Evidence map›Paper›PMID 31251393›Full record

ArticleCancer2019

Survival disparities for second primary malignancies diagnosed among childhood cancer survivors: A population-based assessment.

Austin L Brown, Vidal M Arroyo, Jennifer E Agrusa, Michael E Scheurer, M Monica Gramatges, Philip J Lupo

Open access · bronzeAbstract read
In one paragraph

Article in Cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Late effects of the treatment of childhood cancer.World journal of clinical cases · 2025
    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

6 authors at 1 institution in 1 country.

Austin L BrownHematology-Oncology Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.ORCID 0000-0001-5802-5073
Vidal M ArroyoHematology-Oncology Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
Jennifer E AgrusaHematology-Oncology Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
Michael E ScheurerHematology-Oncology Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
M Monica GramatgesHematology-Oncology Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
Philip J LupoHematology-Oncology Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.ORCID 0000-0003-0978-5863
Baylor College of Medicine · US

Funding

PEDIATRIC ONCOLOGY CLINICAL RESEARCH TRAINING PROGRAMK12CA090433 · NCI · BAYLOR COLLEGE OF MEDICINE · PI CARL E ALLEN, Donald W. Parsons · 2002 to 2026
$18.5M
Integrative Molecular Epidemiology of Neurocognitive Outcomes in Acute Lymphoblastic LeukemiaK07CA218362 · NCI · BAYLOR COLLEGE OF MEDICINE · PI BROWN, AUSTIN L · 2018 to 2022
$758k
NCI NIH HHS K07 CA218362NCI NIH HHS K07CA218362NCI NIH HHS K12 CA090433
6 · The paper itself

Abstract

backgroundCurative therapy places childhood cancer survivors at increased risk for second primary malignancies (SPMs). However, there have been few population-based attempts to characterize differences between outcomes of SPMs in childhood cancer survivors and outcomes of first primary malignancies (FPMs).

methodsClinical and demographic information about childhood cancer survivors who developed SPMs and individuals with comparable FPMs was extracted from the Surveillance, Epidemiology, and End Results program. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated with Cox proportional hazards models comparing the overall survival (OS) of individuals with and without a history of childhood cancer. OS was evaluated both overall and for specific cancers diagnosed in 50 or more childhood cancer survivors. Models accounted for potential confounders, including sex, race, age, treatment decade, histology, and disease stage.

resultsCompared with individuals with FPMs (n = 1,332,203), childhood cancer survivors (n = 1409) with an SPM experienced poorer OS (HR, 1.86; 95% CI, 1.72-2.02) after the study had accounted for cancer type, age, sex, race, and decade of diagnosis. A history of childhood cancer remained a poor prognostic factor for all specific cancers evaluated, including breast cancer (HR, 2.07; 95% CI, 1.63-2.62), thyroid cancer (HR, 3.59; 95% CI, 2.08-6.19), acute myeloid leukemia (HR, 2.38; 95% CI, 1.87-3.05), brain cancer (HR, 2.09; 95% CI, 1.72-2.55), melanoma (HR, 2.57; 95% CI, 1.55-4.27), bone cancer (HR, 1.88; 95% CI, 1.37-2.57), and soft-tissue sarcoma (HR, 2.44; 95% CI, 1.78-3.33).

conclusionsCompared with individuals without a prior cancer diagnosis, survivors of childhood cancer with an SPM experienced inferior outcomes. Survival disparities were observed for the most frequent SPMs diagnosed in childhood cancer survivors.

Indexed as

Cancer SurvivorsAdolescentAdultChildDisease-Free SurvivalFemaleHumansMaleMiddle AgedNeoplasmsNeoplasms, Second PrimaryProportional Hazards ModelsRisk FactorsSEER ProgramYoung Adultchildhood cancer survivorsecond primary malignancysurvival

Identifiers

PMID31251393
PMCPMC6763352
OpenAlexW2954119687

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.