Evidence map›Paper›PMID 41348022›Full record

ReviewHematology. American Society of Hematology. Education Program2025

Could treatment modification based on early response assessment improve results in DLBCL?

Hari S Raman, Jennifer L Crombie

Abstract readReview
In one paragraph

Review in Hematology. American Society of Hematology. Education Program, 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. 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

2 authors.

Hari S RamanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
Jennifer L CrombieDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the curative potential of frontline therapy in diffuse large B-cell lymphoma (DLBCL), nearly a third of patients will have relapsed or refractory disease and thus have a poor prognosis. While potentially curative options exist in the relapsed setting, these treatments are intensive, are not available to all patients, and are associated with high rates of relapse. As such, there is considerable interest in preemptively identifying high-risk patients who could benefit from modifications to initial treatment strategies. Alternatively, there may also be a subset of patients with favorable disease who could benefit from de-escalation strategies and reduction in toxicity. Personalized treatment approaches, including those that incorporate modification of therapy based on early response assessments, have the potential to improve outcomes in DLBCL, though these approaches require further evaluation in clinical practice. Here we review the prognostic role of interim positron emission tomography and the primarily unsuccessful efforts to use this tool to guide response-adaptive treatment strategies thus far. We subsequently review the potential role of evaluating minimal residual disease (MRD) in this context, discussing the available tools, the data to support its role in interim response assessment, and the future directions of MRD use in DLBCL clinical trials.

Indexed as

Lymphoma, Large B-Cell, DiffuseHumansNeoplasm, ResidualPositron-Emission TomographyPrognosis

Identifiers

PMID41348022
PMCPMC12891563

What OpenQuestion holds

Textmetadata
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.