Nizam Aaron, Bustamante Bethany, Shan Weiwei, Shih Karin K, Whyte Jill S, Sakaris Antoinette, Dos Santos Lisa, Frimer Marina, Menzin Andrew W, Truskinovsky Alexander, Goldberg Gary L
Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Zucker School of Medicine at Hofstra/Northwell, Northwell Health, New Hyde Park, NY 11040, USA.
Department of Biostatistics, Northwell Health, New Hyde Park, NY 11040, USA.
Diagnostics (Basel). 2019 Nov 22;9(4):200. doi: 10.3390/diagnostics9040200.
Carcinosarcoma of the ovary (CSO) is a rare and aggressive variant of ovarian cancer. Due to the rare nature of the disease there is insufficient evidence to make recommendations regarding standard management and overall prognosis.
An Institutional Review Board-approved study identified all our patients with CSO between January 2011 and May 2018. Demographic and outcome measures were abstracted from the medical records and tumor board files. Cox proportional hazard models, log rank tests, and comparisons of means were used to calculate significance ( < 0.05).
27 women with CSO were identified. The median age at diagnosis was 65 years (range 48-91). Five women (18%) presented with early stage disease (Stage I or II) and 22 patients (82%) presented with late stage III or IV disease. Twenty patients (74%) received intravenous platinum-based combination chemotherapy. Seven patients did not receive chemotherapy during their treatment course. The median overall survival was 23 months (range 2-68 months). Overall survival was not significantly worsened by the stage of disease at diagnosis. There was no difference in survival based on the age at diagnosis, tobacco status or ethnicity ( > 0.05).
This is one of the largest single institution experiences with CSO. The majority of our patients presented with advanced stage disease and received adjuvant platinum-based chemotherapy after cytoreductive surgery. The median overall survival of 23 months was not affected by the stage of the disease. The optimal management of this rare disease needs further study with collaborative, prospective multi-institutional trials.
卵巢癌肉瘤(CSO)是一种罕见且侵袭性强的卵巢癌变体。由于该疾病罕见,尚无足够证据就标准治疗和总体预后提出建议。
一项经机构审查委员会批准的研究确定了2011年1月至2018年5月期间我们所有患有CSO的患者。从病历和肿瘤委员会文件中提取人口统计学和结局指标。使用Cox比例风险模型、对数秩检验和均值比较来计算显著性(<0.05)。
确定了27例患有CSO的女性。诊断时的中位年龄为65岁(范围48 - 91岁)。5名女性(18%)表现为早期疾病(I期或II期),22名患者(82%)表现为晚期III期或IV期疾病。20名患者(74%)接受了静脉铂类联合化疗。7名患者在治疗过程中未接受化疗。中位总生存期为23个月(范围2 - 68个月)。诊断时疾病分期并未使总生存期显著恶化。基于诊断时年龄、吸烟状况或种族的生存率无差异(>0.05)。
这是关于CSO的最大单机构经验之一。我们的大多数患者表现为晚期疾病,在减瘤手术后接受了辅助铂类化疗。23个月的中位总生存期不受疾病分期影响。这种罕见疾病的最佳治疗需要通过协作性、前瞻性多机构试验进行进一步研究。