EUCTR2017-003631-12-NL进行中（未招募）1 期
A phase II study evaluating the effect of DA-EPOCH-R induction followed by nivolumab consolidation in patients with newly diagnosed high grade B cell lymphoma (HGBL) with MYC and BCL2 and/or BCL6 rearrangements - HOVON 152 DLBC
HOVON Foundation0 个研究点目标入组 97 人开始时间: 2018年5月23日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 97
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
- 性别
- All
入选标准
- •? High-grade B-cell lymphoma, with MYC in combination with BCL2 and/or BCL6 rearrangements as assessed by FISH according to the WHO 2016 classification including high-grade B-cell lymphoma with MYC and BCL2 rearrangements, transformed from previously untreated FL.
- •? Age = 18 year
- •? Patient started with or has received one course of full dose R-CHOP or DA-EPOCH-R (cycle 1). Starting with DA-EPOCH-R in cycle 1 is only allowed when FISH results (confirming DH/TH diagnosis) are directly available at diagnosis. [Reversed R-CHOP (cyclophosphamide, vincristine and doxorubicin on day 5) is allowed; local radiation or short course (max 7 days) of steroids (max 100 mg/day) before R-CHOP is allowed. Mini-R-CHOP is not allowed].
- •? WHO performance status 0-3 during or after induction cycle 1 (see appendix C).
- •? Ann Arbor stage II-IV at diagnosis (see appendix A).
- •? 18F-FDG PET scan and contrast enhanced CT-scan performed preferably within 28 days before start first induction cycle. When the PET or CT-scan is performed outsite the 28-day window, consultation and written approval by the Principal Investigator for potential patient inclusion are necessary.
- •? Measurable disease: on contrast enhanced CT-scan at least 1 lesion/node with a long axis of >1.5 cm and at least one 18F-FDG avid lesion.
- •? Negative pregnancy test at study entry.
- •? Patient is willing and able to use adequate contraception until 6 months post last treatment administration.
- •? Written informed consent.
- •? Patient is capable of giving informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 51
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 51
排除标准
- •? All histopathological diagnoses other than DH/TH-HGBL (like testicular large B-cell lymphoma or primary mediastinal B-cell lymphoma) according to WHO 2016 classification.
- •? Known history of indolent lymphoma previously treated with immunochemotherapy.
- •? Inadequate renal function or creatinine clearance < 30 mL/min (after rehydration). Creatinine clearance may be calculated by Cockcroft –Gault formula:
- •CrCl = (140 - age [in years]) x weight [kg] (x 0.85 for females)
- •(0.815 x serum creatinine [µmol/L])
- •? Inadequate hepatic function: bilirubin > 3 times ULN (total) except patients with Gilbert's syndrome as defined by > 80% unconjugated bilirubin.
- •? Inadequate hematological function: ANC < 1.0x109/L or platelets < 75x109 /L before induction cycle 1 unless lymphoma related.
- •? CNS localization of the lymphoma. CSF analysis before start of treatment is only necessary in case of suspicion of CNS localization.
- •? Female subject pregnant or breast-feeding.
- •? History of active malignancy during the past 5 years with the exception of basal carcinoma of the skin or stage 0 cervical carcinoma.
- •? Active symptomatic ischemic heart disease, myocardial infarction, or congestive heart failure within the past year. In case of cardiac history, an echo or MUGA should be obtained and LVEF should exceed 40% to be eligible.
- •? Concurrent severe and/or uncontrolled medical condition (e.g. uncontrolled diabetes, infection, hypertension, cancer, etc.) that would jeopardize the patient's ability to receive the regimen with reasonable safety.
- •? HIV positivity.
- •? Active Hepatitis B or C infection as defined by positive serology and transaminitis. Non-active Hepatitis B carriers may be included if protected (see 9.2.3).
- •? Severe pulmonary dysfunction (CTCAE grade III-IV, see appendix D).
- •? Subjects with active, known or suspected autoimmune disease. Subjects with vitiligo, type I diabetes mellitus, residual hypothyroidism due to autoimmune condition only requiring hormone replacement, psoriasis not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger are permitted to enroll.
- •? Subjects with a condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalents) or other immunosuppressive medications within 14 days of study drug administration. Inhaled or topical steroids, and adrenal replacement doses > 10 mg daily prednisone equivalents are permitted in the absence of active autoimmune disease.
- •? Prior treatment with an anti-PD1, anti-PDL1, anti-PDL2, or anti-CTLA-4 antibody, or any other antibody or drug specifically targeting T-cell costimulation or immune checkpoint pathways.
- •? Severe neurological or psychiatric disease.
- •? Current participation in another clinical trial interfering with this trial.
- •? Any psychological, familial, sociological and geographical condition potentially hampering compliance with the study protocol and follow-up schedule.
- •? Claustrophobia precluding PET-CT.
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