Agenda
Wednesday, February 3, 2010 | |
3:00–8:00 p.m. | Registration |
Thursday, February 4, 2010 | |
7:30–8:00 a.m. | Registration/Continental Breakfast |
Session I: Basic Biology and Preclinical Data | |
Moderator: Lee M. Ellis, MD | |
8:00–8:30 | Opening Remarks/Overview |
8:30–8:55 | Breaking VEGF to Pieces: Can the Tail of VEGF be the Beginning of a New Therapy? |
8:55–9:20 | Reduction of Tumor Invasiveness and Metastasis and Prolongation of Survival After Inhibition of VEGFR plus c-Met in Preclinical Models |
9:20–9:35 | Identification and Characterization of a Novel Anti-Angiogenic & Anti-Tumorigenic Peptide Derived From Tissue Inhibitor of Metalloproteinases-3* |
9:35–10:00 | PI3 Kinase Gamma Control of Tumor Inflammation, Angiogenesis and Progression |
10:00–10:20 | Break |
10:20–10:45 | Will Anti-Angiogenic Drugs be More Effective for Metastatic Disease Than as Neoadjuvant or Adjuvant Therapies? |
10:45–11:10 | Notch Ligands as Therapeutic Targets in Tumor Angiogenesis |
11:10–11:35 | Targeting the PHD/HIF/VHL Pathway Therapeutically |
11:35–12:00 p.m. | Tumor Stroma and Targeted Delivery via Endothelial Caveolae |
12:00–1:00 | Lunch |
Session II: Biomarkers/Resistance Mechanisms | |
Moderator: Robert S. Kerbel, PhD | |
1:00–1:25 | Circulating Cytokines and Endothelial Cells |
1:25–1:40 | SNPs and Anti-VEGF Therapy |
1:40–2:05 | TKI Therapy RelatedProteomic Patterns in Serum from Patients with Metastatic Renal Cell Carcinoma* |
2:05–2:30 | Pro-invasive Growth of Giloma During VEGF Inhibition |
| 2:30–2:45 | Inhibition of Vasculogenesis, but not Angiogenesis, Prevents the Recurrence of Glioblastoma Following Irradiation* Mitomu Kioi, DDS, PhD |
2:45–3:10 | The Biology and Treatment of Acquired VEGF Pathway Resistance in RCC |
3:10–3:30 | Break |
3:30–4:00 | Panel Discussion: Does Anti-Angiogenic Therapy Accelerate Tumor Growth & Metastasis in the Clinic? |
| Chairs: |
| Panelists: |
4:00–5:30 p.m. | Welcome/Poster Reception |
Friday, February 5, 2010 | |
7:30–8:00 a.m. | Registration/Continental Breakfast |
Session III: Controversies in Anti-Angiogenic Therapy | |
Moderator: George W. Sledge, Jr., MD | |
8:00–8:05 | Introduction |
8:05–8:30 | Why Do Drugs Fail? |
8:30–8:55 | Do We Need Another VEGF Targeted TKI? |
8:55–9:20 | Development of Hypertension is a BioMarker of Clinical Efficacy for VEGF Inhibiting Agents in Metastatic RCC |
9:20–9:35 | Updated Activity and Dafety Results of Phase 2 Randomized Discontinuation Trial (RDT) of Tivozanib (AV-951), a Potent and Selective VEGFR1, 2 and 3 Kinase Inhibitor, in Patients Wwith Renal Cell Carcinoma (RCC)* |
9:35–10:00 | Novel Clinical Trial Designs for Anti-Angiogenic Therapy |
10:00–10:25 | Pharmacoeconomics of Anti-VEGF Therapy |
10:25–10:45 | Break |
Session IV: Early Drug Development | |
Moderators: Helen X. Chen, MD and George W. Sledge, Jr., MD | |
10:45–11:00 | A Phase I Study of Jl-101, a Multikinase Oral VEGFR TKI with Activity Targeting EphB4 |
11:00–11:15 | A Phase I Study of the Safety and Phamacokinetics of MEGF0444A (MoAB to EGFL7) Administered IV to Patients with Advanced Solid Tumors |
11:15–11:30 | Targeting the Delta-like Ligand 4 (DII4) as a Novel Notch Pathway-Mediated Anti-Angiogenic Strategy: A First-in-Human Study |
11:30–11:45 | Phase I Trial With PTC299 in Patients with Advanced Solid Tumors |
11:45–12:10 p.m. | Combinations With Anti-Angiogenic Therapy |
12:10–1:10 | Lunch |
Session V: Clinical Trial Results | |
Moderator: Helen X. Chen, MD | |
1:10–1:35 | Anti-Angiogenic Therapy for the Treatment of Breast Cancer |
1:35–2:00 | Anti-Angiogenic Therapy for Hepatocellular Carcinoma |
2:00–2:15 | A Phase II Study of Neoadjuvant Bevacizumab and Radiation Therapy for Resectable Soft Tissue Sarcomas* |
2:15–2:35 | Break |
2:35–3:00 | Anti-Angiogenic Therapy for NETS |
3:00–3:25 | Anti-Angiogenic Therapy for Metastatic Melanoma: First Wave of Results From Randomized Trials With VEGF-Targeted Therapy in Melanoma |
3:25–3:50 | Imaging of Anti-Angiogenic Therapy |
4:00 | Adjourn |
Saturday, February 6, 2010 | |
7:30 - 8:00 a.m. | Registration/Continental Breakfast |
Session VI: Clinical Trial Results | |
Moderator: Michael S. Gordon, MD | |
8:00–8:05 | Introduction |
8:05–8:30 | Anti-Angiogenic Therapy for the Treatment of Ovarian & Endometrial Cancers |
8:30–8:55 | Vascular Disrupting Agents |
8:55 –9:20 | VEGF Targeted Drugs Piling Up in Renal Cell Carcinoma: What Will be the Next Innovation? |
9:20–9:40 | Break |
9:40–10:05 | Anti-Angiogenic Therapy for the Treatment of CNS Malignancies |
10:05–10:30 | Anti-Angiogenic Therapy for the Treatment of Lung Cancer |
10:30–10:55 | Anti-Angiogenic Therapy for the Treatment of Gastric/Esophageal Cancer |
10:55–11:20 | Anti-Angiogenic Therapy for the Treatment of CRC |
11:20–11:25 | Closing Remarks |
11:30 | Adjourn |
*selected from poster abstract submissions
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The University of Texas M. D. Anderson Cancer Center has implemented a process whereby everyone who is in a position to control the content of an educational activity must disclose all relevant financial relationships with any commercial interest that could potentially affect the information presented. M. D. Anderson also requires that all faculty disclose any unlabeled use or investigational use (not yet approved for any purpose) of pharmaceutical and medical device products. Specific disclosure will be made to the participants prior to the educational activity.
Agendas are subject to change because we are always striving to improve the quality of your educational experience. M. D. Anderson may substitute faculty with comparable expertise on rare occasions necessitated by illness, scheduling conflicts, and so forth.
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