Literature DB >> 27815356

KTN0158, a Humanized Anti-KIT Monoclonal Antibody, Demonstrates Biologic Activity against both Normal and Malignant Canine Mast Cells.

Cheryl A London1,2, Heather L Gardner2, Sarah Rippy2, Gerald Post3, Krista La Perle4, Linda Crew5, Lori Lopresti-Morrow5, Andrew J Garton5, Gerald McMahon5, Theresa M LaVallee5, Richard Gedrich5.   

Abstract

Purpose: KTN0158 is a novel anti-KIT antibody that potently inhibits wild-type and mutant KIT. This study evaluated the safety, biologic activity, and pharmacokinetic/pharmacodynamics profile of KTN0158 in dogs with spontaneous mast cell tumors (MCT) as a prelude to human clinical applications.Experimental Design: Cell proliferation, KIT phosphorylation, and mast cell degranulation were evaluated in vitro KTN0158 was administered to 4 research dogs to assess clinical effects and cutaneous mast cell numbers. Thirteen dogs with spontaneous MCT were enrolled into a prospective phase I dose-escalating open-label clinical study of KTN0158 evaluating 3 dose levels and 2 schedules and with weekly assessments for response and clinical toxicities.
Results: KTN0158 was a potent inhibitor of human and dog KIT activation and blocked mast cell degranulation in vitro In dogs, KTN0158 was well tolerated and reduced cutaneous mast cell numbers in a dose-dependent manner. Clinical benefit of KTN0158 administration in dogs with MCT (n = 5 partial response; n = 7 stable disease) was observed regardless of KIT mutation status, and decreased KIT phosphorylation was demonstrated in tumor samples. Histopathology after study completion demonstrated an absence of neoplastic cells in the primary tumors and/or metastatic lymph nodes from 4 dogs. Reversible hematologic and biochemical adverse events were observed at doses of 10 and 30 mg/kg. The MTD was established as 10 mg/kg.Conclusions: KTN0158 inhibits KIT phosphorylation, demonstrates an acceptable safety profile in dogs, and provides objective responses in canine MCT patients with and without activating KIT mutations, supporting future clinical evaluation of KTN0158 in people. Clin Cancer Res; 23(10); 2565-74. ©2016 AACR. ©2016 American Association for Cancer Research.

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Year:  2016        PMID: 27815356      PMCID: PMC5418113          DOI: 10.1158/1078-0432.CCR-16-2152

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  45 in total

Review 1.  Cell signaling by receptor tyrosine kinases.

Authors:  J Schlessinger
Journal:  Cell       Date:  2000-10-13       Impact factor: 41.582

2.  Deletion of the KIT gene is associated with liver metastasis and poor prognosis in patients with gastrointestinal stromal tumor in the stomach.

Authors:  Songde Cho; Yasuhiko Kitadai; Shigeto Yoshida; Shinji Tanaka; Masaharu Yoshihara; Kazuhiro Yoshida; Kazuaki Chayama
Journal:  Int J Oncol       Date:  2006-06       Impact factor: 5.650

3.  Spontaneous canine mast cell tumors express tandem duplications in the proto-oncogene c-kit.

Authors:  C A London; S J Galli; T Yuuki; Z Q Hu; S C Helfand; E N Geissler
Journal:  Exp Hematol       Date:  1999-04       Impact factor: 3.084

4.  Acquired resistance to imatinib in gastrointestinal stromal tumor occurs through secondary gene mutation.

Authors:  Cristina R Antonescu; Peter Besmer; Tianhua Guo; Knarik Arkun; Glory Hom; Beata Koryotowski; Margaret A Leversha; Philip D Jeffrey; Diann Desantis; Samuel Singer; Murray F Brennan; Robert G Maki; Ronald P DeMatteo
Journal:  Clin Cancer Res       Date:  2005-06-01       Impact factor: 12.531

Review 5.  Gene of the month: KIT.

Authors:  Riyaadh Roberts; Dhirendra Govender
Journal:  J Clin Pathol       Date:  2015-07-01       Impact factor: 3.411

6.  Response evaluation criteria for solid tumours in dogs (v1.0): a Veterinary Cooperative Oncology Group (VCOG) consensus document.

Authors:  S M Nguyen; D H Thamm; D M Vail; C A London
Journal:  Vet Comp Oncol       Date:  2013-03-28       Impact factor: 2.613

Review 7.  Mast cell tumors in the dog.

Authors:  Cheryl A London; Bernard Seguin
Journal:  Vet Clin North Am Small Anim Pract       Date:  2003-05       Impact factor: 2.093

8.  Structural basis for activation of the receptor tyrosine kinase KIT by stem cell factor.

Authors:  Satoru Yuzawa; Yarden Opatowsky; Zhongtao Zhang; Valsan Mandiyan; Irit Lax; Joseph Schlessinger
Journal:  Cell       Date:  2007-07-27       Impact factor: 41.582

Review 9.  Recent advances in the understanding of mastocytosis: the role of KIT mutations.

Authors:  Alberto Orfao; Andrés C Garcia-Montero; Laura Sanchez; Luis Escribano
Journal:  Br J Haematol       Date:  2007-07       Impact factor: 6.998

10.  Comparing ELISA and surface plasmon resonance for assessing clinical immunogenicity of panitumumab.

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Journal:  J Immunol       Date:  2007-06-01       Impact factor: 5.422

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Review 3.  Introducing fluorescence guided surgery into orthopedic oncology: A systematic review of candidate protein targets for Ewing sarcoma.

Authors:  Sarah E Bosma; Pieter Baa van Driel; Pancras Cw Hogendoorn; Pd Sander Dijkstra; Cornelis Fm Sier
Journal:  J Surg Oncol       Date:  2018-09-13       Impact factor: 3.454

Review 4.  Neuroblastoma Origin and Therapeutic Targets for Immunotherapy.

Authors:  Irina V Kholodenko; Daniel V Kalinovsky; Igor I Doronin; Sergey M Deyev; Roman V Kholodenko
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5.  CD117 (c-Kit) Is Expressed During CD8+ T Cell Priming and Stratifies Sensitivity to Apoptosis According to Strength of TCR Engagement.

Authors:  Guido Frumento; Jianmin Zuo; Kriti Verma; Wayne Croft; Pradeep Ramagiri; Frederick E Chen; Paul Moss
Journal:  Front Immunol       Date:  2019-03-15       Impact factor: 7.561

Review 6.  Canine Cancer: Strategies in Experimental Therapeutics.

Authors:  Douglas H Thamm
Journal:  Front Oncol       Date:  2019-11-15       Impact factor: 6.244

7.  Anti-KIT monoclonal antibody CDX-0159 induces profound and durable mast cell suppression in a healthy volunteer study.

Authors:  Diego Alvarado; Marcus Maurer; Richard Gedrich; Scott B Seibel; Michael B Murphy; Linda Crew; Joel Goldstein; Andrea Crocker; Laura A Vitale; Pamela A Morani; Lawrence J Thomas; Thomas R Hawthorne; Tibor Keler; Diane Young; Elizabeth Crowley; Martin Kankam; Margo Heath-Chiozzi
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  7 in total

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