Department of Internal Medicine, Division of Hematology and Oncology, Naef K. Basile Cancer Institute, American University of Beirut Medical Center, Beirut, Lebanon.
Department of Internal Medicine, Division of Hematology and Oncology, Hammoud Hospital University Medical Center, Saida, Lebanon.
Cancer Treat Res Commun. 2021;26:100275. doi: 10.1016/j.ctarc.2020.100275. Epub 2020 Dec 11.
Sarcomas are uncommon malignancies. No advances have been recently achieved despite multiple efforts. Pazopanib is a safe and effective tyrosine kinase inhibitor used in managing soft tissue sarcomas (STS) after chemotherapy failure. However, its use is limited in developing countries and no efficacy data exist from our region. We aimed to study the efficacy of pazopanib in our population, characterized by response rates of patients with chemotherapy-refractory advanced STS receiving pazopanib. Secondary endpoints included progression-free survival (PFS), overall survival (OS) and toxicity profile.
15 patients (age≥18 year) diagnosed with advanced STS, refractory to first-line chemotherapy, receiving pazopanib as ≥second-line therapy in one tertiary center in Lebanon were included between January 1st, 2014 and October 31st, 2018. Patient and disease characteristics, disease evaluation, as well as tolerance to treatment, were extracted from charts retrospectively. Statistical analysis was done using SPSS version 24.
The mean age was 48.6 [19-66] years. Eleven patients (73.3%) received pazopanib in second-line, whereas four patients (26.7%) received it in third-line. Thirteen patients (86.7%) progressed, and two patients (13.3%) had stable disease. The median PFS was three months [1-19] and the mean OS was 25.4 months [17.2-33.6]. Five patients required dose-reductions due to poor tolerance.
Conclusions cannot be drawn due to small patient numbers. However, given the 3-month PFS, 13% of patients maintaining stable disease, and tolerable safety profile, it is reasonable to incorporate pazopanib in STS treatment. More focused studies with larger patient populations need to be done in Lebanon.
肉瘤是一种罕见的恶性肿瘤。尽管进行了多次努力,但最近仍未取得进展。帕唑帕尼是一种安全有效的酪氨酸激酶抑制剂,用于治疗化疗失败后的软组织肉瘤(STS)。然而,在发展中国家其应用受限,且我们地区尚无疗效数据。我们旨在研究帕唑帕尼在我们人群中的疗效,该人群特征为化疗耐药的晚期 STS 患者接受帕唑帕尼治疗的反应率。次要终点包括无进展生存期(PFS)、总生存期(OS)和毒性特征。
在黎巴嫩的一家三级中心,我们回顾性地纳入了 15 名(年龄≥18 岁)诊断为晚期 STS 的患者,这些患者对一线化疗耐药,在一线化疗后接受帕唑帕尼作为二线治疗。从病历中提取患者和疾病特征、疾病评估以及对治疗的耐受性。使用 SPSS 版本 24 进行统计分析。
患者的平均年龄为 48.6 [19-66] 岁。11 名患者(73.3%)接受帕唑帕尼二线治疗,4 名患者(26.7%)接受三线治疗。13 名患者(86.7%)疾病进展,2 名患者(13.3%)疾病稳定。中位 PFS 为 3 个月[1-19],平均 OS 为 25.4 个月[17.2-33.6]。由于耐受性差,有 5 名患者需要减少剂量。
由于患者数量较少,无法得出结论。然而,鉴于 3 个月的 PFS、13%的患者疾病稳定以及可耐受的安全性特征,将帕唑帕尼纳入 STS 治疗是合理的。需要在黎巴嫩进行更多以更大患者人群为对象的针对性研究。