TY - JOUR
T1 - PAX3/7-FOXO1 fusion status in older rhabdomyosarcoma patient population by Xuorescent in situ hybridization
AU - Dumont, Sarah N.
AU - Lazar, Alexander J.
AU - Bridge, Julia A.
AU - Benjamin, Robert S.
AU - Trent, Jonathan C.
N1 - Funding Information:
Acknowledgments Institutional Physician-Scientist award (J.C.T.), NIH/NCI 1K23CA109060-05 (J.C.T.), Amschwand Sarcoma Cancer Foundation grant (J.C.T.), Nuovo-Soldati Foundation grant (S.N.D.), AstraZeneca France (S.N.D.) and Association pour la Recherche sur le Cancer (S.N.D.). This research is also supported in part by the National Institutes of Health through MD Anderson’s Cancer Center Support Grant CA016672.
PY - 2012/2
Y1 - 2012/2
N2 - Purpose In pediatric alveolar rhabdomyosarcoma, the PAX3-FOXO1 and PAX7-FOXO1 gene fusions are prognostic indicators, while little is known concerning this disease in older patients. To determine whether PAX3/7-FOXO1 fusion gene status correlates with outcome in adolescent, young adult, and adult rhabdomyosarcoma patients, the histological, immunohistochemical, and clinical characteristics of 105 patients followed at The University of Texas MD Anderson Cancer Center from 1957 to 2001 were evaluated. Methods The samples were assembled into a tissue microarray, and fusion gene status was determined by Xuorescence in situ hybridization using PAX3, PAX7, and FOXO1 loci-speciWc probes. The disease characteristics and speciWc gene fusion were correlated with patient outcomes using the log-rank test. Results Fifty-two percent of the samples exhibited a PAX3-FOXO1 fusion, 15% the PAX7-FOXO1 fusion, and 33% were negative for a rearrangement of these loci. The presence of PAX3/7-FOXO1 translocation was signiWcantly associated with a higher frequency of metastatic disease. Although a statistically signiWcant correlation between the PAX3/7-FOXO1 fusion gene status and overall survival was not identiWed, there was a trend toward better outcomes for patients with fusion-negative RMS. Conclusions Therefore, identiWcation of a FOXO1 fusion appears to be an interesting tool for predicting outcomes in older rhabdomyosarcoma patients and is worth further investigations in this rare subgroup of RMS population.
AB - Purpose In pediatric alveolar rhabdomyosarcoma, the PAX3-FOXO1 and PAX7-FOXO1 gene fusions are prognostic indicators, while little is known concerning this disease in older patients. To determine whether PAX3/7-FOXO1 fusion gene status correlates with outcome in adolescent, young adult, and adult rhabdomyosarcoma patients, the histological, immunohistochemical, and clinical characteristics of 105 patients followed at The University of Texas MD Anderson Cancer Center from 1957 to 2001 were evaluated. Methods The samples were assembled into a tissue microarray, and fusion gene status was determined by Xuorescence in situ hybridization using PAX3, PAX7, and FOXO1 loci-speciWc probes. The disease characteristics and speciWc gene fusion were correlated with patient outcomes using the log-rank test. Results Fifty-two percent of the samples exhibited a PAX3-FOXO1 fusion, 15% the PAX7-FOXO1 fusion, and 33% were negative for a rearrangement of these loci. The presence of PAX3/7-FOXO1 translocation was signiWcantly associated with a higher frequency of metastatic disease. Although a statistically signiWcant correlation between the PAX3/7-FOXO1 fusion gene status and overall survival was not identiWed, there was a trend toward better outcomes for patients with fusion-negative RMS. Conclusions Therefore, identiWcation of a FOXO1 fusion appears to be an interesting tool for predicting outcomes in older rhabdomyosarcoma patients and is worth further investigations in this rare subgroup of RMS population.
KW - Chromosomal rearrangement
KW - Fluorescent in situ hybridization
KW - PAX-FOXO1
KW - Rhabdomyosarcoma
KW - Tissue microarray
UR - http://www.scopus.com/inward/record.url?scp=84857048155&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84857048155&partnerID=8YFLogxK
U2 - 10.1007/s00432-011-1089-7
DO - 10.1007/s00432-011-1089-7
M3 - Article
C2 - 22089931
AN - SCOPUS:84857048155
SN - 0171-5216
VL - 138
SP - 213
EP - 220
JO - Journal of Cancer Research and Clinical Oncology
JF - Journal of Cancer Research and Clinical Oncology
IS - 2
ER -