Prognosis of Patients With Early Breast Cancer Receiving 5 Years vs 2 Years of Adjuvant Bisphosphonate Treatment: A Phase 3 Randomized Clinical Trial.


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
01 Aug 2021
Historique:
pubmed: 25 6 2021
medline: 12 3 2022
entrez: 24 6 2021
Statut: ppublish

Résumé

Bisphosphonate treatment in patients with early breast cancer has become part of care, but the optimal treatment duration is still unclear. To compare 2 vs 5 years of zoledronate treatment following adjuvant chemotherapy in patients with early breast cancer. The SUCCESS A phase 3 multicenter randomized open-label clinical trial with a 2 × 2 factorial design enrolled 3754 patients from September 21, 2005, to March 12, 2007 (last patient out, May 7, 2014). Final data analysis was conducted from September 2019 to October 2020. In 250 German study centers, patients were eligible for participation in the SUCCESS A trial if they had either node-positive or high-risk node-negative (defined as at least 1 of the following: tumor size ≥ pT2, histologic grade 3, negative hormone receptor status, or age ≤35 years) primary invasive breast cancer. Patients were first randomized to adjuvant chemotherapy with 3 cycles of fluorouracil, epirubicin, and cyclophosphamide followed by 3 cycles of docetaxel with or without gemcitabine (not presented in this report). After chemotherapy, patients underwent a second randomization of 5 years of zoledronate treatment (4 mg intravenously every 3 months for 2 years, followed by 4 mg intravenously every 6 months for 3 years) vs 2 years of zoledronate treatment (4 mg intravenously every 3 months for 2 years). The primary end point of the study was disease-free survival; secondary end points were overall survival, distant disease-free survival, and the incidence of skeletal-related adverse events. Survival times were measured from 2 years after the start of zoledronate treatment (landmark analysis). Overall, data on 2987 patients were available for analysis; median age was 53 (range, 21-86) years. Disease-free survival, overall survival, and distant disease-free survival did not differ significantly between the 2 treatment arms (5 vs 2 years) as shown by adjusted multivariable Cox proportional hazards regression models (disease-free survival: hazard ratio [HR], 0.97; 95% CI, 0.75-1.25; P = .81; overall survival: HR, 0.98; 95% CI, 0.67-1.42; P = .90; distant disease-free survival: HR, 0.87; 95% CI, 0.65-1.18; P = .38). Adverse events were observed more often in the 5-year (46.2%) vs 2-year (27.2%) zoledronate treatment arm, which was particularly true for the skeletal-related events bone pain (5 years, 8.3% vs 2 years, 3.7%) and arthralgia (5 years, 5.1% vs 2 years, 3.1%). The results of this phase 3 randomized clinical trial indicate that extending the zoledronate treatment beyond 2 years does not improve the prognosis of high-risk patients with early breast cancer receiving chemotherapy, suggesting that the currently recommended bisphosphonate treatment duration of 3 to 5 years could be reduced. ClinicalTrials.gov Identifier: NCT02181101.

Identifiants

pubmed: 34165508
pii: 2781088
doi: 10.1001/jamaoncol.2021.1854
pmc: PMC8227465
doi:

Substances chimiques

Diphosphonates 0

Banques de données

ClinicalTrials.gov
['NCT02181101']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1149-1157

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Auteurs

Thomas W P Friedl (TWP)

Department of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.

Tanja Fehm (T)

Department of Gynecology and Obstetrics, University Hospital Duesseldorf, Heinrich-Heine University, Duesseldorf, Germany.

Volkmar Müller (V)

Department of Gynecology, University Hamburg-Eppendorf, Hamburg, Germany.

Werner Lichtenegger (W)

Charité University Hospital Campus Virchow, Berlin, Germany.

Jens Blohmer (J)

Department of Gynecology and Obstetrics, Charité University Hospital Campus Virchow, Berlin, Germany.

Ralf Lorenz (R)

Gynecologic Practice Dres Lorenz, Hecker, Wesche, Braunschweig, Germany.

Helmut Forstbauer (H)

Hemato-Oncological Practice Dres Forstbauer and Ziske, Troisdorf, Germany.

Visnja Fink (V)

Department of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.

Inga Bekes (I)

Department of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.

Jens Huober (J)

Department of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.

Julia Jückstock (J)

Department of Gynecology and Obstetrics, Ludwig-Maximilians-University Munich, Munich, Germany.

Andreas Schneeweiss (A)

National Center for Tumor Diseases, Heidelberg University Hospital and German Cancer Research Center, Heidelberg, Germany.

Hans Tesch (H)

Department of Oncology, Onkologie Bethanien, Frankfurt, Germany.

Sven Mahner (S)

Department of Gynecology and Obstetrics, Ludwig-Maximilians-University Munich, Munich, Germany.

Sara Y Brucker (SY)

Department of Gynecology and Obstetrics, University Hospital Tübingen, Tübingen, Germany.

Georg Heinrich (G)

Oncological Practice, Fürstenwalde, Germany.

Lothar Häberle (L)

Department of Gynecology and Obstetrics, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nuremberg, Germany.

Peter A Fasching (PA)

Department of Gynecology and Obstetrics, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nuremberg, Germany.

Matthias W Beckmann (MW)

Department of Gynecology and Obstetrics, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nuremberg, Germany.

Robert E Coleman (RE)

Sheffield Cancer Research Centre, Weston Park Hospital, University of Sheffield, Sheffield, United Kingdom.

Wolfgang Janni (W)

Department of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.

Brigitte Rack (B)

Department of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH