Journals / Turkish Journal of Hematology / 2013 / Cilt: 30 - Sayı: 3

Kronik myeloid lösemi güncel tedavisinde tirozin kinaz inhibitörleri

Current management of chronic myeloid leukemia with tyrosine kinase inhibitors

Pages
247–255
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Complete hematological response, early complete cytogenetic response, faster major molecular response, and deeper, more durable molecular responses (MR4, MR4.5, MR5) are the ultimate goals for TKI-receiving patients with CML.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The clinical outcomes and survival of tyrosine kinase inhibitor (TKI)-treated patients with chronic myeloid leukemia (CML) have been significantly improved.
📊
Key Findings & Data:The aim of this editorial is to outline critical steps of TKI administration practices during the long-term clinical course of CML based on data obtained from randomized clinical trials and international recommendations.
💡
Conclusion & Impact:Complete hematological response, early complete cytogenetic response, faster major molecular response, and deeper, more durable molecular responses (MR4, MR4.5, MR5) are the ultimate goals for TKI-receiving patients with CML.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The clinical outcomes and survival of tyrosine kinase inhibitor (TKI)-treated patients with chronic myeloid leukemia (CML) have been significantly improved. The aim of this editorial is to outline critical steps of TKI administration practices during the long-term clinical course of CML based on data obtained from randomized clinical trials and international recommendations. The efficacy of TKI treatment, TKI side effects, off-target complications, and long-term morbidities due to both the disease and the drug are common arguments in the management of CML. Complete hematological response, early complete cytogenetic response, faster major molecular response, and deeper, more durable molecular responses (MR4, MR4.5, MR5) are the ultimate goals for TKI-receiving patients with CML.

Özet

Kronik myeloid lösemi (KML) tedavisinde tirozin kinaz inhibitörü (TKI) grubu ilaçların kullanımı klinik gidişi ve hastaların yaşam süresini son derece olumlu etkilemiştir. Bu yazının amacı, KMLnin uzun klinik seyri boyunca yapılan TKI uygulamalarının kritik basamaklarını randomize klinik çalışma verileri ve uluslararası rehberler ışığında irdelemektir. KML yönetiminde TKI tedavisinin etkinliği, TKI yan etkileri, ilaçların hedef-dışı komplikasyonları, ve hem hastalık seyrine hem de uygulanan ilaçlara bağlı uzun dönem morbiditeler önemli tartışma noktalarını teşkil etmektedir. Tam hematolojik yanıt, erken tam sitogenetik yanıt, daha çabuk gelişen, daha derin (MR4, MR4.5, MR5), ve dayanıklı major moleküler yanıtlar TKI tedavisi alan KML hastalarında klinik seyir boyunca ulaşılması gereken hedefler konumundadırlar.

🔖

Cite This Article

HAZNEDAROĞLU, C. İ. (2013). Kronik myeloid lösemi güncel tedavisinde tirozin kinaz inhibitörleri. Turkish Journal of Hematology, Cilt: 30 - Sayı: 3, 247–255. https://ajindex.com/articles/413314

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (9)

  1. Ferdinand R, Mitchell SA, Batson S, Tumur I. Treatments for chronic myeloid leukemia: a qualitative systematic review. J Blood Med 2012
  2. Koca E, Haznedaroğlu İC. Imatinib mesylate and the management of chronic myeloid leukemia (CML). Turk J Haematol 2005
  3. Anstrom KJ, Reed SD, Allen AS, Glendenning GA, Schulman KA. Long-term survival estimates for imatinib versus interferon-alpha plus low-dose cytarabine for patients with newly diagnosed chronic-phase chronic myeloid leukemia. Cancer 2004
  4. Kantarjian H, Pasquini R, Hamerschlak N, Rousselot P, Holowiecki J, Jootar S, Robak T, Khoroshko N, Masszi T, Skotnicki A, Hellmann A, Zaritsky A, Golenkov A, Radich J, Hughes T, Countouriotis A, Shah N. Dasatinib or high-dose imatinib for chronic-phase chronic myeloid leukemia after failure of first-line imatinib: a randomized phase 2 trial. Blood 2007
  5. Saydam G, Haznedaroglu IC, Temiz Y, Soysal T, Sucak G, Tombuloglu M, Ozdogu H, Yavuz S, Altintas A, Ozet G, Gulbas Z, Ferhanoglu B, Ilhan O. Retrospective evaluation of patients treated with dasatinib for Philadelphia positive leukemias: Turkish experience of 16 months. UHOD 2009
  6. Luciano L, Seneca E, Annunziata M, Pezzullo L, Danise P, Palmieri F Iovine M, Vallone R, Pane F Efficacy of nilotinib in early chronic phase CML patients who have suboptimal cytogenetic or molecular response to imatinib. A multicentric retrospective study. ASH Annual Meeting Abstracts 2012
  7. Cortes JE, Khoury HJ, Lipton JH, Gambacorti-Passerini C, Brümmendorf TH, Kim DW, Leip E, Kelly V, Besson N, Turnbull K, Kantarjian HM. Baseline predictors of response to bosutinib in patients with chronic phase chronic myeloid leukemia following resistance or intolerance to imatinib plus dasatinib and/or nilotinib. ASH Annual Meeting Abstracts 2012
  8. Hochhaus A, Kim DW, Pinilla-Ibarz J, le Coutre P, Paquette R, Chuah C, Nicolini FE, Apperley J, Khoury HJ, Talpaz M, DiPersio JF DeAngelo D, Abruzzese E, Rea D, Baccarani M, Muller MC, Gambacorti-Passerini C, Wong S, Lustgarten S, Rivera VM, Clackson T, Turner CD, Haluska FG, Guilhot F Deininger MW, Hughes TP, Goldman JM, Shah N, Kantarjian HM, Cortes JE, The PACE Study Group. Molecular responses with ponatinib in patients with Philadelphia chromosome positive (Ph+) leukemia: results from the PACE trial. ASH Annual Meeting Abstracts 2012
  9. Simonsson B, Porkka K, Richter J. Second-generation BCR- ABL kinase inhibi