STELLAR: Phase III, Randomized, Open-Label Study of Eflornithine Plus Lomustine Versus Lomustine Alone in Patients With Recurrent Grade 3 Astrocytoma

H Howard Colman G Giuseppe Lombardi (Medical Oncology 1, Veneto Institute of Oncology IOV - IRCCS, Padova, Italy) E Eric T. Wong (The Warren Alpert Medical School of Brown University, Brown University Health Cancer Institute, Rhode Island Hospital, Providence, RI) T Tobias Walbert (Henry Ford Health, Michigan State and Wayne State University, Detroit, MI) M Marica Eoli A 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) D David M. Peereboom (Cleveland Clinic, Cleveland, OH) S Sani H. Kizilbash C Carlos Kamiya-Matsuoka M Marshall W. Pitz (CancerCare, University of Manitoba, Manitoba, MB, Canada) R Roy E. Strowd (Atrium Health Wake Forest Baptist, Winston-Salem, NC) A Annick Desjardins P Priya Kumthekar W Warren Mason (Princess Margaret Cancer Centre, Cancer Clinical Research Unit, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada) A Alessia Pellerino (Division of Neuro-Oncology, Department of Neuroscience “Rita Levi Montalcini”, University and City of Health and Science Hospital, Torino, Italy) R Riccardo Soffietti N Nicholas Butowski (Brain Tumor Center, University of California San Francisco, San Francisco, CA) P Peter A. Forsyth (Department of Neuro-Oncology, H. Lee Moffitt Cancer Center, Tampa, FL) M Mohamed A. Hamza (OhioHealth Physician Group, Neuro-Oncology, Columbus, OH) P Peter Hau E Enrico Lallana (Kaiser Permanente, Sacramento Medical Center, Sacramento, CA) B Burt Nabors (University of Alabama at Birmingham, Birmingham, AL) D David Piccioni (University of California San Diego Health, San Diego, CA) E Erik J. Uhlmann (Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA) L Liam C. Welsh (Neuro-Oncology Unit, Royal Marsden Hospital, Sutton, Surrey, United Kingdom) P Patrick Y. Wen J Jorg Dietrich (3Division of Neuro-Oncology, Department of Neurology, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA) C Chao Wang V Victor A. Levin (Emeritus Professor, Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX)

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

Volume / Issue Vol. 44, Issue 8
Published March 10, 2026
Pages 641-652
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (29)

H

Howard Colman

G

Giuseppe Lombardi

Medical Oncology 1, Veneto Institute of Oncology IOV - IRCCS, Padova, Italy

E

Eric T. Wong

The Warren Alpert Medical School of Brown University, Brown University Health Cancer Institute, Rhode Island Hospital, Providence, RI

T

Tobias Walbert

Henry Ford Health, Michigan State and Wayne State University, Detroit, MI

M

Marica Eoli

A

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

D

David M. Peereboom

Cleveland Clinic, Cleveland, OH

S

Sani H. Kizilbash

C

Carlos Kamiya-Matsuoka

M

Marshall W. Pitz

CancerCare, University of Manitoba, Manitoba, MB, Canada

R

Roy E. Strowd

Atrium Health Wake Forest Baptist, Winston-Salem, NC

A

Annick Desjardins

P

Priya Kumthekar

W

Warren Mason

Princess Margaret Cancer Centre, Cancer Clinical Research Unit, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada

A

Alessia Pellerino

Division of Neuro-Oncology, Department of Neuroscience “Rita Levi Montalcini”, University and City of Health and Science Hospital, Torino, Italy

R

Riccardo Soffietti

N

Nicholas Butowski

Brain Tumor Center, University of California San Francisco, San Francisco, CA

P

Peter A. Forsyth

Department of Neuro-Oncology, H. Lee Moffitt Cancer Center, Tampa, FL

M

Mohamed A. Hamza

OhioHealth Physician Group, Neuro-Oncology, Columbus, OH

P

Peter Hau

E

Enrico Lallana

Kaiser Permanente, Sacramento Medical Center, Sacramento, CA

B

Burt Nabors

University of Alabama at Birmingham, Birmingham, AL

D

David Piccioni

University of California San Diego Health, San Diego, CA

E

Erik J. Uhlmann

Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA

L

Liam C. Welsh

Neuro-Oncology Unit, Royal Marsden Hospital, Sutton, Surrey, United Kingdom

P

Patrick Y. Wen

J

Jorg Dietrich

3Division of Neuro-Oncology, Department of Neurology, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA

C

Chao Wang

V

Victor A. Levin

Emeritus Professor, Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX