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Treatment Patterns and Outcomes in Follicular Lymphoma with POD24: An Analysis from The LEO Consortium

滤泡性淋巴瘤 医学 内科学 美罗华 淋巴瘤 苯达莫司汀 卵泡期 肿瘤科 置信区间
作者
Jonathan R Day,Melissa C. Larson,Urshila Durani,Jean L. Koff,Yucai Wang,Thomas M. Habermann,Izidore S. Lossos,Loretta J. Nastoupil,Christopher Strouse,Dai Chihara,Peter Martin,John P. Leonard,Jonathon B. Cohen,Brad S. Kahl,Jia Ruan,Richard Burack,Jonathan W. Friedberg,James R. Cerhan,Christopher R. Flowers,Brian K. Link,Matthew J. Maurer,Carla Casulo
出处
期刊:Blood Advances [American Society of Hematology]
标识
DOI:10.1182/bloodadvances.2024014053
摘要

Progression of disease within 24 months of initial immunochemotherapy (POD24) is a negative prognostic factor for patients with follicular lymphoma (FL). There is no standard treatment following POD24. Assembling an academic-based cohort from the Lymphoma Epidemiology of Outcomes Consortium for Real World Evidence (LEO CREWE), we evaluated patterns of care and outcomes for 256 FL patients with POD24 and retained FL histology. Therapy after POD24 was heterogeneous, with no treatment category accounting for >25% of the total. Among patients initially treated with bendamustine-rituximab, R-CHOP was the predominant second-line choice (42%). Among patients initially treated with R-CHOP, the predominant second-line choice was aggressive salvage therapy (36%). Overall response rate to therapy following POD24 was 66% (95% confidence interval [CI] 59%-72%); complete response rate was 40% (95% CI 33%-46%). Median EFS for therapy after POD24 was 10.4 months (95% CI 8.4-12.8); 5-year OS was 73% (95% CI 68-80%). OS was inferior for patients aged >70 years (HR 2.31 [95% CI 1.27-4.20]) and those with high-risk FLIPI scores at diagnosis (HR 2.10 [95% CI 1.23-3.60]). Cause of death was predominantly lymphoma related. Patients with follicular histology at their POD24 event had a low cumulative incidence of transformation (1.9% at 5 years). Our study is among the largest cohorts describing contemporary patterns of care for patients with POD24, providing a focused dataset useful for interpreting and designing prospective clinical trials in this population.

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