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

多西紫杉醇 帕唑帕尼 吉西他滨 医学 软组织肉瘤 内科学 肿瘤科 化疗 肉瘤 癌症 病理 舒尼替尼
作者
Jee Hung Kim,Hyung Soon Park,Su Jin Heo,Sang Kyum Kim,Jung Woo Han,Kyoo Ho Shin,Seung Hyun Kim,Hyuk Hur,Seung Il Kim,Young Deuk Choi,Sung Hoon Kim,Young Han Lee,Jin Suck Suh,Joong Bae Ahn,Hyun Cheol Chung,Sung Hoon Noh,Sun Young Rha,Hyo Song Kim
出处
期刊:Oncology [S. Karger AG]
卷期号:96 (2): 59-69 被引量:15
标识
DOI:10.1159/000492597
摘要

<b><i>Background:</i></b> We retrospectively investigated the treatment outcomes of second-line treatment with pazopanib or gemcitabine/docetaxel in patients with advanced soft tissue sarcoma (STS). <b><i>Methods:</i></b> Ninety-one patients who were treated with pazopanib or gemcitabine/docetaxel for advanced STS between 1995 and 2015 were analyzed. <b><i>Results:</i></b> 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 (<i>p</i> = 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 (<i>p</i> = 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%, <i>p</i> = 0.006), histologic grade 1–2 (40.9 vs. 0%, <i>p</i> = 0.001), and poor first-line treatment response (23.3 vs. 3.0%, <i>p</i> = 0.022). Gemcitabine/docetaxel was associated with better ORRs for the following histologic subtypes: leiomyosarcoma (<i>p</i> = 0.624), malignant fibrous histiocytoma/undifferentiated pleomorphic sarcoma (<i>p</i> = 0.055), and angiosarcoma (<i>p</i> = 0.182). However, the ORR of synovial sarcoma favored pazopanib (<i>p</i> = 0.99). <b><i>Conclusions:</i></b> 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.

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