Luis Martínez-Piñeiro1, José A Portillo2, Jesús M Fernández3, José A Zabala4, Iker Cadierno4, José L Moyano5, Eduardo Solsona6, Miguel Unda7, Pastora Beardo8, Jesús Rodríguez-Molina9, Venancio Chantada10, Joan Palou11, Pedro Muntañola12, José M Alonso Dorrego13, Franciso J Pérez-Garcia14, Juan M Silva15, Nicolás Chesa16, Manuel Montesinos17, Antonio Ojea18, Rosario Madero13, José A Martínez-Piñeiro19. 1. Department of Urology, Hospital Universitario Infanta Sofia, Madrid, Spain. Electronic address: luis.mpineiro@salud.madrid.org. 2. Department of Urology, Hospital Valdecilla, Santander, Spain. 3. Department of Urology, Hospital Central de Asturias, Oviedo, Spain. 4. Department of Urology, Hospital de Cruces, Bilbao, Spain. 5. Department of Urology, Hospital Virgen Macarena, Sevilla, Spain. 6. Department of Urology, IVO, Valencia, Spain. 7. Department of Urology, Hospital Civil de Basurto-Osakidetza, Bilbao, Spain. 8. Department of Urology, Hospital del SAS de Jerez de La Frontera, Cádiz, Spain. 9. Department of Urology, Hospital Clínico San Carlos, Madrid, Spain. 10. Department of Urology, Complejo Hospitalario Universitario A Coruña, A Coruña, Spain. 11. Department of Urology, Fundación Puigvert, Barcelona, Spain. 12. Department of Urology, Hospital Alvarez Buylla, Mieres, Spain. 13. Hospital Universitario La Paz, Madrid, Spain. 14. Department of Urology, Hospital San Agustín, Avilés, Spain. 15. Department of Urology, Hospital Universitario de Salamanca, Salamanca, Spain. 16. Department of Urology, Hospital Insular de Gran Canaria, Las Palmas, Spain. 17. Department of Urology, Hospital Virgen del Camino, Pamplona, Spain. 18. Department of Urology, Hospital Xeral-Cíes, Vigo, Spain. 19. Clínica La Luz, Madrid, Spain.
Abstract
BACKGROUND:Bacillus Calmette-Guérin (BCG) maintenance therapy for 3 yr following BCG induction can reduce the progression of urothelial bladder carcinoma versus BCG induction alone, but is associated with high toxicity. OBJECTIVE: To investigate whether a modified 3-yr BCG maintenance regimen following induction therapy is more effective than standard BCG induction therapy alone and exhibits a low toxicity profile. DESIGN, SETTING, AND PARTICIPANTS: Patients from the outpatient clinics of the participating centres with high-risk non-muscle-invasive bladder carcinoma (NMIBC) were randomised between October 1999 and April 2007. INTERVENTION: Participants received BCG induction once-weekly for 6 wk (no maintenance arm) or BCG induction followed by one BCG instillation every 3 mo for 3 yr (maintenance arm). OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Primary endpoints were disease-free interval (DFI) and time to progression (TTP). Secondary endpoints included survival duration and toxicity. Differences between treatment arms were tested using Student's t test and χ(2) and log-rank tests. RESULTS AND LIMITATIONS: A total of 397 patients were randomised, 195 to the no-maintenance and 202 to the maintenance arm. A median time to recurrence was not reached in either treatment arm. DFI was similar between the arms (hazard ration [HR] 0.83; 95% CI 0.61-1.13; p=0.2) with disease relapse at 5 yr of 33.5% and 38.5%, respectively. TTP was also similar between the treatment arms (HR 0.79; 95% CI 0.50-1.26; p=0.3), with a progression rate at 5 yr of 16% and 19.5%, respectively. There were no significant differences between the treatment groups for overall survival and cancer-specific survival at 5 yr. Twenty and five patients in the maintenance and no-maintenance arms, respectively, stopped treatment because of toxicity. The most common local side effects were frequency (65% of patients), dysuria (63%), and haematuria (43%); the most frequent systemic side effects were general malaise (7.2%) and fever (34%). CONCLUSIONS: In NMIBC patients treated with maintenance therapy comprising a single BCG instillation every 3 mo for 3 yr following standard induction BCG, we did not observe a decrease in recurrence and progression rates versus induction therapy alone. PATIENT SUMMARY:Patients who undergo surgery to remove bladder cancer are usually treated with bacillus Calmette-Guérin (BCG) for 6 wk if there is a high risk of disease recurrence. Extending BCG therapy by 3 yr can further minimise disease recurrence and progression, but is associated with more side effects. We report that a modified 3-yr BCG treatment regimen showed low toxicity, but seemed to be no more effective than 6-wk treatment. TRIAL REGISTRATION: CUETO 98013.
RCT Entities:
BACKGROUND: Bacillus Calmette-Guérin (BCG) maintenance therapy for 3 yr following BCG induction can reduce the progression of urothelial bladder carcinoma versus BCG induction alone, but is associated with high toxicity. OBJECTIVE: To investigate whether a modified 3-yr BCG maintenance regimen following induction therapy is more effective than standard BCG induction therapy alone and exhibits a low toxicity profile. DESIGN, SETTING, AND PARTICIPANTS: Patients from the outpatient clinics of the participating centres with high-risk non-muscle-invasive bladder carcinoma (NMIBC) were randomised between October 1999 and April 2007. INTERVENTION: Participants received BCG induction once-weekly for 6 wk (no maintenance arm) or BCG induction followed by one BCG instillation every 3 mo for 3 yr (maintenance arm). OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Primary endpoints were disease-free interval (DFI) and time to progression (TTP). Secondary endpoints included survival duration and toxicity. Differences between treatment arms were tested using Student's t test and χ(2) and log-rank tests. RESULTS AND LIMITATIONS: A total of 397 patients were randomised, 195 to the no-maintenance and 202 to the maintenance arm. A median time to recurrence was not reached in either treatment arm. DFI was similar between the arms (hazard ration [HR] 0.83; 95% CI 0.61-1.13; p=0.2) with disease relapse at 5 yr of 33.5% and 38.5%, respectively. TTP was also similar between the treatment arms (HR 0.79; 95% CI 0.50-1.26; p=0.3), with a progression rate at 5 yr of 16% and 19.5%, respectively. There were no significant differences between the treatment groups for overall survival and cancer-specific survival at 5 yr. Twenty and five patients in the maintenance and no-maintenance arms, respectively, stopped treatment because of toxicity. The most common local side effects were frequency (65% of patients), dysuria (63%), and haematuria (43%); the most frequent systemic side effects were general malaise (7.2%) and fever (34%). CONCLUSIONS: In NMIBC patients treated with maintenance therapy comprising a single BCG instillation every 3 mo for 3 yr following standard induction BCG, we did not observe a decrease in recurrence and progression rates versus induction therapy alone. PATIENT SUMMARY:Patients who undergo surgery to remove bladder cancer are usually treated with bacillus Calmette-Guérin (BCG) for 6 wk if there is a high risk of disease recurrence. Extending BCG therapy by 3 yr can further minimise disease recurrence and progression, but is associated with more side effects. We report that a modified 3-yr BCG treatment regimen showed low toxicity, but seemed to be no more effective than 6-wk treatment. TRIAL REGISTRATION: CUETO 98013.
Authors: Muhammad T Pirzada; Rashid Ghauri; Monis J Ahmed; Muhammad F Shah; Irfan Ul Islam Nasir; Jasim Siddiqui; Irfan Ahmed; Khurram Mir Journal: Cureus Date: 2017-01-05
Authors: Ashish M Kamat; Joaquim Bellmunt; Matthew D Galsky; Badrinath R Konety; Donald L Lamm; David Langham; Cheryl T Lee; Matthew I Milowsky; Michael A O'Donnell; Peter H O'Donnell; Daniel P Petrylak; Padmanee Sharma; Eila C Skinner; Guru Sonpavde; John A Taylor; Prasanth Abraham; Jonathan E Rosenberg Journal: J Immunother Cancer Date: 2017-08-15 Impact factor: 13.751