Bétrian Sarah, Bergeron Christophe, Blay Jean-Yves, Bompas Emmanuelle, Cassier Philippe A, Chevallier Laure, Fayette Jérome, Girodet Magali, Guillemet Cécile, Le Cesne Axel, Marec-Berard Perrine, Ray-Coquard Isabelle, Chevreau Christine
Departments of Oncology and Clinical Research, Institut Claudius Regaud, Institut Universitaire du Cancer, Toulouse Oncopole, 1 avenue Irène Joliot-Curie, 31059 Toulouse Cedex, France.
Departments of Oncology and Clinical Research, Centre Léon Berard and Institut d'Hématologie et d'Oncologie Pédiatrique, Lyon, France.
Clin Sarcoma Res. 2017 May 10;7:10. doi: 10.1186/s13569-017-0076-4. eCollection 2017.
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.
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.
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.
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.
促结缔组织增生性小圆细胞肿瘤(DSRCT)是一种非常罕见的间充质肿瘤,主要影响青少年和年轻成年人,诊断时的平均年龄约为20 - 25岁。尽管初始治疗仍需标准化,但许多中心会采用多模式治疗,包括强化化疗、广泛手术切除后放疗。尽管如此,预后仍然很差,中位总生存期为25个月。复发性疾病主要通过化疗治疗。最近,由于复发性疾病存在未满足的医疗需求,人们对DSRCT的靶向治疗进行了探索。
在本研究中,我们评估了法国国家肉瘤靶向治疗登记处(OUTC)登记的9例进展性DSRCT患者使用抗血管生成靶向药物(舒尼替尼、索拉非尼和贝伐单抗)治疗后的缓解率和无进展生存期。OUTC收集关于肉瘤中使用非标签靶向治疗的数据。
纳入8名男性和1名女性,诊断时的中位年龄为27.3岁(范围为9至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线)治疗。6例患者接受舒尼替尼治疗,2例接受索拉非尼治疗,1例接受贝伐单抗治疗。中位无进展生存期为3.1个月(范围为2至5.5个月),观察到的最佳反应为疾病稳定5.5个月。大多数患者的毒性较低且可控,主要为疲劳、腹痛和皮肤毒性。
尽管在我们的研究中抗血管生成药物的活性非常有限,但对这些罕见肿瘤病例的前瞻性收集以及分子数据应指导治疗决策并改善治疗结果。