Colia Vittoria, Fiore Marco, Provenzano Salvatore, Fumagalli Elena, Bertulli Rossella, Morosi Carlo, Dei Tos Angelo P, Barisella Marta, Gronchi Alessandro, Casali Paolo G, Sanfilippo Roberta
Medical Oncology Unit 2, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milan, Italy.
Department of Surgery, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
Clin Sarcoma Res. 2017 Aug 22;7:16. doi: 10.1186/s13569-017-0082-6. eCollection 2017.
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).
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.
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.
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.
我们报告了在意大利米兰国家肿瘤研究所及意大利罕见癌症网络(RTR)中接受治疗的晚期黏液纤维肉瘤患者的回顾性系列研究中,基于蒽环类药物和高剂量延长输注异环磷酰胺化疗的活性。
回顾性分析2001年11月至2016年12月期间接受蒽环类药物+异环磷酰胺以及高剂量延长输注异环磷酰胺单药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专家病理学家进行集中复审。采用RECIST评估反应,并计算生存函数。
在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(男性/女性=6/7,中位年龄54岁,范围33 - 72岁)。总体最佳反应为:4例部分缓解,3例病情稳定,6例病情进展,中位无进展生存期为4个月。28例患者接受二线/后续高剂量延长输注异环磷酰胺治疗(男性/女性=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。
这项回顾性分析表明,蒽环类药物和异环磷酰胺的联合应用在黏液纤维肉瘤中具有活性。在已经接受蒽环类药物和异环磷酰胺联合治疗的患者中,高剂量延长输注异环磷酰胺也显示出活性。