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卵巢原发性肉瘤:临床病理特征、预后因素和治疗评估。

Primary sarcoma of the ovary: clinicopathological characteristics, prognostic factors and evaluation of therapy.

机构信息

Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100730, China.

出版信息

Chin Med J (Engl). 2011 May;124(9):1316-21.

Abstract

BACKGROUND

The primary ovarian sarcoma is a very rare malignancy. The objective of this study was to further investigate the clinicopathologic features and outcome in patients with primary sarcoma of the ovary.

METHODS

Between 1988 and 2007, 24 patients with primary ovarian sarcoma who underwent treatment at Peking Union Medical Hospital were reviewed retrospectively. Response to treatment, progression and overall survival were analyzed.

RESULTS

Patients with ovarian sarcoma had a mean age of (54.3 ± 10.3) years, and 16 of them were postmenopausal. The most common symptom was abdominal pain, present in 14 patients. Of the 24 patients, 16 patients were pathologically diagnosed as carcinosarcoma (known as malignant mixed mesodermal tumor (MMMT)), 2 as ovarian leiomyosarcoma (LS) and 6 patients as ovarian endometrial stromal sarcoma (ESS). The patients in optimal debulking group had a median survival period of 28 months and 1-year survival rate of 71%. The patients in suboptimal debulking group had a significantly lower median survival of 6 months (P = 0.02) and 1-year survival rate of 29%. Among the patients, 23 patients received chemotherapy and most of regimens were based on platinum, 3 patients received chemoradiation. The mean number of courses of combined chemotherapy was 6.6 ± 5.0, and the response was unsatisfactory. The median survival for the entire group was 18.7 months. The one-year survival rate was 58%, and two-year survival rate only 29%.

CONCLUSIONS

Ovarian primary sarcoma has a poor overall prognosis. Optimal debulking surgery appears to be of prognostic significance. There is a clear need for further study to explore the role and the regimen of platinum-based chemotherapy in primary ovarian sarcoma.

摘要

背景

原发性卵巢肉瘤是一种非常罕见的恶性肿瘤。本研究旨在进一步探讨原发性卵巢肉瘤患者的临床病理特征和预后。

方法

回顾性分析 1988 年至 2007 年在北京协和医院治疗的 24 例原发性卵巢肉瘤患者。分析治疗反应、进展和总生存情况。

结果

卵巢肉瘤患者的平均年龄为(54.3±10.3)岁,16 例绝经后。最常见的症状是腹痛,14 例患者有此症状。24 例患者中,16 例病理诊断为癌肉瘤(又称恶性混合性中胚叶肿瘤(MMMT)),2 例为卵巢平滑肌肉瘤(LS),6 例为卵巢子宫内膜间质肉瘤(ESS)。最佳肿瘤细胞减灭术组患者的中位生存时间为 28 个月,1 年生存率为 71%。肿瘤细胞减灭术不理想组患者的中位生存时间明显缩短至 6 个月(P=0.02),1 年生存率为 29%。23 例患者接受了化疗,大多数方案以铂类为基础,3 例患者接受了放化疗。联合化疗的平均疗程数为 6.6±5.0,疗效不佳。全组患者的中位生存时间为 18.7 个月,1 年生存率为 58%,2 年生存率仅为 29%。

结论

卵巢原发性肉瘤总体预后较差。最佳肿瘤细胞减灭术似乎具有预后意义。显然需要进一步研究探索铂类为基础的化疗在原发性卵巢肉瘤中的作用和方案。

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