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Updated: Jun 10, 2026

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A Real-time Potency Assay for Chimeric Antigen Receptor T Cells Targeting Solid and Hematological Cancer Cells
Published on: November 12, 2019
MAGE A3 antigen-specific cancer immunotherapeutic
Nir Peled1, Ana B Oton, Fred R Hirsch
1University of Colorado, Aurora, CO, USA.
Immunotherapy
|July 20, 2010
Summary
A MAGE A3 vaccine shows promise for treating non-small-cell lung cancer (NSCLC) and melanoma. Postoperative MAGE A3 vaccination is being investigated in Phase III trials for these recurrent diseases.
Area of Science:
- Oncology
- Immunotherapy
- Vaccine Development
Background:
- Non-small-cell lung cancer (NSCLC) and melanoma have high recurrence rates.
- Adjuvant chemotherapy is standard for NSCLC stages II-IIIA, but its benefit in stage IB is debated.
- Melanoma-specific antigen A3 (MAGE A3) is a tumor antigen expressed in NSCLC and melanoma, but not in normal tissues (except testis/placenta).
Purpose of the Study:
- To review recent developments and clinical experience with the MAGE A3 vaccine.
- To summarize the potential of MAGE A3 as a therapeutic target in NSCLC and melanoma.
- To discuss the transition of MAGE A3 vaccine trials from Phase II to Phase III.
Main Methods:
- Review of recent Phase II and ongoing Phase III clinical trials involving the MAGE A3 vaccine.
- Analysis of MAGE A3 antigen expression in relation to tumor burden and prognosis.
- Summary of clinical data on MAGE A3 vaccine efficacy in NSCLC and melanoma.
Main Results:
- Phase II trials indicated a clinical benefit of postoperative MAGE A3 vaccination in NSCLC and stage IV melanoma.
- MAGE A3 expression correlates with disease burden and prognosis in these cancers.
- The promising results from Phase II trials have led to the initiation of Phase III trials.
Conclusions:
- The MAGE A3 vaccine represents a novel immunotherapeutic approach for NSCLC and melanoma.
- Further investigation in Phase III trials is warranted to confirm the efficacy and safety of MAGE A3 vaccination.
- MAGE A3 holds potential as a targeted therapy for cancers expressing this tumor-specific antigen.

