(76%)和22例非原发性肿瘤(15例隐匿性原发性肿瘤、3例转移性肿瘤、4例复发性肿瘤)(24%)。细胞角蛋白20(CK20)表达与总生存期(风险比[HR]2.92,95%置信区间[CI]1.04至8.16)和疾病特异性生存期降低相关(HR 4.62,95%CI 1.31至16.28)。用于治疗其他合并症的免疫调节方案与疾病特异性生存期(HR 2.15,95%CI 1.06至4.36)和无复发生存期降低相关(HR 3.08,95%CI 1.44至6.57)。医源性免疫调节是与预后受损相关的主要因素。CK20表达缺失与更好的生存期相关。