Duke University

Johns Hopkins University

The United States of America, As Represented by the Secretary, Department of Health and Human Services

Other

Cornell Research Foundation Inc.

US Government As Represented by the Secretary of the Army

The University of Texas System

St. Jude Children's Research Hospital

O. Michael Colvin

Henry S. Friedman

Darell D. Bigner

Darell D Bigner

Bert Vogelstein

Hai Yan

Chien-Tsun Kuan

Kenneth W Kinzler

Ira H Pastan

Nickolas Papadopoulos

John Howard Sampson

Matthias Gromeier

Henry S Friedman

Victor E Velculescu

Gregory J Riggins

Sian Jones

Rebecca J Leary

Xiaosong Zhang

D Williams Parsons

Jimmy Cheng-Ho Lin

Giovanni Parmigiani

Philipp Angenendt

Annick Desjardins

Rachel Karchin

Smita K Nair

Chetan Bettegowda

Yuchen Jiao

Vidyalakshmi Chandramohan

Bryan Daehahn Choi

Owen W Griffith

Luis Diaz

Ralph Hruban

Michael R Zalutsky

Nishant Agrawal

Zachary James Reitman

Alan Meeker

Roger McLendon

Hailan Piao

Mingqing Cai

Patrick C Gedeon

Charles Pegram

Patrick J Killela

Partha S Chowdhury

Meng Li

Patrick Y Lu

Duane A Mitchell

Richard Beers

Bryan Choi

Amy Heimberger

Laura P Hale

David H Ashley

O Michael Colvin

Bill H Diplas

Allan H Friedman

Michael Brown

Yiping He

Rui Yang

Landon Hansen

Xuhui Bao

Genglin Jin

Donald Williams Parsons

Charles Peagram

Christopher Gentry Duncan

Robert J Schmittling

Gary E Archer

David M Ashley

Thomas P Brent

Smita Nair

Mathias Gromeier

Bryan D Choi

John Sampson

Zachary J Reitman

Williams Parsons

Kenneth Kinzler

Nickolas Papadapoulos

Human clinical use of a chimeric poliovirus construct has demonstrated excellent anti-tumor effect. The mechanism of action is believed to involve both viral oncolysis as well as immune recruitment, both of which lead to necrosis in the area of the tumor. No adverse effects have been observed.

Oncolytic poliovirus for human tumors

A reliable assay to specifically detect CD155 in tissue sections has widespread use because CD155 is expressed widely among tumor types. Additionally, detected expression of CD 155 in glioblastoma cells is at levels commensurate with susceptibility to PVSRIPO (a poliovirus construct) infection and killing. An anti-CD155 antibody can achieve mono-specific detection of CD155 in immunoblots of tumor homogenates and immunohistochemistry of tumor formalin fixed, paraffin embedded sections. The assay can be used to determine appropriate use of PVSRIPO in oncolytic immunotherapy against cancers.

Detection of CD-155, the poliovirus receptor

Methods of testing tumor samples for mutational burden and/or for expression profiles permit the prediction of responsiveness of an individual to immunotherapy comprising PVSRIPO. Those predicted to respond are treated with PVSRIPO and those predicted not to respond are treated with other agents.

Methods for predicting tumor response to immunotherapy

Chimeric poliovirus is capable of activating antigen presenting cells. The activation of the antigen presenting cells may be in vitro, ex vivo, or in vivo. The activated antigen presenting cells may be administered alone or with an antigen or vaccine. The activated antigen may be loaded in vitro or ex vivo with antigen to form antigen-loaded, activated, antigen presenting cells. These may be administered therapeutically. Therapeutic administration of antigen presenting cells may be used as an adjuvant to other therapies.

Compositions and methods for activating antigen presenting cells with chimeric poliovirus

D2C7-(scdsFv)-PE38KDEL (D2C7-IT) is a recombinantexotoxin A-based immunotoxin (IT), targeting both wild-type epidermal growth factor receptor (EGFRwt) and mutant EGFR variant III (EGFRvIII) proteins overexpressed in glioblastomas. A good laboratory practice (GLP) manufacturing process was developed to produce sufficient material for a Phase I/II clinical trial. D2C7-IT was expressed under the control of the T7 promoter inBLR (&#x3bb; DE31). D2C7-IT was produced by a 10 L batch fermentation process and was then purified from inclusion bodies using anion exchange, size exclusion, and an endotoxin removal process that achieved a yield of over 300 mg of purified protein.

Production of immunotoxin D2C7&#x2014;(scdsFv)&#x2014;PE38KDEL

We surveyed 1,230 tumors of 60 different types and found that tumors could be divided into types with low (&#x3c;15%) and high (&#x2265;15%) frequencies of TERT promoter mutations. The nine TERT-high tumor types almost always originated in tissues with relatively low rates of self renewal, including melanomas, liposarcomas, hepatocellular carcinomas, urothelial carcinomas, squamous cell carcinomas of the tongue, medulloblastomas, and subtypes of gliomas (including 83% of primary glioblastoma, the most common brain tumor type). TERT and ATRX mutations were mutually exclusive, suggesting that these two genetic mechanisms confer equivalent selective growth advantages. In addition to their implications for understanding the relationship between telomeres and tumorigenesis, TERT mutations provide a biomarker for the early detection of urinary tract and liver tumors and aid in the classification and prognostication of brain tumors.

promoter mutations in gliomas and a subset of tumors

We determined the sequence of ATRX and DAXX in 447 cancers from various sites. We found mutations most commonly in pediatric glioblastoma multiformae (GBM) (11.1%), adult GBM (6.5%), oligodendrogliomas (7.7%) and medulloblastomas (1.5%); and showed that Alternative Lengthening of Telomeres (ALT), a telomerase-independent telomere maintenance mechanism found in cancers that have not activated telomerase, perfectly correlated with somatic mutations of either gene. In contrast, neuroblastomas, and adenocarcinomas of the ovary, breast, and pancreas were negative for mutations in ATRX and DAXX. Alterations in ATRX or DAXX define a specific molecular pathway that is closely associated with an alternative telomere maintenance function in human cancers.

Somatic mutations in ATRX in brain cancer

Regional, tumor-targeted, cytotoxic therapy, such as D2C7-immunotoxin (D2C7-IT), not only specifically target and destroy tumor cells, but in the process initiate immune events that promote an in situ vaccine effect. The antitumor effects are amplified by immune checkpoint blockade which engenders a long-term systemic immune response that effectively eliminates all tumor cells.

Combination therapy of immunotoxin and checkpoint inhibitor

We found mutations of the R132 residue of isocitrate dehydrogenase 1 (IDH1) in the majority of grade II and III astrocytomas and oligodendrogliomas as well as in glioblastomas that develop from these lower grade lesions. Those tumors without mutations in IDH1 often had mutations at the analogous R172 residue of the closely related IDH2 gene. These findings have important implications for the pathogenesis and diagnosis of malignant gliomas.

Genetic alterations in isocitrate dehydrogenase and other genes in malignant glioma

We found mutations of the R132 residue of isocitrate dehydrogenase 1 (IDH1) in the majority of grade II and III astrocytomas and oligodendrogliomas as well as in gliblastomas that develop from these lower grade lesions. Those tumors without mutations in IDH1 often had mutations at the analogous R172 residue of the closely related IDH2 gene. These findings have important implications for the pathogenesis and diagnosis of malignant gliomas.

Human clinical use of a chimeric poliovirus construct has demonstrated excellent anti-tumor effect. Combination with immune checkpoint inhibitors increases the anti-tumor effect. Tumors of different types are susceptible to the combination treatment, including but not limited to melanoma, glioglastoma, renal cell carcinoma, prostate cancer, breast cancer, lung cancer, medulloblastoma, and colorectal cancer.

Combination treatment

Human clinical use of a chimeric poliovirus construct has demonstrated excellent anti-tumor effect. Sequential treatment with the virus construct followed by chemotherapy drugs increases the anti-tumor effect. Tumors of different types are susceptible to the combination treatment, including but not limited to melanoma, glioblastoma, renal cell carcinoma, prostate cancer, breast cancer, lung cancer, medulloblastoma, and colorectal cancer.

Sequential anti-cancer treatment

Tert promoter mutations in gliomas and a subset of tumors

Growing community of inventors

Mebane, NC, United States of America

Darell D Bigner