Effect of Doxorubicin Plus Olaratumab vs Doxorubicin Plus Placebo on Survival in Patients With Advanced Soft Tissue Sarcomas: The ANNOUNCE Randomized Clinical Trial.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
07 04 2020
Historique:
entrez: 8 4 2020
pubmed: 8 4 2020
medline: 15 4 2020
Statut: ppublish

Résumé

Patients with advanced soft tissue sarcoma (STS) have a median overall survival of less than 2 years. In a phase 2 study, an overall survival benefit in this population was observed with the addition of olaratumab to doxorubicin over doxorubicin alone. To determine the efficacy of doxorubicin plus olaratumab in patients with advanced/metastatic STS. ANNOUNCE was a confirmatory, phase 3, double-blind, randomized trial conducted at 110 sites in 25 countries from September 2015 to December 2018; the final date of follow-up was December 5, 2018. Eligible patients were anthracycline-naive adults with unresectable locally advanced or metastatic STS, an Eastern Cooperative Oncology Group performance status of 0 to 1, and cardiac ejection fraction of 50% or greater. Patients were randomized 1:1 to receive doxorubicin, 75 mg/m2 (day 1), combined with olaratumab (n = 258), 20 mg/kg in cycle 1 and 15 mg/kg in subsequent cycles, or placebo (n = 251) on days 1 and 8 for up to 8 21-day cycles, followed by olaratumab/placebo monotherapy. Dual primary end points were overall survival with doxorubicin plus olaratumab vs doxorubicin plus placebo in total STS and leiomyosarcoma (LMS) populations. Among the 509 patients randomized (mean age, 56.9 years; 58.2% women; 46.0% with LMS), all were included in the primary analysis and had a median length of follow-up of 31 months. No statistically significant difference in overall survival was observed between the doxorubicin plus olaratumab group vs the doxorubicin plus placebo group in either population (total STS: hazard ratio, 1.05 [95% CI, 0.84-1.30], P = .69, median overall survival, 20.4 months vs 19.7 months; LMS: hazard ratio, 0.95 [95% CI, 0.69-1.31], P = .76, median overall survival, 21.6 months vs 21.9 months). Adverse events of grade 3 or greater reported in 15% or more of total patients with STS were neutropenia (46.3% vs 49.0%), leukopenia (23.3% vs 23.7%), and febrile neutropenia (17.5% vs 16.5%). In this phase 3 clinical trial of patients with advanced STS, treatment with doxorubicin plus olaratumab vs doxorubicin plus placebo resulted in no significant difference in overall survival. The findings did not confirm the overall survival benefit observed in the phase 2 trial. ClinicalTrials.gov Identifier: NCT02451943.

Identifiants

pubmed: 32259228
pii: 2764181
doi: 10.1001/jama.2020.1707
pmc: PMC7139275
doi:

Substances chimiques

Antibiotics, Antineoplastic 0
Antibodies, Monoclonal 0
Placebos 0
Doxorubicin 80168379AG
olaratumab TT6HN20MVF

Banques de données

ClinicalTrials.gov
['NCT02451943']

Types de publication

Clinical Trial, Phase III Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1266-1276

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

William D Tap (WD)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Department of Medicine, Weill Cornell Medical College, New York, New York.

Andrew J Wagner (AJ)

Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.

Patrick Schöffski (P)

University Hospitals Leuven, Department of General Medical Oncology, Leuven Cancer Institute, Leuven, Belgium.

Javier Martin-Broto (J)

Medical Oncology Department in University Hospital Virgen del Rocio and Institute of Biomedicine of Sevilla (IBIS) (HUVR, CSIC, University of Sevilla), Sevilla, Spain.

Anders Krarup-Hansen (A)

University of Copenhagen, Copenhagen, Denmark.

Kristen N Ganjoo (KN)

Stanford University, Stanford, California.

Chueh-Chuan Yen (CC)

Division of Medical Oncology, Center for Immuno-oncology, Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
National Yang-Ming University School of Medicine, Taipei, Taiwan.

Albiruni R Abdul Razak (AR)

Princess Margaret Cancer Center, Toronto, Ontario, Canada.

Alexander Spira (A)

Virginia Cancer Specialists, Fairfax.

Akira Kawai (A)

National Cancer Center Hospital, Tokyo, Japan.

Axel Le Cesne (A)

Institut Gustave Roussy, Villejuif, France.

Brian A Van Tine (BA)

Department of Internal Medicine, Washington University in St Louis School of Medicine, St Louis, Missouri.

Yoichi Naito (Y)

National Cancer Center Hospital East, Kashiwa, Japan.

Se Hoon Park (SH)

Sungkyunkwan University Samsung Medical Center, Seoul, Republic of Korea.

Alexander Fedenko (A)

Blokhin Cancer Research Center, Moscow, Russian Federation.

Zsuzsanna Pápai (Z)

Magyar Honvedseg Eu Kp, Budapest, Hungary.

Victoria Soldatenkova (V)

Eli Lilly and Company, Indianapolis, Indiana.

Ashwin Shahir (A)

Eli Lilly and Company, Windlesham, United Kingdom.

Gary Mo (G)

Eli Lilly and Company, Indianapolis, Indiana.

Jennifer Wright (J)

Eli Lilly and Company, Indianapolis, Indiana.

Robin L Jones (RL)

Sarcoma Unit, Royal Marsden NHS Foundation Trust and Institute of Cancer Research, London, United Kingdom.

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