Literature DB >> 11870180

Phase III trial of fluorouracil, interferon alpha-2b, and cisplatin versus methotrexate, vinblastine, doxorubicin, and cisplatin in metastatic or unresectable urothelial cancer.

Arlene O Siefker-Radtke1, Randall E Millikan, Shi-Ming Tu, Dennis F Moore, Terry L Smith, Dallas Williams, Christopher J Logothetis.   

Abstract

PURPOSE: Previously, we developed a novel biochemotherapy regimen combining interferon alpha-2b with fluorouracil and cisplatin (FAP). We now report the results of a prospective randomized trial comparing FAP with methotrexate, vinblastine, doxorubicin, and cisplatin (M-VAC), the standard chemotherapy regimen for locally advanced and metastatic urothelial cancer. The purpose of this study was to compare the response rates and overall survival of patients with metastatic or unresectable urothelial cancer treated with these two chemotherapy regimens. PATIENTS AND METHODS: Between October 1992 and September 1999, 172 previously untreated patients were registered and randomly assigned to treatment with either FAP or M-VAC. Patients were followed until their death.
RESULTS: The pretreatment clinical characteristics of the groups were similar except for sex (P <.01). Sex did not affect prognosis or survival. The objective response rate for patients assigned to FAP was 42% (35 of 83 patients), with complete response observed in eight (10%) of 83 patients. Among the patients assigned to M-VAC, 51 (59%) of 86 had an objective response, with complete response observed in 21 (24%) of 86. The Kaplan-Meier estimate of median survival was 12.5 months for both groups. Both regimens were quite toxic, with more mucocutaneous toxicity in the FAP arm and more myelosuppression in the M-VAC arm.
CONCLUSION: Although overall survival was not significantly different, patients assigned to M-VAC had a much better chance of responding to front-line therapy. Thus, FAP is very likely to be inferior to M-VAC and is certainly no less toxic. FAP cannot be recommended as part of the standard armamentarium for urothelial cancer.

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Year:  2002        PMID: 11870180     DOI: 10.1200/JCO.2002.20.5.1361

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  12 in total

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Journal:  Curr Oncol Rep       Date:  2020-01-27       Impact factor: 5.075

2.  Bladder cancer: can we move beyond chemotherapy?

Authors:  Arlene Siefker-Radtke
Journal:  Curr Oncol Rep       Date:  2010-07       Impact factor: 5.075

Review 3.  Immunotherapy in metastatic urothelial carcinoma: focus on immune checkpoint inhibition.

Authors:  Arlene Siefker-Radtke; Brendan Curti
Journal:  Nat Rev Urol       Date:  2017-12-05       Impact factor: 14.432

4.  Expression and function of SIRT6 in muscle invasive urothelial carcinoma of the bladder.

Authors:  Minghui Wu; Shohreh Iravani Dickinson; Xue Wang; Jingsong Zhang
Journal:  Int J Clin Exp Pathol       Date:  2014-09-15

5.  Could salvage surgery after chemotherapy have clinical impact on cancer survival of patients with metastatic urothelial carcinoma?

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Journal:  Int J Clin Oncol       Date:  2011-11-18       Impact factor: 3.402

6.  Clinical response to induction chemotherapy predicts improved survival outcome in urothelial carcinoma with clinical lymph nodal metastasis treated by consolidative surgery.

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7.  [Complete resection of urothelial cancer metastases with curative intent].

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Review 8.  Management of bladder cancer: current and emerging strategies.

Authors:  Neeraj Agarwal; Maha Hussain
Journal:  Drugs       Date:  2009-06-18       Impact factor: 9.546

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Authors:  Mohammad Abufaraj; Kilian Gust; Marco Moschini; Beat Foerster; Francesco Soria; Romain Mathieu; Shahrokh F Shariat
Journal:  Transl Androl Urol       Date:  2016-10

Review 10.  Programmed cell death, redox imbalance, and cancer therapeutics.

Authors:  Xiaofeng Dai; Danjun Wang; Jianying Zhang
Journal:  Apoptosis       Date:  2021-07-08       Impact factor: 4.677

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