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SWOG 1918:一项在 75 岁或以上新诊断侵袭性非霍奇金淋巴瘤患者中进行的 R-miniCHOP 联合或不联合口服阿扎胞苷(CC-486)的 II/III 期随机研究-旨在改善治疗、结局,并验证一个前瞻性虚弱工具。

SWOG 1918: A phase II/III randomized study of R-miniCHOP with or without oral azacitidine (CC-486) in participants age 75 years or older with newly diagnosed aggressive non-Hodgkin lymphomas - Aiming to improve therapy, outcomes, and validate a prospective frailty tool.

机构信息

Chao Family Comprehensive Cancer Center, University of California, Irvine, Orange, CA, USA.

SWOG Statistics and Data Management Center, Seattle, WA, USA; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

出版信息

J Geriatr Oncol. 2022 Mar;13(2):258-264. doi: 10.1016/j.jgo.2021.10.003. Epub 2021 Oct 20.


DOI:10.1016/j.jgo.2021.10.003
PMID:34686472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9879719/
Abstract

Diffuse large B cell lymphoma (DLBCL) is an aggressive but potentially curable malignancy; however, cure is highly dependent on the ability to deliver intensive, anthracycline-based chemoimmunotherapy. Nearly one third of cases of DLBCL occur in patients over age 75 years, and advanced age is an important adverse feature in prognostic models. Despite this incidence in older patients, there is no clear accepted standard of care due to under-representation of this group in large randomized clinical trials. Furthermore, insufficient assessments of baseline frailty and prediction of toxicity hamper clinical decision-making. Here, we present an ongoing randomized study of R-miniCHOP chemoimmunotherapy with or without oral azacitidine (CC-486, Onureg) for patients age 75 and older with newly diagnosed DLBCL and associated aggressive lymphomas. The incorporation of an oral hypomethylating agent is based on increased tumor methylation as a biologic feature of older patients with DLBCL and a desire to minimize the injection burden for this population. This is the first randomized study in this population conducted in North America by the National Clinical Trials Network (NCTN) and will enroll up to 422 patients including 40 patients in a safety run-in phase. This study incorporates an objective assessment of baseline frailty (the FIL Tool) and a serial comprehensive geriatric assessment (CGA). Key correlative tests will include circulating tumor DNA (ctDNA) assays at pre-specified timepoints to explore if ctDNA quantity and methylation patterns correlate with response. S1918 has the potential to impact future trial design and to change the standard of care for patients 75 years and older with aggressive lymphoma given its randomized design, prospective incorporation of geriatric assessments, and exploration of ctDNA correlatives. Trial registration: The trial is registered with ClinicalTrial.gov Identifier NCT04799275.

摘要

弥漫性大 B 细胞淋巴瘤(DLBCL)是一种侵袭性但可治愈的恶性肿瘤;然而,治愈高度依赖于提供强化、蒽环类药物为基础的化疗免疫治疗的能力。近三分之一的 DLBCL 病例发生在 75 岁以上的患者中,年龄增长是预后模型中的一个重要不利特征。尽管老年患者发病率较高,但由于该组在大型随机临床试验中的代表性不足,因此没有明确的公认标准治疗方法。此外,对基线虚弱程度的评估不足和毒性预测阻碍了临床决策。在这里,我们提出了一项正在进行的 R-miniCHOP 化疗免疫治疗联合或不联合口服阿扎胞苷(CC-486,Onureg)用于新诊断的 DLBCL 且伴有侵袭性淋巴瘤的 75 岁及以上患者的随机研究。口服低甲基化剂的纳入是基于肿瘤甲基化增加作为 DLBCL 老年患者的生物学特征,以及为该人群减少注射负担的愿望。这是北美国家临床试验网络(NCTN)在该人群中进行的第一项随机研究,将招募多达 422 名患者,包括 40 名患者参加安全预试验阶段。该研究纳入了基线虚弱程度的客观评估(FIL 工具)和连续全面老年评估(CGA)。关键的相关测试将包括在预定时间点进行循环肿瘤 DNA(ctDNA)检测,以探索 ctDNA 数量和甲基化模式是否与反应相关。鉴于其随机设计、前瞻性纳入老年评估以及对 ctDNA 相关性的探索,S1918 有可能影响未来的试验设计并改变 75 岁及以上侵袭性淋巴瘤患者的标准治疗方法。

试验注册:该试验在 ClinicalTrials.gov 标识符 NCT04799275 下注册。

相似文献

[1]
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J Geriatr Oncol. 2022-3

[2]
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[6]
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[2]
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[3]
Advances in epigenetic therapies for B-cell non-hodgkin lymphoma.

Ann Hematol. 2024-12

[4]
Circulating tumor DNA methylation detection as biomarker and its application in tumor liquid biopsy: advances and challenges.

MedComm (2020). 2024-11-9

[5]
The current landscape of frontline large B-cell lymphoma trials.

Blood. 2025-1-9

[6]
Age-adjusted high-dose chemotherapy followed by autologous stem cell transplantation or conventional chemotherapy with R-MP as first-line treatment in elderly primary CNS lymphoma patients - the randomized phase III PRIMA-CNS trial.

BMC Cancer. 2023-8-18

[7]
Diffuse Large B-Cell Lymphoma (DLBCL): Early Patient Management and Emerging Treatment Options.

Onco Targets Ther. 2022-12-6

[8]
How I treat older patients with DLBCL in the frontline setting.

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[9]
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本文引用的文献

[1]
Improving Survival and Predicting Toxicity in Older Patients With DLBCL: A Delicate Balance.

J Clin Oncol. 2021-4-10

[2]
Simplified Geriatric Assessment in Older Patients With Diffuse Large B-Cell Lymphoma: The Prospective Elderly Project of the Fondazione Italiana Linfomi.

J Clin Oncol. 2021-4-10

[3]
Subcutaneous Rituximab-MiniCHOP Compared With Subcutaneous Rituximab-MiniCHOP Plus Lenalidomide in Diffuse Large B-Cell Lymphoma for Patients Age 80 Years or Older.

J Clin Oncol. 2021-4-10

[4]
Obinutuzumab and miniCHOP for unfit patients with diffuse large B-cell lymphoma. A phase II study by Fondazione Italiana Linfomi.

J Geriatr Oncol. 2020-1

[5]
The roles of DNA, RNA and histone methylation in ageing and cancer.

Nat Rev Mol Cell Biol. 2019-7-3

[6]
Comprehensive geriatric assessment is useful in an elderly Australian population with diffuse large B-cell lymphoma receiving rituximab-chemotherapy combinations.

Br J Haematol. 2019-6-17

[7]
Circulating Tumor DNA Measurements As Early Outcome Predictors in Diffuse Large B-Cell Lymphoma.

J Clin Oncol. 2018-8-20

[8]
Combination of ofatumumab and reduced-dose CHOP for diffuse large B-cell lymphomas in patients aged 80 years or older: an open-label, multicentre, single-arm, phase 2 trial from the LYSA group.

Lancet Haematol. 2017-1

[9]
Epigenomic evolution in diffuse large B-cell lymphomas.

Nat Commun. 2015-4-20

[10]
Treatment patterns and comparative effectiveness in elderly diffuse large B-cell lymphoma patients: a surveillance, epidemiology, and end results-medicare analysis.

Oncologist. 2014-12

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