Evidence map›Paper›PMID 38235513›Full record

ArticleHaematologica2024

Autologous stem cell transplant in fit patients with refractory or early relapsed diffuse large B-cell lymphoma that responded to salvage chemotherapy.

Aung M Tun, Yucai Wang, Seth Maliske, Ivana Micallef, David J Inwards, Thomas M Habermann, Luis Porrata, Jonas Paludo, Jose Villasboas Bisneto, Allison Rosenthal and 5 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 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
1.4field-weighted citation impact, top 17% of its field
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, 5 citations in OpenAlex.

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  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

15 authors at 4 institutions in 1 country.

Aung M TunDivision of Hematology, Mayo Clinic, Rochester, Minnesota; Division of Hematologic Malignancies and Cellular Therapeutics, The University of Kansas, Kansas City. atun@kumc.edu.
Yucai WangDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Seth MaliskeDivision of Hematology, Oncology, and Blood and Marrow Transplantation, University of Iowa, Iowa City, Iowa.
Ivana MicallefDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
David J InwardsDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Thomas M HabermannDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Luis PorrataDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Jonas PaludoDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Jose Villasboas BisnetoDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Allison RosenthalInternal Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.
Mohamed A Kharfan-DabajaDivision of Hematology-Oncology and Blood and Marrow Transplantation and Cellular Therapy Program, Mayo Clinic, Jacksonville, Florida.
Stephen M AnsellDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Grzegorz S NowakowskiDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Umar FarooqDivision of Hematology, Oncology, and Blood and Marrow Transplantation, University of Iowa, Iowa City, Iowa.
Patrick B JohnstonDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Mayo Clinic · USUniversity of Iowa · USMayo Clinic in Arizona · USMayo Clinic in Florida · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Jon C.D. Houtman · 2000 to 2026
$70.0M
NCI NIH HHS P30 CA086862
6 · The paper itself

Abstract

Chimeric antigen receptor T-cell therapy is the new standard of care in fit patients with refractory or early relapsed diffuse large B-cell lymphoma (DLBCL). However, there may still be a role for salvage chemotherapy (ST) and autologous stem cell transplant (ASCT) in certain circumstances (e.g., lack of resources for chimeric antigen receptor T-cell therapy, chemosensitive relapses). We retrospectively studied 230 patients with refractory or early relapsed DLBCL who underwent ST and ASCT. The median line of ST was one (range, 1-3). Best response before ASCT was complete response in 106 (46%) and partial response in 124 (54%) patients. The median follow-up after ASCT was 89.4 months. The median progression-free (PFS) and overall survival (OS) were 16.1 and 43.3 months, respectively. Patients relapsing between 6 to 12 months after frontline therapy had a numerically better median PFS (29.6 months) and OS (88.5 months). Patients who required one line of ST, compared to those requiring more than one line, had a better median PFS (37.9 vs. 3.9 months; P=0.0005) and OS (68.3 vs. 12.0 months; P=0.0005). Patients who achieved complete response had a better median PFS (71.1 vs. 6.3 months; P<0.0001) and OS (110.3 vs. 18.9 months; P<0.0001) than those in partial response. Patients who achieved complete response after one line of ST had the most favorable median PFS (88.5 months) and OS (117.2 months). Post-ASCT survival outcomes of patients with refractory or early relapsed DLBCL appeared reasonable and were particularly favorable in those who required only one line of ST to achieve complete response before ASCT, highlighting the role of this procedure in select patients with chemosensitive disease.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsHematopoietic Stem Cell TransplantationLymphoma, Large B-Cell, DiffuseSalvage TherapyTransplantation, AutologousAdultAgedCombined Modality TherapyDrug Resistance, NeoplasmFemaleHumansMaleMiddle AgedRecurrenceRetrospective StudiesTreatment Outcome

Identifiers

PMID38235513
PMCPMC11215374
OpenAlexW4390984611

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.