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Published on: October 16, 2018
Future prospects for cancer immunotherapy - Strategies for ineffective cancers
Satoshi Wada1,2,3, Shinichi Kobayashi2, Takuya Tsunoda3
1Department of Clinical Diagnostic Oncology, Clinical Research Institute for Clinical Pharmacology & Therapeutics, Showa University, Tokyo, Japan.
Abstract:
With the Nobel Prize in Physiology or Medicine in 2018, cancer immunotherapy is attracting more attention than ever before and is strongly expected to develop in the future. Immune checkpoint inhibitors were developed as drugs with a completely different mechanism from conventional chemotherapy for cancer patients, and their therapeutic effects were characterized not only by tumor shrinkage but also by long-term survival of cancer patients, which had a strong impact on cancer treatment. On the other hand, as a result of numerous clinical trials, it was found that the efficacy of immune checkpoint inhibitors alone is only about 10-30%. Currently, more than 2,500 clinical trials of combined cancer immunotherapy with immune checkpoint inhibitors are being conducted with the hope of further improving therapeutic efficacy. Another new cancer immunotherapy, Chimeric Antigen Receptor (CAR) gene transfer T-cell therapy, has been approved for B-cell hematopoietic tumors. In this article, we will outline the future prospects of cancer immunotherapy developed in this way, especially from the viewpoint of "strategies for ineffective cancer".
Insights
Cancer immunotherapy, including immune checkpoint inhibitors and CAR T-cell therapy, shows promise but has limited efficacy alone. This review explores strategies to improve outcomes for patients with ineffective cancer treatments.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Cancer immunotherapy has gained significant attention following the 2018 Nobel Prize, revolutionizing treatment with immune checkpoint inhibitors (ICIs).
- ICIs offer distinct mechanisms from chemotherapy, leading to tumor shrinkage and long-term survival, significantly impacting cancer care.
- Despite advancements, the efficacy of ICIs as monotherapy remains limited, observed in only 10-30% of patients.
Purpose of the Study:
- To review the future prospects of cancer immunotherapy, focusing on strategies for patients with ineffective responses.
- To discuss the development and potential of combined immunotherapies and Chimeric Antigen Receptor (CAR) T-cell therapy.
Main Methods:
- Review of current literature and clinical trial data on cancer immunotherapy.
- Analysis of the efficacy and limitations of existing immunotherapeutic approaches.
- Exploration of novel combination strategies and emerging therapies like CAR T-cell therapy.
Main Results:
- Over 2,500 clinical trials are investigating combinations with ICIs to enhance therapeutic efficacy.
- Chimeric Antigen Receptor (CAR) gene transfer T-cell therapy has achieved approval for B-cell hematopoietic tumors.
- Monotherapy with ICIs demonstrates response rates between 10% and 30%.
Conclusions:
- Combined cancer immunotherapy approaches are crucial for improving treatment outcomes.
- CAR T-cell therapy represents a significant advancement, particularly for hematological malignancies.
- Future research should focus on developing effective strategies for patients who do not respond to current immunotherapies.
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