| Literature DB >> 25918346 |
Susanne Saussele1, Marie-Paloma Krauss1, Rüdiger Hehlmann1, Michael Lauseker2, Ulrike Proetel1, Lida Kalmanti1, Benjamin Hanfstein1, Alice Fabarius1, Doris Kraemer3, Wolfgang E Berdel4, Martin Bentz5, Peter Staib6, Maike de Wit7, Martin Wernli8, Florian Zettl9, Holger F Hebart10, Markus Hahn11, Jochen Heymanns12, Ingo Schmidt-Wolf13, Norbert Schmitz14, Michael J Eckart15, Winfried Gassmann16, Andrea Bartholomäus17, Antonio Pezzutto18, Elisabeth Oppliger Leibundgut19, Dominik Heim20, Stefan W Krause21, Andreas Burchert22, Wolf-Karsten Hofmann1, Joerg Hasford2, Andreas Hochhaus23, Markus Pfirrmann2, Martin C Müller1.
Abstract
We studied the influence of comorbidities on remission rate and overall survival (OS) in patients with chronic myeloid leukemia (CML). Participants of the CML Study IV, a randomized 5-arm trial designed to optimize imatinib therapy, were analyzed for comorbidities at diagnosis using the Charlson Comorbidity Index (CCI); 511 indexed comorbidities were reported in 1519 CML patients. Age was an additional risk factor in 863 patients. Resulting CCI scores were as follows: CCI 2, n = 589; CCI 3 or 4, n = 599; CCI 5 or 6, n = 229; and CCI ≥ 7, n = 102. No differences in cumulative incidences of accelerated phase, blast crisis, or remission rates were observed between patients in the different CCI groups. Higher CCI was significantly associated with lower OS probabilities. The 8-year OS probabilities were 93.6%, 89.4%, 77.6%, and 46.4% for patients with CCI 2, 3 to 4, 5 to 6, and ≥7, respectively. In multivariate analysis, CCI was the most powerful predictor of OS, which was still valid after removal of its age-related components. Comorbidities have no impact on treatment success but do have a negative effect on OS, indicating that survival of patients with CML is determined more by comorbidities than by CML itself. OS may therefore be inappropriate as an outcome measure for specific CML treatments. The trial was registered at www.clinicaltrials.gov as #NCT00055874.Entities:
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Year: 2015 PMID: 25918346 PMCID: PMC4574015 DOI: 10.1182/blood-2015-01-617993
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113