Qiu Jian, Xu Jiewei, Yao Guorong, Zhu Fengjia, Wang Yanyan, Fu Yunfeng
Department of Obstetrics and Gynaecology, Huzhou Central Hospital, Affiliated Central Hospital Huzhou University, Huzhou, 313000, People's Republic of China.
Department of General Surgery, Huzhou Central Hospital, Affiliated Central Hospital Huzhou University, Huzhou, 313000, People's Republic of China.
Cancer Manag Res. 2022 Jul 22;14:2235-2241. doi: 10.2147/CMAR.S366771. eCollection 2022.
Large cell neuroendocrine carcinoma (LCNEC) is a rare histological subtype of ovarian cancer. A few cases have been reported in the literature with extreme invasiveness and a poor prognosis. However, there still have not been accepted criteria for diagnosis and treatment of LCNEC. Here we report an unmarried 37 year-old woman who was diagnosed with LCNEC associated with clear cell carcinoma and the tumor index was manifested with a specific increase of AFP. The case received six courses of etoposide and carboplatin chemotherapy as an adjuvant therapy after primary curative surgery. However, she relapsed within 6 months after surgery and metastasized rapidly to distant organs despite combined chemotherapy of paclitaxel, cisplatin, and bevacizumab, and died 18 months after primary surgery. This is the first reported case of LCNEC manifested with a specific increase of AFP and characteristically metastasized to the spine as recurrence. Reviewing our case as well as previously reported cases, LCNEC present with aggressive malignancy and vulnerable to distant metastasis through a hematogenous approach, we conjectured that adding Bevacizumab in primary chemotherapy may be beneficial to extend disease-free survival. But so far there is no recommendation of this regimen for treatment of LCNEC in current guidelines. Further research is needed to confirm this view so as to find the best treatment of LCNEC and improve the prognosis of these patients.
大细胞神经内分泌癌(LCNEC)是卵巢癌中一种罕见的组织学亚型。文献中报道了少数几例具有极强侵袭性和不良预后的病例。然而,LCNEC的诊断和治疗标准仍未被广泛接受。在此,我们报告一名37岁未婚女性,她被诊断为LCNEC合并透明细胞癌,肿瘤指标表现为甲胎蛋白(AFP)特异性升高。该病例在初次根治性手术后接受了六个疗程的依托泊苷和卡铂化疗作为辅助治疗。然而,她在术后6个月内复发,尽管接受了紫杉醇、顺铂和贝伐单抗的联合化疗,仍迅速转移至远处器官,并在初次手术后18个月死亡。这是首例报道的以AFP特异性升高为表现且复发时特征性转移至脊柱的LCNEC病例。回顾我们的病例以及先前报道的病例,LCNEC具有侵袭性恶性特征,易通过血行途径发生远处转移,我们推测在一线化疗中添加贝伐单抗可能有助于延长无病生存期。但目前指南中尚无该方案用于治疗LCNEC的推荐。需要进一步研究来证实这一观点,以便找到LCNEC的最佳治疗方法并改善这些患者的预后。