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Occurrence of secondary malignancies in chronic myeloid leukemia during therapy with imatinib mesylate-single institution experience.
Helbig, Grzegorz; Bober, Grazyna; Seweryn, Marek; Wichary, Ryszard; Tukiendorf, Andrzej; Sedlak, Lech; Oleksy, Tomasz; Kyrcz-Krzemien, Slawomira.
Afiliación
  • Helbig G; Department of Hematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland.
  • Bober G; Department of Hematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland.
  • Seweryn M; Department of Hematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland.
  • Wichary R; Department of Hematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland.
  • Tukiendorf A; Department of Statistics, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice, Poland.
  • Sedlak L; Student Research Group, Department of Hematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland.
  • Oleksy T; Student Research Group, Department of Hematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland.
  • Kyrcz-Krzemien S; Department of Hematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland.
Mediterr J Hematol Infect Dis ; 7(1): e2015003, 2015.
Article en En | MEDLINE | ID: mdl-25574362
ABSTRACT

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.

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Mediterr J Hematol Infect Dis Año: 2015 Tipo del documento: Article País de afiliación: Polonia

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Mediterr J Hematol Infect Dis Año: 2015 Tipo del documento: Article País de afiliación: Polonia