Evidence map›Paper›PMID 38669353›Full record

ArticleBlood advances2024

Defining primary refractory large B-cell lymphoma.

Allison M Bock, Raphael Mwangi, Yucai Wang, Arushi Khurana, Matthew J Maurer, Amy Ayers, Brad S Kahl, Peter Martin, Jonathon B Cohen, Carla Casulo and 10 more

Abstract readMulticenter Study
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–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

23 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

20 authors.

Allison M BockDivision of Hematology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-3174-8877
Raphael MwangiDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.
Yucai WangDivision of Hematology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-1576-8341
Arushi KhuranaDivision of Hematology, Mayo Clinic, Rochester, MN.
Matthew J MaurerDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.ORCID 0000-0002-1867-0526
Amy AyersDivision of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
Brad S KahlDivision of Oncology, Washington University in St. Louis, St. Louis, MO.
Peter MartinDivision of Hematology/Oncology, Weill Cornell Medicine, New York, NY.
Jonathon B CohenDepartment of Hematology and Medical Oncology, Emory University, Atlanta, GA.ORCID 0000-0002-2723-6481
Carla CasuloDivision of Hematology/Oncology, University of Rochester Medical Center, Rochester, NY.ORCID 0000-0003-4998-9932
Izidore S LossosDivision of Hematology, University of Miami, Miami, FL.ORCID 0000-0002-9346-9013
Umar FarooqDivision of Hematology, Oncology, and Blood and Marrow Transplantation, University of Iowa, Iowa City, IA.ORCID 0000-0001-7891-9891
Sabarish AyyappanDivision of Hematology, Oncology, and Blood and Marrow Transplantation, University of Iowa, Iowa City, IA.
Tanner ReicksDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.
Thomas M HabermannDivision of Hematology, Mayo Clinic, Rochester, MN.
Thomas E WitzigDivision of Hematology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-4215-6500
Christopher R FlowersDivision of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
James R CerhanDepartment of Hematology and Hematologic Malignancies, Huntsman Cancer Institute/University of Utah, Salt Lake City, UT.ORCID 0000-0002-7482-178X
Loretta J NastoupilDivision of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-6071-8610
Grzegorz S NowakowskiDivision of Hematology, Mayo Clinic, Rochester, MN.

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
NCI NIH HHS U01 CA195568
6 · The paper itself

Abstract

abstractPatients with large B-cell lymphoma (LBCL) that fail to achieve a complete response (CR) or who relapse early after anthracycline-containing immunochemotherapy (IC) have a poor prognosis and are commonly considered to have "primary refractory disease." However, different definitions of primary refractory disease are used in the literature and clinical practice. In this study, we examined variation in the time to relapse used to define refractory status and association with survival outcomes in patients with primary refractory LBCL in a single-center prospective cohort with validation in an independent multicenter cohort. Patients with newly diagnosed LBCL were enrolled in the Molecular Epidemiological Resource cohort (MER; N = 949) or the Lymphoma Epidemiology of Outcomes cohort (LEO; N = 2755) from September 2002 to May 2021. Primary refractory LBCL was defined as no response (stable disease [SD]) or progressive disease (PD) during, or by the end of, frontline (1L) IC (primary PD; PPD); partial response at end of treatment (EOT PR); or relapse within 3 to 12 months after achieving CR at EOT to 1L IC (early relapse). In the MER cohort, patients with PPD had inferior overall survival (OS; 2-year OS rate: 15% MER, 31% LEO) when compared with other subgroups considered in defining primary refractory disease, EOT PR (2-year OS rate: 38% MER, 50% LEO) and early relapse (2-year OS rate: 44% MER, 58% LEO). Among patients receiving 1L IC with curative intent, we identified that patients with PPD are the key subgroup with poor outcomes. We propose a definition of primary refractory LBCL as SD or PD during, or by the end of, 1L treatment.

Indexed as

Lymphoma, Large B-Cell, DiffuseAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisProspective StudiesTreatment Outcome

Identifiers

PMID38669353
PMCPMC11255370

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.