Skip to Content

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
Lee M. Ellis, MD

8:30–8:55

Breaking VEGF to Pieces: Can the Tail of VEGF be the Beginning of a New Therapy?
Luisa Iruela-Arispe, PhD

8:55–9:20

Reduction of Tumor Invasiveness and Metastasis and Prolongation of Survival After Inhibition of VEGFR plus c-Met in Preclinical Models
Donald McDonald, MD, PhD

9:20–9:35

Identification and Characterization of a Novel Anti-Angiogenic & Anti-Tumorigenic Peptide Derived From Tissue Inhibitor of Metalloproteinases-3*
Yung-Yi Chen, PhD

9:35–10:00

PI3 Kinase Gamma Control of Tumor Inflammation, Angiogenesis and Progression
Judith Varner, PhD

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?
Robert S. Kerbel, PhD

10:45–11:10

Notch Ligands as Therapeutic Targets in Tumor Angiogenesis
Jan Kitajewski, PhD

11:10–11:35

Targeting the PHD/HIF/VHL Pathway Therapeutically
Amato J. Giaccia, PhD

11:35–12:00 p.m.

Tumor Stroma and Targeted Delivery via Endothelial Caveolae
Jan E. Schnitzer, MD

12:00–1:00

Lunch

Session II: Biomarkers/Resistance Mechanisms

Moderator: Robert S. Kerbel, PhD

1:00–1:25

Circulating Cytokines and Endothelial Cells
John Heymach, MD, PhD

1:25–1:40

SNPs and Anti-VEGF Therapy
Bryan Schneider, MD

1:40–2:05

TKI Therapy RelatedProteomic Patterns in Serum from Patients with Metastatic Renal Cell Carcinoma*
Kerstin Junker, MD, PhD

2:05–2:30

Pro-invasive Growth of Giloma During VEGF Inhibition
Gabriele Bergers, PhD

2:30–2:45Inhibition 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
Michael B. Atkins, MD

3:10–3:30

Break

3:30–4:00

Panel Discussion: Does Anti-Angiogenic Therapy Accelerate Tumor Growth & Metastasis in the Clinic?

 

Chairs:
Lee M. Ellis, MD
Robert S. Kerbel, PhD

 

Panelists:
Michael B. Atkins, MD
S. Gail Eckhardt, MD
John Heymach, MD, PhD
David A. Reardon, MD
George W. Sledge, Jr., MD

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
George W. Sledge, Jr., MD

8:05–8:30

Why Do Drugs Fail?
George W. Sledge, Jr., MD

8:30–8:55

Do We Need Another VEGF Targeted TKI?
S. Gail Eckhardt, MD

8:55–9:20

Development of Hypertension is a BioMarker of Clinical Efficacy for VEGF Inhibiting Agents in Metastatic RCC
Brian Rini, MD

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)*
Pankaj Bhargava, MD

9:35–10:00

Novel Clinical Trial Designs for Anti-Angiogenic Therapy
Lillian L. Siu, MD

10:00–10:25

Pharmacoeconomics of Anti-VEGF Therapy
Neal J. Meropol, MD

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
Michael S. Gordon, MD

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
Lee S. Rosen, MD

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
Antonio Jimeno, MD, PhD

11:30–11:45

Phase I Trial With PTC299 in Patients with Advanced Solid Tumors
Gary W. Schwartz, MD

11:45–12:10 p.m.

Combinations With Anti-Angiogenic Therapy
Helen X. Chen, MD

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
Mark Pegram, MD

1:35–2:00

Anti-Angiogenic Therapy for Hepatocellular Carcinoma
Melanie B. Thomas, MD

2:00–2:15

A Phase II Study of Neoadjuvant Bevacizumab and Radiation Therapy for Resectable Soft Tissue Sarcomas*
Sam Yoon, MD

2:15–2:35

Break

2:35–3:00

Anti-Angiogenic Therapy for NETS
Lillian L. Siu, MD

3:00–3:25

Anti-Angiogenic Therapy for Metastatic Melanoma: First Wave of Results From Randomized Trials With VEGF-Targeted Therapy in Melanoma
Keith T. Flaherty, MD

3:25–3:50

Imaging of Anti-Angiogenic Therapy
Peter Choyke, MD

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
Michael S. Gordon, MD

8:05–8:30

Anti-Angiogenic Therapy for the Treatment of Ovarian & Endometrial Cancers
Robert Allen Burger, MD

8:30–8:55

Vascular Disrupting Agents
Roberto Pili, MD

8:55 –9:20

VEGF Targeted Drugs Piling Up in Renal Cell Carcinoma: What Will be the Next Innovation?
Keith T. Flaherty, MD

9:20–9:40

Break

9:40–10:05

Anti-Angiogenic Therapy for the Treatment of CNS Malignancies
David A. Reardon, MD

10:05–10:30

Anti-Angiogenic Therapy for the Treatment of Lung Cancer
John Heymach, MD, PhD

10:30–10:55

Anti-Angiogenic Therapy for the Treatment of Gastric/Esophageal Cancer
Manish Shah, MD

10:55–11:20

Anti-Angiogenic Therapy for the Treatment of CRC
Neal J. Meropol, MD

11:20–11:25

Closing Remarks

11:30

Adjourn

*selected from poster abstract submissions

Back to General Information


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.

Photographing, audio taping and videotaping are prohibited.


© 2010 The University of Texas M. D. Anderson Cancer Center