Anti-Angiogenesis Soluble Receptor

Neha Vapiwala, MD
The Abramson Cancer Center of the University of Pennsylvania
Ultima Vez Modificado: 27 de septiembre del 2005

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  • VEGF Trap is a fully human fusion protein designed from components of VEGFR-1 and -2. It is soluble (travels freely in blood) and is able to bind VEGF-A more tightly than monoclonal antibodies. In addition to VEGF-A, this drug also blocks placental growth factor (PIGF), another angiogenic substance that is thought to play a role in tumor angiogenesis.
  • VEGF Trap has a relatively long half-life of approximately two weeks.
  • The MTD has not yet been reached, and the most common adverse events observed were fatigue, pain, and constipation.
  • There is an ongoing phase I, open-label, dose-escalation study of intravenous VEGF Trap in patients with advanced cancers are promising.
    • Preliminary efficacy analysis shows tumor size reduction and prolonged stable disease in some patients after single-agent VEGF Trap. One patient achieved a partial response with disappearance of ascites, two patients had minor responses, and one patient has maintained stable disease for over 11 months to date.
  • Phase I studies now accruing include:
    • Single-agent VEGF Trap in patients with relapsed or refractory advanced solid tumors or non-Hodgkin's lymphoma

Anti-inflammatory drugs reduce colorectal cancer risk in women with high baseline sTNFR-2 levels

Mar 21, 2011 - Higher plasma levels of the soluble tumor necrosis factor receptor 2 (sTNFR-2) appear to be associated with an increased risk of colorectal cancer (CRC) among women, with anti-inflammatory drugs reducing the risk of CRC among women with high baseline sTNFR-2 levels, according to a study published in the March issue of Gastroenterology.

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