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本文引用的文献

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Adjuvant Sunitinib in High-Risk Renal-Cell Carcinoma after Nephrectomy.辅助舒尼替尼治疗肾切除术后高危肾细胞癌。
N Engl J Med. 2016 Dec 8;375(23):2246-2254. doi: 10.1056/NEJMoa1611406. Epub 2016 Oct 9.
2
Olaratumab and doxorubicin versus doxorubicin alone for treatment of soft-tissue sarcoma: an open-label phase 1b and randomised phase 2 trial.奥拉单抗与多柔比星联合治疗与多柔比星单药治疗软组织肉瘤的疗效比较:一项开放标签的1b期和随机2期试验。
Lancet. 2016 Jul 30;388(10043):488-97. doi: 10.1016/S0140-6736(16)30587-6. Epub 2016 Jun 9.
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The off-label use of targeted therapies in sarcomas: the OUTC'S program.肉瘤中靶向治疗的超说明书用药:OUTC项目
BMC Cancer. 2014 Nov 24;14:870. doi: 10.1186/1471-2407-14-870.
4
Abdominal desmoplastic small round cell tumor: multimodal treatment combining chemotherapy, surgery, and radiotherapy is the best option.腹部促结缔组织增生性小圆细胞肿瘤:化疗、手术和放疗相结合的多模式治疗是最佳选择。
Ann Surg Oncol. 2015 Apr;22(4):1073-9. doi: 10.1245/s10434-014-4123-6. Epub 2014 Oct 10.
5
Pazopanib in advanced desmoplastic small round cell tumours: a multi-institutional experience.帕唑帕尼治疗晚期促纤维组织增生性小圆细胞肿瘤:一项多机构经验
Clin Sarcoma Res. 2014 Jul 29;4:7. doi: 10.1186/2045-3329-4-7. eCollection 2014.
6
Trabectedin for desmoplastic small round cell tumours: a possible treatment option?曲贝替定用于促纤维组织增生性小圆细胞肿瘤:一种可能的治疗选择?
Clin Sarcoma Res. 2014 Apr 25;4:3. doi: 10.1186/2045-3329-4-3. eCollection 2014.
7
Desmoplastic small round cell tumor of the ovary: A rare but devastating disease in young women.卵巢促纤维增生性小圆细胞肿瘤:一种在年轻女性中罕见但极具破坏性的疾病。
Gynecol Oncol Case Rep. 2013 Feb 26;7:16-8. doi: 10.1016/j.gynor.2013.02.006. eCollection 2014 Jan.
8
Paratesticular desmoplastic small round cell tumor with metastasis: a report of two cases.伴有转移的睾丸旁促结缔组织增生性小圆细胞肿瘤:两例报告
Kaohsiung J Med Sci. 2014 Feb;30(2):104-5. doi: 10.1016/j.kjms.2013.01.018. Epub 2013 Aug 15.
9
Peritoneal carcinomatosis treated with cytoreductive surgery and Hyperthermic Intraperitoneal Chemotherapy (HIPEC) for advanced ovarian carcinoma: a French multicentre retrospective cohort study of 566 patients.采用细胞减灭术和腹腔热灌注化疗(HIPEC)治疗晚期卵巢癌腹膜癌病:法国多中心回顾性队列研究 566 例患者。
Eur J Surg Oncol. 2013 Dec;39(12):1435-43. doi: 10.1016/j.ejso.2013.09.030. Epub 2013 Oct 17.
10
Complete cytoreduction and HIPEC improves survival in desmoplastic small round cell tumor.完全细胞减灭术和腹腔热灌注化疗可提高促结缔组织增生性小圆细胞肿瘤患者的生存率。
Ann Surg Oncol. 2014 Jan;21(1):220-4. doi: 10.1245/s10434-013-3269-y. Epub 2013 Sep 18.

进展性促结缔组织增生性小圆细胞肿瘤患者的抗血管生成作用:来自法国国家肉瘤超适应证靶向治疗登记处(OUTC's)的数据。

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).

作者信息

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

机构信息

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.

出版信息

Clin Sarcoma Res. 2017 May 10;7:10. doi: 10.1186/s13569-017-0076-4. eCollection 2017.

DOI:10.1186/s13569-017-0076-4
PMID:28491276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5424317/
Abstract

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。