Literature DB >> 12767369

Rational selection of a control arm for randomised trials in metastatic renal cell carcinoma.

G H J Mickisch1.   

Abstract

OBJECTIVE: Immunotherapy, and only immunotherapy, has reproducible, albeit limited efficacy in metastatic renal cell cancer (MRCC). Further improvement is warranted and progress will have to be investigated in randomised clinical trials, because the variable natural history of this disease precludes firm conclusions outside the context of controlled clinical studies. Currently, there is no general accepted standard arm to compare for those randomised clinical protocols. This needs to be established, which is the goal of this project.
MATERIALS AND METHODS: Interferon-alpha (IFN-alpha) or interleukin-2 (Il-2) are registered for the use in MRCC. Taking this regulatory affair into consideration, a systematic literature research using Medline Sources was carried out to identify large controlled clinical studies in MRCC, in which one or both of the registered drugs were involved. Scientific value of the trials was weighed, and the applicability, efficacy, and safety of the control arm was analysed.
RESULTS: 13 large controlled studies qualified for this purpose, and a total of 3065 patients were included. IFN-alpha monotherapy, the combination of IFN-alpha and Il-2, and the combination of IFN-alpha, Il-2 and 5-fluorouracil (5-FU) were used as a standard treatment in decreasing frequency, respectively. There is no valid scientific proof that a combination of immunotherapies prolongs survival over monotherapies, but the combination of surgery and immunotherapy leads to a clear survival benefit over immunotherapy alone. IFN-alpha monotherapy has considerable less side effects than Il-2 based regimens.
CONCLUSION: An appealing safety profile, the applicability in an outpatient regimen, the possibility of less stringent selection criteria, and the proven life prolonging effect will make adjuvant monotherapy, in particular IFN-alpha monotherapy, after a tumournephrectomy currently the control-arm of choice in randomised trials for MRCC.

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Year:  2003        PMID: 12767369     DOI: 10.1016/s0302-2838(03)00105-2

Source DB:  PubMed          Journal:  Eur Urol        ISSN: 0302-2838            Impact factor:   20.096


  7 in total

Review 1.  Combination of surgery and immunotherapy in metastatic renal cell carcinoma.

Authors:  Gerald H Mickisch; Roland H Mattes
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2.  Renal tumor causing haematuria and sepsis.

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3.  Indirect treatment comparison of bevacizumab + interferon-α-2a vs tyrosine kinase inhibitors in first-line metastatic renal cell carcinoma therapy.

Authors:  Gerald Hj Mickisch; Björn Schwander; Bernard Escudier; Joaquim Bellmunt; José P Maroto; Camillo Porta; Stefan Walzer; Uwe Siebert
Journal:  Clinicoecon Outcomes Res       Date:  2011-01-25

4.  Sunitinib for advanced renal cell cancer.

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Journal:  Biologics       Date:  2008-03

Review 5.  Targeted therapy for advanced renal cell carcinoma.

Authors:  C Coppin; L Le; F Porzsolt; T Wilt
Journal:  Cochrane Database Syst Rev       Date:  2008-04-16

6.  Targeted therapy for metastatic renal cell carcinoma.

Authors:  Fabian Hofmann; Eu Chang Hwang; Thomas Bl Lam; Axel Bex; Yuhong Yuan; Lorenzo So Marconi; Börje Ljungberg
Journal:  Cochrane Database Syst Rev       Date:  2020-10-14

Review 7.  Efficacy of targeted therapy for advanced renal cell carcinoma: a systematic review and meta-analysis of randomized controlled trials.

Authors:  Chao Wei; Shen Wang; Zhangqun Ye; Zhiqiang Chen
Journal:  Int Braz J Urol       Date:  2018 Mar-Apr       Impact factor: 1.541

  7 in total

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