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First‐line treatment selection and early monitoring patterns in chronic phase‐chronic myeloid leukemia in routine clinical practice: SIMPLICITY
Authors:Stuart L. Goldberg  Jorge E. Cortes  Carlo Gambacorti‐Passerini  Rüdiger Hehlmann  H. Jean Khoury  Mauricette Michallet  Ron L. Paquette  Bengt Simonsson  Teresa Zyczynski  Aimee Foreman  Elisabetta Abruzzese  David Andorsky  Aart Beeker  Pascale Cony‐Makhoul  Richard Hansen  Elza Lomaia  Eduardo Olavarria  Michael J. Mauro
Affiliation:1. John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey;2. The University of Texas, MD Anderson Cancer Center, Houston, Texas;3. University of Milano Bicocca, San Gerardo Hospital, Monza, Italy;4. Universit?t Heidelberg, Mannheim, Germany;5. Winship Cancer Institute of Emory University, Atlanta, Georgia;6. Centre Hospitalier Lyon‐Sud, Pierre‐Bénite, France;7. UCLA Medical Center, Los Angeles, California;8. Uppsala Universitet, Uppsala, Sweden;9. Bristol‐Myers Squibb, Princeton, New Jersey;10. ICON plc, San Francisco, California;11. S. Eugenio Hospital, Rome, Italy;12. Rocky Mountain Cancer Centers, Boulder, Colorado;13. Spaarne Hospital, Hoofddorp, The Netherlands;14. Centre Hospitalier Annecy‐Genevois, Pringy, France;15. IDGGQ, Institut für med, Kaiserslautern, Germany;16. Federal Almazov North‐West Medical Research Centre, St Petersburg, Russia;17. Hammersmith Hospital, Imperial College London, London, United Kingdom;18. Memorial Sloan‐Kettering Cancer Center, New York City, New York
Abstract:Achieving successful outcomes in chronic phase‐chronic myeloid leukemia (CP‐CML) requires careful monitoring of cytogenetic/molecular responses (CyR/MR). SIMPLICITY (NCT01244750) is an observational study exploring tyrosine kinase inhibitor use and management patterns in patients with CP‐CML receiving first‐line imatinib (n = 416), dasatinib (n = 418) or nilotinib (n = 408) in the US and 6 European countries in routine clinical practice. Twelve‐month follow‐up data of 1242 prospective patients (enrolled October 01 2010‐September 02 2015) are reported. 81% of patients had baseline comorbidities. Treatment selection was based on perceived efficacy over patient comorbidity profile. There was a predominance of imatinib‐treated patients enrolled earlier in the study, with subsequent shift toward dasatinib‐ and nilotinib‐treated patients by 2013/2014. Monitoring for either CyR/MR improved over time and was documented for 36%, 82%, and 95% of patients by 3, 6, and 12 months, respectively; 5% had no documentation of CyR/MR monitoring during the first year of therapy. Documentation of MR/CyR testing was higher in Europe than the US (P < .001) and at academic versus community practices (P = .001). Age <65 years, patients being followed at sites within Europe, those followed at academic centers and patients no longer on first‐line therapy were more likely to be monitored by 12 months. SIMPLICITY demonstrates that the NCCN and ELN recommendations on response monitoring have not been consistently translated into routine clinical practice. In the absence of appropriate monitoring practices, clinical response to TKI therapy cannot be established, any needed changes to treatment strategy will thus not be implemented, and long‐term patient outcomes are likely to be impacted.
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