Literature DB >> 20511160

First-line therapy for chronic myeloid leukemia: new horizons and an update.

Giuseppe Saglio1, Michele Baccarani.   

Abstract

Although imatinib has shown unprecedented efficacy in the treatment of newly diagnosed chronic-phase chronic myeloid leukemia (CP-CML), approximately one third of patients could benefit from a more effective treatment strategy. Several trials of next-generation agents and modified imatinib-based treatments are in progress, with the aim of improving on standard imatinib 400 mg per day therapy. In the post-imatinib era, a range of assessments are available for evaluating novel strategies. Based on existing evidence, achieving a complete cytogenetic response (CCyR) within 12 months provides the best prediction of longer-term benefit, although durable response and freedom from disease progression are the main treatment goals. In phase II studies, first-line treatment with dasatinib 100 mg once daily or nilotinib 400 mg twice daily resulted in high rates of CCyR and major molecular response (MMR) compared with historical data, and separate phase III trials are ongoing to compare each of these agents with imatinib for the treatment of newly diagnosed CP-CML. Preliminary results indicated higher 12-month CCyR and MMR and lower progression rates for nilotinib compared with standard-dose imatinib. Conflicting findings were reported regarding the ability of high-dose imatinib (800 mg per day) or imatinib plus interferon to induce higher response rates compared with standard-dose imatinib, although no improvement in progression-free survival or overall survival was reported. In the absence of trials comparing novel strategies, the synthesis of emerging data from next-generation agents and modified imatinib-based strategies is likely to be a key area of debate during the next few years.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20511160     DOI: 10.3816/CLML.2010.n.026

Source DB:  PubMed          Journal:  Clin Lymphoma Myeloma Leuk        ISSN: 2152-2669


  5 in total

Review 1.  Functional deregulation of KIT: link to mast cell proliferative diseases and other neoplasms.

Authors:  Glenn Cruse; Dean D Metcalfe; Ana Olivera
Journal:  Immunol Allergy Clin North Am       Date:  2014-03-12       Impact factor: 3.479

Review 2.  First-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinib.

Authors:  Guoqing Wei; Shamudheen Rafiyath; Delong Liu
Journal:  J Hematol Oncol       Date:  2010-11-26       Impact factor: 17.388

3.  Cytomegalovirus-induced Hemorrhagic Colitis in a Patient with Chronic Myeloid Leukemia (Chronic Phase) on Dasatinib as an Upfront Therapy.

Authors:  Mohamed A Yassin; Abdulqadir J Nashwan; Ashraf T Soliman; Anil Yousif; Afra Moustafa; Afaf AlBattah; Shehab F Mohamed; Deena S Mudawi; Sarah Elkourashy; Deena-Raiza Asaari; Hope-Love G Gutierrez; Mohamed Almusharaf; Radwa M Hussein; Abbas H Moustafa; Hatim El Derhoubi; Sarra Boukhris; Samah Kohla; Nader AlDewik
Journal:  Clin Med Insights Case Rep       Date:  2015-08-26

Review 4.  Automated synthesis and visualization of a chemotherapy treatment regimen network.

Authors:  Jeremy Warner; Peter Yang; Gil Alterovitz
Journal:  Stud Health Technol Inform       Date:  2013

5.  Association of differential gene expression with imatinib mesylate and omacetaxine mepesuccinate toxicity in lymphoblastoid cell lines.

Authors:  Hemant Kulkarni; Harald H H Göring; Vincent Diego; Shelley Cole; Ken R Walder; Greg R Collier; John Blangero; Melanie A Carless
Journal:  BMC Med Genomics       Date:  2012-08-23       Impact factor: 3.063

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.