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加速儿科癌症药物研发: Venetoclax 治疗复发/难治性恶性肿瘤的新型 I 期研究设计。

Accelerating drug development in pediatric cancer: a novel Phase I study design of venetoclax in relapsed/refractory malignancies.

机构信息

Dana-Farber/Boston Children's Cancer & Blood Disorders Center, Boston, MA, USA.

School of Medicine, Emory University, Atlanta, GA, USA.

出版信息

Future Oncol. 2018 Sep;14(21):2115-2129. doi: 10.2217/fon-2018-0121. Epub 2018 Mar 29.

Abstract

Venetoclax is a highly selective, potent BCL-2 inhibitor that is approved for some patients previously treated for chronic lymphocytic leukemia, and has shown promising activity in adult studies across several hematologic malignancies. Preclinical studies have demonstrated venetoclax activity in pediatric patient-derived xenograft models and cell lines; however, clinical studies in pediatric patients have yet to be conducted. The prognosis is poor for children with most relapsed/refractory malignancies, and limited treatment options result in unmet clinical need. Herein, we describe the rationale and design of the first study of venetoclax in pediatric patients with relapsed/refractory malignancies: a Phase I trial investigating the safety and pharmacokinetics of venetoclax monotherapy followed by the addition of chemotherapy (Trial registration: EudraCT 2017-000439-14; NCT03236857).

摘要

维奈托克是一种高选择性、强效的 BCL-2 抑制剂,已被批准用于某些既往治疗慢性淋巴细胞白血病的患者,在多项血液系统恶性肿瘤的成人研究中显示出有前景的活性。临床前研究已经证明维奈托克在儿科患者来源的异种移植模型和细胞系中有活性;然而,在儿科患者中尚未进行临床研究。大多数复发/难治性恶性肿瘤患儿的预后较差,治疗选择有限,导致临床需求未得到满足。在此,我们描述了维奈托克在复发/难治性恶性肿瘤儿科患者中首次研究的原理和设计:一项评估维奈托克单药治疗安全性和药代动力学的 I 期试验,随后添加化疗(试验注册:EudraCT 2017-000439-14;NCT03236857)。

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