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| Content Provider | Springer Nature : BioMed Central |
|---|---|
| Author | Li, Jun-Yan Chen, Yu-Pei Li, Ying-Qin Liu, Na Ma, Jun |
| Abstract | The development of immune checkpoint blockade (ICB)-based immunotherapy has dramatically changed methods of cancer treatment. This approach triggers a durable treatment response and prolongs patients' survival; however, not all patients can benefit. Accumulating evidence demonstrated that the efficacy of ICB is dependent on a robust antitumor immune response that is usually damaged in most tumors. Conventional chemotherapy and targeted therapy promote the antitumor immune response by increasing the immunogenicity of tumor cells, improving CD8+ T cell infiltration, or inhibiting immunosuppressive cells in the tumor microenvironment. Such immunomodulation provides a convincing rationale for the combination therapy of chemotherapeutics and ICBs, and both preclinical and clinical investigations have shown encouraging results. However, the optimal drug combinations, doses, timing, and sequence of administration, all of which affect the immunomodulatory effect of chemotherapeutics, as well as the benefit of combination therapy, are not yet determined. Future studies should focus on these issues and help to develop the optimal combination regimen for each cancer. |
| Related Links | https://molecular-cancer.biomedcentral.com/counter/pdf/10.1186/s12943-021-01317-7.pdf |
| Ending Page | 21 |
| Page Count | 21 |
| Starting Page | 1 |
| File Format | HTM / HTML |
| ISSN | 14764598 |
| DOI | 10.1186/s12943-021-01317-7 |
| Journal | Molecular Cancer |
| Issue Number | 1 |
| Volume Number | 20 |
| Language | English |
| Publisher | BioMed Central |
| Publisher Date | 2021-02-04 |
| Access Restriction | Open |
| Subject Keyword | Cancer Research Oncology antitumor immune response chemotherapy combination therapy immune checkpoint blockade targeted therapy tumor microenvironment |
| Content Type | Text |
| Resource Type | Review |
| Subject | Oncology Molecular Medicine Cancer Research |
| Journal Impact Factor | 27.7/2023 |
| 5-Year Journal Impact Factor | 31.3/2023 |
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