A phase II study of carboplatin AUC-10 guided by positron emission tomography-defined metabolic response in metastatic seminoma.
Adult
Aged
Antineoplastic Agents
/ administration & dosage
Carboplatin
/ administration & dosage
Clinical Decision-Making
Disease Progression
Humans
London
Male
Middle Aged
Neoplasm Staging
Positron Emission Tomography Computed Tomography
Predictive Value of Tests
Progression-Free Survival
Risk Assessment
Risk Factors
Seminoma
/ diagnostic imaging
Testicular Neoplasms
/ diagnostic imaging
Time Factors
Young Adult
Carboplatin monotherapy
Metastatic seminoma
Journal
European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
received:
13
12
2018
revised:
02
04
2019
accepted:
14
04
2019
pubmed:
29
5
2019
medline:
2
6
2020
entrez:
29
5
2019
Statut:
ppublish
Résumé
Carboplatin monotherapy for metastatic seminoma at a dose of AUC-10 has shown promising activity. Three or four cycles have been given with most haematological side-effects seen with the 4th cycle. An early response might allow de-escalation of therapy. Forty-eight patients with metastatic seminoma (International Germ Cell Cancer Collaborative Group good prognosis) were recruited. Positron emission tomography (PET) scanning was performed before and after one cycle of carboplatin. Those with a Deauville score of 3 or less were given a total of three cycles of carboplatin, the rest received four. PET scanning allowed 44% to receive three cycles of carboplatin. With a median follow-up of 31.2 months, 95.6% (95% confidence interval: 83.5%-98.9%) were progression free. The overall survival at 2-years was 100%. Lower stage (2A and 2B) disease was significantly (P = 0.001) associated with the better metabolic response, but the association was not strong (correlation coefficient = -0.48). Over a third of the blood products given were used to support the 4th cycle. The regimen was well tolerated with a low incidence of grade III neutropenic sepsis or nausea and vomiting (<3% cycles). Carboplatin AUC-10 monotherapy is effective with low toxicity. Early changes during PET scanning may allow de-escalation of therapy in high volume disease-comparison against combination therapy is warranted. CLINICALTRIALS. NCT02272816. 2009-009882-33.
Identifiants
pubmed: 31136925
pii: S0959-8049(19)30267-9
doi: 10.1016/j.ejca.2019.04.013
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Carboplatin
BG3F62OND5
Banques de données
ClinicalTrials.gov
['NCT02272816']
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
128-135Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.