Department of Gynecologic Oncology, National Hospital Organization Shikoku Cancer Center, 160 Kou, Minamiumemotomachi, Matsuyama, Japan.
Department of Clinical Research Center, National Hospital Organization Shikoku Cancer Center, 160 Kou, Minamiumemotomachi, Matsuyama, Japan.
Gynecol Oncol. 2020 Apr;157(1):115-120. doi: 10.1016/j.ygyno.2020.01.022. Epub 2020 Jan 23.
Uterine leiomyosarcoma (uLMS) is a rare gynecologic malignancy for which the currently available treatments do not consistently provide long-term disease control. This study aimed to reveal the current clinical status of uLMS to support future clinical trials.
This study enrolled patients with uLMS treated at 53 Japanese institutions from 2000 to 2012. Central pathological review (CPR) was performed. All cases were confirmed by CPR, and epidemiological features, treatment, and prognosis were analyzed statistically.
A total of 307 patients were enrolled. A diagnosis of uLMS was confirmed in 266 patients (86.6%) of patients after CPR, of whom data for 259 were analyzed. Of these, 186 (71.8%) patients underwent complete gross resection as primary therapy. Ninety-eight patients received no additional adjuvant therapy, while docetaxel and gemcitabine was the most frequent regimen among 155 patients treated with adjuvant chemotherapy. In all cases, the median overall survival (OS) was 44.2 months. Multivariate analyses of prognostic factors in all cases identified stage III and IV disease, high serum lactate dehydrogenase level, and menopausal status as poor prognostic factors. However, in stage I cases, high serum lactate dehydrogenase level and no adjuvant treatment were identified as poor prognostic factors. The 5-year OS of patients with stage I uLMS treated with adjuvant chemotherapy was significantly better than that of those without adjuvant treatment (67.8% vs 46.7%, P = 0.0461).
Despite complete removal of the primary lesion, the clinical course of patients with uLMS was poor due to recurrence of distant metastasis. The application of a suitable biomarker and effective adjuvant chemotherapy are required to improve the prognosis of patients with uLMS.
子宫平滑肌肉瘤(uLMS)是一种罕见的妇科恶性肿瘤,目前的治疗方法并不总能提供长期的疾病控制。本研究旨在揭示 uLMS 的当前临床状况,为未来的临床试验提供支持。
本研究纳入了 2000 年至 2012 年在 53 家日本机构接受治疗的 uLMS 患者。进行了中央病理复查(CPR)。所有病例均经 CPR 证实,对流行病学特征、治疗和预后进行了统计学分析。
共纳入 307 例患者。经 CPR 后,266 例(86.6%)患者确诊为 uLMS,其中 259 例进行了数据分析。在这些患者中,186 例(71.8%)患者接受了完全的大体切除术作为初始治疗。98 例患者未接受任何辅助治疗,而在接受辅助化疗的 155 例患者中,多西他赛和吉西他滨是最常见的方案。所有病例的中位总生存期(OS)为 44.2 个月。所有病例的多因素预后因素分析显示,III 期和 IV 期疾病、高血清乳酸脱氢酶水平和绝经状态为不良预后因素。然而,在 I 期病例中,高血清乳酸脱氢酶水平和未接受辅助治疗被确定为不良预后因素。接受辅助化疗的 I 期 uLMS 患者的 5 年 OS 明显优于未接受辅助治疗的患者(67.8% vs 46.7%,P=0.0461)。
尽管完全切除了原发性病变,但由于远处转移的复发,uLMS 患者的临床病程仍较差。需要应用合适的生物标志物和有效的辅助化疗来改善 uLMS 患者的预后。