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Outcomes of male patients with HR+/HER2- advanced breast cancer receiving palbociclib in the real-world POLARIS study.
Blum, Joanne L; DiCristo, Caroline; Gordon, David; Karuturi, Meghan S; Oubre, David; Jepsen, Erin; Cuevas, Juan; Lakhanpal, Shailendra; Montelongo, Monica Z; Zhang, Zhe; Cappelleri, Joseph C; Wang, Yao; Tripathy, Debu.
Affiliation
  • Blum JL; Baylor-Sammons Cancer Center, Texas Oncology, US Oncology, Dallas, TX, USA. jlblum@att.net.
  • DiCristo C; Pfizer Inc, New York, NY, USA.
  • Gordon D; Munson Medical Center, Traverse City, MI, USA.
  • Karuturi MS; The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Oubre D; Ponchartrain Cancer Center, Hammond, LA, USA.
  • Jepsen E; Novant Health Cancer Institute, Winston-Salem, NC, USA.
  • Cuevas J; St. Louis Cancer Care, St. Louis, MO, USA.
  • Lakhanpal S; Saint Vincent's Birmingham, Birmingham, AL, USA.
  • Montelongo MZ; ICON plc, Blue Bell, PA, USA.
  • Zhang Z; Pfizer Inc, La Jolla, CA, USA.
  • Cappelleri JC; Pfizer Inc, Groton, CT, USA.
  • Wang Y; Pfizer Inc, New York, NY, USA.
  • Tripathy D; The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Breast Cancer Res Treat ; 203(3): 463-475, 2024 Feb.
Article in En | MEDLINE | ID: mdl-37903899
ABSTRACT

PURPOSE:

Data on treatments for male breast cancer patients are limited owing to rarity and underrepresentation in clinical trials. The real-world POLARIS study gathers data on palbociclib use for the treatment of hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer (ABC) in female and male patients. This sub-analysis describes real-world palbociclib treatment patterns, clinical outcomes, and quality of life (QoL) in male patients.

METHODS:

POLARIS is a prospective, noninterventional, multicenter, real-world study of patients with HR+/HER2- ABC receiving palbociclib. Assessments included medical record reviews, patient QoL questionnaires (European Organisation for Research and Treatment of Cancer Quality-of-Life Questionnaire-Core 30), site characteristics questionnaires, and physician treatment selection surveys. Variables included demographics, disease history, global health status/QoL, clinical assessments and adverse events. Analyses were descriptive in nature. For clinical outcomes, real-world tumor responses and progression were determined by physician assessment in routine clinical practice. Real-world progression-free survival (rwPFS) was described using the Kaplan-Meier method.

RESULTS:

At data cutoff, 15 male patients were enrolled (median age, 66 years). Nine patients received palbociclib as a first-line treatment and 6 as a second-line or later treatment. Patients received a median of 20 cycles of palbociclib. Neutropenia was experienced by 2 patients and grade ≥ 3 adverse events were reported in 11 patients. Global health status/QoL scores remained generally consistent during the study. One patient (6.7%) achieved a complete tumor response, 4 (26.7%) a partial response, and 8 (53.3%) stable disease. Median rwPFS was 19.8 months (95% CI, 7.4-38.0). Median follow-up duration was 24.7 months (95% CI, 20.0-35.7).

CONCLUSION:

This real-world analysis showed that palbociclib was well tolerated and provides preliminary data on treatment patterns and outcomes with palbociclib in male patients with HR+/HER2- ABC, helping inform the use of palbociclib in this patient subgroup. TRIAL IDENTIFIER NCT03280303.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperazines / Pyridines / Breast Neoplasms Limits: Aged / Humans / Male Language: En Journal: Breast Cancer Res Treat Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperazines / Pyridines / Breast Neoplasms Limits: Aged / Humans / Male Language: En Journal: Breast Cancer Res Treat Year: 2024 Document type: Article Affiliation country: United States