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REALYSA 中弥漫性大 B 细胞淋巴瘤真实世界数据的质量和利用面临的挑战,这是一个 LYSA 队列。

Challenges for quality and utilization of real-world data for diffuse large B-cell lymphoma in REALYSA, a LYSA cohort.

机构信息

Department of Hematology, Hopital Lyon Sud, Claude Bernard Lyon 1 University, Pierre Benite, France.

Lymphoma Academic Research Organisation, Hopital Lyon Sud, Pierre Benite, France.

出版信息

Blood Adv. 2024 Jan 23;8(2):296-308. doi: 10.1182/bloodadvances.2023010798.

DOI:10.1182/bloodadvances.2023010798
PMID:37874913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10824688/
Abstract

Real-world data (RWD) are essential to complement clinical trial (CT) data, but major challenges remain, such as data quality. REal world dAta in LYmphoma and Survival in Adults (REALYSA) is a prospective noninterventional multicentric cohort started in 2018 that included patients newly diagnosed with lymphoma in France. Herein is a proof-of-concept analysis on patients with first-line diffuse large B-cell lymphoma (DLBCL) to (1) evaluate the capacity of the cohort to provide robust data through a multistep validation process; (2) assess the consistency of the results; and (3) conduct an exploratory transportability assessment of 2 recent phase 3 CTs (POLARIX and SENIOR). The analysis population comprised 645 patients with DLBCL included before 31 March 2021 who received immunochemotherapy and for whom 3589 queries were generated, resulting in high data completeness (<4% missing data). Median age was 66 years, with mostly advanced-stage disease and high international prognostic index (IPI) score. Treatments were mostly rituximab, cyclophosphamide, doxorubicin hydrochloride, vincristine, and prednisone (R-CHOP 75%) and reduced dose R-CHOP (13%). Estimated 1-year event-free survival (EFS) and overall survival rates were 77.9% and 90.0%, respectively (median follow-up, 9.9 months). Regarding transportability, when applying the CT's main inclusion criteria (age, performance status, and IPI), outcomes seemed comparable between patients in REALYSA and standard arms of POLARIX (1-year progression-free survival 79.8% vs 79.8%) and SENIOR (1-year EFS, 64.5% vs 60.0%). With its rigorous data validation process, REALYSA provides high-quality RWD, thus constituting a platform for numerous scientific purposes. The REALYSA study was registered at www.clinicaltrials.gov as #NCT03869619.

摘要

真实世界数据(RWD)对于补充临床试验(CT)数据至关重要,但仍存在许多挑战,例如数据质量。REal world dAta in LYmphoma and Survival in Adults(REALYSA)是一项始于 2018 年的前瞻性非干预性多中心队列研究,纳入了法国新诊断为淋巴瘤的患者。本文旨在对一线弥漫性大 B 细胞淋巴瘤(DLBCL)患者进行概念验证分析,(1)通过多步骤验证过程评估该队列提供可靠数据的能力;(2)评估结果的一致性;(3)对 2 项近期 III 期 CT(POLARIX 和 SENIOR)进行探索性可移植性评估。分析人群包括 2021 年 3 月 31 日前入组的 645 例 DLBCL 患者,他们接受了免疫化疗,共生成了 3589 条查询,数据完整性高(<4%缺失数据)。中位年龄为 66 岁,大多数为晚期疾病和高国际预后指数(IPI)评分。治疗方法主要为利妥昔单抗、环磷酰胺、盐酸多柔比星、长春新碱和泼尼松(R-CHOP75%)和低剂量 R-CHOP(13%)。估计 1 年无事件生存率(EFS)和总生存率分别为 77.9%和 90.0%(中位随访时间 9.9 个月)。关于可移植性,当应用 CT 的主要纳入标准(年龄、表现状态和 IPI)时,REALYSA 中的患者和 POLARIX(1 年无进展生存率 79.8% vs 79.8%)和 SENIOR(1 年 EFS,64.5% vs 60.0%)的标准治疗组的结果似乎相似。REALYSA 通过严格的数据验证过程提供了高质量的 RWD,因此构成了众多科学目的的平台。REALYSA 研究在 www.clinicaltrials.gov 上注册,编号为 #NCT03869619。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc67/10824688/66a5fd9e0306/BLOODA_ADV-2023-010798-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc67/10824688/83ddd38d8ed3/BLOODA_ADV-2023-010798-ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc67/10824688/523fef1aa359/BLOODA_ADV-2023-010798-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc67/10824688/d8d90e277fc6/BLOODA_ADV-2023-010798-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc67/10824688/66a5fd9e0306/BLOODA_ADV-2023-010798-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc67/10824688/83ddd38d8ed3/BLOODA_ADV-2023-010798-ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc67/10824688/523fef1aa359/BLOODA_ADV-2023-010798-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc67/10824688/d8d90e277fc6/BLOODA_ADV-2023-010798-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc67/10824688/66a5fd9e0306/BLOODA_ADV-2023-010798-gr3.jpg

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