Activity of anthracycline- and ifosfamide-based chemotherapy in a series of patients affected by advanced myxofibrosarcoma.

Clinical Sarcoma Research Pub Date : 2017-08-22 eCollection Date: 2017-01-01 DOI:10.1186/s13569-017-0082-6
Vittoria Colia, Marco Fiore, Salvatore Provenzano, Elena Fumagalli, Rossella Bertulli, Carlo Morosi, Angelo P Dei Tos, Marta Barisella, Alessandro Gronchi, Paolo G Casali, Roberta Sanfilippo
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引用次数: 22

Abstract

Background: We report on the activity of anthracycline-based and high-dose prolonged-infusion ifosfamide chemotherapy in a retrospective series of patients affected by advanced myxofibrosarcoma treated at Istituto Nazionale Tumori in Milan, Italy, and within the Italian Rare Cancer Network (RTR).

Methods: Advanced myxofibrosarcoma patients treated with anthracycline + ifosfamide and high-dose prolonged-infusion ifosfamide as a single agent from November 2001 to December 2016 were retrospectively reviewed. All pathological diagnosis were centrally reviewed by at least two expert pathologists. Response was evaluated by RECIST, and survival functions were computed.

Results: Among 34 advanced myxofibrosarcoma patients, 13 were treated with front-line anthracycline + ifosfamide chemotherapy (male/female = 6/7, median age 54 years, range 33-72). Overall best response was: 4 partial responses, 3 stable diseases and 6 progressive diseases, with a median progression-free survival of 4 months. Twenty-eight patients received second/further line high-dose prolonged-infusion ifosfamide (male/female = 17/11, median age 55 years, range 27-75 years). We observed 10 partial responses, 4 stable diseases and 14 progressive diseases, with a median progression-free survival of 4 months. Median overall survival was 12 months.

Conclusions: This retrospective analysis suggests that the combination of anthracyclines and ifosfamide is active in myxofibrosarcoma. In patients already treated with a combination of anthracyclines and ifosfamide, high-dose prolonged-infusion ifosfamide showed activity as well.

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蒽环类和异环磷酰胺为基础的化疗在一系列晚期黏液纤维肉瘤患者中的活性。
背景:我们报告了在意大利米兰国立肿瘤研究所和意大利罕见癌症网络(RTR)治疗的晚期黏液纤维肉瘤患者中蒽环类药物和大剂量长时间输注异环磷酰胺化疗的活性。方法:回顾性分析2001年11月至2016年12月期间接受蒽环类药物+异环磷酰胺及大剂量长时间单药输注异环磷酰胺治疗的晚期黏液纤维肉瘤患者。所有病理诊断均由至少两名病理学专家集中复查。采用RECIST评估疗效,并计算生存函数。结果:34例晚期黏液纤维肉瘤患者中,13例接受一线蒽环类药物+异环磷酰胺化疗(男/女= 6/7,中位年龄54岁,范围33-72岁)。总体最佳缓解为:部分缓解4例,疾病稳定3例,疾病进展6例,中位无进展生存期为4个月。28例患者接受了第二次/进一步大剂量延长输注异环磷酰胺(男/女17/11,中位年龄55岁,范围27-75岁)。我们观察到10例部分缓解,4例病情稳定,14例病情进展,中位无进展生存期为4个月。中位总生存期为12个月。结论:回顾性分析提示蒽环类药物联合异环磷酰胺治疗黏液纤维肉瘤有效。在已经接受蒽环类药物和异环磷酰胺联合治疗的患者中,大剂量长时间输注异环磷酰胺也显示出活性。
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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.
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