Real-World Experience with CDK4/6 Inhibitors for Metastatic HR+/HER2− Breast Cancer at a Single Cancer Center

Author:

Knudsen Erik S1ORCID,Schultz Emily2,Hamilton Deanna2,Attwood Kris3,Edge Stephen4,O’Connor Tracey5,Levine Ellis5,Witkiewicz Agnieszka K26

Affiliation:

1. Department of Molecular and Cellular Biology, Roswell Park Comprehensive Cancer Center , Buffalo, NY , USA

2. Center for Personalized Medicine, Roswell Park Comprehensive Cancer Center , Buffalo, NY , USA

3. Department of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center , Buffalo, NY , USA

4. Department of Surgical Oncology, Roswell Park Comprehensive Cancer Center , Buffalo, NY , USA

5. Department of Medical Oncology, Roswell Park Comprehensive Cancer Center , Buffalo, NY , USA

6. Department of Pathology, Roswell Park Comprehensive Cancer Center , Buffalo, NY , USA

Abstract

Abstract Background A study was initiated at Roswell Park Comprehensive Cancer Center to capture the real-world experience related to the use of CDK4/6 inhibitors (Ciclibs) for the treatment of metastatic hormone receptor-positive and HER2-negative breast cancer (HR+/HER2-). Patients and Methods A total of 222 patients were evaluated who received CDK4/6 inhibitors in the period from 2015 to 2021. Detailed clinical and demographic information was obtained on each patient and used to define clinical and demographic features associated with progression-free survival on CDK4/6 inhibitor-based therapies. Results In this real-world analysis, the majority of patients received palbociclib as the CDK4/6 inhibitor with letrozole or fulvestrant as the predominant endocrine therapies. The median progression-free survival (PFS) in the letrozole (27.6 months) and fulvestrant (17.2 months) groups were comparable to that observed in clinical trials. As expected, age at start of the treatment and menopausal status influenced endocrine therapy utilization but were not associated with PFS. Patients with recurrent disease had shorter PFS (P = .0024) than those presenting with de novo metastasis. The presence of visceral metastasis trended toward shorter PFS (P = .051). Similarly, prior endocrine therapy (P = .003) or chemotherapy (P = .036) was associated with shorter PFS. Body mass index was not associated with PFS or with dose interruption and/or modification. While the number of minorities in this analysis is limited (n = 26), these patients as a group had statistically shorter PFS on treatment (P = .002). Conclusions The real-world progression-free survival with CDK4/6 inhibitors mimics that observed in the clinical trial. A number of clinical and demographic features were associated with PFS on CDK4/6 inhibitor-based therapy. Further studies are ongoing to validate these findings incorporating additional cancer centers.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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5. Current status of estrogen and progesterone receptors in breast cancer.;McGuire;Cancer.,1977

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