Abstract
Neoadjuvant chemotherapy for invasive bladder cancer, involving a regimen of M-VAC,
can manage micrometastasis and improve the prognosis. However, some patients suffer
from severe adverse drug reactions without any effect, and no method yet exists for
predicting the response of an individual patient to chemotherapy. Our purpose in this
study is to establish a method for predicting the response to the M-VAC therapy. We
analyzed gene-expression profiles of biopsy materials from 40 invasive bladder cancers
using a cDNA microarray consisting of 27 648 genes, after populations of cancer cells
had been purified by laser-microbeam microdissection. We identified 14 predictive
genes that were expressed differently between nine responder and nine non-responder
tumors and devised a prediction-scoring system that clearly separated the responder
group from the non-responder group. This system accurately predicted the clinical
response for 19 of the 22 additional test cases. The group of patients with positive
predictive scores had significantly longer survival times than that with negative
scores. As real-time RT-PCR data were highly concordant with the cDNA microarray data
for those 14 genes, we developed a quantitative RT-PCR-based prediction system that
could be feasible for routine clinical use. Taken together, our results suggest that
the sensitivity of an invasive bladder cancer to the M-VAC neoadjuvant chemotherapy
can be predicted by expression patterns in this set of genes, a step toward achievement
of “personalized therapy” for treatment of this disease.
Key words
bladder cancer - chemotherapy - cisplatin
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Dr. R. Takata
Department of Urology · Iwate Medical University
18-1 Uchimaru, Morioka
Iwate 020–8505 Japan
eMail: rtakata@iwate-med.ac.jp