Evidence map›Paper›PMID 42317600›Full record

ArticleBlood neoplasia2026

Autologous transplant for patients with chemotherapy-sensitive late relapse of diffuse large B-cell lymphoma.

Lorenzo Iovino, Ningxin Ma, Mohamed A Kharfan-Dabaja, Alex F Herrera, Craig S Sauter, Mehdi Hamadani, Peter A Riedell, Ajay K Gopal, Leona Holmberg, Qian Vicky Wu and 2 more

Abstract read
In one paragraph

Article in Blood neoplasia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Lorenzo IovinoFred Hutchinson Cancer Center, Seattle, WA.
Ningxin MaFred Hutchinson Cancer Center, Seattle, WA.
Mohamed A Kharfan-DabajaDivision of Hematology and Medical Oncology, Bone Marrow Transplantation Program, Mayo Clinic, Jacksonville, FL.
Alex F HerreraDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA.
Craig S SauterDepartment of Medicine, Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Mehdi HamadaniCenter for International Blood and Marrow Transplant Research/Medical College of Wisconsin, Milwaukee, WI.
Peter A RiedellBiological Sciences Division, The University of Chicago, Chicago, IL.
Ajay K GopalFred Hutchinson Cancer Center, Seattle, WA.
Leona HolmbergFred Hutchinson Cancer Center, Seattle, WA.
Qian Vicky WuFred Hutchinson Cancer Center, Seattle, WA.
Sonali M SmithDepartment of Medicine, The University of Chicago, Chicago, IL.
Mazyar ShadmanFred Hutchinson Cancer Center, Seattle, WA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
NCI NIH HHS P30 CA008748NCI NIH HHS U24 CA076518
6 · The paper itself

Abstract

In the era of chimeric antigen receptor (CAR) T-cell therapy, autologous stem cell transplant (ASCT) for diffuse large B-cell lymphoma (DLBCL) is preferentially offered to patients with late relapse (>12 months) who achieve complete or partial response (CR or PR, respectively) to salvage therapy. We conducted a retrospective cohort study using publicly available data from the Center for International Blood and Marrow Transplant Research in this population. We included adult patients with DLBCL, not otherwise specified, and high-grade large B-cell lymphomas who experienced disease relapsed after remaining on a response to first line of treatment for at least 12 months and who achieved a CR or PR after salvage treatment at the time of relapse. A total of 182 patients treated between 2013 and 2021 were included in the analysis: 100 had CR and 82 had PR before ASCT. Median follow-up after ASCT was 34 months (range, 1-95). Overall survival (OS) at 3 years was 67.6%, and progression-free survival (PFS) was 50.6%. Cumulative incidence of relapse at 3 years was 43.9%. Older age (hazard ratio [HR], 1.03;

Identifiers

PMID42317600
PMCPMC13273701

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Registered trials

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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.