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Occurrence of Secondary Malignancies in Chronic Myeloid Leukemia During Therapy with Imatinib Mesylate-Single Institution Experience

INTRODUCTION: Imatinib mesylate (IM) remains the treatment of choice for chronic myeloid leukemia (CML) showing a remarkable efficacy and offers a perspective for long disease-free survival. Due to prolonged administration of IM, the questions about the possible impact on the development of secondar...

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Autores principales: Helbig, Grzegorz, Bober, Grażyna, Seweryn, Marek, Wichary, Ryszard, Tukiendorf, Andrzej, Sedlak, Lech, Oleksy, Tomasz, Kyrcz-Krzemień, Sławomira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Università Cattolica del Sacro Cuore 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283924/
https://www.ncbi.nlm.nih.gov/pubmed/25574362
http://dx.doi.org/10.4084/MJHID.2015.003
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author Helbig, Grzegorz
Bober, Grażyna
Seweryn, Marek
Wichary, Ryszard
Tukiendorf, Andrzej
Sedlak, Lech
Oleksy, Tomasz
Kyrcz-Krzemień, Sławomira
author_facet Helbig, Grzegorz
Bober, Grażyna
Seweryn, Marek
Wichary, Ryszard
Tukiendorf, Andrzej
Sedlak, Lech
Oleksy, Tomasz
Kyrcz-Krzemień, Sławomira
author_sort Helbig, Grzegorz
collection PubMed
description INTRODUCTION: Imatinib mesylate (IM) remains the treatment of choice for chronic myeloid leukemia (CML) showing a remarkable efficacy and offers a perspective for long disease-free survival. Due to prolonged administration of IM, the questions about the possible impact on the development of secondary malignancies (SM) are raised. OBJECTIVE: To investigate the incidence and clinical outcome of secondary malignancies during IM therapy for CML. MATERIAL AND METHODS: The records of 221 CML patients treated with IM between 2003–2013 in a single institution were reviewed. The Poisson regression model was used to estimate the relative risks for SM and death in CML patients. RESULTS: Secondary malignancies developed in eight out of the 221 patients (3.6%) receiving IM for a median of 61 months (range, 10–137 months). Female/male ratio was 5/3. Two patients were diagnosed with their CML at accelerated phase whereas 6 had chronic phase. The median age at IM initiation was 58 years (range, 31–72 years). Five of these 8 SM patients received IM after other treatments failure: interferon α (n=5), hydroxyurea (n=4) and cytarabine (n=1). Three patients received IM as a frontline therapy. All patients were on IM at 400mg daily at SM occurrence. The therapy for SM included surgery (n=3), chemotherapy only (n=3), and chemotherapy followed by radiotherapy (n=1). One patient did not receive treatment due to disseminated disease. All CML patients were in hematologic and complete cytogenetic response (CCR) at the time of SM development. All of them also met the criteria for major molecular response (BCR-ABL(IS) ≤0.1%). They continued their IM while receiving treatment for SM. Among eight patients with SM, five patients are alive and remain in CCR on IM whereas three patients died due to SM. The risks for SM development as well as death due to SM in CML patients were not statistically increased if compared to age-adjusted population. CONCLUSIONS: The association between IM therapy for CML and SM development has not been found.
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spelling pubmed-42839242015-01-08 Occurrence of Secondary Malignancies in Chronic Myeloid Leukemia During Therapy with Imatinib Mesylate-Single Institution Experience Helbig, Grzegorz Bober, Grażyna Seweryn, Marek Wichary, Ryszard Tukiendorf, Andrzej Sedlak, Lech Oleksy, Tomasz Kyrcz-Krzemień, Sławomira Mediterr J Hematol Infect Dis Original Article INTRODUCTION: Imatinib mesylate (IM) remains the treatment of choice for chronic myeloid leukemia (CML) showing a remarkable efficacy and offers a perspective for long disease-free survival. Due to prolonged administration of IM, the questions about the possible impact on the development of secondary malignancies (SM) are raised. OBJECTIVE: To investigate the incidence and clinical outcome of secondary malignancies during IM therapy for CML. MATERIAL AND METHODS: The records of 221 CML patients treated with IM between 2003–2013 in a single institution were reviewed. The Poisson regression model was used to estimate the relative risks for SM and death in CML patients. RESULTS: Secondary malignancies developed in eight out of the 221 patients (3.6%) receiving IM for a median of 61 months (range, 10–137 months). Female/male ratio was 5/3. Two patients were diagnosed with their CML at accelerated phase whereas 6 had chronic phase. The median age at IM initiation was 58 years (range, 31–72 years). Five of these 8 SM patients received IM after other treatments failure: interferon α (n=5), hydroxyurea (n=4) and cytarabine (n=1). Three patients received IM as a frontline therapy. All patients were on IM at 400mg daily at SM occurrence. The therapy for SM included surgery (n=3), chemotherapy only (n=3), and chemotherapy followed by radiotherapy (n=1). One patient did not receive treatment due to disseminated disease. All CML patients were in hematologic and complete cytogenetic response (CCR) at the time of SM development. All of them also met the criteria for major molecular response (BCR-ABL(IS) ≤0.1%). They continued their IM while receiving treatment for SM. Among eight patients with SM, five patients are alive and remain in CCR on IM whereas three patients died due to SM. The risks for SM development as well as death due to SM in CML patients were not statistically increased if compared to age-adjusted population. CONCLUSIONS: The association between IM therapy for CML and SM development has not been found. Università Cattolica del Sacro Cuore 2015-01-01 /pmc/articles/PMC4283924/ /pubmed/25574362 http://dx.doi.org/10.4084/MJHID.2015.003 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Helbig, Grzegorz
Bober, Grażyna
Seweryn, Marek
Wichary, Ryszard
Tukiendorf, Andrzej
Sedlak, Lech
Oleksy, Tomasz
Kyrcz-Krzemień, Sławomira
Occurrence of Secondary Malignancies in Chronic Myeloid Leukemia During Therapy with Imatinib Mesylate-Single Institution Experience
title Occurrence of Secondary Malignancies in Chronic Myeloid Leukemia During Therapy with Imatinib Mesylate-Single Institution Experience
title_full Occurrence of Secondary Malignancies in Chronic Myeloid Leukemia During Therapy with Imatinib Mesylate-Single Institution Experience
title_fullStr Occurrence of Secondary Malignancies in Chronic Myeloid Leukemia During Therapy with Imatinib Mesylate-Single Institution Experience
title_full_unstemmed Occurrence of Secondary Malignancies in Chronic Myeloid Leukemia During Therapy with Imatinib Mesylate-Single Institution Experience
title_short Occurrence of Secondary Malignancies in Chronic Myeloid Leukemia During Therapy with Imatinib Mesylate-Single Institution Experience
title_sort occurrence of secondary malignancies in chronic myeloid leukemia during therapy with imatinib mesylate-single institution experience
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283924/
https://www.ncbi.nlm.nih.gov/pubmed/25574362
http://dx.doi.org/10.4084/MJHID.2015.003
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