Seonggyu Byeon, Haa-Na Song, Hee Kyung Kim, Jun Soo Ham, Su Jin Lee, Jeeyun Lee, Se Hoon Park
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We excluded patients who were enrolled in clinical trials to ensure the results would reflect the real-world outcomes obtained in a daily clinical setting. Endpoints included efficacy in terms of response rate, progression-free survival (PFS), overall survival (OS) and safety.</p><p><strong>Results: </strong>Among 21 patients, 15 (71 %) were male and the median age was 53 years (range, 24-76). Primary sites of angiosarcoma were the visceral organs (33 %), scalp (29 %) and heart (23 %). The median number of metastatic sites was two (range, 1-5) with the lungs being the most frequently involved site. Weekly paclitaxel was generally well tolerated: the major hematologic toxicity was grade 1/2 anemia (24 %). Among non-hematologic toxicities, grade 1/2 peripheral neuropathy was most commonly observed (67 %). Objective response was observed in 11 (52 %) patients (4 complete and 7 partial responses). With a median follow-up of 21 months, the estimated median PFS and OS were 5.7 months (95 % CI 5.1-6.3) and 18.6 months (95 % CI 9.9-27.3), respectively.</p><p><strong>Conclusions: </strong>In this retrospective study, first-line chemotherapy with weekly paclitaxel demonstrated clinically relevant efficacy and tolerability in unselected Korean patients with metastatic angiosarcoma. 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引用次数: 10
摘要
背景:血管肉瘤是一种罕见的预后不良的软组织肉瘤亚群,但紫杉醇已被证明在治疗前的转移性疾病中有活性。我们研究了每周一次紫杉醇作为转移性血管肉瘤成人患者一线化疗的有效性和安全性。方法:对2008年10月至2014年12月期间连续21例血管肉瘤患者进行回顾性研究,这些患者每周接受紫杉醇治疗,作为转移性疾病的一线治疗。我们排除了参加临床试验的患者,以确保结果能反映在日常临床环境中获得的真实结果。终点包括有效率、无进展生存期(PFS)、总生存期(OS)和安全性方面的疗效。结果:21例患者中,男性15例(71%),中位年龄53岁(范围24 ~ 76岁)。血管肉瘤的原发部位为内脏(33%)、头皮(29%)和心脏(23%)。转移部位的中位数为2个(范围1-5),肺是最常见的转移部位。每周紫杉醇通常耐受良好:主要的血液学毒性是1/2级贫血(24%)。在非血液学毒性中,1/2级周围神经病变最常见(67%)。11例(52%)患者观察到客观缓解(4例完全缓解,7例部分缓解)。中位随访为21个月,估计中位PFS和OS分别为5.7个月(95% CI 5.1-6.3)和18.6个月(95% CI 9.9-27.3)。结论:在这项回顾性研究中,一线化疗每周紫杉醇显示临床相关的疗效和耐受性在转移性血管肉瘤未选择的韩国患者。令人鼓舞的是,韩国患者的缓解率和PFS与西方报道的相似。
A Korean single-center, real-world, retrospective study of first-line weekly paclitaxel in patients with metastatic angiosarcoma.
Background: Angiosarcoma is a rare subgroup of soft tissue sarcomas associated with poor prognosis, but paclitaxel has been shown to be active in pretreated metastatic disease. We investigated the efficacy and safety of weekly paclitaxel as first-line chemotherapy in adult patients with metastatic angiosarcoma.
Methods: A retrospective study using the Samsung Medical Center (Seoul, Korea) cancer chemotherapy registry was performed on 21 consecutive patients with angiosarcoma who were treated with weekly paclitaxel as first-line therapy for metastatic disease between Oct. 2008 and Dec. 2014. We excluded patients who were enrolled in clinical trials to ensure the results would reflect the real-world outcomes obtained in a daily clinical setting. Endpoints included efficacy in terms of response rate, progression-free survival (PFS), overall survival (OS) and safety.
Results: Among 21 patients, 15 (71 %) were male and the median age was 53 years (range, 24-76). Primary sites of angiosarcoma were the visceral organs (33 %), scalp (29 %) and heart (23 %). The median number of metastatic sites was two (range, 1-5) with the lungs being the most frequently involved site. Weekly paclitaxel was generally well tolerated: the major hematologic toxicity was grade 1/2 anemia (24 %). Among non-hematologic toxicities, grade 1/2 peripheral neuropathy was most commonly observed (67 %). Objective response was observed in 11 (52 %) patients (4 complete and 7 partial responses). With a median follow-up of 21 months, the estimated median PFS and OS were 5.7 months (95 % CI 5.1-6.3) and 18.6 months (95 % CI 9.9-27.3), respectively.
Conclusions: In this retrospective study, first-line chemotherapy with weekly paclitaxel demonstrated clinically relevant efficacy and tolerability in unselected Korean patients with metastatic angiosarcoma. It is encouraging that response rate and PFS for Korean patients were similar to those reported in Western reports.
期刊介绍:
Clinical Sarcoma Research considers for publication articles related to research on sarcomas, including both soft tissue and bone. The journal publishes original articles and review articles on the diagnosis and treatment of sarcomas along with new insights in sarcoma research, which may be of immediate or future interest for diagnosis and treatment. The journal also considers negative results, especially those from studies on new agents, as it is vital for the medical community to learn whether new agents have been proven effective or ineffective within subtypes of sarcomas. The journal also aims to offer a forum for active discussion on topics of major interest for the sarcoma community, which may be related to both research results and methodological topics.