⭐️⭐️⭐️⭐️⭐️ "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 A Study on the Timing of FOLFOX for Patients With Operable, Node Positive 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: A Study on the Timing of FOLFOX for Patients With Operable, Node Positive Rectal Cancer

Official Title: An Adaptative Randomized Phase II Study on the Timing of FOLFOX for Patients With Operable Stage III Rectal Cancer

Study ID: NCT01274962

Study Description

Brief Summary: This study is proposed to evaluate whether giving part of the chemotherapy prior to radiotherapy and surgery (as opposed to standard of care, which involves giving all the chemotherapy after radiotherapy and surgery) for patients with node positive operable rectal cancer will result in higher patient compliance to chemotherapy.

Detailed Description: In recent randomized studies with preoperative combined chemotherapy and external beam radiation (EBRT/CT) with total mesorectal excision (TME surgery), the compliance to adjuvant chemotherapy ranged from 42.9% to 70%. This low compliance rate could influence the efficacy of chemotherapy. This is quite unique to patients with rectal cancer, since compliance is not a major issue in patients with colon cancer, belonging to the same age group. Therefore, it is reasonable to postulate that this difference might due to the additive toxicity burden of neoadjuvant EBRT/CT and TME. In this randomized phase II study, compliance to chemotherapy will be compared in the two groups: In the first group, patients will receive half of their chemotherapy regimen in neoadjuvant and half in adjuvant; and, in the second group, patients will be receiving all their chemotherapy in adjuvant. Furthermore, brachytherapy will be used to deliver radiotherapy.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Hôpital de Gatineau, Gatineau, Quebec, Canada

Hôpital Charles LeMoyne, Greenfield Park, Quebec, Canada

Centre Hospitalier Pierre-Boucher, Longueuil, Quebec, Canada

Sir Mortimer B. Davis - Jewish General Hospital, Montreal, Quebec, Canada

CHUM-Hôpital St-Luc, Montréal, Quebec, Canada

Hôpital Honoré-Mercier, Saint-Hyacinthe, Quebec, Canada

Hôpital du Suroît, Salaberry-De-Valleyfield, Quebec, Canada

CHUQ - Hôtel-Dieu de Québec, Québec, , Canada

Contact Details

Name: Te Vuong, MD

Affiliation: Sir Mortimer B. Davis - Jewish General Hospital

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: