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BEST: A Randomized Phase II Study of Vascular Endothelial Growth Factor, RAF Kinase, and Mammalian Target of Rapamycin Combination Targeted Therapy With Bevacizumab, Sorafenib, and Temsirolimus in Advanced Renal Cell Carcinoma--A Trial of the ECOG-ACRIN Cancer Research Group (E2804).

Publication ,  Journal Article
Flaherty, KT; Manola, JB; Pins, M; McDermott, DF; Atkins, MB; Dutcher, JJ; George, DJ; Margolin, KA; DiPaola, RS
Published in: J Clin Oncol
July 20, 2015

PURPOSE: On the basis of evidence that resistance to vascular endothelial growth factor (VEGF) receptor inhibition is caused by hypoxia-driven residual VEGF and other proangiogenic factors, combinations of agents from these classes were hypothesized to improve treatment outcomes relative to single-agent VEGF pathway blockade. PATIENTS AND METHODS: A total of 361 patients with metastatic clear cell renal cell carcinoma were randomly assigned equally to arm A (bevacizumab monotherapy 10 mg/kg intravenously [IV] every 2 weeks), B (bevacizumab 10 mg/kg IV every 2 weeks and temsirolimus 25 mg IV every week), C (bevacizumab 5 mg/kg IV every 2 weeks and sorafenib 200 mg orally twice daily on days 1 to 5, 8 to 12, 15 to 19, and 22 to 26), or D (sorafenib 200 mg twice daily and temsirolimus 25 mg IV weekly). Progression-free survival was the primary end point. RESULTS: Among 331 eligible treated patients, median PFS was 7.5 months for bevacizumab alone (90% CI, 5.8 to 10.8 months), 7.6 months for bevacizumab plus temsirolimus (90% CI, 6.7 to 9.2 months), 9.2 months for bevacizumab plus sorafenib (90% CI, 7.5 to 11.4 months), and 7.4 months for sorafenib plus temsirolimus (90% CI, 5.6 to 7.9 months). Hazard ratios from stratified Cox proportional hazards models were 1.01, 0.89, and 1.07 (with respective P values of .95, .49, and .68) for the three combinations, respectively, compared with bevacizumab alone. Adverse events did not differ significantly among treatment arms. CONCLUSION: The activity of sorafenib, temsirolimus, and bevacizumab administered in doublet combinations did not significantly improve median progression-free survival in comparison with bevacizumab monotherapy.

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Published In

J Clin Oncol

DOI

EISSN

1527-7755

Publication Date

July 20, 2015

Volume

33

Issue

21

Start / End Page

2384 / 2391

Location

United States

Related Subject Headings

  • raf Kinases
  • Vascular Endothelial Growth Factor A
  • Treatment Outcome
  • TOR Serine-Threonine Kinases
  • Sorafenib
  • Sirolimus
  • Phenylurea Compounds
  • Oncology & Carcinogenesis
  • Niacinamide
  • Middle Aged
 

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Flaherty, K. T., Manola, J. B., Pins, M., McDermott, D. F., Atkins, M. B., Dutcher, J. J., … DiPaola, R. S. (2015). BEST: A Randomized Phase II Study of Vascular Endothelial Growth Factor, RAF Kinase, and Mammalian Target of Rapamycin Combination Targeted Therapy With Bevacizumab, Sorafenib, and Temsirolimus in Advanced Renal Cell Carcinoma--A Trial of the ECOG-ACRIN Cancer Research Group (E2804). J Clin Oncol, 33(21), 2384–2391. https://doi.org/10.1200/JCO.2015.60.9727
Flaherty, Keith T., Judith B. Manola, Michael Pins, David F. McDermott, Michael B. Atkins, Janice J. Dutcher, Daniel J. George, Kim A. Margolin, and Robert S. DiPaola. “BEST: A Randomized Phase II Study of Vascular Endothelial Growth Factor, RAF Kinase, and Mammalian Target of Rapamycin Combination Targeted Therapy With Bevacizumab, Sorafenib, and Temsirolimus in Advanced Renal Cell Carcinoma--A Trial of the ECOG-ACRIN Cancer Research Group (E2804).J Clin Oncol 33, no. 21 (July 20, 2015): 2384–91. https://doi.org/10.1200/JCO.2015.60.9727.

Published In

J Clin Oncol

DOI

EISSN

1527-7755

Publication Date

July 20, 2015

Volume

33

Issue

21

Start / End Page

2384 / 2391

Location

United States

Related Subject Headings

  • raf Kinases
  • Vascular Endothelial Growth Factor A
  • Treatment Outcome
  • TOR Serine-Threonine Kinases
  • Sorafenib
  • Sirolimus
  • Phenylurea Compounds
  • Oncology & Carcinogenesis
  • Niacinamide
  • Middle Aged