Evidence map›Paper›PMID 40260947›Full record

ArticleHematological oncology2025

Impact of Age on Biology, Presentation and Outcomes in Marginal Zone Lymphoma: Results From a Multicenter Cohort Study.

Pallawi Torka, Natalie S Grover, Timothy J Voorhees, Reem Karmali, Kaitlin Annunzio, Marcus P Watkins, Andrea Anampa-Guzmán, Heather Reves, Montreh Tavakkoli, Beth Christian and 7 more

Abstract readMulticenter Study
In one paragraph

Article in Hematological oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

17 authors.

Pallawi TorkaDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Natalie S GroverDepartment of Medicine, Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Timothy J VoorheesDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0001-7603-6454
Reem KarmaliDepartment of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0003-0984-4376
Kaitlin AnnunzioDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, Ohio, USA.
Marcus P WatkinsDepartment of Medicine, Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, USA.
Andrea Anampa-GuzmánDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Heather RevesDepartment of Medicine, Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas, USA.
Montreh TavakkoliDepartment of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Beth ChristianDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, Ohio, USA.
Colin ThomasDepartment of Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Stefan K BartaDepartment of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Praveen Ramakrishnan GeethakumariDepartment of Medicine, Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas, USA.
Nancy L BartlettDepartment of Medicine, Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, USA.
Geoffrey ShouseDepartment of Medicine, City of Hope National Medical Center, Duarte, California, USA.
Adam J OlszewskiDepartment of Medicine, Brown University Providence, Providence, Rhode Island, USA.ORCID https://orcid.org/0000-0002-6472-6658
Narendranath EpperlaDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0002-8216-3457

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Given the paucity of age-specific data about biology, presentation, and treatment outcomes in adults with MZL, we sought to evaluate differences between younger (≤ 70 years) and older (> 70 years) patients with MZL in a large retrospective cohort treated in the contemporary era (2010 onwards). The primary objective was progression-free survival (PFS), while secondary objectives included the evaluation of overall survival (OS) and the cumulative incidence of transformation between the 2 groups. A total of 598 patients were included in the analysis and among these 32% were > 70 years of age. There were no age-based differences in the prevalence of NMZL, SMZL, and EMZL. Older patients had a higher incidence of adverse prognostic features at diagnosis such as worse performance status, advanced stage disease, and bone marrow involvement, yet were more likely to be treated with single-agent rituximab than chemoimmunotherapy. Age > 70 years was associated with inferior PFS and OS after controlling for clinically relevant risk factors and accounting for differences in first-line treatment. Receipt of rituximab monotherapy was associated with significantly inferior PFS overall, however, the type of first-line therapy did not impact OS in any group. Our data suggests that despite the development of new drugs for MZL, age remains an independent predictor of inferior outcomes. Investigation of targeted therapy combinations in the first-line setting may yield the required balance of efficacy and toxicity in older adults with MZL.

Indexed as

Lymphoma, B-Cell, Marginal ZoneAdultAgedAged, 80 and overAge FactorsFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesRituximabSurvival RateTreatment OutcomeRituximabElderlymarginal zone lymphomanon‐Hodgkin lymphomaoverall survivalprogression‐free survival

Identifiers

PMID40260947
PMCPMC12013245

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.