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临床试验/CTIS2022-502887-19-00
CTIS2022-502887-19-00招募中1 期

R-MINI-CHOP versus R-MINI-CHP in combination with polatuzumab-vedotin, as primary treatment for patients with diffuse large B-cell lymphoma, =80 years, or frail =75 years – an open label randomized Nordic Lymphoma Group phase III trial - NLG-LBC7 (POLAR BEAR) - NLG-LBC7

Region Skane0 个研究点目标入组 305 人开始时间: 2023年6月16日最近更新:

试验速览

阶段
1 期
状态
招募中
发起方
Region Skane
入组人数
305

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

年龄范围
65 至 65+(—)
性别
All

入选标准

  • Age =80 years or frail =75 years, according to simplified comprehensive geriatric assessment, Histologically confirmed lymphoma belonging to one of the following subtypes: a. Diffuse large B-cell lymphoma, including transformation from an indolent lymphoma; b. Follicular lymphoma grade 3B; c. T-cell/histiocyte-rich LBCL; d. Primary cutaneous DLBCL, leg type; e. EBV-positive DLBCL, NOS; f. Primary mediastinal LBCL; g. High grade B-cell lymphoma with MYC/BCL2 rearrangement, Stage II-IV disease, At least 1 measurable site of disease (>1.5 cm long axis), No previous treatment for lymphoma, WHO performance status 0 – 3 (Grade 3 if related to DLBCL), Written informed consent

排除标准

  • Severe cardiac disease: NYHA grade 3-4, CNS involvement at diagnosis, Uncontrolled serious infection, Impaired liver (transaminases > 3x normal upper limit or bilirubin > 1.5 x normal upper limit, unless due to Gilbert´s syndrome), renal (GFR<30ml/min) or other organ function not caused by lymphoma, which will interfere with the treatment, Absolute neutrophil count (ANC) <1000 cells/µL or platelets <100,000 cells/µL, unless due to lymphoma, Any other prior malignancy than non-melanoma skin cancer or stage 0 (in situ) cervical carcinoma, unless treated with curative intent, and without relapse since 2 years, or low grade prostate cancer, not in need of treatment, Psychiatric illness or condition which could interfere with their ability to understand the requirements of the study, Known hypersensitivity to rituximab, polatuzumab vedotin, cyclophosphamide, vincristine or doxorubicin, or to additives in the formulations above, or known hypersensitivity to other human, humanized, chimeric or porcine monoclonal antibodies, or HACA against rituximab, Peripheral neuropathy grade = 2

研究者

发起方
Region Skane

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