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帕唑帕尼与吉西他滨/多西他赛二线治疗转移性软组织肉瘤疗效的差异。

Differences in the Efficacies of Pazopanib and Gemcitabine/Docetaxel as Second-Line Treatments for Metastatic Soft Tissue Sarcoma.

机构信息

Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.

College of Medicine, Yonsei University Graduate School, Seoul, Republic of Korea.

出版信息

Oncology. 2019;96(2):59-69. doi: 10.1159/000492597. Epub 2018 Oct 18.

Abstract

BACKGROUND

We retrospectively investigated the treatment outcomes of second-line treatment with pazopanib or gemcitabine/docetaxel in patients with advanced soft tissue sarcoma (STS).

METHODS

Ninety-one patients who were treated with pazopanib or gemcitabine/docetaxel for advanced STS between 1995 and 2015 were analyzed.

RESULTS

Forty-six and 45 patients received pazopanib and gemcitabine/docetaxel, respectively. The median progression-free survival for the group treated with pazopanib was 4.5 months compared with 3.0 months for the gemcitabine/docetaxel group (p = 0.593). The median overall survival for the group treated with pazopanib was 12.6 months compared with 14.2 months for the gemcitabine/docetaxel group (p = 0.362). The overall response rates (ORRs) were 6.5 and 26.7% in the pazopanib and gemcitabine/docetaxel groups, respectively. The following parameters had ORRs favoring gemcitabine/docetaxel: age ≥50 years (31.6 vs. 2.9%, p = 0.006), histologic grade 1-2 (40.9 vs. 0%, p = 0.001), and poor first-line treatment response (23.3 vs. 3.0%, p = 0.022). Gemcitabine/docetaxel was associated with better ORRs for the following histologic subtypes: leiomyosarcoma (p = 0.624), malignant fibrous histiocytoma/undifferentiated pleomorphic sarcoma (p = 0.055), and angiosarcoma (p = 0.182). However, the ORR of synovial sarcoma favored pazopanib (p = 0.99).

CONCLUSIONS

The efficacies of pazopanib and gemcitabine/docetaxel as second-line treatments after doxorubicin or ifosfamide failure differed among clinical and histologic subgroups and appeared to facilitate a more personalized treatment approach for advanced STS.

摘要

背景

我们回顾性研究了二线使用帕唑帕尼或吉西他滨/多西他赛治疗晚期软组织肉瘤(STS)患者的治疗效果。

方法

分析了 1995 年至 2015 年间接受帕唑帕尼或吉西他滨/多西他赛治疗的 91 例晚期 STS 患者。

结果

46 例和 45 例患者分别接受了帕唑帕尼和吉西他滨/多西他赛治疗。与吉西他滨/多西他赛组相比,帕唑帕尼组的中位无进展生存期为 4.5 个月(p=0.593)。与吉西他滨/多西他赛组相比,帕唑帕尼组的中位总生存期为 12.6 个月(p=0.362)。帕唑帕尼组的总缓解率(ORR)为 6.5%,吉西他滨/多西他赛组为 26.7%。吉西他滨/多西他赛组有利于 ORR 的参数有:年龄≥50 岁(31.6% vs. 2.9%,p=0.006)、组织学分级 1-2 级(40.9% vs. 0%,p=0.001)和一线治疗反应不佳(23.3% vs. 3.0%,p=0.022)。吉西他滨/多西他赛治疗以下组织学亚型的 ORR 更好:平滑肌肉瘤(p=0.624)、恶性纤维组织细胞瘤/未分化多形性肉瘤(p=0.055)和血管肉瘤(p=0.182)。然而,滑膜肉瘤对帕唑帕尼的 ORR 更有利(p=0.99)。

结论

在多柔比星或异环磷酰胺失败后,作为二线治疗,帕唑帕尼和吉西他滨/多西他赛的疗效在临床和组织学亚组之间存在差异,这似乎为晚期 STS 提供了更个性化的治疗方法。

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