R-CHOP联合b细胞受体/NF-κ b双靶向的I/II期一线研究,以分子评估治疗反应。

Sophy Denker, Aitomi Bittner, Il-Kang Na, Julia Kase, Mareike Frick, Ioannis Anagnostopoulos, Michael Hummel, Clemens A Schmitt
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引用次数: 8

摘要

ImbruVeRCHOP试验是一项研究者发起的、多中心、单臂、开放标签的I/II期研究,针对61-80岁新诊断的CD20+弥漫性大b细胞淋巴瘤和高风险患者(国际预后指数≥2)。患者接受标准化疗(CHOP)加免疫治疗(利妥昔单抗)、生物制剂(蛋白酶体抑制剂硼替佐米)和信号抑制剂(靶向布鲁顿酪氨酸激酶的治疗性伊鲁替尼)。ImbruVeRCHOP采用全身性方法,但在第一周期免疫化疗药物暴露下对患者进行另一次淋巴瘤活检,旨在确定一种无偏倚的分子反应标志,标志着弥漫性大b细胞淋巴瘤患者处于危险之中,并可能从该方案中获益,作为当前R-CHOP标准护理的双,近端和远端b细胞受体/NF-κ b共同靶向扩展。EudraCT-Number: 2015-003429-32;ClinicalTrials.gov识别码:NCT03129828。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Phase I/II first-line study of R-CHOP plus B-cell receptor/NF-κB-double-targeting to molecularly assess therapy response.

A Phase I/II first-line study of R-CHOP plus B-cell receptor/NF-κB-double-targeting to molecularly assess therapy response.

The ImbruVeRCHOP trial is an investigator-initiated, multicenter, single-arm, open label Phase I/II study for patients 61-80 years of age with newly diagnosed CD20+ diffuse large B-cell lymphoma and a higher risk profile (International Prognostic Index ≥2). Patients receive standard chemotherapy (CHOP) plus immunotherapy (Rituximab), a biological agent (the proteasome inhibitor Bortezomib) and a signaling inhibitor (the Bruton's Tyrosine Kinase-targeting therapeutic Ibrutinib). Using an all-comers approach, but subjecting patients to another lymphoma biopsy acutely under first-cycle immune-chemo drug exposure, ImbruVeRCHOP seeks to identify an unbiased molecular responder signature that marks diffuse large B-cell lymphoma patients at risk and likely to benefit from this regimen as a double, proximal and distal B-cell receptor/NF-κB-co-targeting extension of the current R-CHOP standard of care. EudraCT-Number: 2015-003429-32; ClinicalTrials.gov identifier: NCT03129828.

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来源期刊
自引率
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发文量
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审稿时长
13 weeks
期刊介绍: International Journal of Hematologic Oncology welcomes unsolicited article proposals. Email us today to discuss the suitability of your research and our options for authors, including Accelerated Publication. Find out more about publishing open access with us here.
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