Evidence map›Paper›PMID 40098231›Full record

ArticlePediatric blood & cancer2025

Standard-Dose Versus High-Dose Cisplatin for Intermediate/Poor-Risk Extracranial Malignant Germ Cell Tumors: Re-Analysis of Pediatric Oncology Group 9049 and Children's Cancer Group 8882 Trial Using Updated MaGIC Risk Stratification.

Daniel Prior, Jingye Yang, Michelle M Nuño, Furqan Shaikh, A Lindsay Frazier, Farzana Pashankar

Abstract readComparative Study
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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Daniel PriorDepartment of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.ORCID https://orcid.org/0009-0007-0697-6871
Jingye YangChildren's Oncology Group, Monrovia, California, USA.
Michelle M NuñoChildren's Oncology Group, Monrovia, California, USA.
Furqan ShaikhThe Hospital for Sick Children, Toronto, Ontario, Canada.ORCID https://orcid.org/0000-0001-7069-0359
A Lindsay FrazierDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-4748-8552
Farzana PashankarDepartment of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.ORCID https://orcid.org/0000-0003-2883-0957

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 CA180899NCTN Operations Center U10CA180886NCTN Statistics & Data Center U10CA180899
6 · The paper itself

Abstract

backgroundCisplatin, etoposide, and bleomycin (PEb) have been the standard of care for patients with germ cell tumors (GCT). In the 1990s, an intergroup trial (POG9049/CCG8882) randomized patients with high-risk GCT, as defined by the 1990 criteria, to high-dose (HDPEb) versus standard-dose PEb. HDPEb resulted in improved event-free survival (EFS), but no difference in overall survival (OS), thus standard-dose PEb has remained the standard of care. Subsequently, the Malignant Germ Cell International Consortium (MaGIC) updated the risk stratification for pediatric and adolescent patients with GCT. Currently, patients are categorized as intermediate or poor risk if they are ≥11 years of age with Stage IV ovarian GCT, or testicular, mediastinal, or retroperitoneal GCT with intermediate or poor prognosis using the International Germ Cell Consensus Classification criteria.

methodsWe re-analyzed data from the POG9049/CCG8882 trial using the updated MaGIC risk stratification to determine whether HDPEb improved outcomes over PEb in patients with intermediate/poor-risk GCTs.

resultsAmong 299 patients in the trial, 57 patients (48 males, nine females) met the inclusion criteria for this analysis. There were no statistically significant differences in 5-year EFS (0.72 vs. 0.70, p-value = 0.82) or OS (0.76 vs. 0.74, p-value = 0.91) among patients treated with HDPEb versus PEb, respectively. Also, of note patients with mediastinal primaries had significantly worse 5-year EFS (0.51 vs. 0.83, p-value = 0.0062) and OS (0.49 vs. 0.89, p-value = 0.0013) compared to other sites, with no difference in outcome between HDPEb and PEb.

conclusionsTreatment with HDPEb did not improve outcomes for intermediate/poor-risk GCT patients compared to standard-dose PEb.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCisplatinMediastinal NeoplasmsNeoplasms, Germ Cell and EmbryonalOvarian NeoplasmsRetroperitoneal NeoplasmsTesticular NeoplasmsAdolescentBleomycinChildChild, PreschoolClinical Trials, Phase II as TopicEtoposideFemaleFollow-Up StudiesHumansBleomycinCisplatinEtoposidegerm cell tumorhigh‐dose cisplatinMalignant Germ Cell International Consortiumrisk stratification

Identifiers

PMID40098231
PMCPMC12018124

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Registered trials

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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.