1. 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
- Author
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Breccia, M, Luciano, L, Latagliata, R, Castagnetti, F, Ferrero, D, Cavazzini, F, Trawinska, Mm, Annunziata, M, Stagno, F, Tiribelli, M, Binotto, G, Crisà, E, Musto, P, Gozzini, A, Cavalli, L, Montefusco, E, Iurlo, A, Russo, S, Cedrone, M, Rossi, Ar, Pregno, P, Endri, M, Spadea, A, Molica, M, Giglio, G, Celesti, F, Sora', Federica, Storti, Sergio, D'Addosio, A, Cambrin, Gr, Isidori, A, Sica, Simona, Abruzzese, E, Speccha, G, Rosti, G, Alimena, G., Sora', Federica (ORCID:0000-0002-9607-5298), Storti, S (ORCID:0000-0002-4374-3985), Sica, Simona (ORCID:0000-0003-2426-3465), Breccia, M, Luciano, L, Latagliata, R, Castagnetti, F, Ferrero, D, Cavazzini, F, Trawinska, Mm, Annunziata, M, Stagno, F, Tiribelli, M, Binotto, G, Crisà, E, Musto, P, Gozzini, A, Cavalli, L, Montefusco, E, Iurlo, A, Russo, S, Cedrone, M, Rossi, Ar, Pregno, P, Endri, M, Spadea, A, Molica, M, Giglio, G, Celesti, F, Sora', Federica, Storti, Sergio, D'Addosio, A, Cambrin, Gr, Isidori, A, Sica, Simona, Abruzzese, E, Speccha, G, Rosti, G, Alimena, G., Sora', Federica (ORCID:0000-0002-9607-5298), Storti, S (ORCID:0000-0002-4374-3985), and Sica, Simona (ORCID:0000-0003-2426-3465)
- 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
- Published
- 2014