Randomized Study of Two Chemotherapy Regimens for Treatment of Low-Grade Glioma in Young Children: A Report From the Children's Oncology Group

Author:

Ater Joann L.1,Zhou Tianni1,Holmes Emiko1,Mazewski Claire M.1,Booth Timothy N.1,Freyer David R.1,Lazarus Ken H.1,Packer Roger J.1,Prados Michael1,Sposto Richard1,Vezina Gilbert1,Wisoff Jeffrey H.1,Pollack Ian F.1

Affiliation:

1. Joann L. Ater, University of Texas MD Anderson Cancer Center, Houston; Timothy N. Booth, University of Texas Southwestern Medical Center, Dallas, TX; Tianni Zhou and Emiko Holmes, Children's Oncology Group Operations Center, Arcadia; David R. Freyer and Richard Sposto, Children's Hospital Los Angeles, Los Angeles; Michael Prados, University of California, San Francisco, San Francisco, CA; Claire M. Mazewski, Children's Health Care Atlanta, Atlanta, GA; Ken H. Lazarus, Indiana University Medical Center,...

Abstract

Purpose Surgery is curative therapy for pediatric low-grade gliomas (LGGs) in areas of the brain amenable to complete resection. However, LGGs located in areas where complete resection is not possible can threaten both function and life. The purpose of this study was to compare two chemotherapy regimens for LGGs in children younger than age 10 years for whom radiotherapy was felt by the practitioner to pose a high risk of neurodevelopmental injury. Patients and Methods Previously untreated children younger than age 10 years with progressive or residual LGGs were eligible. Children were randomly assigned to receive carboplatin and vincristine (CV) or thioguanine, procarbazine, lomustine, and vincristine (TPCV). Children with neurofibromatosis are reported separately. Results Of 274 randomly assigned patients who met eligibility requirements, 137 received CV and 137 received TPCV. The 5-year event-free survival (EFS) and overall survival (OS) rates for all eligible patients were 45% ± 3.2% and 86% ± 2.2%, respectively. The 5-year EFS rates were 39% ± 4% for CV and 52% ± 5% for TPCV (stratified log-rank test P = .10; cure model analysis P = .007). On multivariate analysis, factors independently predictive of worse EFS and OS were younger age and tumor size greater than 3 cm2. Tumor location in the thalamus was also associated with poor OS. Conclusion The difference in EFS between the regimens did not reach significance on the basis of the stratified log-rank test. The 5-year EFS was higher for TPCV on the basis of the cure model analysis. Differences in toxicity may influence physician choice of regimens.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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