Evidence map›Paper›PMID 39602301›Full record

ArticleBlood advances2025

Treatment patterns and outcomes in follicular lymphoma with POD24: an analysis from the LEO Consortium.

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 and 12 more

Abstract read
In one paragraph

Article in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. FLIPI24: A Modern Prognostic Model and Clinical Trial Enrichment Tool for Newly Diagnosed Follicular Lymphoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Jonathan R DayDepartment of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA.
Melissa C LarsonDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.
Urshila DuraniDivision of Hematology, Mayo Clinic, Rochester, MN.
Jean L KoffDepartment of Medicine, Winship Cancer Institute, Emory University, Atlanta, GA.ORCID 0000-0003-4414-0489
Yucai WangDivision of Hematology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-1576-8341
Thomas M HabermannDivision of Hematology, Mayo Clinic, Rochester, MN.
Izidore S LossosDepartment of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Health System, Miami, FL.ORCID 0000-0002-9346-9013
Loretta J NastoupilDepartment of Lymphoma and Myeloma, MD Anderson Cancer Center, The University of Texas, Houston, TX.ORCID 0000-0001-6071-8610
Christopher StrouseDepartment of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA.
Dai ChiharaDepartment of Lymphoma and Myeloma, MD Anderson Cancer Center, The University of Texas, Houston, TX.ORCID 0000-0002-1153-2294
Peter MartinDepartment of Medicine, Weill Cornell Medicine, New York-Presbyterian Hospital, New York, NY.
John P LeonardDepartment of Medicine, Weill Cornell Medicine, New York-Presbyterian Hospital, New York, NY.
Jonathon B CohenDepartment of Medicine, Winship Cancer Institute, Emory University, Atlanta, GA.ORCID 0000-0002-2723-6481
Brad S KahlDepartment of Medicine, Siteman Cancer Center, Washington University School of Medicine in St. Louis, St. Louis, MO.ORCID 0000-0003-0459-6609
Jia RuanDepartment of Medicine, Weill Cornell Medicine, New York-Presbyterian Hospital, New York, NY.
W Richard BurackDepartment of Medicine, James P. Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY.ORCID 0000-0002-5584-584X
Jonathan W FriedbergDepartment of Medicine, James P. Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY.
James R CerhanDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.ORCID 0000-0002-7482-178X
Christopher R FlowersDepartment of Lymphoma and Myeloma, MD Anderson Cancer Center, The University of Texas, Houston, TX.
Brian K LinkDepartment of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA.ORCID 0000-0001-5084-0698
Matthew J MaurerDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.ORCID 0000-0002-1867-0526
Carla CasuloDepartment of Medicine, James P. Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY.ORCID 0000-0003-4998-9932

Funding

The Role of Monocytes in non-Hodgkin LymphomaP50CA097274 · NCI · UNIVERSITY OF IOWA · PI LENTZ, STEVEN R · 2002 to 2021
$45.7M
The Lymphoma Epidemiology of Outcomes (LEO) Cohort Study (Supplement)U01CA195568 · NCI · MAYO CLINIC ROCHESTER · PI CERHAN, JAMES R, FLOWERS, CHRISTOPHER R · 2015 to 2025
$22.1M
Iowa StARR Scholars ProgramR38HL150208 · NHLBI · UNIVERSITY OF IOWA · PI PAUL B MCCRAY, DAVID A STOLTZ · 2021 to 2026
$1.5M
NCI NIH HHS P50 CA097274NCI NIH HHS U01 CA195568NHLBI NIH HHS R38 HL150208
6 · The paper itself

Abstract

abstractProgression 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 after POD24. Assembling an academic-based cohort from the Lymphoma Epidemiology of Outcomes Consortium for Real World Evidence, we evaluated patterns of care and outcomes for 220 patients with FL 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, rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone (R-CHOP) was the predominant second-line choice (48%). Among patients initially treated with R-CHOP, aggressive salvage therapy was the predominant second-line choice (38%). Overall response rate to therapy after POD24 was 64% (95% confidence interval [CI], 56-70); complete response rate was 39% (95% CI, 32-46). The median event-free survival for therapy after POD24 was 9.8 months (95% CI, 7.3-12.1); 5-year overall survival (OS) was 71% (95% CI, 65-78). OS was inferior for patients aged >70 years (hazard ratio [HR], 2.31; 95% CI, 1.27-4.20) and those with high-risk FL International Prognostic Index scores at diagnosis (HR, 2.10; 95% CI, 1.23-3.60). No treatment category stood out with more favorable results. Cause of death was predominantly lymphoma related. Patients with follicular histology at their POD24 event had a low cumulative incidence of transformation (1.1% at 5 years). Our study is among the largest cohorts describing contemporary patterns of care for patients with POD24, providing a focused data set useful for interpreting and designing prospective clinical trials in this population.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, FollicularAdultAgedAged, 80 and overCyclophosphamideDoxorubicinFemaleHumansMaleMiddle AgedPrednisonePrognosisRituximabTreatment OutcomeVincristineCyclophosphamideDoxorubicinPrednisoneRituximabVincristine

Identifiers

PMID39602301
PMCPMC11909426

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.