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  1. Book ; Online: Our Journey Beyond Sunset Boulevard

    Gordon, Erlinda M / Hall, Frederick L

    Evidence-based Analysis of Tumor-Targeted Gene- and Immuno-Therapies Shine a Critical Spotlight on "True" Long-Term Cancer-Free Survival

    2021  

    Keywords Oncology ; cancer immunotherapy
    Language English
    Size 1 electronic resource (56 pages)
    Publisher IntechOpen
    Document type Book ; Online
    Note English
    HBZ-ID HT030647931
    ISBN 9781839694172 ; 1839694173
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  2. Article ; Online: The advent of a pan-collagenous CLOVIS POINT for pathotropic targeting and cancer gene therapy, a retrospective

    Erlinda M. Gordon / Frederick L. Hall

    Frontiers in Molecular Medicine, Vol

    2023  Volume 3

    Abstract: The ‘Clovis Point’—an enabling prehistoric gain-of-function in stone-age tool technologies which empowered the Paleoindian-Americans to hunt, to strike-deep, and to kill designated target megafauna more efficiently—was created biochemically by molecular- ... ...

    Abstract The ‘Clovis Point’—an enabling prehistoric gain-of-function in stone-age tool technologies which empowered the Paleoindian-Americans to hunt, to strike-deep, and to kill designated target megafauna more efficiently—was created biochemically by molecular-genetic bio-engineering. This Biomedical “Clovis Point” was crafted by adapting a broad-spectrum Pan-Collagen Binding Domain (Pan-Coll/CBD) found within the immature pre-pro-peptide segment of Von Willebrand Factor into a constructive series of advanced medical applications. Developed experimentally, preclinically, and clinically into a cutting-edge Biotechnology Platform, the Clovis Point is suitable for 1) solid-state binding of growth factors on collagenous scaffolds for improved orthopedic wound healing, 2) promoting regeneration of injured/diseased tissues; and 3) autologous stem cell capture, expansion, and gene-based therapies. Subsequent adaptations of the high-affinity Pan-Coll/CBD (exposed-collagen-seeking/surveillance function) for intravenous administration in humans, enabled the physiological delivery, aka Pathotropic Targeting to diseased tissues via the modified envelopes of gene vectors; enabling 4) precision tumor-targeting for cancer gene therapy and 5) adoptive/localized immunotherapies, demonstrating improved long-term survival value—thus pioneering a proximal and accessible cell cycle control point for cancer management—empowering modern medical oncologists to address persistent problems of chemotherapy resistance, recurrence, and occult progression of metastatic disease. Recent engineering adaptations have advanced the clinical utility to include the targeted delivery of small molecule APIs: including taxanes, mAbs, and RNA-based therapeutics.
    Keywords pan-collagen-binding domain ; wound healing ; stem cell capture ; cancer gene therapy ; immunotherapy ; deltarex-G ; Computer applications to medicine. Medical informatics ; R858-859.7
    Subject code 610
    Language English
    Publishing date 2023-02-01T00:00:00Z
    Publisher Frontiers Media S.A.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: From Mendel to Gene Therapy.

    Jeffrey, Samantha L / Brigham, Don A / Chawla, Sant P / Federman, Noah / Hall, Frederick L / Gordon, Erlinda M

    Anticancer research

    2023  Volume 43, Issue 10, Page(s) 4257–4261

    Language English
    Publishing date 2023-04-03
    Publishing country Greece
    Document type Letter
    ZDB-ID 604549-2
    ISSN 1791-7530 ; 0250-7005
    ISSN (online) 1791-7530
    ISSN 0250-7005
    DOI 10.21873/anticanres.16620
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: A Phase I/II Investigation of Safety and Efficacy of Nivolumab and

    Gordon, Erlinda M / Angel, Nicole L / Omelchenko, Nadezhda / Chua-Alcala, Victoria S / Moradkhani, Ania / Quon, Doris / Wong, Steven

    Anticancer research

    2023  Volume 43, Issue 5, Page(s) 1993–2002

    Abstract: ... doses of nab-sirolimus at 56, 75 or 100 mg/m: Results: The maximum-tolerated dose was 100 mg/m ...

    Abstract Background/aim: Advanced sarcoma has a poor prognosis. Dysregulation of the mammalian target of rapamycin (mTOR) occurs in various types of cancer. We aimed to determine the safety and efficacy of mTOR inhibitor nab-sirolimus when combined with the immune checkpoint inhibitor nivolumab.
    Patients and methods: Previously treated patients ≥18 years with confirmed diagnosis of advanced sarcoma or tumor with mutations in the mTOR pathway were treated with 3 mg/kg nivolumab intravenously every 3 weeks; escalating doses of nab-sirolimus at 56, 75 or 100 mg/m
    Results: The maximum-tolerated dose was 100 mg/m
    Conclusion: The data indicate that (i) treatment with nivolumab plus nab-sirolimus is safe with no unexpected adverse events; (ii) treatment outcome parameters were not improved by combining nivolumab with nab-sirolimus; and (iii) best responders were patients with undifferentiated pleomorphic sarcoma with PTEN loss and TSC2 mutation and estrogen receptor-positive leiomyosarcoma. Future direction in sarcoma research with nab-sirolimus will be biomarker-based (TSC1/2/mTOR, tumor mutational burden/mismatch repair deficiency etc.).
    MeSH term(s) Humans ; Nivolumab/adverse effects ; Leiomyosarcoma/drug therapy ; Receptors, Estrogen ; Sirolimus/pharmacology ; TOR Serine-Threonine Kinases/genetics ; Sarcoma/drug therapy ; Angiogenesis Inhibitors/therapeutic use ; Mutation ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use
    Chemical Substances Nivolumab (31YO63LBSN) ; Receptors, Estrogen ; Sirolimus (W36ZG6FT64) ; TOR Serine-Threonine Kinases (EC 2.7.11.1) ; Angiogenesis Inhibitors ; MTOR protein, human (EC 2.7.1.1)
    Language English
    Publishing date 2023-04-03
    Publishing country Greece
    Document type Clinical Trial, Phase II ; Clinical Trial, Phase I ; Journal Article
    ZDB-ID 604549-2
    ISSN 1791-7530 ; 0250-7005
    ISSN (online) 1791-7530
    ISSN 0250-7005
    DOI 10.21873/anticanres.16360
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Phase II Trial of

    Wagner, Andrew J / Ravi, Vinod / Riedel, Richard F / Ganjoo, Kristen / Van Tine, Brian A / Chugh, Rashmi / Cranmer, Lee / Gordon, Erlinda M / Hornick, Jason L / Du, Heng / Ding, Li / Schmid, Anita N / Navarro, Willis H / Kwiatkowski, David J / Dickson, Mark A

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology

    2024  Volume 42, Issue 13, Page(s) 1472–1476

    Abstract: Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial ... ...

    Abstract Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in
    MeSH term(s) Humans ; Female ; Male ; Middle Aged ; Perivascular Epithelioid Cell Neoplasms/drug therapy ; Adult ; Aged ; Sirolimus/therapeutic use ; Sirolimus/adverse effects ; Sirolimus/administration & dosage ; Progression-Free Survival ; Antibiotics, Antineoplastic/therapeutic use ; Antibiotics, Antineoplastic/adverse effects
    Chemical Substances Sirolimus (W36ZG6FT64) ; Antibiotics, Antineoplastic
    Language English
    Publishing date 2024-03-01
    Publishing country United States
    Document type Journal Article ; Clinical Trial, Phase II ; Research Support, Non-U.S. Gov't ; Multicenter Study ; Research Support, N.I.H., Extramural
    ZDB-ID 604914-x
    ISSN 1527-7755 ; 0732-183X
    ISSN (online) 1527-7755
    ISSN 0732-183X
    DOI 10.1200/JCO.23.02266
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Tumor protein p53 mutation in archived tumor samples from a 12-year survivor of stage 4 pancreatic ductal adenocarcinoma may predict long-term survival with DeltaRex-G: A case report and literature review.

    Morse, Michael A / Chawla, Sant P / Wong, Terence Z / Bruckner, Howard W / Hall, Frederick L / Gordon, Erlinda M

    Molecular and clinical oncology

    2021  Volume 15, Issue 3, Page(s) 186

    Abstract: DeltaRex-G is a replication-incompetent amphotropic murine leukemia virus-based retroviral vector that displays a collagen-matrix-targeting decapeptide on its surface envelope protein, gp70, and encodes a cytocidal 'dominant negative', i.e. a truncated ... ...

    Abstract DeltaRex-G is a replication-incompetent amphotropic murine leukemia virus-based retroviral vector that displays a collagen-matrix-targeting decapeptide on its surface envelope protein, gp70, and encodes a cytocidal 'dominant negative', i.e. a truncated construct of the executive cyclin G1 (
    Language English
    Publishing date 2021-07-08
    Publishing country England
    Document type Journal Article
    ZDB-ID 2796865-0
    ISSN 2049-9469 ; 2049-9450
    ISSN (online) 2049-9469
    ISSN 2049-9450
    DOI 10.3892/mco.2021.2348
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Exploiting Oncogenic Drivers along the

    Al-Shihabi, Ahmad / Chawla, Sant P / Hall, Frederick L / Gordon, Erlinda M

    Molecular therapy oncolytics

    2018  Volume 11, Page(s) 122–126

    Language English
    Publishing date 2018-12-12
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 2372-7705
    ISSN 2372-7705
    DOI 10.1016/j.omto.2018.11.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Early-stage

    Chawla, Sant P / Olevsky, Olga / Iyengar, Geeta / Brigham, Don A / Omelchenko, Nadezhda / Thomas, Sonu / Suryamohan, Kushal / Foshag, Leland / Hall, Frederick L / Gordon, Erlinda M

    Anticancer research

    2023  Volume 43, Issue 6, Page(s) 2383–2391

    Abstract: Women with HR+HER2+ early-stage breast cancer are disadvantaged by the lack of clinical trials focused on women ≥70 years of age. In the past years, there has been increasing controversy on the use of toxic chemotherapy as standard of care treatment for ... ...

    Abstract Women with HR+HER2+ early-stage breast cancer are disadvantaged by the lack of clinical trials focused on women ≥70 years of age. In the past years, there has been increasing controversy on the use of toxic chemotherapy as standard of care treatment for early- stage HR+ HER2+ breast carcinoma in older women. With precision medicine coming of age, molecular profiling of tumors and circulating tumor DNA has identified target oncogenes that could be used in designing an optimal treatment for this group of women. This article reviews the current treatment of early-stage triple receptor positive breast cancer, the risks of chemotherapy in older women, and CCNG1, a novel biomarker in development for the use of DeltaRex-G, a CCNG1 inhibitor. Further, future perspectives for DeltaRex-G in older women with early stage CCNG1+ HR+ HER2+ breast cancer are discussed.
    MeSH term(s) Female ; Humans ; Aged ; Receptor, ErbB-2 ; Breast Neoplasms/drug therapy ; Breast Neoplasms/pathology ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Trastuzumab ; Cyclin G1
    Chemical Substances retrovector encoding mutant anti-cyclin G1 ; Receptor, ErbB-2 (EC 2.7.10.1) ; Trastuzumab (P188ANX8CK) ; CCNG1 protein, human ; Cyclin G1
    Language English
    Publishing date 2023-05-27
    Publishing country Greece
    Document type Journal Article ; Review
    ZDB-ID 604549-2
    ISSN 1791-7530 ; 0250-7005
    ISSN (online) 1791-7530
    ISSN 0250-7005
    DOI 10.21873/anticanres.16406
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Activity of TNT: a phase 2 study using talimogene laherparepvec, nivolumab and trabectedin for previously treated patients with advanced sarcomas (NCT# 03886311).

    Chawla, Sant P / Tellez, Walter Andree / Chomoyan, Hripsime / Valencia, Chrysler / Ahari, Amir / Omelchenko, Nadezhda / Makrievski, Stefan / Brigham, Don A / Chua-Alcala, Victoria / Quon, Doris / Moradkhani, Ania / Gordon, Erlinda M

    Frontiers in oncology

    2023  Volume 13, Page(s) 1116937

    Abstract: ... Trabectedin intravenously (1.2 mg/m: Results: Median time of follow-up: 15.2 months. Efficacy analysis ...

    Abstract Background: Intratumoral injection of talimogene laherparepvec evokes a cytotoxic immune response. Therefore, the combination of talimogene laherparepvec with trabectedin and nivolumab may have synergistic effects in advanced sarcomas.
    Patients and methods: This phase 2 trial was conducted from May 30, 2019 to January 31, 2022. Endpoints: Primary: Progression free survival rate at month 12. Secondary: Best overall response, progression free survival rate at 6 and 9 months, overall survival rate at 6, 9, and 12 months, incidence of conversion of an unresectable tumor to a resectable tumor, and incidence of adverse events. Eligible patients had to be ≥ 18 years of age, have advanced histologically proven sarcoma, at least 1 previous chemotherapy regimen, and at least one accessible tumor for intratumoral injection. Treatment: Trabectedin intravenously (1.2 mg/m
    Results: Median time of follow-up: 15.2 months. Efficacy analysis: Thirty-nine patients who had completed at least one treatment cycle and had a follow-up computerized tomography were evaluable for efficacy analysis. Median number of prior therapies: 4 (range 1-11). Progression free survival rate at month 12, 36.7%. Confirmed Best Overall Response by Response Evaluation Criteria in Solid Tumors v1.1 = 3 partial responses, 30 stable disease, 6 progressive disease. Best Overall Response Rate, 7.7%, Disease Control Rate, 84.6%; median progression free survival, 7.8 (95% Confidence Intervals: 4.1-13.1) months; 6-, 9-, 12-month progression free survival rates, 54.5%/45.9%/36.7%; median overall survival 19.3 (95% Confidence Intervals: 12.8 -.) months; 6-, 9- and 12-month overall survival rate, 86.9%/73.3%/73.3%. One patient had a complete surgical resection. Fifty percent of patients had a ≥ grade 3 treatment related adverse events which included anemia (6%), thrombocytopenia (6%), neutropenia (4%), increased alanine transaminase (4%), decreased left ventricular ejection fraction (4%), dehydration (4%), hyponatremia (4%).
    Conclusions: Taken together these data suggest that the TNT regimen is effective and safe for advanced previously treated sarcomas, and is worth being further studied in a randomized phase 3 trial as first- or second- line treatment for patients with advanced sarcomas.
    Language English
    Publishing date 2023-05-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2649216-7
    ISSN 2234-943X
    ISSN 2234-943X
    DOI 10.3389/fonc.2023.1116937
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: A Phase I-II Study Using Rexin-G Tumor-Targeted Retrovector Encoding a Dominant-Negative Cyclin G1 Inhibitor for Advanced Pancreatic Cancer.

    Chawla, Sant P / Bruckner, Howard / Morse, Michael A / Assudani, Nupur / Hall, Frederick L / Gordon, Erlinda M

    Molecular therapy oncolytics

    2018  Volume 12, Page(s) 56–67

    Abstract: Rexin-G is a replication-incompetent retroviral vector displaying a ... ...

    Abstract Rexin-G is a replication-incompetent retroviral vector displaying a cryptic
    Language English
    Publishing date 2018-12-14
    Publishing country United States
    Document type Journal Article
    ISSN 2372-7705
    ISSN 2372-7705
    DOI 10.1016/j.omto.2018.12.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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