Evidence map›Paper›PMID 36966871›Full record

ArticleTransplantation and cellular therapy2023

Access to Chimeric Antigen Receptor T Cell Clinical Trials in Underrepresented Populations: A Multicenter Cohort Study of Pediatric and Young Adult Acute Lymphobastic Leukemia Patients.

Anurekha G Hall, Lena E Winestone, Erin M Sullivan, Qian Wu, Adam J Lamble, Mark C Walters, Paibel Aguayo-Hiraldo, Lourdes Baez Conde, Tumaini R Coker, Dana Dornsife and 5 more

Open access · greenAbstract readMulticenter Study
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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 29 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

15 authors at 8 institutions in 1 country.

Anurekha G HallDivision of Hematology and Oncology, University of Washington, Seattle Children's Hospital, Seattle, Washington; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington. Electronic address: Anurekha.Hall@seattlechildrens.org.
Lena E WinestoneDivision of Pediatric Allergy, Immunology, and Blood & Marrow Transplantation, UCSF Benioff Children's Hospitals, San Francisco, California.
Erin M SullivanCore for Biostatistics, Epidemiology, and Analytics in Research, Seattle Children's Research Institute, Seattle, Washington.
Qian WuClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Adam J LambleDivision of Hematology and Oncology, University of Washington, Seattle Children's Hospital, Seattle, Washington.
Mark C WaltersDivision of Oncology, UCSF Benioff Children's Hospitals, Oakland, California.
Paibel Aguayo-HiraldoCancer and Blood Disease Institute, Children's Hospital Los Angeles, Los Angeles, California; USC Norris Comprehensive Cancer Center, University of Southern California, Keck School of Medicine, Los Angeles, California.
Lourdes Baez CondeUSC Norris Comprehensive Cancer Center, University of Southern California, Keck School of Medicine, Los Angeles, California.
Tumaini R CokerDepartment of Pediatrics, Seattle Children's Research Institute, University of Washington School of Medicine, Seattle, Washington.
Dana DornsifeLazarex Foundation, Danville, California.
Amy K KeatingPediatric Blood and Marrow Transplantation, University of Colorado School of Medicine, Aurora, Colorado.
Diana M MerinoFriends of Cancer Research, Washington, DC.
Bonnie RamseyDepartment of Pediatrics, Seattle Children's Hospital, University of Washington School of Medicine, Seattle, Washington.
Julie R ParkDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Anurag K AgrawalDivision of Oncology, UCSF Benioff Children's Hospitals, Oakland, California.
Seattle Children's Hospital · USUCSF Benioff Children's Hospital · USUniversity of Southern California · USFred Hutch Cancer Center · USFriends of Cancer Research · USLazarex Cancer Foundation · USSt. Jude Children's Research Hospital · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Prospective evaluation of barriers to patient referral and enrollment in emerging cellular therapy trials: determining methods and structure to improve equity in future trial designU01TR002487 · NCATS · SEATTLE CHILDREN'S HOSPITAL · PI PARK, JULIE R, RAMSEY, BONNIE W · 2018 to 2022
$7.2M
NCATS NIH HHS U01 TR002487NCATS NIH HHS UL1 TR002319
6 · The paper itself

Abstract

Chimeric antigen receptor T cell (CAR-T) therapy is a promising approach to improve survival for children and adults with relapsed/refractory (r/r) B cell acute lymphoblastic leukemia (B-ALL), but these clinical trials might not be equally accessible to patients of low socioeconomic status (SES) or to patients from racial or ethnic minority groups. We sought to describe the sociodemographic characteristics of pediatric and adolescent and young adult (AYA) patients enrolled in CAR-T clinical trials and to compare these characteristics to those of other patients with r/r B-ALL. We conducted a multicenter retrospective cohort study at 5 pediatric consortium sites to compare the sociodemographic characteristics of patients treated and enrolled in CAR-T trials at their home institution, other patients with r/r B-ALL treated at these sites, and patients referred from an external hospital for CAR-T trials. The patients were age 0 to 27 years with r/r B-ALL treated at 1 of the consortium sites between 2012 and 2018. Clinical and demographic data were collected from the electronic health record. We calculated distance from home to treating institution and assigned SES scores based on census tract. Among the 337 patients treated for r/r B-ALL, 112 were referred from an external hospital to a consortium site and enrolled in a CAR-T trial and 225 were treated primarily at a consortium site, with 34% enrolled in a CAR-T trial. Patients treated primarily at a consortium site had similar characteristics regardless of trial enrollment. Lower proportions of Hispanic patients (37% versus 56%; P = .03), patients whose preferred language was Spanish (8% versus 22%; P = .006), and publicly insured patients (38% versus 65%; P = .001) were referred from an external hospital than were treated primarily at a consortium site and enrolled in a CAR-T trial. Patients who are Hispanic, Spanish-speaking, or publicly insured are underrepresented in referrals from external hospitals to CAR-T centers. External provider implicit bias also may influence referral of these patients. Establishing partnerships between CAR-T centers and external hospital sites may improve provider familiarity, patient referral, and patient access to CAR-T clinical trials.

Indexed as

Leukemia, Myeloid, AcutePrecursor Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenAdolescentAdultChildChild, PreschoolClinical Trials as TopicEthnicityHumansInfantInfant, NewbornMinority GroupsRetrospective StudiesT-LymphocytesYoung AdultReceptors, Chimeric AntigenAccess to careB-ALLCAR-T cellsClinical trialsDisparitiesPediatric

Identifiers

PMID36966871
PMCPMC10247402
OpenAlexW4360860829

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.