TY - JOUR
T1 - Predictive value of microtubule associated proteins tau and stathmin in patients with nonmuscle invasive bladder cancer receiving adjuvant intravesical taxane therapy
AU - Wosnitzer, Matthew S.
AU - Domingo-Domenech, Josep
AU - Castillo-Martin, Mireia
AU - Ritch, Chad
AU - Mansukhani, Mahesh
AU - Petrylack, Daniel P.
AU - Benson, Mitchell C.
AU - McKiernan, James M.
AU - Cordon-Cardo, Carlos
N1 - Funding Information:
Supported by National Institutes of Health Grant CA-087497 .
PY - 2011/11
Y1 - 2011/11
N2 - Purpose: After encouraging results from 2 clinical trials performed at our institution to test intravesical taxane based chemotherapy for bacillus Calmette-Guérin refractory, nonmuscle invasive bladder cancer we designed a study to identify molecular markers linked to the optimal response to such treatment modality. Materials and Methods: Included in the institutional review board approved study were 32 patients with nonmuscle invasive, bacillus Calmette-Guérin refractory bladder cancer who received intravesical taxane chemotherapy, that is docetaxel or nanoparticle albumin-bound paclitaxel. Immunophenotype analysis on tissue samples obtained before intravesical taxane therapy was done using a panel of molecular markers, including Ki-67, p53, and the microtubule associated proteins tau and stathmin. Results: Increased total tau (cytoplasmic and nuclear) and stathmin expression before intravesical taxane therapy was significantly associated with decreased recurrence-free survival (p <0.0001 and 0.007, respectively). A tau positive phenotype was an independent prognostic factor for recurrence-free survival on multivariate analysis (HR 15.66, 95% CI 2.6891.71, p = 0.002). Neither the proliferation index assessed by Ki-67 expression nor p53 status was significantly associated with recurrence-free survival. Conclusions: Assessment of tau and stathmin protein expression should be considered to select patients before intravesical taxane based chemotherapy for nonmuscle invasive, bacillus Calmette- Guérin refractory bladder cancer since those who have tumors with low tau/stathmin protein expression show a better response to therapy.
AB - Purpose: After encouraging results from 2 clinical trials performed at our institution to test intravesical taxane based chemotherapy for bacillus Calmette-Guérin refractory, nonmuscle invasive bladder cancer we designed a study to identify molecular markers linked to the optimal response to such treatment modality. Materials and Methods: Included in the institutional review board approved study were 32 patients with nonmuscle invasive, bacillus Calmette-Guérin refractory bladder cancer who received intravesical taxane chemotherapy, that is docetaxel or nanoparticle albumin-bound paclitaxel. Immunophenotype analysis on tissue samples obtained before intravesical taxane therapy was done using a panel of molecular markers, including Ki-67, p53, and the microtubule associated proteins tau and stathmin. Results: Increased total tau (cytoplasmic and nuclear) and stathmin expression before intravesical taxane therapy was significantly associated with decreased recurrence-free survival (p <0.0001 and 0.007, respectively). A tau positive phenotype was an independent prognostic factor for recurrence-free survival on multivariate analysis (HR 15.66, 95% CI 2.6891.71, p = 0.002). Neither the proliferation index assessed by Ki-67 expression nor p53 status was significantly associated with recurrence-free survival. Conclusions: Assessment of tau and stathmin protein expression should be considered to select patients before intravesical taxane based chemotherapy for nonmuscle invasive, bacillus Calmette- Guérin refractory bladder cancer since those who have tumors with low tau/stathmin protein expression show a better response to therapy.
KW - BCG vaccine
KW - carcinoma
KW - stathmin
KW - tau proteins
KW - transitional cell
KW - urinary bladder
UR - http://www.scopus.com/inward/record.url?scp=80053958687&partnerID=8YFLogxK
U2 - 10.1016/j.juro.2011.06.051
DO - 10.1016/j.juro.2011.06.051
M3 - Article
C2 - 21944130
AN - SCOPUS:80053958687
SN - 0022-5347
VL - 186
SP - 2094
EP - 2100
JO - Journal of Urology
JF - Journal of Urology
IS - 5
ER -