进进性结丝增生性小圆细胞肿瘤患者的抗血管生成作用:来自法国国家登记处的数据,专门用于肉瘤(OUTC)的非标记靶向治疗。

Clinical Sarcoma Research Pub Date : 2017-05-10 eCollection Date: 2017-01-01 DOI:10.1186/s13569-017-0076-4
Sarah Bétrian, Christophe Bergeron, Jean-Yves Blay, Emmanuelle Bompas, Philippe A Cassier, Laure Chevallier, Jérome Fayette, Magali Girodet, Cécile Guillemet, Axel Le Cesne, Perrine Marec-Berard, Isabelle Ray-Coquard, Christine Chevreau
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引用次数: 14

摘要

背景:结缔组织增生小圆细胞瘤(DSRCT)是一种非常罕见的间充质肿瘤,主要发生在青少年和青壮年,平均诊断年龄在20-25岁左右。虽然最初的管理仍需要标准化,但许多中心将采用多模式治疗,包括强化化疗,广泛手术切除和放疗。尽管如此,预后仍然很差,中位总生存期为25个月。复发性疾病主要以化疗治疗。近年来,由于复发性疾病的医疗需求未得到满足,人们开始探索针对DSRCT的靶向治疗。方法:在这项研究中,我们评估了纳入OUTC登记的9例进展性DSRCT的缓解率和无进展生存率,并使用抗血管生成靶向药物(舒尼替尼、索拉非尼和贝伐单抗)治疗。OUTC’s是法国的一个国家注册机构,收集关于在肉瘤中使用标签外靶向治疗的数据。结果:包括8名男性和1名女性,诊断时的中位年龄为27.3岁(范围从9岁到48岁)。在开始使用抗血管生成药物之前,他们平均接受了3线(2-5)的治疗。6名患者接受舒尼替尼治疗,2名接受索拉非尼治疗,1名接受贝伐单抗治疗。中位无进展生存期为3.1个月(范围2-5.5个月),观察到的最佳反应为5.5个月的疾病稳定。大多数患者有可控制的低度毒性,主要是疲劳、腹痛和皮肤毒性。结论:尽管我们的研究中抗血管生成药物的活性非常有限,但前瞻性收集这些罕见肿瘤的病例以及分子数据应该指导治疗决策并提高疗效。
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Antiangiogenic effects in patients with progressive desmoplastic small round cell tumor: data from the French national registry dedicated to the use of off-labeled targeted therapy in sarcoma (OUTC's).

Background: Desmoplastic small round cell tumor (DSRCT) is a very rare mesenchymal tumor that mainly affects teenagers and young adults with a mean age at diagnosis around 20-25 years. Although initial management still needs standardization, many centers will use multimodal treatment including intensive chemotherapy, extensive surgical resection followed by radiotherapy. Despite this, prognosis remains very poor and the median overall survival is 25 months. Recurrent disease is mainly treated by chemotherapy. Recently, due to the unmet medical need for recurrent disease, targeted therapies were explored for DSRCT.

Methods: In this study, we assessed the response rate and progression free survival in nine cases of progressive DSRCT included in the OUTC's registry and treated with antiangiogenics targeted agents (sunitinib, sorafenib and bevacizumab). OUTC's, a French national registry, collects data about the use of off-label targeted therapy in sarcoma.

Results: Eight males and one woman were included, with median age at diagnosis of 27.3 years (range from 9 to 48 years). They received a mean 3 lines (2-5) of treatment before antiangiogenic agent initiation. Six patients received sunitinib, two received sorafenib and one bevacizumab. Median progression free survival was 3.1 months (range 2-5.5 months) and best response observed was 5.5 months stable disease. Most patients had manageable low-grade toxicities, mainly fatigue, abdominal pain and skin toxicity.

Conclusions: Despite very limited activity of antiangiogenics in our study, prospective collection of cases of these rare tumors together with molecular data should guide therapeutic decision and enhance outcome.

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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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