TY - JOUR
T1 - Effect of Doxorubicin Plus Olaratumab vs Doxorubicin Plus Placebo on Survival in Patients with Advanced Soft Tissue Sarcomas
T2 - The ANNOUNCE Randomized Clinical Trial
AU - Tap, William D.
AU - Wagner, Andrew J.
AU - Schöffski, Patrick
AU - Martin-Broto, Javier
AU - Krarup-Hansen, Anders
AU - Ganjoo, Kristen N.
AU - Yen, Chueh Chuan
AU - Abdul Razak, Albiruni R.
AU - Spira, Alexander
AU - Kawai, Akira
AU - Le Cesne, Axel
AU - Van Tine, Brian A.
AU - Naito, Yoichi
AU - Park, Se Hoon
AU - Fedenko, Alexander
AU - Pápai, Zsuzsanna
AU - Soldatenkova, Victoria
AU - Shahir, Ashwin
AU - Mo, Gary
AU - Wright, Jennifer
AU - Jones, Robin L.
N1 - Funding Information:
Conflict of Interest Disclosures: Dr Tap reported receiving a standard budget from Eli Lilly and Company for site participation for this trial. Apart from the submitted work, Dr Tap reported receiving personal fees from Eli Lilly and Company, EMD Serono, Novartis, Eisai, Janssen, Immune Design, Adaptimmune, Daiichi Sankyo, Blueprint, Loxo, GlaxoSmithKline, Agios Pharmaceuticals, and NanoCarrier. In addition, Dr Tap reported having a patent pending to MSKCC/SKI for Companion Diagnostic for CDK4 inhibitors 14/854,329; participating on an advisory board for and having stock ownership of both Certis Oncology Solutions and Atropos Therapeutics; and consulting for Daiichi Sankyo’s FDA Oncologic Drugs Advisory Committee meeting on pexidartinib. All research at Memorial Sloan Kettering is supported in part by a grant from the National Institutes of Health, National Cancer Institute (No. P30 CA008748). Dr Wagner reported receiving grants and personal fees from Eli Lilly and Company for participation in this trial. Apart from the submitted work, Dr Wagner reported receiving personal fees and grants from Daiichi Sankyo and Five Prime Therapeutics; personal fees from Novartis, Deciphera, NanoCarrier, and Epizyne; and grants from Karyopharm, Aadi Bioscience, Plexxikon, and Celldex. Dr Schöffski reported grants to Leuven Cancer Institute from Eli Lilly and Company for participation in this trial. Apart from the submitted work, Dr Schöffski reported payments to Leuven Cancer Institute for consulting or advisory role from Eli Lilly and Company, Plexxikon, Eisai, Loxo, Blueprint Medicines, Ellipses Pharma, Deciphera, Merck, Servier, Genmab, Adaptimmune, Intellisphere, and Transgene and research funding to Leuven Cancer Institute from Eli Lilly and Company, Blueprint Medicines, Boehringer Ingelheim, CoBioRes NV, Eisai, Exelixis, G1 Therapeutics, Novartis, PharmaMar, and Plexxikon. Dr Martin-Broto reported receiving personal fees for consulting or an advisory role from Eli Lilly and Company, PharmaMar, Bayer, Roche, and Daichii; for speakers’ bureaus from PharmaMar; and for research from Novartis, PharmaMar, Eisai, Pfizer, and Bristol-Myers Squibb outside of this work. Dr Ganjoo reported receiving personal fees from Eli Lilly and Company for advisory board participation for this trial. Apart from the submitted work, Dr Ganjoo reported receiving personal fees from Daiichi Sankyo for advisory board participation. Dr Yen reported receiving grants and personal fees, in addition to grants to Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, from Eli Lilly and Company for participation in this trial. Apart from the submitted work, Dr Yen reported receiving grants from Eli Lilly and Company, ONO, TLC, Eisai, and EffPha for clinical trial participation; personal fees from Merck, Deciphera, and Athenex; and personal fees for travel, accommodations, and other meeting expenses from Merck, Roche, ONO, and Eisai. Dr Abdul Razak reported receiving personal fees, in addition to grants to Princess Margaret Cancer Center, from Eli Lilly and Company for participation in this trial. Apart from the submitted work, Dr Abdul Razak reported providing expert testimony to Eli Lilly and Company. Dr Spira reported grants and provision of writing assistance, medicines, equipment, or administrative support to Virginia Cancer Specialists from Eli Lilly and Company for participation in this trial. Dr Spira also reported receiving grants from Eli Lilly during the conduct of the study and grants from Bristol-Myers Squibb, CytomX, Novartis, Roche, Trovagene, Arch, Merck, AbbVie, LAM Pharmaceuticals, Arcus, Loxo, and Amgen; grants, personal fees, and nonfinancial support from Takeda; and grants and personal fees from AstraZeneca outside the submitted work. Dr Kawai reported receiving personal fees for travel to meetings and participation in review activities from Eli Lilly and Company for this trial. Dr Kawai also reported receiving personal fees from Novartis and Eisai outside the submitted work. Dr Le Cesne reported receiving personal fees from Eli Lilly and Company for participation in this trial. Apart from the submitted work, Dr Le Cesne reported receiving personal fees for board membership and lectures from PharmaMar and for lectures from Pfizer, Eisai, and Bayer. Dr Van Tine reported receiving personal fees for travel expenses and study support for this trial from Eli Lilly and Company. Apart from the submitted work, Dr Van Tine reported receiving personal fees for consulting from Eli Lilly and Company, Epizyme, CytRx, Janssen, Bayer, Adaptimmune, Immune Design, Daiichi Sankyo, Plexxikon, and Pfizer; grants to Washington University in St Louis School of Medicine from Pfizer, Merck, and Tracon; personal fees for lectures from Eli Lilly and Company, Janssen, Caris, and Adaptimmune; and travel and research expenses from GlaxoSmithKline. Dr Naito reported receiving personal fees for advisory board participation for this trial from Eli Lilly and Company. Apart from the submitted work, Dr Naito reported receiving personal fees for advisory board participation from Daiichi Sankyo; research grants from Roche; personal fees for participation on speakers’ bureaus from Eli Lilly and Company, Pfizer, Chugai, Eisai, Merck Serono, Taiho, AstraZeneca, Nihon Kayaku, Fuji RI, Roche, Novartis, and Bayer; and personal fees from Mieji Seika. Dr Fedenko reported receiving personal fees for advisory board participation for this trial from Eli Lilly and Company. Apart from the submitted work, Dr Fedenko reported receiving personal fees for participation on speakers’ bureaus from Eli Lilly and Company, Eisai, Merck Serono, AstraZeneca, Roche, and Novartis. Ms Soldatenkova and Drs Shahir, Mo, and Wright are employees and stockholders of Eli Lilly and Company. In addition, Dr Mo reported receiving payment for a patent for dosing regimen assigned to ImClone LCC, a wholly owned subsidiary of Eli Lilly and Company. Dr Jones reported receiving personal fees for consulting apart from the submitted work from Eli Lilly and Company, Adaptimmune, Blueprint, Clinigen, Eisai, Epizyme, Daiichi Sankyo, Deciphera, Immunedesign, Merck, and PharmaMar and personal fees from UpToDate, as well as serving as an unpaid consultant for Tracon. No other disclosures were reported.
Publisher Copyright:
© 2020 American Medical Association. All rights reserved.
PY - 2020/4/7
Y1 - 2020/4/7
N2 - Importance: 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. Objective: To determine the efficacy of doxorubicin plus olaratumab in patients with advanced/metastatic STS. Design, Setting, and Participants: 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. Interventions: 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. Main Outcomes and Measures: Dual primary end points were overall survival with doxorubicin plus olaratumab vs doxorubicin plus placebo in total STS and leiomyosarcoma (LMS) populations. Results: 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%). Conclusions and Relevance: 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. Trial Registration: ClinicalTrials.gov Identifier: NCT02451943.
AB - Importance: 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. Objective: To determine the efficacy of doxorubicin plus olaratumab in patients with advanced/metastatic STS. Design, Setting, and Participants: 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. Interventions: 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. Main Outcomes and Measures: Dual primary end points were overall survival with doxorubicin plus olaratumab vs doxorubicin plus placebo in total STS and leiomyosarcoma (LMS) populations. Results: 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%). Conclusions and Relevance: 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. Trial Registration: ClinicalTrials.gov Identifier: NCT02451943.
UR - http://www.scopus.com/inward/record.url?scp=85083022636&partnerID=8YFLogxK
U2 - 10.1001/jama.2020.1707
DO - 10.1001/jama.2020.1707
M3 - Article
C2 - 32259228
AN - SCOPUS:85083022636
SN - 0098-7484
VL - 323
SP - 1266
EP - 1276
JO - Journal of the American Medical Association
JF - Journal of the American Medical Association
IS - 13
ER -