Evidence map›Paper›PMID 42100396›Full record

ArticleFrontiers in oncology2026

Autologous and allogeneic hematopoietic cell transplantation in children and adults with high-risk anaplastic large cell lymphoma.

Natalie L Smith, Corinne Summers, Ted Gooley, Andrei Shustov, Rachel Salit, Rebecca A Gardner, Ann Dahlberg, Marie Bleakley, Mohamed L Sorror, Leona Holmberg and 4 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 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

14 authors.

Natalie L Smith *Fred Hutchinson Cancer Center, Seattle, WA, United States.
Corinne Summers *Fred Hutchinson Cancer Center, Seattle, WA, United States.
Ted GooleyFred Hutchinson Cancer Center, Seattle, WA, United States.
Andrei ShustovDepartment of Pediatrics, University of Washington School of Medicine, Seattle, WA, United States.
Rachel SalitFred Hutchinson Cancer Center, Seattle, WA, United States.
Rebecca A GardnerDepartment of Pediatrics, University of Washington School of Medicine, Seattle, WA, United States.
Ann DahlbergFred Hutchinson Cancer Center, Seattle, WA, United States.
Marie BleakleyFred Hutchinson Cancer Center, Seattle, WA, United States.
Mohamed L SorrorFred Hutchinson Cancer Center, Seattle, WA, United States.
Leona HolmbergFred Hutchinson Cancer Center, Seattle, WA, United States.
Paul A CarpenterFred Hutchinson Cancer Center, Seattle, WA, United States.
Brenda M SandmaierFred Hutchinson Cancer Center, Seattle, WA, United States.
David MaloneyFred Hutchinson Cancer Center, Seattle, WA, United States.
Monica S ThakarFred Hutchinson Cancer Center, Seattle, WA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Both autologous and allogeneic hematopoietic cell transplantation (HCT) have been used to treat high-risk anaplastic large cell lymphoma (ALCL) that has failed conventional chemotherapy. However, many patients are not able to fully eradicate disease prior to HCT, making the role of either form of HCT unclear. The aim of this study was to collect characteristics and outcomes of patients who underwent either autologous and/or allogeneic HCT and determine the role that disease status at HCT plays in overall survival (OS). Methods: To address this, we collected data on 41 patients with ALCL that underwent autologous (n=24) and/or allogeneic (n=17) HCT at our center between 1997-2020. Results: The 5-year estimated progression-free survival (PFS) and OS for the autologous HCT group was 40% (95% confidence interval, 20-59%) and 53% (31-71%), while for the allogeneic HCT group it was 65% (38-92%) and 65% (38-82%), respectively. For transplants performed in 2009 or later, 5-year OS was 91% (51-99%) in the allogeneic HCT group, and 51% (23-73%) in the autologous HCT group. Notable was that for those who entered transplant with detectable disease, 5-year OS was 50% (15-77%) with allogeneic HCT whereas it was 27% (7-54%) for autologous HCT. Discussion: These data confirm that HCT is a potentially curative therapy, and allogeneic HCT may have a survival advantage over autologous HCT when there is detectable disease prior to HCT.

Indexed as

allogeneic transplantationanaplastic large cell lymphomaautologous transplantationhematopoietic cell transplantationlymphoma

Identifiers

PMID42100396
PMCPMC13147282

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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.