A Systematic Review of Sequencing and Combinations of Systemic Therapy in Metastatic Renal Cancer

被引:123
作者
Albiges, Laurence [1 ]
Choueiri, Toni [2 ]
Escudier, Bernard [1 ]
Galsky, Matthew [3 ]
George, Dan [4 ]
Hofmann, Fabian [5 ]
Lam, Thomas [6 ]
Motzer, Robert [7 ]
Mulders, Peter [8 ]
Porta, Camillo [9 ]
Powles, Thomas [10 ]
Sternberg, Cora [11 ]
Bex, Axel [12 ]
机构
[1] Inst Gustave Roussy, F-94805 Villejuif, France
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY 10029 USA
[4] Duke Univ, Med Ctr, Durham, NC USA
[5] Sunderby Hosp, Dept Urol, Sunderby, Sweden
[6] Univ Aberdeen, Acad Urol Unit, Aberdeen, Scotland
[7] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[8] Radboud Univ Nijmegen, Dept Urol, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[9] IRCCS San Matteo Univ Hosp Fdn, Pavia, Italy
[10] Barts Canc Inst, London, England
[11] San Camillo & Forlanini Hosp Padiglione Flajani, Dept Med Oncol, Rome, Italy
[12] Netherlands Canc Inst, Div Surg Oncol, Dept Urol, Amsterdam, Netherlands
关键词
Renal cell carcinoma; Tyrosine kinase inhibitor; Sequence of systemic therapies; Combination of systemic therapies; RANDOMIZED DISCONTINUATION TRIAL; VEGF-TARGETED THERAPY; BLIND PHASE-III; CELL CARCINOMA; INTERFERON-ALPHA; SORAFENIB; BEVACIZUMAB; TEMSIROLIMUS; SUNITINIB; SURVIVAL;
D O I
10.1016/j.eururo.2014.04.006
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
Context: The introduction of novel molecular-targeted agents has revolutionised the management of patients with metastatic renal cell carcinoma (mRCC). However, uncertainties remain over sequential or simultaneous combination therapies. Objective: To systematically review relevant literature comparing the clinical effectiveness and harms of different sequencing and combinations of systemic targeted therapies for mRCC. Evidence acquisition: Relevant databases (including Medline, Cochrane Library, trial registries, and conference proceedings) were searched (January 2000 to September 2013) including only randomised controlled trials (RCTs). Risk of bias assessment was performed. A qualitative and quantitative synthesis of the evidence was presented. Evidence synthesis: The literature search identified 5149 articles. A total of 24 studies reporting on 9589 patients were eligible for inclusion; data from four studies were included for meta-analysis. There were generally low risks of bias across studies; however, clinical and methodological heterogeneity prevented pooling of data for most studies. Overall, the data showed several targeted therapies were associated with an improvement in progression-free survival in patients with mRCC. There were limited data from RCTs regarding the issue of sequencing; studies on combination therapies have been hampered by difficulties with tolerability and safety. Conclusions: Although the role of vascular endothelial growth factor/vascular endothelial growth factor receptor targeting therapies and mammalian target of rapamycin inhibition in the management of mRCC is now established, limited reliable data are available regarding sequencing and combination therapies. Although data from retrospective cohort studies suggest a potential benefit for sequencing systemic therapies, significant uncertainties remain. Presently, mRCC systemic treatment should follow international guidelines (such as the European Society for Medical Oncology, National Comprehensive Cancer Network, and European Association of Urology) for patients fit to receive several lines of systemic therapies. Patient summary: We thoroughly examined the literature on the benefits and harms of combining drugs for the treatment of kidney cancer that has spread and on the sequence in which the drugs should be given. (C) 2014 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:100 / 110
页数:11
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