Intravesical instillation of epirubicin, bacillus Calmette-Guerin and bacillus Calmette-Guerin plus isoniazid for intermediate and high risk Ta, T1 papillary carcinoma of the bladder: A European organization for research andtreatment of cancer genito-urinary group randomized phase III trial
Apm. Van Der Meijden et al., Intravesical instillation of epirubicin, bacillus Calmette-Guerin and bacillus Calmette-Guerin plus isoniazid for intermediate and high risk Ta, T1 papillary carcinoma of the bladder: A European organization for research andtreatment of cancer genito-urinary group randomized phase III trial, J UROL, 166(2), 2001, pp. 476-481
Purpose: After transurethral resection, we compared the efficacy and side e
ffects of weekly intravesical instillations of epirubicin, bacillus Calmett
e-Guerin (BCG), and BCG plus isoniazid during a 6-week interval followed by
3 weekly maintenance instillations at months 3, 6, 12, 18, 24, 30 and 36 i
n patients with intermediate and high risk Ta, T1 bladder cancer.
Materials and Methods: A total of 957 patients were randomized at 44 instit
utions in a phase III multicenter trial.
Results: The time to first recurrence was significantly longer in patients
treated with BCG and BCG plus isoniazid compared to epirubicin (p = 0.0001)
but there was no difference between the 2 BCG regimens (p = 0.27). Progres
sion to muscle invasive cancer was rare (5%) and did not differ significant
ly among the 3 arms (p = 0.12). Drug induced cystitis was observed in 31% o
f the patients treated with epirubicin, 42% BCG and 45% BCG plus isoniazid.
Systemic side effects, such as fever and malaise, were not observed in pat
ients treated with epirubicin, but were noted in 31% BCG and 36% BCG plus i
soniazid.
Conclusions: Intravesical BCG with or without isoniazid provokes more side
effects than epirubicin. Prophylactic isoniazid does not reduce the side ef
fects of BCG, while BCG with or without isoniazid prolongs the time to firs
t recurrence compared to epirubicin. Further followup is required before lo
ng-term conclusions can be made for progression-to-muscle invasive disease
and survival.