Progression of Disease after Bacillus Calmette-Guerin Therapy: Refining Patient Selection for Neoadjuvant Chemotherapy before Radical Cystectomy

被引:9
作者
Hensley, Patrick J. [1 ]
Bree, Kelly K. [1 ]
Campbell, Matthew T. [2 ]
Alhalabi, Omar [2 ]
Kokorovic, Andrea [1 ]
Miest, Tanner [1 ]
Nogueras-Gonzalez, Graciela M. [3 ]
Gao, Jianjun [2 ]
Siefker-Radtke, Arlene O. [2 ]
Guo, Charles C. [4 ]
Navai, Neema [1 ]
Dinney, Colin P. [1 ]
Kamat, Ashish M. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Urol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
关键词
urinary bladder neoplasms; neoadjuvant therapy; cystectomy; mycobacterium bovis; INVASIVE BLADDER-CANCER; HIGH-RISK; UROTHELIAL CARCINOMA; DEFERRED CYSTECTOMY; SURVIVAL; TUMORS;
D O I
10.1097/JU.0000000000001943
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Data from the pre-neoadjuvant chemotherapy (NAC) era suggests patients who progress on bacillus Calmette-Guerin (BCG) to muscle-invasive bladder cancer (P-MIBC) exhibit worse outcomes compared to de novo MIBC (D-MIBC). Herein, we investigate whether P-MIBC is an independent poor risk factor in the setting of contemporary NAC use. Materials and Methods: A review of patients who underwent radical cystectomy (RC) for cT2-3 MIBC from 2005 to 2018 was performed. Patients were stratified into high risk (lymphovascular invasion, variant histology, hydronephrosis, cT3b) vs low risk (no risk factors) and P-MIBC (<= pT1 treated with at least induction BCG who progressed to >= cT2) vs D-MIBC. Results: Among 801 patients who underwent RC 20.3% had P-MIBC and 79.7% had D-MIBC. In low-risk patients treated without NAC, P-MIBC was associated with pathological upstaging (64.9% vs 42.7%, p=0.004) and worse overall (OS, p=0.006) and cancer-specific survival (CSS, p=0.001) compared to D-MIBC. P-MIBC status conferred uniformly poor survival outcomes to patients who did not receive NAC compared to D-MIBC without NAC (median OS 51.5 months [95% CI 40.0-81.0] vs 85.1 months [95% CI 62.8-96.0], p=0.040; median CSS not reached, p=0.014). However, P-MIBC status did not remain a negative prognostic factor in the setting of NAC (median OS 90.5 months [95% CI 34.0-not estimable] vs 87.8 months [95% CI 68.7enot estimable], p=0.606; median CSS not reached, p=0.448). Conclusions: P-MIBC confers a poor prognosis when managed with RC alone. Treatment with NAC results in equivalent pathological response and survival outcomes compared to D-MIBC. P-MIBC should be included in risk-stratified approaches to NAC selection.
引用
收藏
页码:1259 / 1266
页数:8
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