Evidence map›Paper›PMID 33496737›Full record

ArticleBlood advances2021

Genetic ancestry and skeletal toxicities among childhood acute lymphoblastic leukemia patients in the DFCI 05-001 cohort.

Song Yao, Qianqian Zhu, Peter D Cole, Kristen Stevenson, Marian H Harris, Emily Schultz, Justine M Kahn, Elena J Ladas, Uma H Athale, Luis A Clavell and 8 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Interplay between Genetic Ancestry, Self-reported Race and Ethnicity, and Clinical Factors in Pediatric Acute Lymphoblastic Leukemia: A REDIAL Consortium Report.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. The Role ofGenes · 2022
    Article
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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

18 authors at 11 institutions in 3 countries.

Song YaoDepartment of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
Qianqian ZhuDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
Peter D ColeDivision of Pediatric Hematology/Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ.
Kristen StevensonDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
Marian H HarrisDepartment of Pathology, Boston Children's Hospital, Boston, MA.
Emily SchultzDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
Justine M KahnDivision of Pediatric Hematology/Oncology/Stem Cell Transplantation, Columbia University Irving Medical Center, New York, NY.
Elena J LadasDivision of Pediatric Hematology/Oncology/Stem Cell Transplantation, Columbia University Irving Medical Center, New York, NY.
Uma H AthaleDivision of Pediatric Hematology/Oncology, McMaster University, Hamilton, ON, Canada.
Luis A ClavellDivision of Pediatric Oncology, San Jorge Children's Hospital, San Juan, Puerto Rico.
Caroline LaverdiereDivision of Hematology and Oncology, Hospital Sainte-Justine, University of Montreal, Montreal, QC, Canada.
Jean-Marie LeclercDivision of Hematology and Oncology, Hospital Sainte-Justine, University of Montreal, Montreal, QC, Canada.
Bruno MichonDivision of Hematology-Oncology, Centre Hospitalier de l'Université Laval, Quebec City, QC, Canada.
Marshall A SchorinInova Fairfax Hospital for Children, Falls Church, VA.
Jennifer J G WelchDivision of Pediatric Hematology-Oncology, Hasbro Children's Hospital, Warren Alpert Medical School of Brown University, Providence, RI.
Stephen E SallanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.
Lewis B SilvermanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.
Kara M KellyJacob School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY.
Roswell Park Comprehensive Cancer Center · USBoston Children's Hospital · USCentre Hospitalier Universitaire Sainte-Justine · CAColumbia University Irving Medical Center · USBrown University · USCentre hospitalier de l'Université Laval · CAHarvard University · USInova Fairfax Hospital · USMcMaster University · CARutgers, The State University of New Jersey · USSan Juan City Hospital · PR

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
Institutional Career Development CoreKL2TR001874 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GENKINGER, JEANINE M., SHIMBO, DAICHI · 2016 to 2025
$13.6M
Genetic underpinnings of ethnic disparities in bone toxicities between Hispanic and non-Hispanic children treated for acute lymphoblastic leukemiaR03CA223730 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI KELLY, KARA M, YAO, SONG · 2018 to 2019
$174k
NCATS NIH HHS KL2 TR001874NCI NIH HHS P30 CA016056NCI NIH HHS R03 CA223730
6 · The paper itself

Abstract

Hispanic children have a higher incidence of acute lymphoblastic leukemia (ALL) and inferior treatment outcomes relative to non-Hispanic White children. We previously reported that Hispanic children with ALL had lower risk of fracture and osteonecrosis. To unravel the genetic root of such ethnic differences, we genotyped 449 patients from the DFCI 05-001 cohort and analyzed their ancestry. Patients with discordant clinical and genetic ancestral groups were reclassified, and those with unknown ancestry were reassigned on the basis of genetic estimates. Both clinical and genetic ancestries were analyzed in relation to risk of bone toxicities and survival outcomes. Consistent with clinically reported race/ethnicity, genetically defined Hispanic and Black patients had significantly lower risk of fracture (Hispanic: subdistribution hazard ratio [SHR], 0.42; 95% confidence interval [CI], 0.22-0.81; P = .01; Black: SHR, 0.28; 95% CI, 0.10-0.75; P = .01), and osteonecrosis (Hispanic: SHR, 0.12; 95% CI, 0.02-0.93; P = .04; Black: SHR, 0.24; 95% CI, 0.08-0.78; P = .02). The lower risk was driven by African but not Native American or Asian ancestry. In addition, patients with a higher percentage of Native American ancestry had significantly poorer overall survival and event-free survival. Our study revealed that the lower risk of bone toxicities among Black and Hispanic children treated for ALL was attributed, in part, to the percentage of African ancestry in their genetic admixture. The findings provide suggestive evidence for the protective effects of genetic factors associated with African decent against bone damage caused by ALL treatment and clues for future studies to identify underlying biological mechanisms.

Indexed as

Precursor Cell Lymphoblastic Leukemia-LymphomaWhite PeopleBlack or African AmericanChildEthnicityHispanic or LatinoHumans

Identifiers

PMID33496737
PMCPMC7839368
OpenAlexW2988451298

What OpenQuestion holds

Textmetadata
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.