Vascular endothelial growth factor targeted therapy in the perioperative setting: implications for patient care

被引:107
作者
Bose, Debashish [1 ,3 ]
Meric-Bernstam, Funda [1 ]
Hofstetter, Wayne [2 ]
Reardon, David A. [4 ,5 ]
Flaherty, Keith T. [6 ]
Ellis, Lee M. [1 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77230 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Thorac Surg, Houston, TX 77230 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77230 USA
[4] Duke Univ, Sch Med, Dept Pediat, Durham, NC USA
[5] Duke Univ, Sch Med, Dept Surg, Durham, NC USA
[6] Massachusetts Gen Hosp, Dept Med, Ctr Canc, Boston, MA 02114 USA
关键词
METASTATIC COLORECTAL-CANCER; BEVACIZUMAB PLUS IRINOTECAN; RENAL-CELL CARCINOMA; OXALIPLATIN-BASED CHEMOTHERAPY; TYROSINE KINASE INHIBITOR; PHASE-II TRIAL; GASTROINTESTINAL PERFORATION; PREOPERATIVE CHEMOTHERAPY; LIVER-REGENERATION; INCREASE MORBIDITY;
D O I
10.1016/S1470-2045(09)70341-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Vascular endothelial growth factor (VEGF) targeted therapy, either alone or in combination with chemotherapy, has become the standard of care in several solid tumours, including colorectal cancer, renal-cell carcinoma, breast cancer, non-small-cell lung cancer, and glioblastoma. VEGF is crucial in the process of angiogenesis and wound healing and, thus, its inhibition has the potential to affect wound healing in patients undergoing surgery. In this review, we summarise the data available on the use of VEGF-targeted therapies, and their effect on perioperative wound complications. Surgery in patients receiving VEGF-targeted therapies seems to be safe when an appropriate interval of time is allowed between surgical procedures and treatment. Recommendations regarding this interval are provided in a disease and agent site-specific manner. We also discuss complications arising from the use of VEGF-directed therapies that might require surgical intervention and the considerations important in their management. At this juncture, safety data on the use of VEGF-targeted therapies in the perioperative period are sparse, and investigators are urged to continue to study this issue prospectively in current and future clinical trials to establish firm guidelines.
引用
收藏
页码:373 / 382
页数:10
相关论文
共 95 条
[1]   Initial Safety Report of NSABP C-08: A Randomized Phase III Study of Modified FOLFOX6 With or Without Bevacizumab for the Adjuvant Treatment of Patients With Stage II or III Colon Cancer [J].
Allegra, Carmen J. ;
Yothers, Greg ;
O'Connell, Michael J. ;
Sharif, Saima ;
Colangelo, Linda H. ;
Lopa, Samia H. ;
Petrelli, Nicholas J. ;
Goldberg, Richard M. ;
Atkins, James N. ;
Seay, Thomas E. ;
Fehrenbacher, Louis ;
O'Reilly, Seamus ;
Chu, Luis ;
Azar, Catherine A. ;
Wolmark, Norman .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (20) :3385-3390
[2]   Subcutaneous implantable venous access device erosion through the skin in patients treated with anti-vascula endothelial growth factor therapy: a case series [J].
Almhanna, Khaldoun ;
Pelley, Robert J. ;
Budd, G. Thomas ;
Davidson, Jon ;
Moore, Halle C. F. .
ANTI-CANCER DRUGS, 2008, 19 (02) :217-219
[3]   Preoperative tyrosine kinase inhibition as an adjunct to debulking nephrectomy [J].
Amin, Chirag ;
Wallen, Eric ;
Pruthi, Raj S. ;
Calvo, Benjamin F. ;
Godley, Paul A. ;
Rathmell, W. Kimryn .
UROLOGY, 2008, 72 (04) :864-868
[4]   Management of bevacizumab-associated bowel perforation: a case series and review of the literature [J].
Badgwell, B. D. ;
Camp, E. R. ;
Feig, B. ;
Wolff, R. A. ;
Eng, C. ;
Ellis, L. M. ;
Cormier, J. N. .
ANNALS OF ONCOLOGY, 2008, 19 (03) :577-582
[5]   AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients [J].
Batchelor, Tracy T. ;
Sorensen, A. Gregory ;
di Tomaso, Emmanuelle ;
Zhang, Wei-Ting ;
Duda, Dan G. ;
Cohen, Kenneth S. ;
Kozak, Kevin R. ;
Cahill, Daniel P. ;
Chen, Poe-Jou ;
Zhu, Mingwang ;
Ancukiewicz, Marek ;
Mrugala, Maciej M. ;
Plotkin, Scott ;
Drappatz, Jan ;
Louis, David N. ;
Ivy, Percy ;
Scadden, David T. ;
Benner, Thomas ;
Loeffler, Jay S. ;
Wen, Patrick Y. ;
Jain, Rakesh K. .
CANCER CELL, 2007, 11 (01) :83-95
[6]   Modes of resistance to anti-angiogenic therapy [J].
Bergers, Gabriele ;
Hanahan, Douglas .
NATURE REVIEWS CANCER, 2008, 8 (08) :592-603
[7]   Renal cell carcinoma: A model system for novel drug development? [J].
Bukowski, Ronald M. .
CLINICAL GENITOURINARY CANCER, 2008, 6 (01) :7-8
[8]   Reversible tumor growth acceleration following bevacizumab interruption in metastatic colorectal cancer patients scheduled for surgery [J].
Cacheux, W. ;
Boisserie, T. ;
Staudacher, L. ;
Vignaux, O. ;
Dousset, B. ;
Soubrane, O. ;
Terris, B. ;
Mateus, C. ;
Chaussade, S. ;
Goldwasser, F. .
ANNALS OF ONCOLOGY, 2008, 19 (09) :1659-1661
[9]   A meta-analysis of randomized controlled trials comparing chemotherapy plus bevacizumab with chemotherapy alone in metastatic colorectal cancer [J].
Cao, Yunfei ;
Tan, Aihua ;
Gao, Feng ;
Liu, Lidan ;
Liao, Cun ;
Mo, Zengnan .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2009, 24 (06) :677-685
[10]   Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele [J].
Carmeliet, P ;
Ferreira, V ;
Breier, G ;
Pollefeyt, S ;
Kieckens, L ;
Gertsenstein, M ;
Fahrig, M ;
Vandenhoeck, A ;
Harpal, K ;
Eberhardt, C ;
Declercq, C ;
Pawling, J ;
Moons, L ;
Collen, D ;
Risau, W ;
Nagy, A .
NATURE, 1996, 380 (6573) :435-439