Evidence map›Paper›PMID 30537212›Full record

ArticleBritish journal of haematology2019

Allogeneic haematopoietic cell transplantation impacts on outcomes of mantle cell lymphoma with TP53 alterations.

Richard J Lin, Caleb Ho, Patrick D Hilden, Juliet N Barker, Sergio A Giralt, Paul A Hamlin, Ann A Jakubowski, Hugo R Castro-Malaspina, Kevin S Robinson, Esperanza B Papadopoulos and 2 more

Abstract read
In one paragraph

Article in British journal of haematology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 3 pooled it
–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

37 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Guideline
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  3. Pooled it
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  9. Review
  10. Your chemo is no good here: management of high-risk MCL.Hematology. American Society of Hematology. Education Program · 2024
    Review
  11. Article
  12. Article
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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.

Richard J LinAdult BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0002-0834-7880
Caleb HoDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Patrick D HildenDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Juliet N BarkerAdult BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Sergio A GiraltAdult BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Paul A HamlinLymphoma Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Ann A JakubowskiAdult BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Hugo R Castro-MalaspinaAdult BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Kevin S RobinsonAdult BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Esperanza B PapadopoulosAdult BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Miguel-Angel PeralesAdult BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Craig S SauterAdult BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
T LYMPHOCYTE SUBSET FUNCTION POST-TRANSPLANTATIONP01CA023766 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SCHEINBERG, DAVID A · 1985 to 2023
$59.0M
NCI NIH HHS P01 CA023766NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

TP53 alterations portend extremely poor prognosis in patients with mantle cell lymphoma treated with standard treatment modalities. We reviewed outcomes of 42 patients with available TP53 status who had received a reduced-intensity or non-myeloablative allogeneic haematopoietic cell transplant at our institution. We demonstrated a 2-year overall survival and progression-free survival of 78% [95% confidence interval (CI) 60-88] and 61% (95% CI 43-75), respectively. The 2-year cumulative incidences of relapse and non-relapse mortality were 19% and 20%, respectively. Importantly, there is no significant difference among patients with and without TP53 alterations, suggesting for the first time a beneficial treatment modality for these high-risk patients.

Indexed as

AdultAgedFemaleHematopoietic Stem Cell TransplantationHumansLymphoma, Mantle-CellMaleMiddle AgedPrognosisTransplantation ConditioningTransplantation, HomologousTumor Suppressor Protein p53Tumor Suppressor Protein p53allogeneic hematopoietic cell transplantmantle cell lymphomaTP53

Identifiers

PMID30537212
PMCPMC6399037

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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.