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Biooncology R-VEGF
Related Resources for this page:
- Clinical Trials
- Future Directions
- Antibody-Drug Conjugates
- High VEGF expression
- Hypoxic tumor environment promotes angiogenesis
- MVD and progression
- Regulation of VEGF expression
- Serum VEGF as a clinical marker
- Summary
- Summary
- Summary
- Summary
- VEGF and MVD
- VEGF in bladder cancer
- VEGF in gastric cancer
- VEGF in pancreatic cancer
- VEGF and prognosis
- VEGF and prognosis in multiple myeloma
- VEGF and prognosis in pancreatic cancer
- VEGF and progression in urothelial carcinoma
- VEGF and tumor progression in gastric cancer
- VEGF and tumor progression in pancreatic cancer
- VEGF expression and liver metastases
- VEGF expression in gastric cancer
- VEGF expression in multiple myeloma
- VEGF in multiple myeloma
- VEGF pathways in multiple myeloma
- VEGF, MVD, and metastases in gastric carcinoma
- Glycoengineered Antibodies
- High VEGF expression
- Hypoxic tumor environment promotes angiogenesis
- MVD and progression
- Regulation of VEGF expression
- Serum VEGF as a clinical marker
- Summary
- Summary
- Summary
- Summary
- VEGF and MVD
- VEGF in bladder cancer
- VEGF in gastric cancer
- VEGF in pancreatic cancer
- VEGF and prognosis
- VEGF and prognosis in multiple myeloma
- VEGF and prognosis in pancreatic cancer
- VEGF and progression in urothelial carcinoma
- VEGF and tumor progression in gastric cancer
- VEGF and tumor progression in pancreatic cancer
- VEGF expression and liver metastases
- VEGF expression in gastric cancer
- VEGF expression in multiple myeloma
- VEGF in multiple myeloma
- VEGF pathways in multiple myeloma
- VEGF, MVD, and metastases in gastric carcinoma
- Non-Antibody Biologics
- High VEGF expression
- Hypoxic tumor environment promotes angiogenesis
- MVD and progression
- Regulation of VEGF expression
- Serum VEGF as a clinical marker
- Summary
- Summary
- Summary
- Summary
- What are the strategies for inhibiting the VEGF pathway?
- VEGF and MVD
- VEGF in bladder cancer
- VEGF in gastric cancer
- VEGF in pancreatic cancer
- VEGF and prognosis
- VEGF and prognosis in multiple myeloma
- VEGF and prognosis in pancreatic cancer
- VEGF and progression in urothelial carcinoma
- VEGF and tumor progression in gastric cancer
- VEGF and tumor progression in pancreatic cancer
- VEGF expression and liver metastases
- VEGF expression in gastric cancer
- VEGF expression in multiple myeloma
- VEGF in multiple myeloma
- VEGF pathways in multiple myeloma
- VEGF, MVD, and metastases in gastric carcinoma
- Targeted Small Molecules
- High VEGF expression
- Hypoxic tumor environment promotes angiogenesis
- MVD and progression
- Regulation of VEGF expression
- Serum VEGF as a clinical marker
- Summary
- Summary
- Summary
- Summary
- Slide decks and videos
- What are the strategies for inhibiting the VEGF pathway?
- VEGF and MVD
- VEGF in bladder cancer
- VEGF in gastric cancer
- VEGF in pancreatic cancer
- VEGF and prognosis
- VEGF and prognosis in multiple myeloma
- VEGF and prognosis in pancreatic cancer
- VEGF and progression in urothelial carcinoma
- VEGF and tumor progression in gastric cancer
- VEGF and tumor progression in pancreatic cancer
- VEGF expression and liver metastases
- VEGF expression in gastric cancer
- VEGF expression in multiple myeloma
- VEGF in multiple myeloma
- VEGF pathways in multiple myeloma
- VEGF, MVD, and metastases in gastric carcinoma
- Traditional Monoclonal Antibodies
- Glossary
- High VEGF expression
- Hypoxic tumor environment promotes angiogenesis
- MVD and progression
- Regulation of VEGF expression
- Serum VEGF as a clinical marker
- Summary
- Summary
- Summary
- Summary
- Slide decks and videos
- What are the strategies for inhibiting the VEGF pathway?
- VEGF and MVD
- VEGF in bladder cancer
- VEGF in gastric cancer
- VEGF in pancreatic cancer
- VEGF and prognosis
- VEGF and prognosis in multiple myeloma
- VEGF and prognosis in pancreatic cancer
- VEGF and progression in urothelial carcinoma
- VEGF and tumor progression in gastric cancer
- VEGF and tumor progression in pancreatic cancer
- VEGF expression and liver metastases
- VEGF expression in gastric cancer
- VEGF expression in multiple myeloma
- VEGF in multiple myeloma
- VEGF pathways in multiple myeloma
- VEGF, MVD, and metastases in gastric carcinoma
- Antibody-Drug Conjugates
VEGF and progression in bladder cancer
VEGF and relapse-free/stage progression-free survival1
Kaplan-Meier survival curves demonstrating relapse free (A) and stage progression free (B) survival in 55 T1G1 and T1G2 bladder cancers expressing low VEGF mRNA (below the median, n=27), high VEGF mRNA (above the median) and p53 negative (n=15), and high VEGF mRNA and p53 positive (n=13). All but 1 p53-positive tumor expressed high levels of VEGF mRNA.
Crew et al investigated the relationship between vascular endothelial growth factor (VEGF) mRNA levels and relapse and progression status in 55 patients (37 male and 18 female with a median age of 73 years) with primary transitional cell carcinomas of the bladder. High median levels of VEGF expression (>10 units) directly correlated with lower rates of relapse-free and progression-free survival (hazard ratios 1.11 and 1.14, respectively).1
Adapted with permission from Crew JP, O'Brien T, Bradburn M, et al. Cancer Res. 1997;57:5281-5285. Figure 2.
Significance of VEGF in risk of relapse and progression
The same study by Crew et al showed VEGF as a predictor of relapse (P<0.001) and progression (P=0.02) in superficial bladder cancer. Increased risk was significantly associated with high levels of VEGF expression (>10 units), which were found in tumors that had recurred within 6 months or underwent stage progression. Crew et al also determined that presence of VEGF mRNA was associated with shortened time to recurrence and shortened progression-free survival.1
A clinical study by Bernardini et al involving 58 patients with superficial or invasive tumors reported similar findings. In this study, the authors described a significant association of VEGF levels with tumor stage (P<0.0001), grade (P<0.002), vascular invasion (P<0.001), and carcinoma in situ (P<0.01). Levels of VEGF were also significantly higher in patients with metastases (582 pg/mL) compared with localized disease (194 pg/mL).2
References:
- 1.
- Crew JP, O'Brien T, Bradburn M, et al. Cancer Res. 1997;57:5281-5285.
- 2.
- Bernardini S, Fauconnet S, Chabannes E, et al. J Urol. 2001;166:1275-1279.