Evidence map›Paper›PMID 29263438›Full record

ArticleLeukemia2018

Early relapse after autologous hematopoietic cell transplantation remains a poor prognostic factor in multiple myeloma but outcomes have improved over time.

S K Kumar, A Dispenzieri, R Fraser, F Mingwei, G Akpek, R Cornell, M Kharfan-Dabaja, C Freytes, S Hashmi, G Hildebrandt and 17 more

Abstract read
In one paragraph

Article in Leukemia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

52 citing papers in PubMed.

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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

27 authors.

S K KumarMayo Clinic Rochester, Rochester, MN, USA.
A DispenzieriMayo Clinic Rochester, Rochester, MN, USA.
R FraserCIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
F MingweiCIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
G AkpekDepartment of Internal Medicine, Rush University, Chicago, IL, USA.
R CornellDivision of Hematology/Oncology Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
M Kharfan-DabajaDepartment of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
C FreytesSouth Texas Veterans Health Care System and University of Texas Health Science Center San Antonio, San Antonio, TX, USA.
S HashmiMayo Clinic Rochester, Rochester, MN, USA.
G HildebrandtDepartment of Medicine, University of Kentucky, Lexington, KY, USA.
L HolmbergFred Hutchinson Cancer Research Center, Seattle, WA, USA.
R KyleMayo Clinic Rochester, Rochester, MN, USA.
H LazarusSeidman Cancer Center, University Hospitals Case Medical Center, Cleveland, OH, USA.
C LeeRoyal Adelaide Hospital, Adelaide, South Australia, Australia.
J MikhaelMayo Clinic Arizona, Scottsdale, AZ, USA.
T NishihoriDepartment of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.ORCID 0000-0002-2621-7924
J TayUniversity of Ottawa, Ottawa, ON, Canada.
S UsmaniDepartment of Hematology and Medical Oncology, Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC, USA.
D VesoleJohn Theurer Cancer Center at Hackensack UMC, Hackensack, NJ, USA.
R VijDivision of Oncology, Washington University, St Louis, MS, USA.
B WirkDivision of Bone Marrow Transplant, Seattle Cancer Care Alliance, Seattle, WA, USA.
A KrishnanCity of Hope National Medical Center, Duarte, CA, USA.
C GasparettoDuke University Medical Center, Durham, NC, USA.
T MarkDivision of Hematology, University of Colorado-Anschutz Medical College, Aurora, CO, USA.
Y NietoMayo Clinic Arizona, Scottsdale, AZ, USA.
P HariCIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
A D'SouzaCIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.

Funding

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
Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Peter Leif Bergsagel · 2015 to 2026
$25.5M
Institutional Career Development CoreKL2TR001438 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI WIDLANSKY, MICHAEL E · 2015 to 2024
$2.9M
Clinical and Translational Science AwardKL2TR000056 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI SHAKER, REZA NONE · 2012 to 2015
$609k
NCATS NIH HHS KL2 TR000056NCATS NIH HHS KL2 TR001438NCI NIH HHS P50 CA186781NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294
6 · The paper itself

Abstract

Duration of initial disease response remains a strong prognostic factor in multiple myeloma (MM) particularly for upfront autologous hematopoietic cell transplant (AHCT) recipients. We hypothesized that new drug classes and combinations employed prior to AHCT as well as after post-AHCT relapse may have changed the natural history of MM in this population. We analyzed the Center for International Blood and Marrow Transplant Research database to track overall survival (OS) of MM patients receiving single AHCT within 12 months after diagnosis (N=3256) and relapsing early post-AHCT (<24 months), and to identify factors predicting for early vs late relapses (24-48 months post-AHCT). Over three periods (2001-2004, 2005-2008, 2009-2013), patient characteristics were balanced except for lower proportion of Stage III, higher likelihood of one induction therapy with novel triplets and higher rates of planned post-AHCT maintenance over time. The proportion of patients relapsing early was stable over time at 35-38%. Factors reducing risk of early relapse included lower stage, chemosensitivity, transplant after 2008 and post-AHCT maintenance. Shorter post-relapse OS was associated with early relapse, IgA MM, Karnofsky <90, stage III, >1 line of induction and lack of maintenance. Post-AHCT early relapse remains a poor prognostic factor, even though outcomes have improved over time.

Indexed as

AdultAgedAged, 80 and overFemaleHematopoietic Stem Cell TransplantationHumansImmunoglobulin AMaleMiddle AgedMultiple MyelomaNeoplasm Recurrence, LocalPrognosisRecurrenceTransplantation, AutologousYoung AdultImmunoglobulin A

Identifiers

PMID29263438
PMCPMC5871538

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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.