Talimogene Laherparepvec (T-VEC) and Other Oncolytic Viruses for the Treatment of Melanoma DOI
Praveen K. Bommareddy,

Anand Patel,

Saamia Hossain

et al.

American Journal of Clinical Dermatology, Journal Year: 2016, Volume and Issue: 18(1), P. 1 - 15

Published: Dec. 17, 2016

Language: Английский

Approaches to treat immune hot, altered and cold tumours with combination immunotherapies DOI
Jérôme Galon, Daniela Bruni

Nature Reviews Drug Discovery, Journal Year: 2019, Volume and Issue: 18(3), P. 197 - 218

Published: Jan. 4, 2019

Language: Английский

Citations

2639

Cancer immunotherapy: the beginning of the end of cancer? DOI Creative Commons
Sofia Farkona, Eleftherios P. Diamandis, Ivan M. Blasutig

et al.

BMC Medicine, Journal Year: 2016, Volume and Issue: 14(1)

Published: May 5, 2016

These are exciting times for cancer immunotherapy. After many years of disappointing results, the tide has finally changed and immunotherapy become a clinically validated treatment cancers. Immunotherapeutic strategies include vaccines, oncolytic viruses, adoptive transfer ex vivo activated T natural killer cells, administration antibodies or recombinant proteins that either costimulate cells block so-called immune checkpoint pathways. The recent success several immunotherapeutic regimes, such as monoclonal antibody blocking cytotoxic lymphocyte-associated protein 4 (CTLA-4) programmed cell death 1 (PD1), boosted development this modality, with consequence new therapeutic targets schemes which combine various immunological agents now being described at breathtaking pace. In review, we outline some main in (cancer cellular immunotherapy, blockade, viruses) discuss progress synergistic design immune-targeting combination therapies.

Language: Английский

Citations

1073

Cold Tumors: A Therapeutic Challenge for Immunotherapy DOI Creative Commons
Paola Bonaventura, Tala Shekarian, Vincent Alcazer

et al.

Frontiers in Immunology, Journal Year: 2019, Volume and Issue: 10

Published: Feb. 7, 2019

Therapeutic monoclonal antibodies targeting immune checkpoints (ICPs) have changed the treatment landscape of many tumors. However, response rate remains relatively low in most cases. A major factor involved initial resistance to ICP inhibitors is lack or paucity tumor T cell infiltration, characterizing so-called "cold tumors". In this review, we describe main mechanisms absence including antigens, defect antigen presentation, activation and deficit homing into bed. We discuss then different therapeutic approaches that could turn cold hot way, specific therapies are proposed according their mechanism action. addition, "supra-physiological" therapies, such as recruiting bispecific Chimeric Antigen Receptor (CAR) cells, may be active regardless involved, especially MHC class I negative The determination factors implicated preexisting infiltration crucial for development adapted algorithms treatments

Language: Английский

Citations

932

A Review of Cancer Immunotherapy: From the Past, to the Present, to the Future DOI Creative Commons
Khashayar Esfahani,

Liya Roudaia,

Najwa Buhlaiga

et al.

Current Oncology, Journal Year: 2020, Volume and Issue: 27(12), P. 87 - 97

Published: April 1, 2020

Compared with previous standards of care (including chemotherapy, radiotherapy, and surgery), cancer immunotherapy has brought significant improvements for patients in terms survival quality life. Immunotherapy now firmly established itself as a novel pillar care, from the metastatic stage to adjuvant neoadjuvant settings numerous types. In this review article, we highlight how history paved way discoveries that are part standard care. We also current pitfalls limitations checkpoint research fields personalized vaccines, autoimmunity, microbiome, tumour microenvironment, metabolomics is aiming solve those challenges.

Language: Английский

Citations

806

The future of cancer immunotherapy: microenvironment-targeting combinations DOI Creative Commons
Yonina R. Murciano‐Goroff, Allison Betof Warner, Jedd D. Wolchok

et al.

Cell Research, Journal Year: 2020, Volume and Issue: 30(6), P. 507 - 519

Published: May 28, 2020

Abstract Immunotherapy holds the potential to induce durable responses, but only a minority of patients currently respond. The etiologies primary and secondary resistance immunotherapy are multifaceted, deriving not from tumor intrinsic factors, also complex interplay between cancer its microenvironment. In addressing frontiers in clinical immunotherapy, we describe two categories approaches design novel drugs combination therapies: first involves direct modification tumor, while second indirectly enhances immunogenicity through alteration By systematically factors that mediate resistance, able identify mechanistically-driven improve outcomes.

Language: Английский

Citations

617

Integrating oncolytic viruses in combination cancer immunotherapy DOI
Praveen K. Bommareddy, Megha Shettigar, Howard L. Kaufman

et al.

Nature reviews. Immunology, Journal Year: 2018, Volume and Issue: 18(8), P. 498 - 513

Published: May 9, 2018

Language: Английский

Citations

563

Autophagy, Inflammation, and Immunity: A Troika Governing Cancer and Its Treatment DOI Creative Commons
Zhenyu Zhong, Elsa Sánchez‐López, Michael Karin

et al.

Cell, Journal Year: 2016, Volume and Issue: 166(2), P. 288 - 298

Published: July 1, 2016

Language: Английский

Citations

548

Oncolytic Viruses in Cancer Treatment DOI Open Access
Sean E. Lawler, Maria C. Speranza,

Choi-Fong Cho

et al.

JAMA Oncology, Journal Year: 2016, Volume and Issue: 3(6), P. 841 - 841

Published: July 21, 2016

Oncolytic viruses (OVs) are emerging as important agents in cancer treatment. offer the attractive therapeutic combination of tumor-specific cell lysis together with immune stimulation, therefore acting potential situ tumor vaccines. Moreover, OVs can be engineered for optimization selectivity and enhanced stimulation readily combined other agents. The effectiveness has been demonstrated many preclinical studies recently humans, US Food Drug Administration approval oncolytic herpesvirus talimogene laherparepvec advanced melanoma, a major breakthrough field. Thus, OV approach to therapy is becoming more interesting scientists, clinicians, public. main purpose this review give basic overview clinical development provide description current status trials.In 2016 approximately 40 trials recruiting patients, using range multiple types. There also planning stages. Therefore, we now most active period history several currently being tested additional derivatives. In trials, there number specific areas that should considered, including viral pharmacokinetics pharmacodynamics, toxic effects, monitoring patients' status. Clinical increasingly focused on their stimulatory properties, which may work synergistically checkpoint inhibitors strategies treatment human cancer.Oncolytic an area research. ability these harness antitumor immunity appears key success. Combinatorial blockade have started results awaited great interest.

Language: Английский

Citations

506

Cancer vaccines as promising immuno-therapeutics: platforms and current progress DOI Creative Commons
Jian Liu,

Minyang Fu,

Manni Wang

et al.

Journal of Hematology & Oncology, Journal Year: 2022, Volume and Issue: 15(1)

Published: March 18, 2022

Abstract Research on tumor immunotherapy has made tremendous progress in the past decades, with numerous studies entering clinical evaluation. The cancer vaccine is considered a promising therapeutic strategy of solid tumors. Cancer stimulates anti-tumor immunity antigens, which could be delivered form whole cells, peptides, nucleic acids, etc . Ideal vaccines overcome immune suppression tumors and induce both humoral cellular immunity. In this review, we introduced working mechanism summarized four platforms for development. We also highlighted research vaccines, especially focusing their application efficacy, might hopefully facilitate future design vaccine.

Language: Английский

Citations

488

Emerging Concepts for Immune Checkpoint Blockade-Based Combination Therapies DOI Creative Commons
Roberta Zappasodi, Taha Merghoub, Jedd D. Wolchok

et al.

Cancer Cell, Journal Year: 2018, Volume and Issue: 33(4), P. 581 - 598

Published: April 1, 2018

Language: Английский

Citations

469