Literature DB >> 25047978

Age influences initial dose and compliance to imatinib in chronic myeloid leukemia elderly patients but concomitant comorbidities appear to influence overall and event-free survival.

Massimo Breccia1, Luigiana Luciano2, Roberto Latagliata3, Fausto Castagnetti4, Dario Ferrero5, Francesco Cavazzini6, Malgorzata Monica Trawinska7, Mario Annunziata8, Fabio Stagno9, Mario Tiribelli10, Gianni Binotto11, Elena Crisà5, Pellegrino Musto12, Antonella Gozzini13, Laura Cavalli14, Enrico Montefusco15, Alessandra Iurlo16, Sabina Russo17, Michele Cedrone18, Antonella Russo Rossi19, Patrizia Pregno20, Mauro Endri21, Antonio Spadea22, Matteo Molica3, Gianfranco Giglio23, Francesca Celesti24, Federica Sorà25, Sergio Storti26, Ada D'Addosio27, Giovanna Rege Cambrin28, Alessandro Isidori29, Simona Sica25, Elisabetta Abruzzese7, Giorgina Speccha19, Gianantonio Rosti4, Giuliana Alimena3.   

Abstract

We applied Charlson comorbidity index (CCI) stratification on a large cohort of chronic myeloid leukemia (CML) very elderly patients (>75 years) treated with imatinib, in order to observe the impact of concomitant diseases on both compliance and outcome. One hundred and eighty-one patients were recruited by 21 Italian centers. There were 95 males and 86 females, median age 78.6 years (range 75-93.6). According to Sokal score, 106 patients were classified as intermediate risk and 55 as high risk (not available in 20 patients). According to CCI stratification, 71 patients had score 0 and 110 a score ≥ 1. Imatinib standard dose was reduced at start of therapy (200-300 mg/day) in 68 patients independently from the evaluation of baseline comorbidities, but based only on physician judgement: 43.6% of these patients had score 0 compared to 34% of patients who had score ≥ 1. Significant differences were found in terms of subsequent dose reduction (39% of patients with score 0 compared to 53% of patients with score ≥ 1) and in terms of drug discontinuation due to toxicity (35% of patients with score 0 vs 65% of patients with score ≥ 1). We did not find significant differences as regards occurrence of hematologic side effects, probably as a consequence of the initial dose reduction: 39% of patients with score 0 experienced grade 3/4 hematologic toxicity (most commonly anemia) compared to 42% of patients with score ≥ 1. Independently from the initial dose, comorbidities again did not have an impact on development of grade 3/4 non-hematologic side effects (most commonly skin rash, muscle cramps and fluid retention): 62% of patients with score 0 compared to 52.5% of patients with score ≥ 1. Notwithstanding the reduced dose and the weight of comorbidities we did not find significant differences but only a trend in terms of efficacy: 66% of patients with score 0 achieved a CCyR compared to 54% of patients with score ≥ 1. Comorbidities appeared to have an impact on median OS (40.8 months for patients with score 0 vs 20.16 months for patients with score ≥ 1) on EFS and on non-CML death rate. Our results suggest that treatment of very elderly CML patients might be influenced by personal physician perception: evaluation at baseline of comorbidities according to CCI should improve initial decision-making in this subset of patients.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Age; Chronic myeloid leukemia; Comorbidities; Overall survival

Mesh:

Substances:

Year:  2014        PMID: 25047978     DOI: 10.1016/j.leukres.2014.06.020

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  8 in total

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Journal:  Pharmacol Res Perspect       Date:  2022-10

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7.  The impact of comorbid disease history on all-cause and cancer-specific mortality in myeloid leukemia and myeloma - a Swedish population-based study.

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8.  Imatinib and polypharmacy in very old patients with chronic myeloid leukemia: effects on response rate, toxicity and outcome.

Authors:  Alessandra Iurlo; Alessandro Nobili; Roberto Latagliata; Cristina Bucelli; Fausto Castagnetti; Massimo Breccia; Elisabetta Abruzzese; Daniele Cattaneo; Carmen Fava; Dario Ferrero; Antonella Gozzini; Massimiliano Bonifacio; Mario Tiribelli; Patrizia Pregno; Fabio Stagno; Paolo Vigneri; Mario Annunziata; Francesco Cavazzini; Gianni Binotto; Giovanna Mansueto; Sabina Russo; Franca Falzetti; Enrico Montefusco; Gabriele Gugliotta; Sergio Storti; Ada M D'Addosio; Luigi Scaffidi; Laura Cortesi; Michele Cedrone; Antonella Russo Rossi; Paolo Avanzini; Endri Mauro; Antonio Spadea; Francesca Celesti; Gianfranco Giglio; Alessandro Isidori; Monica Crugnola; Elisabetta Calistri; Federica Sorà; Giovanna Rege-Cambrin; Simona Sica; Luigiana Luciano; Sara Galimberti; Ester M Orlandi; Monica Bocchia; Mauro Tettamanti; Giuliana Alimena; Giuseppe Saglio; Gianantonio Rosti; Pier Mannuccio Mannucci; Agostino Cortelezzi
Journal:  Oncotarget       Date:  2016-11-29
  8 in total

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