Evidence map›Paper›PMID 39321424›Full record

SynthesisBlood advances2024

Transformation in marginal zone lymphoma: results from a prospective cohort and a meta-analysis of the literature.

Côme Bommier, Brian K Link, Brianna J Gysbers, Matthew J Maurer, Melissa C Larson, Arushi Khurana, Yucai Wang, Carrie A Thompson, Dai Chihara, Juan P Alderuccio and 9 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
  4. Article
  5. Article
  6. Review
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

19 authors.

Côme BommierDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.ORCID 0000-0002-5695-911X
Brian K LinkDivision of Hematology, Oncology, and Blood and Marrow Transplantation, Department of Internal Medicine, University of Iowa, Iowa City, IA.ORCID 0000-0001-5084-0698
Brianna J GysbersDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.ORCID 0000-0001-7592-8952
Matthew J MaurerDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.ORCID 0000-0002-1867-0526
Melissa C LarsonDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.ORCID 0000-0002-5430-8161
Arushi KhuranaDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0001-5645-0949
Yucai WangDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0002-1576-8341
Carrie A ThompsonDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.
Dai ChiharaDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-1153-2294
Juan P AlderuccioDivision of Hematology, Sylvester Comprehensive Cancer Center, University of Miami School of Medicine, Miami, FL.ORCID 0000-0002-2690-3377
Jean L KoffDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0003-4414-0489
Narendranath EpperlaHuntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0002-8216-3457
Annarita ConconiStruttura Semplice a Valenza Dipartimentale di Ematologia, Ospedale degli Infermi, Ponderano, Italy.
Izidore S LossosDivision of Hematology, Sylvester Comprehensive Cancer Center, University of Miami School of Medicine, Miami, FL.ORCID 0000-0002-9346-9013
Grzegorz S NowakowskiDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0002-6955-9393
Andrew L FeldmanDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.ORCID 0000-0001-5009-4808
Thomas M HabermannDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0003-3532-9132
Rebecca L KingDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
James R CerhanDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.ORCID 0000-0002-7482-178X

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI AKHILESH PANDEY · 1985 to 2026
$151.3M
Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
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 P30 CA015083NCI NIH HHS P50 CA097274NCI NIH HHS U01 CA195568
6 · The paper itself

Abstract

abstractMarginal zone lymphoma (MZL) includes extranodal MZL (EMZL), splenic MZL (SMZL), and nodal MZL (NMZL) subtypes. Histologic transformation (HT) to large B-cell lymphomas is well documented but with a large variability in published cumulative incidence rates. We report results from the Molecular Epidemiology Resource (MER) cohort on the cumulative incidence of HT (with death as competing risk) and the associated risk factors and outcomes. We also conducted a meta-analysis of available studies on the cumulative incidence of HT. From 2002 to 2015, 529 patients with MZL were enrolled in the MER study (69% EMZL, 16% SMZL, and 15% NMZL). The 10-year overall survival (OS) from diagnosis was 66%. HT occurred in 21 patients with a 5-year and 10-year cumulative incidence of 2.7% (95% confidence interval [CI], 0.02-0.05) and 3.6% (95% CI, 0.02-0.06), respectively. HT was associated with an increased risk for death (subdistribution hazard ratio [HR], 3.95; 95% CI, 2.06-7.55). Predictors of HT were ≥2 extranodal sites and mucosa-associated lymphoid tissue International Prognostic Index score ≥2. The OS was 79% at 5 years and 55% at 10 years after HT. In the meta-analysis of 12 studies (6161 patients), the 5- and 10-year cumulative incidence of HT across all subtypes were 5% (95% CI, 0.05-0.06) and 8% (95% CI, 0.07-0.09), respectively. These rates were lower in EMZL (3% and 5%) than in SMZL (7% and 13%) and NMZL (9% and 13%). Although HT is relatively uncommon in the first decade after MZL diagnosis, it is associated with an inferior outcome and needs new approaches for prevention and management.

Indexed as

Lymphoma, B-Cell, Marginal ZoneAdultAgedCell Transformation, NeoplasticFemaleHumansIncidenceMaleMiddle AgedPrognosisProspective StudiesRisk Factors

Identifiers

PMID39321424
PMCPMC11629267

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.