STELLAR: Phase III, Randomized, Open-Label Study of Eflornithine Plus Lomustine Versus Lomustine Alone in Patients With Recurrent Grade 3 Astrocytoma
Abstract
PURPOSE STELLAR (ClinicalTrials.gov identifier: NCT02796261 ) was a phase III, randomized, open-label trial of eflornithine + lomustine versus lomustine monotherapy in patients with recurrent grade 3 astrocytoma. METHODS At trial initiation, eligibility criteria included: age ≥18 years, anaplastic astrocytoma (2016 WHO CNS Tumor classification [WHO CNS4]), first recurrence ≥6 months after radiation and temozolomide (TMZ), Karnofsky performance status ≥70, and no imaging findings consistent with grade 4 glioblastoma. Random assignment (1:1) was stratified by isocitrate dehydrogenase ( IDH ) mutation, age, resection extent, and geography. Patients received eflornithine (2.8 g/m 2 orally, every 8 hours [2 weeks on, 1 week off]) + lomustine (90 mg/m 2 orally, once every 6 weeks), or lomustine monotherapy (110 mg/m 2 once every 6 weeks). The primary end point was overall survival (OS). RESULTS Among 343 patients randomly assigned across 74 sites in eight countries, there was no difference in survival between eflornithine + lomustine and lomustine monotherapy (median OS 23.4 v 20.3 months, hazard ratio [HR], 0.94). Following changes in classification and grading in the 2021 WHO CNS5, a subset analysis of patients with IDH- mutant, grade 3 astrocytoma (n = 196), defined in 2024, before unblinding, showed clinically meaningful improvements in median OS with eflornithine + lomustine versus lomustine monotherapy (34.9 v 23.5 months, HR, 0.64) and median progression-free survival (PFS, 15.8 v 7.2 months, HR, 0.57). No differences were observed among patients with CNS grade 4 disease. Grade ≥3 treatment-emergent adverse events of relevance were related to reversible myelosuppression (eflornithine + lomustine 42% v lomustine monotherapy 29% of patients) and hearing impairment (24% v 0%). No new safety signals were identified. CONCLUSION Clinically meaningful improvements were observed; eflornithine + lomustine doubled PFS and improved OS in patients with recurrent IDH -mutant, grade 3 astrocytoma, but not grade 4 tumors, after prior radiotherapy and TMZ, consistent with its cytostatic mechanism of action.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (29)
Howard Colman
Giuseppe Lombardi
Medical Oncology 1, Veneto Institute of Oncology IOV - IRCCS, Padova, Italy
Eric T. Wong
The Warren Alpert Medical School of Brown University, Brown University Health Cancer Institute, Rhode Island Hospital, Providence, RI
Tobias Walbert
Henry Ford Health, Michigan State and Wayne State University, Detroit, MI
Marica Eoli
Andrew B. Lassman
Division of Neuro-Oncology, Department of Neurology, Columbia University Vagelos College of Physicians and Surgeons, Herbert Irving Comprehensive Cancer Center, New York-Presbyterian, New York, NY
David M. Peereboom
Cleveland Clinic, Cleveland, OH
Sani H. Kizilbash
Carlos Kamiya-Matsuoka
Marshall W. Pitz
CancerCare, University of Manitoba, Manitoba, MB, Canada
Roy E. Strowd
Atrium Health Wake Forest Baptist, Winston-Salem, NC
Annick Desjardins
Priya Kumthekar
Warren Mason
Princess Margaret Cancer Centre, Cancer Clinical Research Unit, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada
Alessia Pellerino
Division of Neuro-Oncology, Department of Neuroscience “Rita Levi Montalcini”, University and City of Health and Science Hospital, Torino, Italy
Riccardo Soffietti
Nicholas Butowski
Brain Tumor Center, University of California San Francisco, San Francisco, CA
Peter A. Forsyth
Department of Neuro-Oncology, H. Lee Moffitt Cancer Center, Tampa, FL
Mohamed A. Hamza
OhioHealth Physician Group, Neuro-Oncology, Columbus, OH
Peter Hau
Enrico Lallana
Kaiser Permanente, Sacramento Medical Center, Sacramento, CA
Burt Nabors
University of Alabama at Birmingham, Birmingham, AL
David Piccioni
University of California San Diego Health, San Diego, CA
Erik J. Uhlmann
Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA
Liam C. Welsh
Neuro-Oncology Unit, Royal Marsden Hospital, Sutton, Surrey, United Kingdom
Patrick Y. Wen
Jorg Dietrich
3Division of Neuro-Oncology, Department of Neurology, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA
Chao Wang
Victor A. Levin
Emeritus Professor, Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX