首页> 美国卫生研究院文献>BMC Cancer >The STELLAR trial protocol: a prospective multicentre trial for Richter’s syndrome consisting of a randomised trial investigation CHOP-R with or without acalabrutinib for newly diagnosed RS and a single-arm platform study for evaluation of novel agents in relapsed disease
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The STELLAR trial protocol: a prospective multicentre trial for Richter’s syndrome consisting of a randomised trial investigation CHOP-R with or without acalabrutinib for newly diagnosed RS and a single-arm platform study for evaluation of novel agents in relapsed disease

机译:STELLAR试验方案:一项针对Richter综合征的前瞻性多中心试验包括一项随机试验CHOP-R(有或没有acalabrutinib用于新诊断的RS)和单臂平台研究以评估复发性疾病中的新药

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摘要

BackgroundTransformation of chronic lymphocytic leukaemia (CLL) to diffuse large B-cell lymphoma (DLCBL) type Richter’s syndrome (RS) carries a dismal prognosis. Standard-of-care chemoimmunotherapy for de novo RS is inadequate with median survival of less than one year. Patients are frequently elderly or have co-morbidities limiting dose-intense chemotherapy. Treatment of relapsed/refractory (R/R) RS and RS emerging after CLL-directed therapy represent urgent unmet clinical needs.Agents targeting Bruton’s tyrosine kinase (BTK) deliver improved outcomes for patients with high-risk CLL and expand effective treatments to frailer patients. Acalabrutinib is an oral, second-generation BTK inhibitor with a favourable toxicity profile and demonstrated activity in CLL and B-cell lymphomas. Combination of acalabrutinib with standard-of-care CHOP-R chemoimmunotherapy offers a sound rationale to test in a prospective trial for de novo RS.
机译:背景:慢性淋巴细胞性白血病(CLL)转变为弥散性大B细胞淋巴瘤(DLCBL)型里氏综合征(RS)的预后很差。从头开始的RS的标准护理化学免疫疗法不足,中位生存期不到一年。患者常年老或患有合并症,限制了剂量密集的化疗。针对CLL指导的治疗后出现的复发/难治性RS和RS代表了迫切的临床需求,针对布鲁顿酪氨酸激酶(BTK)的代理商可为高危CLL患者提供更好的治疗效果,并为体弱的患者提供有效的治疗方法。 Acalabrutinib是口服第二代BTK抑制剂,具有良好的毒性特征,并在CLL和B细胞淋巴瘤中显示出活性。 acalabrutinib与护理标准CHOP-R化学免疫疗法的结合为从头RS的前瞻性试验提供了合理的理由。

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