Ponatinib efficacy and safety in Philadelphia chromosome–positive leukemia: final 5-year results of the phase 2 PACE trial

Jörge E. Cortes(The University of Texas MD Anderson Cancer Center), Dong‐Wook Kim(The Catholic University of Korea Seoul St. Mary's Hospital), Javier Pinilla‐Ibarz(Moffitt Cancer Center), Philipp D. le Coutre(Charité - Universitätsmedizin Berlin), Ronald Paquette(Cedars-Sinai Medical Center), Charles Chuah(National University of Singapore), Franck E. Nicolini(Hôpital Lyon Sud), Jane F. Apperley(Imperial College London), H. Jean Khoury(Emory University), Moshe Talpaz(University of Michigan), Daniel J. DeAngelo(Dana-Farber Cancer Institute), Elisabetta Abruzzese(St. Eugenio Hospital), Delphine Réa(Hôpital Saint-Louis), Michele Baccarani(University of Bologna), Martin C. Müller(Heidelberg University), Carlo Gambacorti‐Passerini(University of Milano-Bicocca), Stephanie Lustgarten(Takeda (United States)), Victor M. Rivera(Takeda (United States)), Frank G. Haluska(Takeda (United States)), François Guilhot(Inserm), Michael W. Deininger(University of Utah), Andreas Hochhaus(Jena University Hospital), Timothy P. Hughes(South Australian Health and Medical Research Institute), Neil P. Shah(University of California, San Francisco), Hagop M. Kantarjian(The University of Texas MD Anderson Cancer Center)
Blood
March 22, 2018
Cited by 581Open Access
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Abstract

This analysis focuses on chronic-phase CML (CP-CML) patients (n = 270) with 56.8-month median follow-up. Among 267 evaluable patients, 60%, 40%, and 24% achieved major cytogenetic response (MCyR), major molecular response (MMR), and 4.5-log molecular response, respectively. The probability of maintaining MCyR for 5 years was 82% among responders. Dose reductions were implemented in October 2013 to decrease the risk of arterial occlusive events (AOEs); ≥90% of CP-CML patients who had achieved MCyR or MMR maintained response 40 months after elective dose reductions. Estimated 5-year overall survival was 73%. In CP-CML patients, the most common treatment-emergent adverse events were rash (47%), abdominal pain (46%), thrombocytopenia (46%), headache (43%), dry skin (42%), and constipation (41%). The cumulative incidence of AOEs in CP-CML patients increased over time to 31%, while the exposure-adjusted incidence of new AOEs (15.8 and 4.9 per 100 patient-years in years 1 and 5, respectively) did not increase over time. These final PACE results demonstrate ponatinib provides durable and clinically meaningful responses, irrespective of dose reductions, in this population of heavily pretreated CP-CML patients. This trial was registered at www.clinicaltrials.gov as #NCT01207440.


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