1. Efficacy and safety of palbociclib in patients with estrogen receptor–positive/human epidermal growth factor receptor 2–negative advanced breast cancer with preexisting conditions: A post hoc analysis of PALOMA-2
- Author
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Reshma Mahtani, Janice M. Walshe, Eustratios Bananis, Meghan Sri Karuturi, D. Lu, Sindy T. Kim, Patrick Schnell, Anil A. Joy, Karen A. Gelmon, Patrick Neven, and Lee S. Schwartzberg
- Subjects
Oncology ,medicine.medical_specialty ,Pyridines ,Receptor, ErbB-2 ,MedDRA ,Estrogen receptor ,Breast Neoplasms ,Palbociclib ,Placebo ,Piperazines ,Internal medicine ,Post-hoc analysis ,Antineoplastic Combined Chemotherapy Protocols ,medicine ,Humans ,Progression-free survival ,Adverse effect ,Preexisting condition ,RC254-282 ,Science & Technology ,business.industry ,Letrozole ,Obstetrics & Gynecology ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,General Medicine ,Receptors, Estrogen ,OLDER WOMEN ,Surgery ,Female ,Original Article ,Advanced breast cancer ,Safety ,COMORBIDITY ,business ,Life Sciences & Biomedicine ,medicine.drug - Abstract
Objective In the PALOMA-2 trial, palbociclib in combination with letrozole prolonged progression-free survival (PFS) and exhibited an acceptable safety profile in patients with estrogen receptor–positive/human epidermal growth factor receptor 2–negative advanced breast cancer (ABC). This post hoc analysis of PALOMA-2 evaluated the efficacy and safety of palbociclib plus letrozole in patients with preexisting conditions grouped by Medical Dictionary for Regulatory Activities (MedDRA) System Organ Class (SOC). Methods Postmenopausal patients without prior treatment for ABC were randomized 2:1 to receive palbociclib (125 mg/d on a 3 weeks on/1 week off schedule) plus letrozole (2.5 mg/d, continuous) or placebo plus letrozole. Patients were grouped by the following MedDRA SOC preexisting conditions: gastrointestinal, musculoskeletal, metabolic, and vascular/cardiac. Median PFS was estimated by the Kaplan-Meier method, and treatment emergent adverse events (AEs) were compared between treatment arms within each preexisting condition subgroup. Results At baseline, 276 (41.4 %) patients had preexisting gastrointestinal disorders, 390 (58.6 %) had musculoskeletal disorders, 259 (38.9 %) had metabolic disorders, and 382 (57.4 %) had vascular/cardiac disorders. Baseline characteristics were similar between subgroups and between each arm within subgroups. Regardless of baseline preexisting condition, palbociclib plus letrozole prolonged PFS compared with placebo plus letrozole. Treatment-emergent AEs associated with palbociclib plus letrozole and dose modifications due to AEs were similar across preexisting condition subgroups. Conclusion This post hoc analysis of PALOMA-2 demonstrated a favorable effect of palbociclib on PFS and a safety profile consistent with previous observations, regardless of underlying preexisting condition. Pfizer Inc (NCT01740427)., Highlights • Preexisting conditions can affect the safety and efficacy of breast cancer therapies. • This is a post hoc analysis of patients with preexisting conditions from PALOMA-2. • Palbociclib prolonged median PFS, regardless of preexisting condition. • Within each treatment arm, AEs were similar regardless of preexisting condition.
- Published
- 2021