Evidence map›Paper›PMID 30908863›Full record

ReviewPediatric blood & cancer2019

Development of acute lymphoblastic leukemia following treatment for acute myeloid leukemia in children with Down syndrome: A case report and retrospective review of Children's Oncology Group acute myeloid leukemia trials.

Brianna R Murphy, Michael Roth, E Anders Kolb, Todd Alonzo, Robert Gerbing, Robert J Wells

Open access · greenAbstract readCase ReportsReview
In one paragraph

Review in Pediatric blood & cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

6 authors at 4 institutions in 1 country.

Brianna R MurphyM. D. Anderson Children's Cancer Hospital, University of Texas, Houston, Texas.ORCID 0000-0002-9396-5842
Michael RothM. D. Anderson Children's Cancer Hospital, University of Texas, Houston, Texas.
E Anders KolbNemours/Alfred I DuPont Hospital for Children, Division of Pediatric Hematology/Oncology, Wilmington, Delaware.
Todd AlonzoKeck School of Medicine, University of Southern California, Los Angeles, California.
Robert GerbingChildren's Oncology Group, Monrovia, California.
Robert J WellsM. D. Anderson Children's Cancer Hospital, University of Texas, Houston, Texas.
The University of Texas MD Anderson Cancer Center · USChildren's Oncology Group · USDuPont (United States) · USUniversity of Southern California · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

Children with Down syndrome have a 150-fold increased risk of developing acute myeloid leukemia (AML) and 20-fold increased risk of developing acute lymphoblastic leukemia (ALL). Although the risk of developing AML and ALL is significantly increased in children with Down syndrome, the development of both malignancies in the same patient is very rare. We describe a patient with Down syndrome who developed ALL 6 years after being diagnosed with AML. We performed a literature review and Children's Oncology Group query and discovered eight published cases and five cases of ALL following AML in pediatric patients with Down syndrome, as well as six cases of ALL following AML in non-Down syndrome patients. There was a similar cumulative incidence of ALL after treatment for AML in the Down syndrome and non-Down syndrome populations. Overall survival in patients with Down syndrome who developed ALL after treatment for AML was comparable to overall survival for patients with Down syndrome with de novo ALL with an average follow-up of 7 years after ALL diagnosis. Clinical data collected were used to discuss whether this phenomenon represents a secondary leukemia, second primary cancer, or mixed-lineage leukemia.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBone Marrow TransplantationChildClinical Trials as TopicCombined Modality TherapyDown SyndromeFemaleHumansLeukemia, Myeloid, AcuteNeoplasms, Second PrimaryPrecursor Cell Lymphoblastic Leukemia-LymphomaPrognosisRetrospective Studiesacute lymphoblastic leukemiaacute myeloid leukemiaDown syndrome

Identifiers

PMID30908863
PMCPMC6941434
OpenAlexW2960198286

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.