TY - JOUR
T1 - Impact of carcinoma in situ on the outcome of intravesical Bacillus Calmette-Guérin therapy for non-muscle-invasive bladder cancer
T2 - a comparative analysis of large real-world data
AU - the Japanese Urological Oncology Group
AU - Tomida, Ryotaro
AU - Miyake, Makito
AU - Minato, Ryoei
AU - Sawada, Yuichiro
AU - Matsumura, Masafumi
AU - Iida, Kota
AU - Hori, Shunta
AU - Fukui, Shinji
AU - Ohyama, Chikara
AU - Miyake, Hideaki
AU - Hongo, Fumiya
AU - Taoka, Rikiya
AU - Kobayashi, Takashi
AU - Kojima, Takahiro
AU - Matsui, Yoshiyuki
AU - Nishiyama, Naotaka
AU - Kitamura, Hiroshi
AU - Nishiyama, Hiroyuki
AU - Fujimoto, Kiyohide
AU - Hashine, Katsuyoshi
N1 - Publisher Copyright:
© 2022, The Author(s) under exclusive licence to Japan Society of Clinical Oncology.
PY - 2022/5
Y1 - 2022/5
N2 - Background: This study investigated the clinical impact of carcinoma in situ (CIS) in intravesical Bacillus Calmette-Guérin (BCG) therapy for patients with non-muscle-invasive bladder cancer (NMIBC). Methods: This study retrospectively evaluated 3035 patients who were diagnosed with NMIBC and treated by intravesical BCG therapy between 2000 and 2019 at 31 institutions. Patients were divided into six groups according to the presence of CIS as follows: low-grade Ta without concomitant CIS, high-grade Ta without concomitant CIS, high-grade Ta with concomitant CIS, high-grade T1 without concomitant CIS, high-grade T1 with concomitant CIS, and pure CIS (without any papillary lesion). The endpoints were recurrence- and progression-free survival after the initiation of BCG therapy. We analyzed to identify factors associated with recurrence and progression. Results: At a median follow-up of 44.4 months, recurrence and progression were observed in 955 (31.5%) and 316 (10.4%) patients, respectively. Comparison of six groups using univariate and multivariate analysis showed no significant association of CIS. However, CIS in the prostatic urethra was an independent factors associated with progression. Conclusion: Concomitant CIS did not show a significant impact in the analysis of Ta and T1 tumors which were treated using intravesical BCG. Concomitant CIS in the prostatic urethra was associated with high risk of progression. Alternative treatment approaches such as radical cystectomy should be considered for patients with NMIBC who have a risk of progression.
AB - Background: This study investigated the clinical impact of carcinoma in situ (CIS) in intravesical Bacillus Calmette-Guérin (BCG) therapy for patients with non-muscle-invasive bladder cancer (NMIBC). Methods: This study retrospectively evaluated 3035 patients who were diagnosed with NMIBC and treated by intravesical BCG therapy between 2000 and 2019 at 31 institutions. Patients were divided into six groups according to the presence of CIS as follows: low-grade Ta without concomitant CIS, high-grade Ta without concomitant CIS, high-grade Ta with concomitant CIS, high-grade T1 without concomitant CIS, high-grade T1 with concomitant CIS, and pure CIS (without any papillary lesion). The endpoints were recurrence- and progression-free survival after the initiation of BCG therapy. We analyzed to identify factors associated with recurrence and progression. Results: At a median follow-up of 44.4 months, recurrence and progression were observed in 955 (31.5%) and 316 (10.4%) patients, respectively. Comparison of six groups using univariate and multivariate analysis showed no significant association of CIS. However, CIS in the prostatic urethra was an independent factors associated with progression. Conclusion: Concomitant CIS did not show a significant impact in the analysis of Ta and T1 tumors which were treated using intravesical BCG. Concomitant CIS in the prostatic urethra was associated with high risk of progression. Alternative treatment approaches such as radical cystectomy should be considered for patients with NMIBC who have a risk of progression.
KW - Bacillus Calmette-Guérin
KW - Bladder cancer
KW - Carcinoma in situ
KW - Non-muscle-invasive bladder cancer
UR - http://www.scopus.com/inward/record.url?scp=85127444841&partnerID=8YFLogxK
U2 - 10.1007/s10147-022-02127-7
DO - 10.1007/s10147-022-02127-7
M3 - 学術論文
C2 - 35142962
AN - SCOPUS:85127444841
SN - 1341-9625
VL - 27
SP - 958
EP - 968
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 5
ER -