Cyclin-Dependent Kinase 4/6 Inhibitors Plus Endocrine Therapy versus Endocrine Therapy Alone for HR-Positive, HER-2-Negative Early Breast Cancer: Meta-Analysis of Phase III Randomized Clinical Trials

Author:

Moraes Francisco Cezar Aquino de1ORCID,de Oliveira Almeida Gustavo2ORCID,Alves Vinícius Freire Costa3,Priantti Jonathan N.4ORCID,Gomes Giovanna da Conceição5,Carnevalli Sarah Vitória Bristot6,Madeira Thiago7,Vilbert Maysa8ORCID,Stecca Carlos9ORCID,Figueroa Magalhães Maria Cristina9ORCID,Fernandes Marianne Rodrigues1ORCID,dos Santos Ney Pereira Carneiro1

Affiliation:

1. Oncology Research Center, Federal University of Pará, Belem 66073-005, Brazil

2. School of Medicine, Federal University of Triângulo Mineiro, Uberaba 38025-180, Brazil

3. School of Medicine, University of São Paulo, São Paulo 01246-903, Brazi

4. School of Medicine, Federal University of Amazonas, Manaus 69080-900, Brazil

5. School of Medicine, Catholic University of Minas Gerais, Belo Horizonte 32010-025, Brazil

6. School of Medicine, Federal University of Santa Catarina, Florianópolis 88040-900, Brazil

7. School of Medicine, Federal University of Minas Gerais, Belo Horizonte 31270-901, Brazil

8. Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2C4, Canada

9. Mackenzie Evangelical University Hospital, Curitiba 80730-150, Brazil

Abstract

Background: Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors are approved for advanced breast cancer combined with endocrine therapy (ET). The efficacy of CDK4/6 inhibitors plus ET in hormone estrogen-positive, human epidermal growth factor 2-negative (HR+/HER2−) early-stage breast cancer (esBC) is still to be confirmed. Methods: We performed a systematic review and a meta-analysis to investigate the efficacy of CDK4/6i plus ET in esBC. Main outcomes included invasive disease-free survival (iDFS), distant relapse-free survival (DRFS), and overall survival (OS). We included only phase III randomized controlled trials. We used RStudio version 4.2.3, and we considered p < 0.05 to be statistically significant. Results: Four studies were selected, including 14,168 patients, of which 7089 were treated with CDK4/6i plus ET and 7079 received ET monotherapy. Regarding patient characteristics, 6828 (48.2%) were premenopausal. Compared with ET alone, iDFS rates (HR 0.81; 95% CI: 0.67, 0.98; p = 0.034) were significantly in favor of CDK4/6 inhibitors plus ET. However, there were no significant differences in DRFS (HR 0.79; 95% CI: 0.58, 1.07; p = 0.132) nor OS (HR 0.96; 95% CI: 0.69, 1.35; p = 0.829). Conclusions: Our results show that the addition of CDK4/6 inhibitors is associated with a significant benefit for HR+/HER2− esBC patients in iDFS. More studies and longer follow-up are needed to assess overall survival benefits.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Pró-Reitoria de Pesquisa e Pós-Graduação da UFPA

Federal University of Pará

the Center for Research in Oncology

Publisher

MDPI AG

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