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Do age, fitness, and concomitant medications influence management and outcomes of patients with CLL treated with ibrutinib?
Tedeschi, Alessandra; Frustaci, Anna Maria; Mauro, Francesca Romana; Chiarenza, Annalisa; Coscia, Marta; Ciolli, Stefania; Reda, Gianluigi; Laurenti, Luca; Varettoni, Marzia; Murru, Roberta; Baratè, Claudia; Sportoletti, Paolo; Greco, Antonino; Borella, Chiara; Rossi, Valentina; Deodato, Marina; Biagi, Annalisa; Zamprogna, Giulia; Pelle, Angelo Curto; Lapietra, Gianfranco; Vitale, Candida; Morelli, Francesca; Cassin, Ramona; Fresa, Alberto; Cavalloni, Chiara; Postorino, Massimiliano; Ielo, Claudia; Cairoli, Roberto; Di Raimondo, Francesco; Montillo, Marco; Del Poeta, Giovanni.
Afiliação
  • Tedeschi A; Department of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
  • Frustaci AM; Department of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
  • Mauro FR; Hematology, Department of Translational and Precision Medicine, Sapienza University, Policlinico Umberto I, Rome, Italy.
  • Chiarenza A; Division of Hematology, AOU "Policlinico-Vittorio Emanuele," University of Catania, Catania, Italy.
  • Coscia M; Division of Hematology, AOU Città della Salute e della Scienza di Torino, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
  • Ciolli S; Department of Hematology, Università degli Studi di Firenze, Firenze, Italy.
  • Reda G; Department of Hematology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milano, Italy.
  • Laurenti L; Hematology Institute, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Roma, Italy.
  • Varettoni M; Division of Hematology Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Murru R; Hematology and Stem Cell Transplantation Unit, Ospedale A. Businco, ARNAS "G. Brotzu," Cagliari, Italy.
  • Baratè C; Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
  • Sportoletti P; Division of Hematology and Clinical Immunology, Department of Medicine, University of Perugia, Perugia, Italy.
  • Greco A; Department of Hematology, Azienda Ospedaliera Giovanni Panìco, Tricase, Italy.
  • Borella C; Department of Hematology, Ospedale San Gerardo, Monza, Italy.
  • Rossi V; Hematology & Transfusion Medicine L. Sacco University Hospital and School of Medicine, Milano, Italy; and.
  • Deodato M; Department of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
  • Biagi A; Hematology, Department of Biomedicine and Prevention, University Tor Vergata, Rome, Italy.
  • Zamprogna G; Department of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
  • Pelle AC; Division of Hematology, AOU "Policlinico-Vittorio Emanuele," University of Catania, Catania, Italy.
  • Lapietra G; Hematology, Department of Translational and Precision Medicine, Sapienza University, Policlinico Umberto I, Rome, Italy.
  • Vitale C; Division of Hematology, AOU Città della Salute e della Scienza di Torino, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
  • Morelli F; Department of Hematology, Università degli Studi di Firenze, Firenze, Italy.
  • Cassin R; Department of Hematology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milano, Italy.
  • Fresa A; Hematology Institute, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Roma, Italy.
  • Cavalloni C; Division of Hematology Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Postorino M; Hematology, Department of Biomedicine and Prevention, University Tor Vergata, Rome, Italy.
  • Ielo C; Hematology, Department of Translational and Precision Medicine, Sapienza University, Policlinico Umberto I, Rome, Italy.
  • Cairoli R; Department of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
  • Di Raimondo F; Division of Hematology, AOU "Policlinico-Vittorio Emanuele," University of Catania, Catania, Italy.
  • Montillo M; Department of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
  • Del Poeta G; Hematology, Department of Biomedicine and Prevention, University Tor Vergata, Rome, Italy.
Blood Adv ; 5(24): 5490-5500, 2021 12 28.
Article em En | MEDLINE | ID: mdl-34525181
ABSTRACT
Functional reserve of organs and systems is known to be relevant in predicting immunochemotherapy tolerance. Age and comorbidities, assessed by the cumulative illness rating scale (CIRS), have been used to address chemotherapy intensity. In the ibrutinib era, it is still unclear whether age, CIRS, and Eastern Cooperative Oncology Group performance status (ECOG-PS) retain their predictive role on treatment vulnerability. In this series of 712 patients with chronic lymphocytic leukemia (CLL) treated with ibrutinib outside clinical trials, baseline ECOG-PS and neutropenia resulted as the most accurate predictors of treatment feasibility and outcomes. Age did not independently influence survival and ibrutinib tolerance, indicating that not age per se, but age-related conditions, may affect drug management. We confirmed the role of CIRS > 6 as a predictor of a poorer progression- and event-free survival (PFS, EFS). The presence of a severe comorbidity was significantly associated with permanent dose reductions (PDRs), not translating into worse outcomes. As expected, del(17p) and/or TP53mut and previous therapies affected PFS, EFS, and overall survival. No study so far has analyzed the influence of concomitant medications and CYP3A inhibitors with ibrutinib. In our series, these factors had no impact, although CYP3A4 inhibitors use correlated with Cox regression analysis, with an increased risk of PDR. Despite the limitation of its retrospective nature, this large study confirmed the role of ECOG-PS as the most accurate predictor of ibrutinib feasibility and outcomes, and importantly, neutropenia emerged as a relevant tool influencing patients' vulnerability. Although CIRS > 6 retained a significant impact on PFS and EFS, its value should be confirmed by prospective studies.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Preparações Farmacêuticas / Leucemia Linfocítica Crônica de Células B Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Preparações Farmacêuticas / Leucemia Linfocítica Crônica de Células B Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article