Li Shuzhan, Zhang Jiali, Du Weijiao, Ren Xiubao, Zhang Xinwei
Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin, China.
Tianjin's Clinical Research Center for Cancer, Tianjin, China.
Gland Surg. 2022 Sep;11(9):1562-1567. doi: 10.21037/gs-22-420.
Ovarian clear cell carcinoma (OCCC) is a subtype of ovarian cancer with unique features at histological and molecular levels. The prevalence of OCCC is higher in east Asia than in Western countries. As cases are usually chemo-resistant, treatment effects of platinum-based chemotherapy are not satisfactory, especially for patients with stage III or IV disease. Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of patients with advanced-stage cancers. However, whether advanced OCCC patients benefit from ICIs remains elusive.
Herein, we report a Chinese patient with stage IIIB inoperable OCCC who was resistant to platinum-based chemotherapy and anlotinib. Next-generation sequencing (NGS) revealed a pathogenic polymerase epsilon () P286R mutation and a high level of tumor mutation burden (TMB) in tissue and plasma samples. The ICI sintilimab was then used with bevacizumab as third-line treatment. Tumor reduction was observed, and the patient underwent surgical resection which indicated a pathologic complete response (pCR). Maintenance therapy with sintilimab and bevacizumab was applied, and the patient has achieved overall survival (OS) of 35 months since the diagnosis. They have also achieved a progression-free survival (PFS) of 29 months since commencing ICI treatment and have been disease-free for 24 months after surgical resection.
The treatment effect of ICI in -mutant OCCC patients has been rarely reported. The treatment benefits observed in the stage IIIB OCCC patient who was resistant to platinum-based chemotherapy may be associated with the presence of mutation and a high level of TMB. Comprehensive genomic profiling could contribute to appropriate treatment decisions for OCCC.
卵巢透明细胞癌(OCCC)是卵巢癌的一种亚型,在组织学和分子水平上具有独特特征。OCCC在东亚的患病率高于西方国家。由于病例通常对化疗耐药,铂类化疗的治疗效果并不理想,尤其是对于III期或IV期疾病的患者。免疫检查点抑制剂(ICI)彻底改变了晚期癌症患者的治疗方式。然而,晚期OCCC患者是否能从ICI中获益仍不明确。
在此,我们报告一名中国III B期不可切除的OCCC患者,该患者对铂类化疗和安罗替尼耐药。二代测序(NGS)显示组织和血浆样本中存在致病性聚合酶ε()P286R突变和高水平的肿瘤突变负荷(TMB)。然后使用ICI信迪利单抗联合贝伐单抗作为三线治疗。观察到肿瘤缩小,患者接受了手术切除,显示病理完全缓解(pCR)。应用信迪利单抗和贝伐单抗进行维持治疗,自诊断以来患者已实现35个月的总生存期(OS)。自开始ICI治疗以来,他们还实现了29个月的无进展生存期(PFS),并且在手术切除后已无病生存24个月。
ICI在携带突变的OCCC患者中的治疗效果鲜有报道。在对铂类化疗耐药的III B期OCCC患者中观察到的治疗益处可能与突变的存在和高水平的TMB有关。全面的基因组分析有助于为OCCC做出合适的治疗决策。