TY - JOUR
T1 - First-line treatment selection and early monitoring patterns in chronic phase-chronic myeloid leukemia in routine clinical practice
T2 - SIMPLICITY
AU - Goldberg, Stuart L.
AU - Cortes, Jorge E.
AU - Gambacorti-Passerini, Carlo
AU - Hehlmann, Rüdiger
AU - Khoury, H. Jean
AU - Michallet, Mauricette
AU - Paquette, Ron L.
AU - Simonsson, Bengt
AU - Zyczynski, Teresa
AU - Foreman, Aimee
AU - Abruzzese, Elisabetta
AU - Andorsky, David
AU - Beeker, Aart
AU - Cony-Makhoul, Pascale
AU - Hansen, Richard
AU - Lomaia, Elza
AU - Olavarria, Eduardo
AU - Mauro, Michael J.
N1 - Funding Information:
Novartis, and Pfizer. JC has received grants and/or consultancy fees from Ariad, BMS, Novartis, Pfizer and Teva. CGP has received grants and consultany fees from BMS, and honoraria/grants from Pfizer. RH has received consultancy fees from BMS and grants from Novartis. JK has received grants from BMS, Pfizer, Ariad and Teva. MMichallet reports grants from BMS, consultant fees/honoraria from BMS, Pfizer, Novartis, Astellas Pharma, MSD and Genzyme. RP and BS declare no conflict of interest. TZ is a BMS employee, and AF an employee of ICON Clinical Research. EA has received grants from BMS, and consultancy fees from Novartis, Wyeth, Ariad, and Takeda. DA received grants from BMS and Celgene, and consultancy feeds from Gilead, CTI, Janssen and Celgene. AB has received grants from BMS. PCM has received grants/honoraria from BMS and Novartis, and consultancy fees from Pfizer. RHansen has received grants/honoraria from BMS. EL reports consultant fees/honoraria from Novartis, BMS and Pfizer. EO declares no conflict of interest. MMauro has received grants from Novartis Oncology and Ariad/ Takeda, and consultancy fees from BMS, Ariad/Takeda and Pfizer.
Publisher Copyright:
© 2017 The Authors American Journal of Hematology Published by Wiley Periodicals, Inc.
PY - 2017/11
Y1 - 2017/11
N2 - 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.
AB - 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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U2 - 10.1002/ajh.24887
DO - 10.1002/ajh.24887
M3 - Article
C2 - 28815757
AN - SCOPUS:85030213233
SN - 0361-8609
VL - 92
SP - 1214
EP - 1223
JO - American Journal of Hematology
JF - American Journal of Hematology
IS - 11
ER -