Evidence map›Paper›PMID 29275139›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2018

Pretransplant Consolidation Is Not Beneficial for Adults with ALL Undergoing Myeloablative Allogeneic Transplantation.

Nelli Bejanyan, Mei-Jie Zhang, Hai-Lin Wang, Aleksandr Lazaryan, Marcos de Lima, David I Marks, Brenda M Sandmaier, Veronika Bachanova, Jacob Rowe, Martin Tallman and 17 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 19% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
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

27 authors at 20 institutions in 7 countries.

Nelli BejanyanDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota. Electronic address: nbejanya@umn.edu.
Mei-Jie ZhangDivision of Biostatistics, Insitute for Health and Society, Medical College of Wisconsin, Milwaukee, Wisconsin; CIBMTR (Center for International Blood and Marrrow Trasnsplantation), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Hai-Lin WangCIBMTR (Center for International Blood and Marrrow Trasnsplantation), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Aleksandr LazaryanDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota.
Marcos de LimaDepartment of Medicine, Seidman Cancer Center, University Hospitals Case Medical Center, Cleveland, Ohio.
David I MarksAdult Bone Marrow Transplant, University Hospitals Bristol NHS Trust, Bristol, United Kingdom.
Brenda M SandmaierDivision of Medical Oncology, University of Washington and Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Veronika BachanovaDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota.
Jacob RoweDepartment of Hematology, Shaare Zedek Medical Center, Jerusalem, Israel.
Martin TallmanLeukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Partow KebriaeiDepartment of Stem Cell Transplantation, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Mohamed Kharfan-DabajaDepartment of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Robert Peter GaleHematology Research Centre, Division of Experimental Medicine, Department of Medicine, Imperial College London, London, United Kingdom.
Hillard M LazarusSeidman Cancer Center, University Hospitals Cleveland Medical Center, Cleveland, Ohio.
Celalettin UstunDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota.
Edward CopelanDepartment of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Carolinas HealthCare System, Charlotte, North Carolina.
Betty Ky HamiltonBlood & Marrow Transplant Program, Cleveland Clinic Taussig Cancer Institute, Cleveland, Ohio.
Gary SchillerHematological Malignancy/Stem Cell Transplant Program, David Geffen School of Medicine at UCLA, Los Angeles, California.
William HoganDepartments of Hematology and Transplant Center, Mayo Clinic Rochester, Rochester, Minnesota.
Shahrukh HashmiDepartment of Internal Medicine, Mayo Clinic, Minnesota; Oncology Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Matthew SeftelDepartment of Medical Oncology and Hematology, CancerCare Manitoba, Winnipeg, Canada.
Christopher G KanakryExperimental Transplantation and Immunology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Richard F OlssonDivision of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden; Centre for Clinical Research Sormland, Uppsala University, Uppsala, Sweden.
Rodrigo MartinoDivison of Clinical Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Wael SaberCIBMTR (Center for International Blood and Marrrow Trasnsplantation), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
H Jean KhouryEmory University Hospital, Atlanta, Georgia.
Daniel J WeisdorfDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota.
University of Minnesota · USMedical College of Wisconsin · USCancerCare Manitoba · CACenter for Cancer Research · USCleveland Clinic · USEmory University Hospital · USHospital de Sant Pau · ESImperial College London · GBKarolinska Institutet · SEKing Faisal Specialist Hospital & Research Centre · SALevine Cancer Institute · USMayo Clinic · USMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USShaare Zedek Medical Center · ILThe University of Texas MD Anderson Cancer Center · USUniversity Hospitals Case Medical Center · USUniversity Hospitals Seidman Cancer Center · USUniversity of California, Los Angeles · USUniversity of Washington · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
Deciphering the efficacy of posttransplant cyclophosphamide in haplo transplantZIABC011659 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KANAKRY, CHRISTOPHER · 2015 to 2025
$18.5M
NCI NIH HHS P30 CA008748NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294
6 · The paper itself

Abstract

Allogeneic hematopoietic cell transplantation (alloHCT) is curative for patients with acute lymphoblastic leukemia (ALL) who achieve complete remission (CR1) with chemotherapy. However, the benefit of consolidation chemotherapy remains uncertain in patients undergoing alloHCT. We compared clinical outcomes of 524 adult patients with ALL in CR1 who received ≥2 (n = 109), 1 (n = 93), or 0 cycles (n = 322) of consolidation before myeloablative alloHCT from 2008 to 2012. As expected, time to alloHCT was longer with increasing cycles of consolidation. Patients receiving ≥2, 1, or 0 cycles of consolidation had an adjusted 3-year cumulative incidence of relapse of 20%, 27%, and 22%; 1-year transplant-related mortality (TRM) of 16%, 18%, and 23%; adjusted 3-year leukemia-free survival (LFS) of 54%, 48%, and 47%; and 3-year overall survival (OS) of 63%, 59%, and 54% (all P values >.40). Multivariable analysis confirmed that consolidation was not prognostic for LFS (relative risk, 1.20, 95% confidence interval, .86 to 1.67; P = .28 for no consolidation; RR, 1.18, 95% confidence interval, .79 to 1.76; P = .41 for 1 cycle versus ≥2 cycles = reference). Similarly, consolidation was not associated with OS, relapse, TRM, or graft-versus-host disease. We conclude that consolidation chemotherapy does not appear to provide added benefit in adult ALL patients with available donors who undergo myeloablative alloHCT in CR1.

Indexed as

Consolidation ChemotherapyAdultAgedGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansMiddle AgedMyeloablative AgonistsPrecursor Cell Lymphoblastic Leukemia-LymphomaRecurrenceSurvival AnalysisTime FactorsTransplantation, HomologousTreatment OutcomeYoung AdultMyeloablative AgonistsALLAllogeneic transplantConsolidation chemotherapyMyeloablative conditioning

Identifiers

PMID29275139
PMCPMC5953798
OpenAlexW2776743851

What OpenQuestion holds

Textmetadata
LicenceTDM
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.