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PTCH1 is a reliable marker for predicting imatinib response in chronic myeloid leukemia patients in chronic phase

Authors :
Eduardo Anguita
Pilar Llamas
Valentín García-Gutiérrez
Santiago Osorio
Ignacio Mahillo-Fernández
Luis Felipe Casado
Carmen Burgaleta
Juan M. Alonso-Domínguez
Ismael Buño
Pedro Sánchez-Godoy
Juan Luis Steegmann
Alicia Arenas
Joaquin Martinez-Lopez
Rafael Del Orbe
María Teresa Gómez-Casares
Rocio N. Salgado
Francisca Ferrer-Marín
Rosa Ayala
Source :
PLoS ONE, Vol 12, Iss 7, p e0181366 (2017), PLoS ONE, Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid, Consejería de Sanidad de la Comunidad de Madrid
Publication Year :
2017
Publisher :
Public Library of Science (PLoS), 2017.

Abstract

Patched homolog 1 gene (PTCH1) expression and the ratio of PTCH1 to Smoothened (SMO) expression have been proposed as prognostic markers of the response of chronic myeloid leukemia (CML) patients to imatinib. We compared these measurements in a realistic cohort of 101 patients with CML in chronic phase (CP) using a simplified qPCR method, and confirmed the prognostic power of each in a competing risk analysis. Gene expression levels were measured in peripheral blood samples at diagnosis. The PTCH1/SMO ratio did not improve PTCH1 prognostic power (area under the receiver operating characteristic curve 0.71 vs. 0.72). In order to reduce the number of genes to be analyzed, PTCH1 was the selected measurement. High and low PTCH1 expression groups had significantly different cumulative incidences of imatinib failure (IF), which was defined as discontinuation of imatinib due to lack of efficacy (5% vs. 25% at 4 years, P = 0.013), probabilities of achieving a major molecular response (81% vs. 53% at first year, P = 0.02), and proportions of early molecular failure (14% vs. 43%, P = 0.015). Every progression to an advanced phase (n = 3) and CML-related death (n = 2) occurred in the low PTCH1 group (P

Details

Language :
English
ISSN :
19326203
Volume :
12
Issue :
7
Database :
OpenAIRE
Journal :
PLoS ONE
Accession number :
edsair.doi.dedup.....173bc9f081eed1d38f0becbe19905359