Literature DB >> 20302388

Dasatinib and nilotinib in imatinib-resistant Philadelphia-positive chronic myelogenous leukemia: a 'head-to-head comparison'.

Gianantonio Rosti1, Fausto Castagnetti, Gabriele Gugliotta, Francesca Palandri, Giovanni Martinelli, Michele Baccarani.   

Abstract

Imatinib has revolutionized the treatment of patients with chronic myeloid leukemia (CML). However, some patients may experience resistance or intolerance to imatinib over time. For these patients, two excellent therapeutic options are available. Dasatinib, approved in 2006 for the treatment of patients with CML in all phases who experience imatinib resistance or intolerance, has displayed significant efficacy, with a 2-year follow-up showing durable hematologic and cytogenetic responses, as well as prolonged progression-free and overall survival. Nilotinib was approved in 2007 for the treatment of patients with CML in chronic phase or CML in accelerated phase, resistant or intolerant to prior therapy including imatinib, based on strong efficacy as well as a favorable safety profile. Several factors, including mutation status, patient history, and existing comorbidities can impact the decision to use dasatinib or nilotinib, or pursue other options such as allogeneic stem cell transplant. The purpose of this review article is to shed light on a further consideration when deciding which agent to use, based on the efficacy and safety of dasatinib and nilotinib. This consideration involves the differences in both the imatinib-resistant and -intolerant patients enrolled in the pivotal studies for each agent, as well as other trial criteria.

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Year:  2010        PMID: 20302388     DOI: 10.3109/10428191003637282

Source DB:  PubMed          Journal:  Leuk Lymphoma        ISSN: 1026-8022


  11 in total

1.  Reduced intensity conditioning is superior to nonmyeloablative conditioning for older chronic myelogenous leukemia patients undergoing hematopoietic cell transplant during the tyrosine kinase inhibitor era.

Authors:  Erica Warlick; Kwang Woo Ahn; Tanya L Pedersen; Andrew Artz; Marcos de Lima; Michael Pulsipher; Gorgun Akpek; Mahmoud Aljurf; Jean-Yves Cahn; Mitchell Cairo; Yi-Bin Chen; Brenda Cooper; Abhinav Deol; Sergio Giralt; Vikas Gupta; H Jean Khoury; Holbrook Kohrt; Hillard M Lazarus; Ian Lewis; Richard Olsson; Joseph Pidala; Bipin N Savani; Matthew Seftel; Gerard Socié; Martin Tallman; Celaettin Ustun; Ravi Vij; Lars Vindeløv; Daniel Weisdorf
Journal:  Blood       Date:  2012-03-09       Impact factor: 22.113

Review 2.  Jakinibs: a new class of kinase inhibitors in cancer and autoimmune disease.

Authors:  Apostolos Kontzias; Alexander Kotlyar; Arian Laurence; Paul Changelian; John J O'Shea
Journal:  Curr Opin Pharmacol       Date:  2012-07-19       Impact factor: 5.547

3.  Tyrosine kinase inhibitors: Multi-targeted or single-targeted?

Authors:  Fleur Broekman; Elisa Giovannetti; Godefridus J Peters
Journal:  World J Clin Oncol       Date:  2011-02-10

4.  The N550K/H mutations in FGFR2 confer differential resistance to PD173074, dovitinib, and ponatinib ATP-competitive inhibitors.

Authors:  Sara A Byron; Huaibin Chen; Andreas Wortmann; David Loch; Michael G Gartside; Farhad Dehkhoda; Steven P Blais; Thomas A Neubert; Moosa Mohammadi; Pamela M Pollock
Journal:  Neoplasia       Date:  2013-08       Impact factor: 5.715

5.  Extensive pleural and pericardial effusion in chronic myeloid leukemia during treatment with dasatinib at 100 mg or 50 mg daily.

Authors:  Maria-Theresa Krauth; Susanne Herndlhofer; Maria-Theresa Schmook; Gerlinde Mitterbauer-Hohendanner; Ernst Schlögl; Peter Valent
Journal:  Haematologica       Date:  2010-10-07       Impact factor: 9.941

6.  The CRKL gene encoding an adaptor protein is amplified, overexpressed, and a possible therapeutic target in gastric cancer.

Authors:  Hiroko Natsume; Kazuya Shinmura; Hong Tao; Hisaki Igarashi; Masaya Suzuki; Kiyoko Nagura; Masanori Goto; Hidetaka Yamada; Matsuyoshi Maeda; Hiroyuki Konno; Satoki Nakamura; Haruhiko Sugimura
Journal:  J Transl Med       Date:  2012-07-03       Impact factor: 5.531

7.  Nilotinib-induced vasculopathy: identification of vascular endothelial cells as a primary target site.

Authors:  E Hadzijusufovic; K Albrecht-Schgoer; K Huber; G Hoermann; F Grebien; G Eisenwort; W Schgoer; S Herndlhofer; C Kaun; M Theurl; W R Sperr; U Rix; I Sadovnik; B Jilma; G H Schernthaner; J Wojta; D Wolf; G Superti-Furga; R Kirchmair; P Valent
Journal:  Leukemia       Date:  2017-07-31       Impact factor: 11.528

8.  Analysis of adverse events associated with dasatinib and nilotinib treatments in chronic-phase chronic myeloid leukemia patients outside clinical trials.

Authors:  Koung Jin Suh; Ji Yun Lee; Dong-Yeop Shin; Youngil Koh; Soo-Mee Bang; Sung-Soo Yoon; Seonyang Park; Inho Kim; Jeong-Ok Lee
Journal:  Int J Hematol       Date:  2017-04-04       Impact factor: 2.490

9.  Nilotinib exacerbates diabetes mellitus by decreasing secretion of endogenous insulin.

Authors:  Yoshikiyo Ito; Toshihiro Miyamoto; Yong Chong; Toshinobu Maki; Koichi Akashi; Tomohiko Kamimura
Journal:  Int J Hematol       Date:  2012-11-23       Impact factor: 2.490

10.  Machine Learning Approaches to Predict Hepatotoxicity Risk in Patients Receiving Nilotinib.

Authors:  Jung-Sun Kim; Ji-Min Han; Yoon-Sook Cho; Kyung-Hee Choi; Hye-Sun Gwak
Journal:  Molecules       Date:  2021-05-31       Impact factor: 4.411

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