Guida Michele, D'Alò Alessandro, Mangia Anita, Di Pinto Federica, Sonnessa Margherita, Albano Anna, Sciacovelli Angela, Asabella Artor Niccoli, Fucci Livia
Department of Medical Oncology, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.
Functional Biomorphology Laboratory, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.
Front Oncol. 2020 Jul 7;10:1073. doi: 10.3389/fonc.2020.01073. eCollection 2020.
Merkel-cell carcinoma (MCC) is a rare, highly aggressive skin cancer typically involving elderly people. Surgery is usually the first treatment for primary tumor. In adjuvant setting, radiotherapy is effective in reducing local recurrence and in improving overall survival. Regarding advanced disease, systemic chemotherapy ended up disappointing results whereas antiPD1/antiPD-L1 immunotherapy recently gave relevant clinical benefits. Interestingly, about the half of MCC patients expresses high somatostatin receptors (SRs) to possibly represent a target for the therapeutic use of somatostatin analogs (SSAs). Nevertheless, SSAs have been little studied in MCC and cases treated with SSAs in association with checkpoint inhibitor immunotherapy have not been published yet. We report the case of a 73-year-old man affected by metastatic MCC of right arm previously treated with surgery and adjuvant radio and chemotherapy. Three years later the patient presented loco-regional relapse involving lateral-cervical, mediastinal, and submandibular lymph nodes with high value of chromogranin A and neuron specific enolase. Due to the high expression of SRs at octreoscan and immunoistochemistry, patient started octreotide 30 mg i.m. every 28 days with a good control of disease for about 2 years. A widespread progression of disease was reported afterwards. The patient started the antiPD-L1 avelumab immunotherapy, only recently available in Italy, while still taking SSA. The patient showed an impressive regression of the disease after only four cycles of avelumab until complete remission. SSA could be a valid therapeutic option in patients with MCC with high SR expression. When combined with PD-1/PD-L1 immune-checkpoint inhibition, SSA is likely to enhance antiproliferative activity. Our case report provides the rationale to conduct a prospective trial and translational research to verify the efficacy and safety of combined SSA and checkpoint inhibitors for advanced MCC.
默克尔细胞癌(MCC)是一种罕见的、侵袭性很强的皮肤癌,通常发生于老年人。手术通常是原发性肿瘤的首选治疗方法。在辅助治疗中,放疗可有效降低局部复发率并提高总生存率。对于晚期疾病,全身化疗最终结果令人失望,而抗PD1/抗PD-L1免疫疗法最近带来了显著的临床益处。有趣的是,大约一半的MCC患者表达高生长抑素受体(SRs),这可能使其成为生长抑素类似物(SSAs)治疗应用的靶点。然而,SSAs在MCC中的研究较少,且SSAs与检查点抑制剂免疫疗法联合治疗的病例尚未见报道。我们报告一例73岁男性患者,患有右臂转移性MCC,此前接受过手术及辅助放化疗。三年后,患者出现局部区域复发,累及颈外侧、纵隔及下颌下淋巴结,嗜铬粒蛋白A和神经元特异性烯醇化酶水平升高。由于奥曲肽扫描和免疫组化显示SRs高表达,患者开始每28天肌内注射30 mg奥曲肽,疾病得到了约2年的良好控制。此后报告疾病广泛进展。患者开始使用抗PD-L1阿维鲁单抗免疫疗法(该疗法最近才在意大利可用),同时仍服用SSA。仅在接受四个周期的阿维鲁单抗治疗后,患者疾病就出现了显著消退,直至完全缓解。对于SR高表达的MCC患者,SSA可能是一种有效的治疗选择。当与PD-1/PD-L1免疫检查点抑制联合使用时,SSA可能会增强抗增殖活性。我们的病例报告为开展前瞻性试验和转化研究以验证SSA与检查点抑制剂联合用于晚期MCC的疗效和安全性提供了理论依据。