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First-, second-, third-line therapy for mRCC: benchmarks for trial design from the IMDC.
Ko, J J; Choueiri, T K; Rini, B I; Lee, J-L; Kroeger, N; Srinivas, S; Harshman, L C; Knox, J J; Bjarnason, G A; MacKenzie, M J; Wood, L; Vaishampayan, U N; Agarwal, N; Pal, S K; Tan, M-H; Rha, S Y; Yuasa, T; Donskov, F; Bamias, A; Heng, D Y C.
Afiliação
  • Ko JJ; Tom Baker Cancer Center, University of Calgary, Calgary, Alberta, Canada.
  • Choueiri TK; Dana Farber Cancer Institute, Boston, Massachusetts, USA.
  • Rini BI; Cleveland Clinic Taussig Cancer Institute, Cleveland, Ohio, USA.
  • Lee JL; Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Kroeger N; 1] Tom Baker Cancer Center, University of Calgary, Calgary, Alberta, Canada [2] Department of Urology, Universitätsmedizin Greifswald, Greifswald, Germany.
  • Srinivas S; Division of Oncology, Stanford Medical Center, Stanford, California, USA.
  • Harshman LC; Division of Oncology, Stanford Cancer Institute, Stanford School of Medicine, Stanford, California, USA.
  • Knox JJ; Department of Medicine, Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, Ontario, Canada.
  • Bjarnason GA; Sunnybrook Odette Cancer Centre, University of Toronto, Toronto, Ontario, Canada.
  • MacKenzie MJ; London Health Sciences Center, London, Ontario, Canada.
  • Wood L; Queen Elizabeth II Health Sciences Centre and Dalhousie University, Halifax, Nova Scotia, Canada.
  • Vaishampayan UN; Karmanos Cancer Institute, Wayne State University, Detroit, Michigan, USA.
  • Agarwal N; Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
  • Pal SK; City of Hope Comprehensive Cancer Center, Medical Oncology & Experimental Therapeutics, Duarte, California, USA.
  • Tan MH; National Cancer Center, Institute of Bioengineering and Nanotechnology, Singapore, Singapore.
  • Rha SY; Yonsei University Hospital, Seoul, South Korea.
  • Yuasa T; Department of Urology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Donskov F; Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  • Bamias A; Alexandra Peripheral General Hospital, Athens, Greece.
  • Heng DY; Tom Baker Cancer Center, University of Calgary, Calgary, Alberta, Canada.
Br J Cancer ; 110(8): 1917-22, 2014 Apr 15.
Article em En | MEDLINE | ID: mdl-24691425
ABSTRACT

BACKGROUND:

Limited data exist on outcomes for metastatic renal cell carcinoma (mRCC) patients treated with multiple lines of therapy. Benchmarks for survival are required for patient counselling and clinical trial design.

METHODS:

Outcomes of mRCC patients from the International mRCC Database Consortium database treated with 1, 2, or 3+ lines of targeted therapy (TT) were compared by proportional hazards regression. Overall survival (OS) and progression-free survival (PFS) were calculated using different population inclusion criteria.

RESULTS:

In total, 2705 patients were treated with TT of which 57% received only first-line TT, 27% received two lines of TT, and 16% received 3+ lines of TT. Overall survival of patients who received 1, 2, or 3+ lines of TT were 14.9, 21.0, and 39.2 months, respectively, from first-line TT (P<0.0001). On multivariable analysis, 2 lines and 3+ lines of therapy were each associated with better OS (HR=0.738 and 0.626, P<0.0001). Survival outcomes for the subgroups were as follows for all patients, OS 20.9 months and PFS 7.2 months; for those similar to eligible patients in the first-line ADAPT trial, OS 14.7 months and PFS 5.6 months; for those similar to patients in first-line TIVO-1 trial, OS 24.8 months and PFS 8.2 months; for those similar to patients in second-line INTORSECT trial, OS 13.0 months and PFS 3.9 months; and for those similar to patients in the third-line GOLD trial, OS 18.0 months and PFS 4.4 months.

CONCLUSIONS:

Patients who are able to receive more lines of TT live longer. Survival benchmarks provide context and perspective when interpreting and designing clinical trials.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Fator A de Crescimento do Endotélio Vascular / Serina-Treonina Quinases TOR / Terapia de Alvo Molecular Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Cancer Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Fator A de Crescimento do Endotélio Vascular / Serina-Treonina Quinases TOR / Terapia de Alvo Molecular Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Cancer Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Canadá