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Concurrent use of proton pump inhibitors or H2 blockers did not adversely affect nilotinib efficacy in patients with chronic myeloid leukemia
Authors:Ophelia Q P Yin  Frank J Giles  Michele Baccarani  Philipp le Coutre  Ovidiu Chiparus  Neil Gallagher  Giuseppe Saglio  Timothy P Hughes  Andreas Hochhaus  Hagop M Kantarjian  Richard A Larson
Institution:Oncology Clinical Pharmacology, Novartis Pharmaceuticals Corporation, Florham Park, NJ 07932, USA. ophelia.yin@novartis.com
Abstract:

Purpose

The impact of proton pump inhibitors (PPIs) and histamine H2 receptor antagonists (H2 blockers) on the efficacy of nilotinib was evaluated.

Methods

Retrospective analyses were performed in patients with newly diagnosed Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia in chronic phase (CML-CP; N?=?492) and in patients with imatinib-resistant or imatinib-intolerant Ph+ CML-CP (N?=?256) treated with nilotinib.

Results

In the newly diagnosed population, 87 (17.7?%) and 49 (10.0?%) patients received PPIs and H2 blockers, respectively. Major molecular response at 12?months was achieved by 59 (49.6?%) patients who received at least one PPI or H2 blocker (n?=?119) and 153 (41.0?%) patients who did not receive any comedication (n?=?373; P?=?0.13). PPIs and H2 blockers were used by 77 (30.1?%) and 17 (6.6?%) patients with imatinib-resistant or imatinib-intolerant CML-CP, respectively. Major cytogenetic response by 12?months was achieved by 55 (64.0?%) patients who received at least one PPI or H2 blocker (n?=?86) versus 98 (57.6?%) patients who did not receive any comedication (n?=?170; P?=?0.40); 39 (45.3?%) versus 65 (38.2?%), respectively, achieved complete cytogenetic response by 12?months (P?=?0.34). Similar findings were observed in patients who received comedication for >50?% of the time on nilotinib therapy. Nilotinib steady-state trough concentration was not affected by the presence of PPIs or H2 blockers.

Conclusions

Concurrent use of PPIs or H2 blockers did not affect the pharmacokinetics and efficacy of nilotinib in patients with Ph+ CML-CP.
Keywords:
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