Evidence map›Paper›PMID 37086851›Full record

ArticleTransplantation and cellular therapy2023

Transplantation Referral Patterns for Patients with Newly Diagnosed Higher-Risk Myelodysplastic Syndromes and Acute Myeloid Leukemia at Academic and Community Sites in the Connect® Myeloid Disease Registry: Potential Barriers to Care.

Benjamin Tomlinson, Marcos de Lima, Christopher R Cogle, Michael A Thompson, David L Grinblatt, Daniel A Pollyea, Rami S Komrokji, Gail J Roboz, Michael R Savona, Mikkael A Sekeres and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Transplantation and cellular therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

25 authors at 19 institutions in 1 country.

Benjamin TomlinsonSeidman Cancer Center, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, Ohio. Electronic address: Benjamin.Tomlinson@UHhospitals.org.
Marcos de LimaDepartment of Hematology, Ohio State University, Columbus, Ohio.
Christopher R CogleDivision of Hematology and Oncology, Department of Medicine, University of Florida, Gainesville, Florida.
Michael A ThompsonAurora Research Institute, Advocate Aurora Health, Milwaukee, Wisconsin.
David L GrinblattNorthShore Medical Group, NorthShore University Health System, Evanston, Illinois.
Daniel A PollyeaUniversity of Colorado Cancer Center, Aurora, Colorado.
Rami S KomrokjiDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center, Tampa, Florida.
Gail J RobozWeill Cornell College of Medicine and New York-Presbyterian Hospital, New York, New York.
Michael R SavonaVanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee.
Mikkael A SekeresSylvester Comprehensive Cancer Center, University of Miami, Miami, Florida.
Mehrdad AbediUniversity of California Davis, Comprehensive Cancer Center, Sacramento, California.
Guillermo Garcia-ManeroDepartment of Leukemia, University of Texas MD Anderson Cancer Center, Houston, Texas.
Sandra E KurtinUniversity of Arizona Cancer Center, Tucson, Arizona.
Jaroslaw P MaciejewskiSylvester Comprehensive Cancer Center, University of Miami, Miami, Florida.
Jay L PatelDepartment of Pathology, University of Utah and ARUP Laboratories, Salt Lake City, Utah.
Dennis A RevickiOutcomes Research Consulting, Sarasota, Florida.
Tracy I GeorgeDepartment of Pathology, University of Utah and ARUP Laboratories, Salt Lake City, Utah.
E Dawn FlickBristol Myers Squibb, Princeton, New Jersey.
Pavel KiselevBristol Myers Squibb, Princeton, New Jersey.
Chrystal U LouisBristol Myers Squibb, Princeton, New Jersey.
Irene S DeGutisBristol Myers Squibb, Princeton, New Jersey.
Melissa NifeneckerBristol Myers Squibb, Princeton, New Jersey.
Harry P ErbaDuke Cancer Institute, North Carolina.
David P SteensmaDana-Farber Cancer Institute, Boston, Massachusetts.
Bart L ScottFred Hutchinson Cancer Research Center, Seattle, Washington.
Bristol-Myers Squibb (United States) · USUniversity of Miami · USUniversity of Utah · USAurora Health Care · USDana-Farber Cancer Institute · USDuke Medical Center · USFred Hutch Cancer Center · USHealth Outcomes Solutions (United States) · USMoffitt Cancer Center · USNewYork–Presbyterian Hospital · USNorthShore University HealthSystem · USThe Ohio State University · USThe University of Texas MD Anderson Cancer Center · USUC Davis Comprehensive Cancer CenterUniversity Hospitals of Cleveland · USUniversity of Arizona · USUniversity of Colorado Cancer Center · USUniversity of Florida · USVanderbilt University · US

Funding

Therapeutic Implications of Molecular Defects in Bone Marrow FailureR35HL135795 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI MACIEJEWSKI, JAROSLAW P. · 2017 to 2023
$5.7M
NHLBI NIH HHS R35 HL135795
6 · The paper itself

Abstract

Hematopoietic stem cell transplantation (HCT) is indicated for patients with higher-risk (HR) myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML). Age, performance status, patient frailty, comorbidities, and nonclinical factors (eg, cost, distance to site) are all recognized as important clinical factors that can influence HCT referral patterns and patient outcomes; however, the proportion of eligible patients referred for HCT in routine clinical practice is largely unknown. This study aimed to assess patterns of consideration for HCT among patients with HR-MDS and AML enrolled in the Connect® Myeloid Disease Registry at community/government (CO/GOV)- or academic (AC)-based sites, as well as to identify factors associated with rates of transplantation referral. We assessed patterns of consideration for and completion of HCT in patients with HR-MDS and AML enrolled between December 12, 2013, and March 6, 2020, in the Connect Myeloid Disease Registry at 164 CO/GOV and AC sites. Registry sites recorded whether patients were considered for transplantation at baseline and at each follow-up visit. The following answers were possible: "considered potentially eligible," "not considered potentially eligible," or "not assessed." Sites also recorded whether patients subsequently underwent HCT at each follow-up visit. Rates of consideration for HCT between CO/GOV and AC sites were compared using multivariable logistic regression analysis with covariates for age and comorbidity. Among the 778 patients with HR-MDS or AML enrolled in the Connect Myeloid Disease Registry, patients at CO/GOV sites were less likely to be considered potentially eligible for HCT than patients at AC sites (27.9% versus 43.9%; P < .0001). Multivariable logistic regression analysis with factors for age (<65 versus ≥65 years) and ACE-27 comorbidity grade (<2 versus ≥2) showed that patients at CO/GOV sites were significantly less likely than those at AC sites to be considered potentially eligible for HCT (odds ratio, 1.6, 95% confidence interval, 1.1 to 2.4; P = .0155). Among patients considered eligible for HCT, 45.1% (65 of 144) of those at CO/GOV sites and 35.7% (41 of 115) of those at AC sites underwent transplantation (P = .12). Approximately one-half of all patients at CO/GOV (50.1%) and AC (45.4%) sites were not considered potentially eligible for HCT; the most common reasons were age at CO/GOV sites (71.5%) and comorbidities at AC sites (52.1%). Across all sites, 17.4% of patients were reported as not assessed (and thus not considered) for HCT by their treating physician (20.7% at CO/GOV sites and 10.7% at AC sites; P = .0005). These findings suggest that many patients with HR-MDS and AML who may be candidates for HCT are not receiving assessment or consideration for transplantation in clinical practice. In addition, treatment at CO/GOV sites and age remain significant barriers to ensuring that all potentially eligible patients are assessed for HCT.

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteMyelodysplastic SyndromesAgedHealth Services AccessibilityHumansRegistriesAcute myeloid leukemiaBone marrow transplantationClinical practiceHematologic malignanciesManagement and treatmentMyelodysplastic syndromes

Identifiers

PMID37086851
PMCPMC11104018
OpenAlexW4366607243

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.