Evidence map›Paper›PMID 42489639›Full record

ArticleHematological oncology2026

Autologous Stem Cell Transplant Consolidation Is Associated With Improved Overall Survival in Angioimmunoblastic T-Cell Lymphoma: A Real-World National Cancer Database Study.

Yu Tao, Huijun Li, Ayo S Falade, Richard C Godby, Steven R Hwang, Grzegorz S Nowakowski, Urshila Durani, Yun Kyoung Tiger, N Nora Bennani, Stephen M Ansell and 2 more

Abstract read
In one paragraph

Article in Hematological 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

12 authors.

Yu TaoDepartment of Hematology, The First Affiliated Hospital, School of Medicine, Southern University of Science and Technology, Shenzhen, China.
Huijun LiDepartment of Hematology, Shenzhen People's Hospital, The Second Clinical Medical College of Jinan University, The First Affiliated Hospital of Southern University of Science and Technology, Shenzhen, Guangdong, China.
Ayo S FaladeDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0001-9201-6998
Richard C GodbyDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Steven R HwangDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0002-6536-1291
Grzegorz S NowakowskiDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Urshila DuraniDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0003-1860-2424
Yun Kyoung TigerDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
N Nora BennaniDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Stephen M AnsellDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0003-1244-6758
Yucai WangDivision of Hematology, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0002-1576-8341
Jihao ZhouDepartment of Hematology, Shenzhen People's Hospital, The Second Clinical Medical College of Jinan University, The First Affiliated Hospital of Southern University of Science and Technology, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0002-2684-192X

Funding

National Natural Science Foundation of China 82500213Shenzhen Outstanding Scientific and Technological Innovation Talent Training Program RCBS20221008093314036Shenzhen Science and Technology Program JCYJ20250604141706008
6 · The paper itself

Abstract

Angioimmunoblastic T-cell lymphoma (AITL) is an aggressive peripheral T-cell lymphoma with poor outcomes, and the role of autologous stem cell transplantation (ASCT) as consolidation after frontline therapy remains controversial. We conducted a retrospective cohort study using the National Cancer Database, including adults diagnosed with AITL between 2004 and 2020 who received frontline systemic therapy. Patients were categorized as chemotherapy alone (Chemo) or chemotherapy followed by ASCT (Chemo + ASCT). To mitigate immortal time bias, prespecified landmark analyses were performed, with a 6-month landmark analysis as the primary approach and a 9-month landmark analysis as a sensitivity analysis. Multivariable Cox regression and propensity score weighting using inverse probability of treatment weighting for the average treatment effect were used to address measured confounding. Among 3996 patients receiving systemic therapy, 686 (17.2%) underwent ASCT. In the 6-month landmark analysis, ASCT was associated with improved overall survival (HR, 0.53; 95% CI, 0.45-0.62; p < 0.001). Findings were consistent in the 9-month landmark analysis (HR, 0.58; 95% CI, 0.49-0.69; p < 0.001) and IPTW-adjusted model (HR, 0.51; 95% CI, 0.44-0.60; p < 0.001). In this large real-world cohort, ASCT consolidation was consistently associated with improved survival in patients with AITL. Although treatment-response data were unavailable and residual confounding cannot be excluded, these findings provide supportive real-world evidence and warrant prospective studies with treatment-timing and response data to better define patient selection.

Indexed as

Hematopoietic Stem Cell TransplantationImmunoblastic LymphadenopathyLymphoma, T-CellLymphoma, T-Cell, PeripheralAdultAgedDatabases, FactualFemaleHumansMaleMiddle AgedRetrospective StudiesSurvival RateTransplantation, Autologousangioimmunoblastic T‐cell lymphomaautologous stem cell transplantationimmortal time biaslandmark analysisnational cancer databaseoverall survival

Identifiers

PMID42489639
PMCPMC13394240

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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.