ReviewHematology. American Society of Hematology. Education Program2025
Could treatment modification based on early response assessment improve results in DLBCL?
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.
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.
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.
Who cites it
1 citing paper in PubMed.
- Minimal residual disease in diffuse large B-cell lymphoma after first-line therapy: Defining the continuum from metabolic remission to molecular clearance.British journal of haematology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
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.
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Registered trials
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.