Abstract 1589
Background
Recently, palbociclib plus exemestane with GnRH agonist demonstrated a statistically significant improvement in progression-free survival (PFS) compared with that of the capecitabine for premenopausal women with hormone receptor-positive metastatic breast cancer (median PFS 20·1 vs. 14·4 months, p = 0·0235 ; HR 0·659 [95% C.I. 0·437–0·994])(Park YH et al, J Clin Oncol 37, 2019 [suppl; abstr 1007]). We evaluated PROs in YoungPEARL phase ll trial.
Methods
Pts (N = 189) were randomized 1:1 to receive palbociclib plus exemestane with GnRH agonist or capecitabine. PROs were assessed at day 1 (baseline), every 6 weeks, and at the end of treatment, using European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-30). Repeated-measures mixed-effect analyses were carried out to compare on-treatment overall scores and changes from baseline between the treatment groups while controlling for baseline.
Results
Questionnaire completion rates were 100% at baseline and during treatment from baseline to 84 weeks in each group. Global health status/QoL scores were maintained from baseline to the end of treatment across all time points within each cohort. Between-treatment comparison in the change from baseline functioning scale scores showed trends favoring palbociclib arm for physical functioning (0.12 vs -3.66, p = 0.1201) while favoring capecitabine arm for emotional (0.87 vs 2.61, p = 0.5963) and social functioning (2.63 vs 5.97, p = 0.3234). There was a trend to improve appetite loss (-5.27 vs 0.72, p = 0.1484) and insomnia tended to get worse (3.81 vs -2.65, p = 0.0736) in palbociclib arm while capecitabine arm showed the greater improvement in pain (-2.80 vs -5.83, p = 0.3200) but worsening in diarrhea (1.17 vs 7.37, p = 0.0598) without statistical significance.
Conclusions
These findings show that palbociclib plus endocrine therapy maintained high PRO scores with some different function and symptom profiles compared with capecitabine arm.
Clinical trial identification
NCT02592746.
Editorial acknowledgement
Legal entity responsible for the study
Korea Cancer Study Group.
Funding
Pfizer.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
Poster Discussion - Breast cancer, metastatic - Invited Discussant 311PD and LBA25
Presenter: Miguel Martín
Session: Poster Discussion - Breast cancer, metastatic
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