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


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 Nov 2023
Historique:
medline: 17 11 2023
pubmed: 9 8 2023
entrez: 9 8 2023
Statut: ppublish

Résumé

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. 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. 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). 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.

Identifiants

pubmed: 37556775
doi: 10.1200/JCO.23.00126
doi:

Substances chimiques

palbociclib G9ZF61LE7G
Receptor, ErbB-2 EC 2.7.10.1

Banques de données

ClinicalTrials.gov
['NCT02513394']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

5118-5130

Auteurs

Georg Pfeiler (G)

Department of Gynecology and Gynecological Oncology, Medical University of Vienna, Vienna, Austria.

Dominik Hlauschek (D)

Austrian Breast and Colorectal Cancer Study Group, Vienna, Austria.

Erica L Mayer (EL)

Dana-Farber/Partners Cancer Care, Boston, MA.

Christine Deutschmann (C)

Department of Gynecology and Gynecological Oncology, Medical University of Vienna, Vienna, Austria.

Stephanie Kacerovsky-Strobl (S)

Breast Health Center, St Francis Hospital, Vienna, Austria.

Miguel Martin (M)

Hospital General Universitario Gregorio Marañón, Universidad Complutense, Madrid, Spain.

Jane Lowe Meisel (JL)

Winship Cancer Institute, Emory University, Atlanta, GA.

Nicholas Zdenkowski (N)

University of Newcastle, Newcastle, NSW, Australia.

Sibylle Loibl (S)

German Breast Group, Neu-Isenburg, Germany.
Goethe University Frankfurt/M, Frankfurt/M, Germany.
Centre for Haematology and Oncology/Bethanien, Frankfurt/M, Germany.

Marija Balic (M)

Division of Oncology, Department of Internal Medicine, Medical University Graz, Graz, Austria.

Haeseong Park (H)

Siteman Cancer Center, Washington University, St Louis, MO.

Aleix Prat (A)

Department of Medical Oncology, Hospital Clinic, IDIBAPS, University of Barcelona, Barcelona, Spain.

Claudine Isaacs (C)

Georgetown University, Washington, DC.

Emilio Bajetta (E)

Gruppo I.T.M.O., Monza, Italy.
Fondazione Policlinico di Monza, Monza, Italy.

Justin M Balko (JM)

Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN.

Merixtell Bellet-Ezquerra (M)

Hospital Universitari Son Espases, Palma de Mallorca, Spain.

Judith Bliss (J)

The Institute of Cancer Research, London, United Kingdom.

Harold Burstein (H)

Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.

Fatima Cardoso (F)

Breast Unit, Champalimaud Clinical Center/Champalimaud Foundation, Lisbon, Portugal.

Hannes Fohler (H)

Austrian Breast and Colorectal Cancer Study Group, Vienna, Austria.

Theodoros Foukakis (T)

Breast Center, Theme Cancer, Karolinska University Hospital, Stockholm, Sweden.
Department of Oncology/Pathology, Karolinska Institute, Stockholm, Sweden.

Karen A Gelmon (KA)

BC Cancer, Vancouver, BC, Canada.

Tufia C Haddad (TC)

Mayo Clinic College of Medicine and Science, Rochester, MN.

Hiroji Iwata (H)

Aichi Cancer Center Hospital, Nagoya, Japan.

Jacek Jassem (J)

Department of Oncology and Radiotherapy, Medical University of Gdańsk, Gdańsk, Poland.

Soo-Chin Lee (SC)

Department of Haematology-Oncology, National University Cancer Institute (NCIS), Singapore, Singapore.
Cancer Science Institute (CSI), Singapore, Singapore.
National University of Singapore (NUS), Singapore, Singapore.

Barbro Linderholm (B)

Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Oncology, Institution of Clinical Sciences, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.

Maartje Los (M)

St Antonius Ziekenhuis Nieuwegein, Utrecht, the Netherlands.

Eleftherios P Mamounas (EP)

Orlando Health Cancer Institute, Orlando, FL.

Kathy D Miller (KD)

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN.

Patrick G Morris (PG)

Cancer Trials Ireland, Dublin, Ireland.
Beaumont RCSI Cancer Centre, Dublin, Ireland.

Elisabetta Munzone (E)

European Institute of Oncology IRCCS, Milan, Italy.

Einav Nili Gal-Yam (EN)

The Talpiot Medical Leadership Program, Breast Oncology Institute, Sheba Medical Center, Ramat-Gam, Israel.

Alistair Ring (A)

Royal Marsden Hospital, NHS Foundation Trust, London, United Kingdom.

Lois Shepherd (L)

Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada.

Christian Singer (C)

Department of Gynecology and Gynecological Oncology, Medical University of Vienna, Vienna, Austria.
Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.

Christoph Thomssen (C)

Martin-Luther-University Halle-Wittenberg, Halle/S, Germany.

Ling-Ming Tseng (LM)

Taipei-Veterans General Hospital, National Yang Ming Chiao Tung University, Taipei, Taiwan.

Pinuccia Valagussa (P)

Fondazione Michelangelo, Milano, Italy.

Eric P Winer (EP)

Yale Cancer Center, Smilow Cancer Network, Yale University, New Haven, CT.

Antonio C Wolff (AC)

Johns Hopkins University, Baltimore, MD.

Gabriele Zoppoli (G)

Gruppo Oncologico Italiano di Ricerca Clinica (GOIRC), Università degli Studi di Genova, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Jana Machacek-Link (J)

Austrian Breast and Colorectal Cancer Study Group, Vienna, Austria.

Celine Schurmans (C)

Breast International Group (BIG), Brussels, Belgium.

Xin Huang (X)

Pfizer, Inc, San Francisco, CA.

Eric Gauthier (E)

Pfizer, Inc, San Francisco, CA.

Christian Fesl (C)

Austrian Breast and Colorectal Cancer Study Group, Vienna, Austria.

Amylou C Dueck (AC)

Alliance Statistics and Data Center, Mayo Clinic, Phoenix, AZ.

Angela DeMichele (A)

University of Pennsylvania, Philadelphia, PA.

Michael Gnant (M)

Austrian Breast and Colorectal Cancer Study Group, Vienna, Austria.
Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.

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