Evidence map›Paper›PMID 40947516›Full record

ArticlePediatric blood & cancer2025

Outcome of Children With Intermediate-Risk Extracranial Malignant Germ Cell Tumors by Response Status at the End of Induction Chemotherapy: A Report From the Children's Oncology Group.

Adriana Fonseca, Doojduen Villaluna, Mark Krailo, Thomas A Olson, Farzana Pashankar, Marcio H Malogolowkin, James F Amatruda, Deborah F Billmire, Frederick J Rescorla, Jonathan H Ross and 4 more

Abstract read
In one paragraph

Article in Pediatric blood & cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Adriana FonsecaCenter For Cancer and Blood Disorders, Children's National Hospital, Washington, District of Columbia, USA.ORCID 0000-0002-6382-6833
Doojduen VillalunaChildren's Oncology Group, Monrovia, California, USA.
Mark KrailoChildren's Oncology Group, Monrovia, California, USA.
Thomas A OlsonChildren's Healthcare of Atlanta, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-6691-5380
Farzana PashankarYale University School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0003-2883-0957
Marcio H MalogolowkinUniversity of California Davis Comprehensive Cancer Center, Sacramento, California, USA.
James F AmatrudaUniversity of Southern California Keck School of Medicine, Los Angeles, California, USA.ORCID 0000-0002-9901-2137
Deborah F BillmireRiley Hospital for Children, Indianapolis, Indiana, USA.
Frederick J RescorlaRiley Hospital for Children, Indianapolis, Indiana, USA.
Jonathan H RossRush University, Chicago, Illinois, USA.
Bryan J DickenStollery Children's Hospital, Edmonton, Alberta, Canada.ORCID 0000-0001-5058-5973
Carlos Rodriguez-GalindoSt. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID 0000-0002-2360-8946
Lindsay FrazierDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0003-4748-8552
Furqan ShaikhDivision of Hematology Oncology, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0001-7069-0359

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 CA180899NIH HHS U10CA180886NIH HHS U10CA180899St. Baldrick's Grant
6 · The paper itself

Abstract

backgroundIn many pediatric malignant germ cell tumor (MGCT) protocols, patients who do not achieve a complete response (CR; normal tumor markers, no radiological/histological residual) after three cisplatin-etoposide-bleomycin (PEb) cycles receive two to three "consolidation" cycles of the same regimen. Evidence for this practice is limited, and historical outcomes for non‑CR patients remain poor.

methodsWe retrospectively reviewed patients diagnosed with intermediate-risk MGCT, enrolled in AGCT0132, between 2003 and 2011. All patients received three cycles of PEb and underwent response assessment at the end of induction. Patients not in CR were prescribed three additional cycles of PEb as consolidation. We compared event-free survival (EFS) and overall survival (OS) for patients who did and did not receive consolidation.

resultsAmong 210 patients enrolled, two patients were excluded from analyses: one without complete information, and one had rapid progressive disease (PD) and did not complete induction therapy. Out of 208 patients, 193 had a CR after three cycles of induction chemotherapy, and their post-induction 4-year EFS and OS were 93% and 99%. Fifteen patients were not in CR at the end of the first three cycles. Twelve received consolidated chemotherapy as mandated per protocol, and their 4-year EFS and OS were 61% and 65%, respectively. Three patients were deemed to have progressive disease at the end of induction and received second-line therapy.

conclusionChildren with MGCTs who did not achieve CR after the first three cycles of chemotherapy had an inferior outcome compared to those with a CR, despite receiving additional cycles of PEb chemotherapy. We conclude that consolidation is of unclear benefit. We suggest that pediatric MGCT patients who fail to achieve a CR after standard induction chemotherapy may receive a salvage regimen with different agents rather than consolidation with more of the same chemotherapy.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsInduction ChemotherapyNeoplasms, Germ Cell and EmbryonalAdolescentBleomycinChildChild, PreschoolCisplatinEtoposideFemaleFollow-Up StudiesHumansInfantMalePrognosisRetrospective StudiesBleomycinCisplatinEtoposideconsolidationgerm cell tumorsoutcomesrelapse

Identifiers

PMID40947516
PMCPMC13086527

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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.