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Peripheral blood lymphocytes predict clinical outcomes in hormone receptor-positive HER2-negative advanced breast cancer patients treated with CDK4/6 inhibitors.
Zattarin, Emma; Mariani, Luigi; Menichetti, Alice; Leporati, Rita; Provenzano, Leonardo; Ligorio, Francesca; Fucà, Giovanni; Lobefaro, Riccardo; Lalli, Luca; Vingiani, Andrea; Nichetti, Federico; Griguolo, Gaia; Sirico, Marianna; Bernocchi, Ottavia; Marra, Antonio; Corti, Chiara; Zagami, Paola; Agostinetto, Elisa; Jacobs, Flavia; Di Mauro, Pierluigi; Presti, Daniele; Sposetti, Caterina; Giorgi, Carlo Alberto; Guarneri, Valentina; Pedersini, Rebecca; Losurdo, Agnese; Generali, Daniele; Curigliano, Giuseppe; Pruneri, Giancarlo; de Braud, Filippo; Dieci, Maria Vittoria; Vernieri, Claudio.
Affiliation
  • Zattarin E; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Mariani L; Unit of Clinical Epidemiology and Trial Organization, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Menichetti A; Oncology 2, Istituto Oncologico Veneto IOV - IRCCS, Padova, Italy.
  • Leporati R; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Provenzano L; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Ligorio F; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Fucà G; IFOM ETS, the AIRC Institute of Molecular Oncology, Milan, Italy.
  • Lobefaro R; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Lalli L; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Vingiani A; Unit of Clinical Epidemiology and Trial Organization, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Nichetti F; Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
  • Griguolo G; Pathology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Sirico M; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Bernocchi O; Computational Oncology, Molecular Diagnostics Program, National Center for Tumor Diseases (NCT) and German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Marra A; Oncology 2, Istituto Oncologico Veneto IOV - IRCCS, Padova, Italy.
  • Corti C; Department of Surgery, Oncology and Gastroenterology-DiSCOG, University of Padova, Padova, Italy.
  • Zagami P; Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
  • Agostinetto E; Farmacia Ospedaliera ASST Cremona, Cremona, Lombardia, Italy.
  • Jacobs F; Division of Early Drug Development for Innovative Therapies, IEO, European Institute of Oncology IRCCS, Milan, Italy.
  • Di Mauro P; Breast Medicine Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Presti D; Division of Early Drug Development for Innovative Therapies, IEO, European Institute of Oncology IRCCS, Milan, Italy.
  • Sposetti C; Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
  • Giorgi CA; Division of Early Drug Development for Innovative Therapies, IEO, European Institute of Oncology IRCCS, Milan, Italy.
  • Guarneri V; IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
  • Pedersini R; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
  • Losurdo A; Institut Jules Bordet and l'Université Libre de Bruxelles, Bruxelles, Belgium.
  • Generali D; IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
  • Curigliano G; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
  • Pruneri G; Medical Oncology Unit, ASST Spedali Civili, Brescia, Italy.
  • de Braud F; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Dieci MV; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Vernieri C; Oncology 2, Istituto Oncologico Veneto IOV - IRCCS, Padova, Italy.
Ther Adv Med Oncol ; 15: 17588359231204857, 2023.
Article in En | MEDLINE | ID: mdl-38130467
ABSTRACT

Background:

Cyclin-Dependent Kinase 4/6 inhibitors (CDK4/6i) combined with Endocrine Therapy (ET) are the standard treatment for patients with Hormone Receptor-positive/HER2-negative advanced breast cancer (HR+/HER2- aBC).

Objectives:

While CDK4/6i are known to reduce several peripheral blood cells, such as neutrophils, lymphocytes and platelets, the impact of these modulations on clinical outcomes is unknown.

Design:

A multicenter, retrospective-prospective Italian study.

Methods:

We investigated the association between baseline peripheral blood cells, or their early modifications (i.e. 2 weeks after treatment initiation), and the progression-free survival (PFS) of HR+/HER2- aBC patients treated with ETs plus CDK4/6i. Random Forest models were used to select covariates associated with patient PFS among a large list of patient- and tumor-related variables.

Results:

We evaluated 638 HR+/HER2- aBC patients treated with ET plus CDK4/6i at six Italian Institutions between January 2017 and May 2021. High baseline lymphocyte counts were independently associated with longer PFS [median PFS (mPFS) 20.1 versus 13.2 months in high versus low lymphocyte patients, respectively; adjusted Hazard Ratio (aHR) 0.78; 95% confidence interval (CI) 0.66-0.92; p = 0.0144]. Moreover, patients experiencing a lower early reduction of lymphocyte counts had significantly longer PFS when compared to patients undergoing higher lymphocyte decrease (mPFS 18.1 versus 14.5 months; aHR 0.82; 95% CI 0.73-0.93; p = 0.0037). Patients with high baseline lymphocytes and undergoing a lower reduction, or even an increase, of lymphocyte counts during CDK4/6i therapy experienced the longest PFS, while patients with lower baseline lymphocytes and undergoing a higher decrease of lymphocytes had the lowest PFS (mPFS 21.4 versus 11 months, respectively).

Conclusion:

Baseline and on-treatment modifications of peripheral blood lymphocytes have independent prognostic value in HR+/HER2- aBC patients. This study supports the implementation of clinical strategies to boost antitumor immunity in patients with HR+/HER2- aBC treated with ETs plus CDK4/6i.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ther Adv Med Oncol Year: 2023 Document type: Article Affiliation country: Italia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ther Adv Med Oncol Year: 2023 Document type: Article Affiliation country: Italia