Evidence map›Paper›PMID 35201611›Full record

ArticleCancer2022

Sex-based disparities in outcome in pediatric acute lymphoblastic leukemia: a Children's Oncology Group report.

Sumit Gupta, David T Teachey, Zhiguo Chen, Karen R Rabin, Kimberly P Dunsmore, Eric C Larsen, Kelly W Maloney, Leonard A Mattano, Stuart S Winter, Andrew J Carroll and 9 more

Open access · greenAbstract read
In one paragraph

Article in Cancer, 2022. 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
5.2field-weighted citation impact, top 4% 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, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 16 institutions in 2 countries.

Sumit GuptaDivision of Haematology/Oncology, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0003-1334-3670
David T TeacheyDepartment of Pediatrics and Center for Childhood Cancer Research, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Philadelphia, Philadelphia, Pennsylvania.
Zhiguo ChenDepartment of Biostatistics, Colleges of Medicine, Public Health, and Health Professions, University of Florida, Gainesville, Florida.
Karen R RabinDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas.ORCID 0000-0002-4081-8195
Kimberly P DunsmoreDepartment of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia.
Eric C LarsenDepartment of Pediatrics, Maine Children's Cancer Program, Scarborough, Maine.
Kelly W MaloneyDepartment of Pediatrics, University of Colorado and Children's Hospital Colorado, Aurora, Colorado.
Leonard A MattanoHARP Pharma Consulting, Mystic, Connecticutt.
Stuart S WinterChildren's Hospitals and Clinics of Minnesota, Minneapolis, Minnesota.
Andrew J CarrollDepartment of Genetics, University of Alabama at Birmingham, Birmingham, Alabama.
Nyla A HeeremaDepartment of Pathology, The Ohio State University Wexner School of Medicine, Columbus, Ohio.
Michael J BorowitzDivision of Hematologic Pathology, Johns Hopkins University, Baltimore, Maryland.
Brent L WoodDepartment of Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California.
William L CarrollDepartment of Pediatrics, NYU Langone Health, New York, New York.
Elizabeth A RaetzDepartment of Pediatrics, NYU Langone Health, New York, New York.
Naomi J WinickDepartment of Pediatrics, Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas.
Mignon L LohDivision of Pediatric Hematology, Oncology, Bone Marrow Transplant and Cellular Therapy, Seattle Children's Hospital, Seattle, Washington.
Stephen P HungerDepartment of Pediatrics and Center for Childhood Cancer Research, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Philadelphia, Philadelphia, Pennsylvania.
Meenakshi DevidasDepartment of Global Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, Tennessee.
Children's Hospital of Philadelphia · USNYU Langone Health · USBaylor College of Medicine · USBridge Pharma (United States) · USChildren's Hospital of Los Angeles · USChildren's Minnesota · USHospital for Sick Children · CAJohns Hopkins University · USSeattle Children's Hospital · USSouthwestern Medical Center · USSt. Jude Children's Research Hospital · USThe Ohio State University Wexner Medical Center · USUniversity of Alabama at Birmingham · USUniversity of Colorado Boulder · USUniversity of Florida Health · USUniversity of Virginia · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DEVIDAS, MEENAKSHI · 2003 to 2013
$67.5M
NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

backgroundBoys with acute lymphoblastic leukemia (ALL) have historically experienced inferior survival compared to girls. This study determined whether sex-based disparities persist with contemporary therapy and whether patterns of treatment failure vary by sex.

methodsPatients 1 to 30.99 years old were enrolled on frontline Children's Oncology Group trials between 2004 and 2014. Boys received an additional year of maintenance therapy. Sex-based differences in the distribution of various prognosticators, event-free survival (EFS) and overall survival (OS), and subcategories of relapse by site were explored.

resultsA total of 8202 (54.4% male) B-cell ALL (B-ALL) and 1562 (74.3% male) T-cell ALL (T-ALL) patients were included. There was no sex-based difference in central nervous system (CNS) status. Boys experienced inferior 5-year EFS and OS (EFS, 84.6% ± 0.5% vs 86.0% ± 0.6%, P = .009; OS, 91.3% ± 0.4% vs 92.5% ± 0.4%, P = .02). This was attributable to boys with B-ALL, who experienced inferior EFS (hazard ratio [HR], 1.2; 95% confidence interval [95% CI], 1.1-1.3; P = .004) and OS (HR, 1.2; 95% CI, 1.0-1.4; P = .046) after adjustment for prognosticators. Inferior B-ALL outcomes in boys were attributable to more relapses (5-year cumulative incidence 11.2% ± 0.5% vs 9.6% ± 0.5%; P = .001), particularly involving the CNS (4.2% ± 0.3% vs 2.5% ± 0.3%; P < .0001). There was no difference in isolated bone marrow relapses (5.4% ± 0.4% vs 6.2% ± 0.4%; P = .49). There were no sex-based differences in EFS or OS in T-ALL.

conclusionsSex-based disparities in ALL persist, attributable to increased CNS relapses in boys with B-ALL. Studies of potential mechanisms are warranted. Improved strategies to identify and modify treatment for patients at highest risk of CNS relapse may have particular benefit for boys.

Indexed as

Precursor Cell Lymphoblastic Leukemia-LymphomaPrecursor T-Cell Lymphoblastic Leukemia-LymphomaAdolescentAdultAntineoplastic Combined Chemotherapy ProtocolsBone MarrowChildChild, PreschoolDisease-Free SurvivalFemaleHumansInfantMaleRecurrenceTreatment OutcomeYoung Adultacute lymphoblastic leukemiachildhooddisparitiessexsurvival

Identifiers

PMID35201611
PMCPMC9007837
OpenAlexW4214705541

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.