医学
临床终点
内科学
美罗华
中性粒细胞减少症
贫血
强的松
不利影响
国际预后指标
临床研究阶段
代理终结点
外科
临床试验
存活率
四分位间距
细胞因子释放综合征
发热性中性粒细胞减少症
进行性疾病
随访中值
作者
Lorenzo Falchi,Fritz Offner,Sven de Vos,Joshua Brody,Daniel Morillo,Kim Linton,Sylvia Snauwaert,Michael Roost Clausen,Yasmin Karimi,Catherine Thieblemont,Umberto Vitolo,Lori A. Leslie,Mayur Narkhede,Raúl Córdoba,Toshihiko Oki,Monica Wielgos-Bonvallet,Mina Khoshdeli,Yi Hao,Kimberly Archer,Malene Risum
出处
期刊:Blood
[Elsevier BV]
日期:2026-08-11
标识
DOI:10.1182/blood.2026033839
摘要
Patients with newly diagnosed large B-cell lymphoma (LBCL) and International Prognostic Index (IPI) scores ≥3 have inferior outcomes with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). We evaluated efficacy and safety of epcoritamab plus R-CHOP in newly diagnosed LBCL in Arm 1 of the phase 1b/2 EPCORE NHL-2 trial. Adults with CD20+ LBCL and IPI scores 3-5 received R-CHOP (6 cycles) plus epcoritamab for a total of 1 year of treatment. Primary endpoint was investigator-assessed overall response rate (ORR). Key secondary endpoints included complete response (CR) rate, duration of CR (DOCR), progression-free survival (PFS), overall survival (OS), minimal residual disease (MRD) negativity, and safety. Forty-seven patients were treated. Median age was 64 years, 89% had Ann Arbor stage IV, and 53% had bulky disease (≥7 cm). ORR was 98% (95% CI, 89-100) and CR rate 85% (95% CI, 72-94). At median follow-up of 44.2 months, median DOCR, PFS and OS were not reached (NR; 95% CI, NR-NR); estimated 2-year PFS and OS rates were 80% (95% CI, 65-89) and 87% (95% CI, 73-94), respectively. MRD-negativity was achieved in 100% of MRD-evaluable patients. Most common adverse events were neutropenia (74%), anemia (72%), and cytokine release syndrome (CRS; 60%). CRS events were predominantly grade 1-2; all resolved. Epcoritamab plus R-CHOP induced high response rates in patients with newly diagnosed LBCL and IPI scores 3-5. These promising findings support the ongoing phase 3 evaluation of this treatment regimen. This trial was registered at ClinicalTrials.gov (NCT04663347).
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