Evidence map›Paper›PMID 30576269›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2019

Detection of Relapse by Tumor Markers Versus Imaging in Children and Adolescents With Nongerminomatous Malignant Germ Cell Tumors: A Report From the Children's Oncology Group.

Adriana Fonseca, Caihong Xia, Armando J Lorenzo, Mark Krailo, Thomas A Olson, Farzana Pashankar, Marcio H Malogolowkin, James F Amatruda, Deborah F Billmire, Carlos Rodriguez-Galindo and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 19 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

12 authors at 10 institutions in 2 countries.

Adriana Fonseca1 The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Caihong Xia2 Children's Oncology Group, Monrovia, CA.
Armando J Lorenzo1 The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Mark Krailo2 Children's Oncology Group, Monrovia, CA.
Thomas A Olson4 Emory University, Atlanta, GA.
Farzana Pashankar5 Yale University School of Medicine, New Haven, CT.
Marcio H Malogolowkin6 University of California Davis Comprehensive Cancer Center, Sacramento, CA.
James F Amatruda7 University of Texas Southwestern Medical Center and Children's Medical Center Dallas, Dallas, TX.
Deborah F Billmire8 Riley Hospital for Children, Indianapolis, IN.
Carlos Rodriguez-Galindo9 St Jude Children's Research Hospital, Memphis, TN.
A Lindsay Frazier10 Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
Furqan Shaikh1 The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Children's Oncology Group · USHospital for Sick Children · CADana-Farber Cancer Institute · USEmory University · USRiley Hospital for Children · USSickKids Foundation · CASt. Jude Children's Research Hospital · USThe University of Texas Southwestern Medical Center · USUniversity of California, Davis · USYale University · 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

purposeTo investigate relapse detection methods among children and adolescents with nongerminomatous malignant germ cell tumors (MGCTs) and to determine whether tumor markers alone might be sufficient for surveillance.

methodsWe retrospectively reviewed all patients enrolled in a phase III, single-arm trial for low-risk and intermediate-risk MGCTs. The method used to detect relapse was assessed based on case report forms, tumor markers, imaging, and pathology reports. Relapses were classified into one of two categories on the basis of whether they were (1) detectable by tumor marker elevation or (2) not detectable by tumor markers.

resultsA total of 302 patients were enrolled, and 284 patients had complete data for review. Seven patients had normal tumor markers at initial diagnosis, and none experienced a relapse. At a median follow-up of 5.3 years, 48 patients (16.9%) had experienced a relapse. After central review, 47 of 48 relapses (98%) were detected by tumor marker elevation. Of the 47 patients, 16 (33.3%) had abnormal tumor markers with normal/unknown imaging, 31 patients (64.6%) had abnormal tumor markers with abnormal imaging, and one patient (2.1%) had abnormal imaging with unknown marker levels at relapse.

conclusionTumor marker elevation is a highly sensitive method of relapse surveillance, at least among children and adolescents with tumor marker elevation at initial diagnosis. Eliminating exposure to imaging with ionizing radiation may enhance the safety of relapse surveillance in patients treated for MGCT.

Indexed as

AdolescentAdultBiomarkers, TumorChildChild, PreschoolClinical Trials, Phase III as TopicFemaleHumansInfantInfant, NewbornMaleNeoplasm Recurrence, LocalNeoplasms, Germ Cell and EmbryonalOvarian NeoplasmsRetrospective StudiesTesticular NeoplasmsBiomarkers, Tumor

Identifiers

PMID30576269
PMCPMC6553816
OpenAlexW2906531899

What OpenQuestion holds

Textmetadata
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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.