Li Guiling, Jiang Yao
Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Front Oncol. 2022 Jul 12;12:916790. doi: 10.3389/fonc.2022.916790. eCollection 2022.
Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) is a rare and highly aggressive malignancy with a poor prognosis. Most patients experience recurrence even after surgery and chemotherapy, and there are no standard treatment options for recurrent disease. Here, we report the case of a 36-year-old woman with SCCOHT who underwent primary cytoreductive surgery without adjuvant chemotherapy and remained disease-free for 9 months. She then developed retroperitoneal lymph node metastasis and was treated with two cycles of bleomycin/etoposide/cisplatin chemotherapy. However, the disease progressed and the patient received four cycles of liposomal doxorubicin/ifosfamide chemotherapy, followed by local radiation to the enlarged retroperitoneal lymph nodes. She achieved partial remission for 13 months, after which the disease progressed again. Tumor tissues and blood samples were sent for next-generation sequencing. The results indicated a somatic SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member 4 () mutation, microsatellite stability, and a tumor mutation burden of 1.0 muts/Mb without any germline mutations. An anti-PD-1 antibody, camrelizumab, and an antiangiogenic agent, apatinib, were administered, and the patient achieved partial remission for 28 months. Our study provides the first clinical evidence that the combination therapy of camrelizumab and apatinib could be an effective treatment for recurrent SCCOHT.
卵巢小细胞癌高钙血症型(SCCOHT)是一种罕见且侵袭性很强的恶性肿瘤,预后较差。大多数患者即使在手术和化疗后仍会复发,且复发性疾病没有标准的治疗方案。在此,我们报告一例36岁患有SCCOHT的女性病例,该患者接受了初次肿瘤细胞减灭术但未进行辅助化疗,且无病生存了9个月。随后她出现了腹膜后淋巴结转移,并接受了两个周期的博来霉素/依托泊苷/顺铂化疗。然而,疾病进展,患者又接受了四个周期的脂质体阿霉素/异环磷酰胺化疗,随后对增大的腹膜后淋巴结进行了局部放疗。她获得了13个月的部分缓解,之后疾病再次进展。肿瘤组织和血液样本被送去进行二代测序。结果显示存在一种体细胞SWI/SNF相关、基质相关、肌动蛋白依赖性染色质调节因子A亚家族成员4()突变、微卫星稳定性,肿瘤突变负荷为1.0 muts/Mb,且没有任何胚系突变。给予抗PD-1抗体卡瑞利珠单抗和抗血管生成药物阿帕替尼,患者获得了28个月的部分缓解。我们的研究提供了首个临床证据,表明卡瑞利珠单抗和阿帕替尼联合治疗可能是复发性SCCOHT的有效治疗方法。