⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for Preoperative Panitumumab and Radiotherapy in Rectal Cancer

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Preoperative Panitumumab and Radiotherapy in Rectal Cancer

Official Title: Phase II Study of Preoperative Panitumumab and External Beam Radiotherapy in Patients With Locally Advanced Rectal Cancer

Study ID: NCT00973193

Conditions

Rectal Cancer

Interventions

panitumumab

Study Description

Brief Summary: The purpose of this study is to investigate the activity of panitumumab in combination with standard preoperative radiotherapy in locally advanced rectal cancer, followed by complete surgery and adjuvant chemotherapy. The main hypothesis of the study is that the association of EGFR-targeting agent and radiation therapy could be as effective or even improve the rate of pathological complete tumoral response with fewer toxicities in comparison to the standard of care using chemoradiation therapy.

Detailed Description: Anti-EGFR monoclonal antibodies have radiosensitizing properties. In particular, cetuximab in combination with curative-intent radiotherapy has been reported to increase median overall survival over radiation therapy alone in locally advanced head and neck carcinoma. Similar benefit in rectal cancer is expected. However, preliminary studies revealed that the combination of chemoradiation and cetuximab did not seem to improve the pathological tumor response. However, in the past studies, the selection of patients' population was not optimal since KRAS mutational status was not considered during recruitments. Therefore, new trials to investigate EGFR-targeting therapies in combination with radiotherapy in wild-type KRAS patients are required. Adjuvant chemotherapy has also shown to decrease the risk of local relapse in patients who did not receive chemotherapy during radiotherapy. In our study, since there will be no chemotherapy given during the preoperative setting, the administration of adjuvant chemotherapy postoperatively is highly recommended.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Institute Jules Bordet, Brussels, , Belgium

Cliniques Universitaires Saint Luc - Université Catholique de Louvain, Brussels, , Belgium

Centre Hospitalier Notre Dame et Reine Fabiola, Charleroi, , Belgium

Centre Hospitalier de Jolimont-Lobbes, La Louvière, , Belgium

UZ Gasthuisberg, Leuven, , Belgium

Clinique et Maternité Saint Elizabeth, Namur, , Belgium

Clinique Saint Pierre, Ottignies, , Belgium

Clinique Universitaire de Mont Godinne, Yvoir, , Belgium

Contact Details

Name: Jean-Pascal H Machiels, MD, PhD

Affiliation: Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: