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Impact of BMI in Patients With Early Hormone Receptor-Positive Breast Cancer Receiving Endocrine Therapy With or Without Palbociclib in the PALLAS Trial.

Authors :
Pfeiler G
Hlauschek D
Mayer EL
Deutschmann C
Kacerovsky-Strobl S
Martin M
Meisel JL
Zdenkowski N
Loibl S
Balic M
Park H
Prat A
Isaacs C
Bajetta E
Balko JM
Bellet-Ezquerra M
Bliss J
Burstein H
Cardoso F
Fohler H
Foukakis T
Gelmon KA
Goetz M
Haddad TC
Iwata H
Jassem J
Lee SC
Linderholm B
Los M
Mamounas EP
Miller KD
Morris PG
Munzone E
Gal-Yam EN
Ring A
Shepherd L
Singer C
Thomssen C
Tseng LM
Valagussa P
Winer EP
Wolff AC
Zoppoli G
Machacek-Link J
Schurmans C
Huang X
Gauthier E
Fesl C
Dueck AC
DeMichele A
Gnant M
Source :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology [J Clin Oncol] 2023 Nov 20; Vol. 41 (33), pp. 5118-5130. Date of Electronic Publication: 2023 Aug 09.
Publication Year :
2023

Abstract

Purpose: BMI affects breast cancer risk and prognosis. In contrast to cytotoxic chemotherapy, CDK4/6 inhibitors are given at a fixed dose, irrespective of BMI or weight. This preplanned analysis of the global randomized PALLAS trial investigates the impact of BMI on the side-effect profile, treatment adherence, and efficacy of palbociclib.<br />Methods: Patients were categorized at baseline according to WHO BMI categories. Neutropenia rates were assessed with univariable and multivariable logistic regression. Time to early discontinuation of palbociclib was analyzed with Fine and Gray competing risk models. Unstratified Cox models were used to investigate the association between BMI category and time to invasive disease-free survival (iDFS). 95% CIs were derived.<br />Results: Of 5,698 patients included in this analysis, 68 (1.2%) were underweight, 2,082 (36.5%) normal weight, 1,818 (31.9%) overweight, and 1,730 (30.4%) obese at baseline. In the palbociclib arm, higher BMI was associated with a significant decrease in neutropenia (unadjusted odds ratio for 1-unit change, 0.93; 95% CI, 0.91 to 0.94; adjusted for age, race ethnicity, region, chemotherapy use, and Eastern Cooperative Oncology Group at baseline, 0.93; 95% CI, 0.92 to 0.95). This translated into a significant decrease in treatment discontinuation rate with higher BMI (adjusted hazard ratio [HR] for 10-unit change, 0.75; 95% CI, 0.67 to 0.83). There was no significant improvement in iDFS with the addition of palbociclib to ET in any weight category (normal weight HR, 0.84; 95% CI, 0.63 to 1.12; overweight HR, 1.10; 95% CI, 0.82 to 1.49; and obese HR, 0.95; 95% CI, 0.69 to 1.30) in this analysis early in follow-up (31 months).<br />Conclusion: This preplanned analysis of the PALLAS trial demonstrates a significant impact of BMI on side effects, dose reductions, early treatment discontinuation, and relative dose intensity. Additional long-term follow-up will further evaluate whether BMI ultimately affects outcome.

Details

Language :
English
ISSN :
1527-7755
Volume :
41
Issue :
33
Database :
MEDLINE
Journal :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Publication Type :
Academic Journal
Accession number :
37556775
Full Text :
https://doi.org/10.1200/JCO.23.00126