Your browser doesn't support javascript.
loading
PF-06463922, an ALK/ROS1 Inhibitor, Overcomes Resistance to First and Second Generation ALK Inhibitors in Preclinical Models.
Zou, Helen Y; Friboulet, Luc; Kodack, David P; Engstrom, Lars D; Li, Qiuhua; West, Melissa; Tang, Ruth W; Wang, Hui; Tsaparikos, Konstantinos; Wang, Jinwei; Timofeevski, Sergei; Katayama, Ryohei; Dinh, Dac M; Lam, Hieu; Lam, Justine L; Yamazaki, Shinji; Hu, Wenyue; Patel, Bhushankumar; Bezwada, Divya; Frias, Rosa L; Lifshits, Eugene; Mahmood, Sidra; Gainor, Justin F; Affolter, Timothy; Lappin, Patrick B; Gukasyan, Hovhannes; Lee, Nathan; Deng, Shibing; Jain, Rakesh K; Johnson, Ted W; Shaw, Alice T; Fantin, Valeria R; Smeal, Tod.
Afiliación
  • Zou HY; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Friboulet L; Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.
  • Kodack DP; Department of Radiation Oncology, Edwin L. Steele Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
  • Engstrom LD; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Li Q; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • West M; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Tang RW; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Wang H; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Tsaparikos K; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Wang J; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Timofeevski S; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Katayama R; Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo 135-8550, Japan.
  • Dinh DM; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Lam H; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Lam JL; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Yamazaki S; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Hu W; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Patel B; Department of Radiation Oncology, Edwin L. Steele Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
  • Bezwada D; Department of Radiation Oncology, Edwin L. Steele Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
  • Frias RL; Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.
  • Lifshits E; Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.
  • Mahmood S; Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.
  • Gainor JF; Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.
  • Affolter T; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Lappin PB; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Gukasyan H; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Lee N; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Deng S; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Jain RK; Department of Radiation Oncology, Edwin L. Steele Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
  • Johnson TW; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Shaw AT; Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.
  • Fantin VR; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
  • Smeal T; Pfizer World Wide Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA. Electronic address: tod.smeal@pfizer.com.
Cancer Cell ; 28(1): 70-81, 2015 Jul 13.
Article en En | MEDLINE | ID: mdl-26144315
ABSTRACT
We report the preclinical evaluation of PF-06463922, a potent and brain-penetrant ALK/ROS1 inhibitor. Compared with other clinically available ALK inhibitors, PF-06463922 displayed superior potency against all known clinically acquired ALK mutations, including the highly resistant G1202R mutant. Furthermore, PF-06463922 treatment led to regression of EML4-ALK-driven brain metastases, leading to prolonged mouse survival, in a superior manner. Finally, PF-06463922 demonstrated high selectivity and safety margins in a variety of preclinical studies. These results suggest that PF-06463922 will be highly effective for the treatment of patients with ALK-driven lung cancers, including those who relapsed on clinically available ALK inhibitors because of secondary ALK kinase domain mutations and/or brain metastases.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Proteínas Tirosina Quinasas Receptoras / Resistencia a Antineoplásicos / Lactamas Macrocíclicas / Neoplasias / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: Cancer Cell Asunto de la revista: NEOPLASIAS Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Proteínas Tirosina Quinasas Receptoras / Resistencia a Antineoplásicos / Lactamas Macrocíclicas / Neoplasias / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: Cancer Cell Asunto de la revista: NEOPLASIAS Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos
...