Phase III Study of Molecularly Targeted Adjuvant Therapy in Locally Advanced Urothelial Cancer of the Bladder Based on p53 Status

被引:168
作者
Stadler, Walter M. [1 ]
Lerner, Seth P. [2 ]
Groshen, Susan
Stein, John P. [3 ]
Shi, Shan-Rong [3 ]
Raghavan, Derek [4 ]
Esrig, David [6 ]
Steinberg, Gary [1 ]
Wood, David [7 ]
Klotz, Laurence [8 ]
Hall, Craig [5 ]
Skinner, Donald G. [3 ]
Cote, Richard J. [9 ]
机构
[1] Univ Chicago, Chicago, IL 60637 USA
[2] Baylor Coll Med, Houston, TX 77030 USA
[3] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
[4] Carolinas HealthCare Syst, Levine Canc Inst, Charlotte, NC USA
[5] Piedmont Urol Associates, High Point, NC USA
[6] Oregon Urol Inst, Springfield, OR USA
[7] Univ Michigan, Ann Arbor, MI 48109 USA
[8] Univ Toronto, Sunnybrook Hosp, Toronto, ON, Canada
[9] Univ Miami, Miller Sch Med, Dept Pathol, Miami, FL 33136 USA
关键词
ACCUMULATION; PROGRESSION; CYSTECTOMY; GENE;
D O I
10.1200/JCO.2010.34.4028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Retrospective studies suggest that p53 alteration is prognostic for recurrence in patients with urothelial bladder cancer and predictive for benefit from combination methotrexate, vinblastine, doxorubicin, and cisplatin (MVAC) adjuvant chemotherapy. Patients and Methods Patients with pT1/T2N0M0 disease whose tumors demonstrated >= 10% nuclear reactivity on centrally performed immunohistochemistry for p53 were offered random assignment to three cycles of adjuvant MVAC versus observation; p53-negative patients were observed. By using a log-rank test with one-sided alpha = .05 and beta = .10, 190 p53-positive patients were planned to be randomly assigned to detect an absolute improvement in probability of recurring by 3 years from 0.50 to 0.30. Results A total of 521 patients were registered, 499 underwent p53 assessment, 272 (55%) were positive, and 114 (42%) were randomly assigned. Accrual was halted on the basis of the data and safety monitoring board review of a futility analysis. Overall 5-year probability of recurring was 0.20 (95% CI, 0.16 to 0.24) with no difference on the basis of p53 status. Only 67% of patients randomly assigned to MVAC received all three cycles with 12 patients receiving no treatment. There was no difference in recurrence in the randomly assigned patients (hazard ratio, 0.78; 95% CI, 0.29 to 2.08; P = .62). Conclusion Neither the prognostic value of p53 nor the benefit of MVAC chemotherapy in patients with p53-positive tumors was confirmed, but the high patient refusal rate, lower than expected event rate, and failures to receive assigned therapy severely compromised study power. J Clin Oncol 29:3443-3449. (C) 2011 by American Society of Clinical Oncology
引用
收藏
页码:3443 / 3449
页数:7
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