Toripalimab: the First Domestic Anti-Tumor PD-1 Antibody in China.

Front Immunol

Department of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.

Published: February 2022

AI Article Synopsis

  • Toripalimab (Tuoyi™) is a monoclonal antibody designed to block the PD-1 protein, which is involved in immune response regulation, and was developed by Shanghai Junshi Bioscience Co., Ltd.
  • It has received conditional approval in China for several types of cancer, including melanoma, nasopharyngeal carcinoma, and urothelial carcinoma, and has shown promising anti-tumor effects in various other tumors.
  • Generally well-tolerated among patients, toripalimab may offer new treatment options for different cancers, although direct comparisons with other drugs are limited due to differing study populations.

Article Abstract

Toripalimab (Tuoyi™) is a selective, recombinant, humanized monoclonal antibody against programmed death protein 1 (PD-1) developed by Shanghai Junshi Bioscience Co., Ltd. Toripalimab is able to bind to PD-1 and block the interaction with its ligands. The binding of toripalimab to PD-1 is mainly attributed to the heavy chain of the former and the FG loop of the latter. Toripalimab received a conditional approval in China for the treatment of melanoma (second-line) in December, 2018. It has also received approvals to treat nasopharyngeal carcinoma (first-line and third-line) and urothelial carcinoma (second-line) in 2021. Additionally, several orphan drug designations were granted to toripalimab by the US Food and Drug Administration. Toripalimab has exhibited primary anti-tumor effects in tumors such as melanoma, lung cancer, digestive tract tumors, hepatobiliary and pancreatic tumors, neuroendocrine neoplasms, nasopharyngeal carcinoma and urothelial carcinoma. It showed a satisfactory anti-tumor effect and long-term survival benefits in Chinese melanoma patients, while the combination of axitinib with toripalimab exhibited an impressive result in metastatic mucosal melanoma. As a checkpoint inhibitor, toripalimab was generally well-tolerated in the enrolled patients. Due to different study populations, comparisons could not be made directly between toripalimab and other drugs in most cases. Nevertheless, the introduction of toripalimab may offer a valuable choice for decision-making in the treatment of tumors in the future.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789657PMC
http://dx.doi.org/10.3389/fimmu.2021.730666DOI Listing

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