Bevacizumab and everolimus in renal cancer: a rational way forward.
Publication
, Journal Article
Stadler, WM; Phillips, G; George, DJ; Halabi, S; Small, E
Published in: J Clin Oncol
November 20, 2010
Duke Scholars
Published In
J Clin Oncol
DOI
EISSN
1527-7755
Publication Date
November 20, 2010
Volume
28
Issue
33
Start / End Page
e692 / e693
Location
United States
Related Subject Headings
- Vascular Endothelial Growth Factor A
- Sirolimus
- Oncology & Carcinogenesis
- Kidney Neoplasms
- Humans
- Everolimus
- Carcinoma, Renal Cell
- Bevacizumab
- Antineoplastic Combined Chemotherapy Protocols
- Antibodies, Monoclonal, Humanized
Citation
APA
Chicago
ICMJE
MLA
NLM
Stadler, W. M., Phillips, G., George, D. J., Halabi, S., & Small, E. (2010). Bevacizumab and everolimus in renal cancer: a rational way forward. J Clin Oncol, 28(33), e692–e693. https://doi.org/10.1200/JCO.2010.30.7934
Stadler, Walter M., George Phillips, Daniel J. George, Susan Halabi, and Eric Small. “Bevacizumab and everolimus in renal cancer: a rational way forward.” J Clin Oncol 28, no. 33 (November 20, 2010): e692–93. https://doi.org/10.1200/JCO.2010.30.7934.
Stadler WM, Phillips G, George DJ, Halabi S, Small E. Bevacizumab and everolimus in renal cancer: a rational way forward. J Clin Oncol. 2010 Nov 20;28(33):e692–3.
Stadler, Walter M., et al. “Bevacizumab and everolimus in renal cancer: a rational way forward.” J Clin Oncol, vol. 28, no. 33, Nov. 2010, pp. e692–93. Pubmed, doi:10.1200/JCO.2010.30.7934.
Stadler WM, Phillips G, George DJ, Halabi S, Small E. Bevacizumab and everolimus in renal cancer: a rational way forward. J Clin Oncol. 2010 Nov 20;28(33):e692–e693.
Published In
J Clin Oncol
DOI
EISSN
1527-7755
Publication Date
November 20, 2010
Volume
28
Issue
33
Start / End Page
e692 / e693
Location
United States
Related Subject Headings
- Vascular Endothelial Growth Factor A
- Sirolimus
- Oncology & Carcinogenesis
- Kidney Neoplasms
- Humans
- Everolimus
- Carcinoma, Renal Cell
- Bevacizumab
- Antineoplastic Combined Chemotherapy Protocols
- Antibodies, Monoclonal, Humanized