Evidence map›Paper›PMID 24680975›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2014

Feasibility of treating post-transplantation minimal residual disease in children with acute leukemia.

Nirali N Shah, Michael J Borowitz, Nancy C Robey, Christopher J Gamper, Heather J Symons, David M Loeb, Alan S Wayne, Allen R Chen

Abstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
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  5. 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

8 authors.

Nirali N ShahPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; Pediatric Oncology, Johns Hopkins University, Baltimore, Maryland. Electronic address: Nirali.Shah@nih.gov.
Michael J BorowitzDepartment of Pathology, Johns Hopkins University, Baltimore, Maryland.
Nancy C RobeyPediatric Oncology, Johns Hopkins University, Baltimore, Maryland.
Christopher J GamperPediatric Oncology, Johns Hopkins University, Baltimore, Maryland.
Heather J SymonsPediatric Oncology, Johns Hopkins University, Baltimore, Maryland.
David M LoebPediatric Oncology, Johns Hopkins University, Baltimore, Maryland.
Alan S WaynePediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; Children's Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Allen R ChenPediatric Oncology, Johns Hopkins University, Baltimore, Maryland.

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
BONE MARROW TRANSPLANTATION FOR CHILDHOOD DISEASESK23CA083779 · NCI · JOHNS HOPKINS UNIVERSITY · PI CHEN, ALLEN R · 2000 to 2004
$654k
Intramural NIH HHS Z99 CA999999NCI NIH HHS K23 CA083779NCI NIH HHS P30 CA006973
6 · The paper itself

Abstract

Outcomes are poor for patients with hematologic malignancies who experience overt relapse after allogeneic hematopoietic stem cell transplantation (HCT). Data on outcomes of post-transplantation minimal residual disease (MRD) are limited. In this single-institution, retrospective cohort analysis of children with acute leukemia and myelodysplastic syndrome, we document the pattern of relapse with a primary focus on outcomes of post-transplantation MRD. Forty of 93 patients (43%) who underwent a first allogeneic HCT and had systematic pretransplantation and post-transplantation MRD evaluations at +30, +60, +90, +180 days and +1 and +2 years post-transplantation experienced relapse. The median time to relapse was 4.8 months post-transplantation, with a median survival of 4 months post-relapse. Despite frequent, systematic, routine post-HCT disease restaging evaluation, 31 patients (78%) presented with overt disease at the time of relapse. Seven patients with acute leukemia who had post-transplantation MRD presented at a median of 1 month post-transplantation. Owing to rapid disease progression or treatment-related mortality, there was no improvement in survival in those patients whose leukemia was detected in a state of MRD post-transplantation. Our results suggest that early intervention strategies targeting post-transplantation MRD for relapse prevention in acute leukemia may not be feasible.

Indexed as

Acute DiseaseAdolescentAdultChildChild, PreschoolCohort StudiesFeasibility StudiesFemaleHematopoietic Stem Cell TransplantationHumansInfantInfant, NewbornLeukemiaMaleNeoplasm, ResidualRetrospective StudiesAllogeneic hematopoietic cell transplantationLeukemiaMinimal residual diseasePediatricsRelapse

Identifiers

PMID24680975
PMCPMC4077899

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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.