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Azacitidine followed by R-GDP in transplant-ineligible relapsed/refractory diffuse large B-cell lymphoma: preliminary results from a multicenter, phase II study

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Author(s)
Dong Hyun KimJee Hyun KongJunshik HongJa Min ByunDong-Yeop ShinYoungil KohInho KimJinny ParkYoung Rok DoJeong-A KimWon Seog KimHo-Jin ShinSung-Soo Yoon
Keimyung Author(s)
Do, Young Rok
Department
Dept. of Internal Medicine (내과학)
Journal Title
Ther Adv Hematol
Issued Date
2025
Volume
16
Abstract
Background:
Epigenetic priming prior to chemotherapy represents a promising treatment strategy for refractory or relapsed diffuse large B-cell lymphoma (R/R DLBCL). We conducted a phase II trial to evaluate the efficacy and safety of azacitidine in combination with R-GDP (rituximab/gemcitabine/dexamethasone/cisplatin) in transplant-ineligible R/R DLBCL.

Methods:
Fifteen patients were enrolled and treated with azacitidine and R-GDP regimen (NCT03719989). Azacitidine was administered intravenously at a dose of 25 mg/m2/day for 5 days. Each cycle consisted of 21 days, with patients receiving up to a maximum of six cycles. The primary endpoint was the objective response rate, and the secondary objectives were toxicity, progression-free survival (PFS), and overall survival (OS).

Results:
Overall, 15 patients were enrolled in the study from March 2019 to August 2023, and the median age was 64 years (range: 41–75). The objective response rate was 66.7% with a complete response rate of 53.3%. The most common grade 3 or higher adverse events were hematologic toxicities, including neutropenia (66.7%) and thrombocytopenia (53.3%). Grade 3 or higher non-hematologic toxicities were rare, and most adverse events were transient and manageable. During a median follow-up of 15.8 months, five patients died, all from DLBCL. The median PFS was 12.6 months, while the median OS was not reached.

Conclusion:
Our study suggests that azacitidine followed by R-GDP is an effective and safe strategy for transplant-ineligible patients with R/R DLBCL. This represents the first phase II study to demonstrate the potential of epigenetic priming with azacitidine to enhance chemosensitivity in this patient population.
Keimyung Author(s)(Kor)
도영록
Publisher
School of Medicine (의과대학)
Type
Article
ISSN
2040-6215
Source
https://journals.sagepub.com/doi/10.1177/20406207251349361
DOI
10.1177/20406207251349361
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/46328
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Internal Medicine (내과학)
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