## Abstract Cancer/testis antigens (CTAs) elicit immune response in cancer patients and are therefore targets of immunotherapy. Current information on CTA expression is primarily based on mRNA assays and little is known about their expression at the protein level. The objectives of our study are to
Prognostic value of MAGE-A and NY-ESO-1 expression in pharyngeal cancer
✍ Scribed by Marija Pastorcic-Grgic; Bozena Sarcevic; Danijel Dosen; Antonio Juretic; Giulio C. Spagnoli; Marko Grgic
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 184 KB
- Volume
- 32
- Category
- Article
- ISSN
- 1043-3074
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Background
The prognostic value of cancer testis antigens in pharyngeal cancer is understudied.
Methods
We recruited 90 patients who were treated for pharyngeal cancer. Monoclonal antibodies 57B and B9.8.1.1 were used for detection of MAGE‐A and NY‐ESO‐1 genes.
Results
MAGE‐A and NY‐ESO‐1 gene products were detectable in 70.0% and 33.3% of pharyngeal tumors, respectively. No correlation was established between MAGE‐A and NY‐ESO‐1 expression and TNM staging at presentation. Survival analysis showed a trend toward a shorter 5‐year disease‐free survival in the group of patients with MAGE‐A–positive tumors (log‐rank test, p = .122). In contrast, a trend toward a prolonged 5‐year disease‐free survival was observed in the group of patients with NY‐ESO‐1–positive tumors (log‐rank test, p = .219).
Conclusion
In a large population of patients with pharyngeal cancer and available 5‐year survival data, prognosis tended to be poorer with MAGE‐A expression and better with NY‐ESO‐1 expression, but the correlations did not reach statistical significance. © 2009 Wiley Periodicals, Inc. Head Neck, 2010
📜 SIMILAR VOLUMES
## Abstract The characterization of the expression pattern of different families of cancer/testis (C/T) antigens in different tumors, at the protein level, might be of relevance in the development of multiantigen vaccine preparations for active specific immunotherapy. We have used tissue microarray
## Abstract ## __Background.__ Despite diagnostic and therapeutic advances in head and neck cancer, the 5‐year survival of patients with laryngeal cancer has not improved in the last 30 years. Several recent studies indicate that specific targets for immunotherapeutic approaches can be useful in t
## Abstract ## Background. Certain tumor antigens have been identified that stimulate an immune response, thus making them targets for immunotherapy. NY‐ESO‐1, MAGE‐1, and MAGE‐3 are such antigens. This study was undertaken to determine their presence or absence in head and neck squamous cell canc
Synovial sarcomas are high-grade malignant mesenchymal tumors with biphasic (BSS) and monophasic (MSS) variants that carry a pathognomonic cytogenetic alteration, t(X;18), involving the SYT gene on chromosome 18 and one of several SSX genes on chromosome X, usually SSX1 or SSX2. Cancer/ testis (CT)