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Cancer Immunology Research
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Clinical Trials of Cancer Immunotherapies

Abstract A011: First-in-man clinical trial of intratumoral injection of Clostridiumnovyi-NT spores in patients with treatment-refractory advanced solid tumors: Safety, activity, and immune responses

Filip Janku, Mrinal Gounder, Abdul Mohammad Pezeshki, Ravi Murthy, Andrea Wang-Gillam, Dale Shepard, David S. Hong, Sarina A. Piha-Paul, Anjali Raina, Alexey A. Leontovich, Gary DeCrescenzo, Brent L. Kreider, David Tung, Mary Varterasian, Halle H. Zhang and Khashayarsha Khazaie
Filip Janku
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Mrinal Gounder
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Abdul Mohammad Pezeshki
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Ravi Murthy
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Andrea Wang-Gillam
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Dale Shepard
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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David S. Hong
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Sarina A. Piha-Paul
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Anjali Raina
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Alexey A. Leontovich
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Gary DeCrescenzo
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Brent L. Kreider
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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David Tung
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Mary Varterasian
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Halle H. Zhang
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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Khashayarsha Khazaie
University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Mayo Clinic, Rochester, NY; Washington University School of Medicine Siteman Cancer Center, St. Louis, MO; Cleveland Clinic, Cleveland, OH; BioMed Valley Discoveries, Kansas City, MO.
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DOI: 10.1158/2326-6074.CRICIMTEATIAACR18-A011 Published February 2019
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Abstracts: Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; September 30 - October 3, 2018; New York, NY

Abstract

Bacteriolytic strategies offer unique advantages to combat a broad range of cancers often refractive to conventional chemotherapies and/or radiotherapies. C. novyi-NT is an attenuated strain of Clostridium novyi, a spore-forming, gram-positive, obligate anaerobe that lacks a lethal alpha- toxin, expressed by the parental strain. When administered intravenously or intratumorally with percutaneous injection, C. novyi-NT colonizes and replicates within the hypoxic region of the tumors, eliciting robust, tumor-confined cell lysis. In this first-in-man phase 1 study, patients with injectable treatment-refractory solid tumors received a single intratumoral injection of C. novyi-NT spores across 6 dose cohorts (spore concentrations of 104, 3x104, 105, 3x105, 106, 3x106) using a 3+3 trial design. The primary endpoints were to assess the safety profile, the dose limiting toxicity, and the maximum tolerated dose of C. novyi-NT. Key secondary endpoints included assessments of the preliminary antitumor activity of the injected tumor, an overall response evaluated by RECIST v. 1.1, and the host immune and inflammatory response to C. novyi-NT. Twenty-four patients were enrolled between November, 2013 and April, 2017. A single intratumoral injection of C. novyi-NT led to germination and resultant tumor lysis of injected tumor masses in 46% of patients across all dosing cohorts. The cohort 5 dose of 106 spores was defined as the maximum tolerated dose. Dose-limiting toxicities were grade 4 sepsis and grade 4 gas gangrene (n=1), all in patients with germination. In the 22 evaluable patients, 21 (95%) had stable disease (SD) as the best response for the injected lesion (tumor shrinkage of > 10% was observed in 21% of patients) and 19 (86%) had overall SD as the best response per RECIST 1.1. C. novyi-NT injection resulted in transient serum cytokine responses consistent with inflammasome activity, activation of innate immunity, tissue remodeling, and angiogenesis. Tumor antigen specific ELISPOT assays pre- and post- treatment documented enhanced secretion of IFNγ and TNFα by circulating T-cells, indicating improved systemic tumor specific T-cell responses. Multiparametric in situ immunostaining of core biopsies suggested improved immune cell infiltration in metastatic lesions. These early signs of improved antitumor activity in patients with advanced solid tumors have encouraged a new trial of C. novyi-NT in combination with immune checkpoint inhibitors.

Citation Format: Filip Janku, Mrinal Gounder, Abdul Mohammad Pezeshki, Ravi Murthy, Andrea Wang-Gillam, Dale Shepard, David S. Hong, Sarina A. Piha-Paul, Anjali Raina, Alexey A. Leontovich, Gary DeCrescenzo, Brent L. Kreider, David Tung, Mary Varterasian, Halle H. Zhang, Khashayarsha Khazaie. First-in-man clinical trial of intratumoral injection of Clostridiumnovyi-NT spores in patients with treatment-refractory advanced solid tumors: Safety, activity, and immune responses [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A011.

  • ©2019 American Association for Cancer Research.
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Cancer Immunology Research: 7 (2 Supplement)
February 2019
Volume 7, Issue 2 Supplement
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Abstract A011: First-in-man clinical trial of intratumoral injection of Clostridiumnovyi-NT spores in patients with treatment-refractory advanced solid tumors: Safety, activity, and immune responses
Filip Janku, Mrinal Gounder, Abdul Mohammad Pezeshki, Ravi Murthy, Andrea Wang-Gillam, Dale Shepard, David S. Hong, Sarina A. Piha-Paul, Anjali Raina, Alexey A. Leontovich, Gary DeCrescenzo, Brent L. Kreider, David Tung, Mary Varterasian, Halle H. Zhang and Khashayarsha Khazaie
Cancer Immunol Res February 1 2019 (7) (2 Supplement) A011; DOI: 10.1158/2326-6074.CRICIMTEATIAACR18-A011

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Abstract A011: First-in-man clinical trial of intratumoral injection of Clostridiumnovyi-NT spores in patients with treatment-refractory advanced solid tumors: Safety, activity, and immune responses
Filip Janku, Mrinal Gounder, Abdul Mohammad Pezeshki, Ravi Murthy, Andrea Wang-Gillam, Dale Shepard, David S. Hong, Sarina A. Piha-Paul, Anjali Raina, Alexey A. Leontovich, Gary DeCrescenzo, Brent L. Kreider, David Tung, Mary Varterasian, Halle H. Zhang and Khashayarsha Khazaie
Cancer Immunol Res February 1 2019 (7) (2 Supplement) A011; DOI: 10.1158/2326-6074.CRICIMTEATIAACR18-A011
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