Literature DB >> 27815358

Phase I Study of GDC-0425, a Checkpoint Kinase 1 Inhibitor, in Combination with Gemcitabine in Patients with Refractory Solid Tumors.

Jeffrey R Infante1, Antoine Hollebecque2, Sophie Postel-Vinay2,3, Todd M Bauer4, Elizabeth M Blackwood5, Marie Evangelista5, Sami Mahrus5, Franklin V Peale5, Xuyang Lu5, Srikumar Sahasranaman5, Rui Zhu5, Yuan Chen5, Xiao Ding5, Elaine R Murray5, Jennifer L Schutzman5, Jennifer O Lauchle5, Jean-Charles Soria2,3, Patricia M LoRusso6.   

Abstract

Purpose: Chk1 inhibition potentiates DNA-damaging chemotherapy by overriding cell-cycle arrest and genome repair. This phase I study evaluated the Chk1 inhibitor GDC-0425 given in combination with gemcitabine to patients with advanced solid tumors.Experimental Design: Patients received GDC-0425 alone for a 1-week lead-in followed by 21-day cycles of gemcitabine plus GDC-0425. Gemcitabine was initially administered at 750 mg/m2 (Arm A), then increased to 1,000 mg/m2 (Arm B), on days 1 and 8 in a 3 + 3 + 3 dose escalation to establish maximum tolerated dose (MTD). GDC-0425 was initially administered daily for three consecutive days; however, dosing was abbreviated to a single day on the basis of pharmacokinetics and tolerability. TP53 mutations were evaluated in archival tumor tissue. On-treatment tumor biopsies underwent pharmacodynamic biomarker analyses.
Results: Forty patients were treated with GDC-0425. The MTD of GDC-0425 was 60 mg when administered approximately 24 hours after gemcitabine 1,000 mg/m2 Dose-limiting toxicities included thrombocytopenia (n = 5), neutropenia (n = 4), dyspnea, nausea, pyrexia, syncope, and increased alanine aminotransferase (n = 1 each). Common related adverse events were nausea (48%); anemia, neutropenia, vomiting (45% each); fatigue (43%); pyrexia (40%); and thrombocytopenia (35%). The GDC-0425 half-life was approximately 15 hours. There were two confirmed partial responses in patients with triple-negative breast cancer (TP53-mutated) and melanoma (n = 1 each) and one unconfirmed partial response in a patient with cancer of unknown primary origin.Conclusions: Chk1 inhibition with GDC-0425 in combination with gemcitabine was tolerated with manageable bone marrow suppression. The observed preliminary clinical activity warrants further investigation of this chemopotentiation strategy. Clin Cancer Res; 23(10); 2423-32. ©2016 AACR. ©2016 American Association for Cancer Research.

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Year:  2016        PMID: 27815358     DOI: 10.1158/1078-0432.CCR-16-1782

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


  20 in total

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3.  Evaluation of Prexasertib, a Checkpoint Kinase 1 Inhibitor, in a Phase Ib Study of Patients with Squamous Cell Carcinoma.

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Journal:  Clin Cancer Res       Date:  2018-04-11       Impact factor: 12.531

4.  Phase I Study of LY2606368, a Checkpoint Kinase 1 Inhibitor, in Patients With Advanced Cancer.

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Journal:  J Clin Oncol       Date:  2016-04-04       Impact factor: 44.544

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Journal:  Invest New Drugs       Date:  2016-06-27       Impact factor: 3.651

6.  A phase II study to evaluate LY2603618 in combination with gemcitabine in pancreatic cancer patients.

Authors:  Berta Laquente; Jose Lopez-Martin; Donald Richards; Gerald Illerhaus; David Z Chang; George Kim; Philip Stella; Dirk Richel; Cezary Szcylik; Stefano Cascinu; G L Frassineti; Tudor Ciuleanu; Karla Hurt; Scott Hynes; Ji Lin; Aimee Bence Lin; Daniel Von Hoff; Emiliano Calvo
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7.  Combinatorial drug screening of mammary cells with induced mesenchymal transformation to identify drug combinations for triple-negative breast cancer.

Authors:  Sierra A Colavito; James T Platt; Matthew A Held; Zongzhi Liu; Ryan Sokup; David F Stern
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8.  Small-molecule screen reveals synergy of cell cycle checkpoint kinase inhibitors with DNA-damaging chemotherapies in medulloblastoma.

Authors:  Raelene Endersby; Jacqueline Whitehouse; Allison Pribnow; Mani Kuchibhotla; Hilary Hii; Brooke Carline; Suresh Gande; Jennifer Stripay; Mathew Ancliffe; Meegan Howlett; Tobias Schoep; Courtney George; Clara Andradas; Patrick Dyer; Marjolein Schluck; Brett Patterson; Silvia K Tacheva-Gigorova; Matthew N Cooper; Giles Robinson; Clinton Stewart; Stefan M Pfister; Marcel Kool; Till Milde; Amar Gajjar; Terrance Johns; Robert J Wechsler-Reya; Martine F Roussel; Nicholas G Gottardo
Journal:  Sci Transl Med       Date:  2021-01-20       Impact factor: 19.319

9.  Cell cycle perturbation induced by gemcitabine in human tumor cells in cell culture, xenografts and bladder cancer patients: implications for clinical trial designs combining gemcitabine with a Chk1 inhibitor.

Authors:  Ryan Montano; Nadeem Khan; Huagang Hou; John Seigne; Marc S Ernstoff; Lionel D Lewis; Alan Eastman
Journal:  Oncotarget       Date:  2017-06-28

Review 10.  Novel DNA targeted therapies for head and neck cancers: clinical potential and biomarkers.

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Journal:  Oncotarget       Date:  2017-09-16
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