Project 452378
Nicotinamide chemoprevention for keratinocyte carcinoma in solid organ transplant recipients: a multicentre, pragmatic randomized trial
Nicotinamide chemoprevention for keratinocyte carcinoma in solid organ transplant recipients: a multicentre, pragmatic randomized trial
Project Information
| Study Type: | Unclear |
| Research Theme: | Clinical |
Institution & Funding
| Principal Investigator(s): | Chan, An-Wen; Kim, Sang J |
| Co-Investigator(s): | Au, Sheila; Beecker, Jennifer; Chih, Sharon S; Gill, John S; Gourishankar, Sita; Jafarian, Fatemeh; Johnston, Olwyn; Kalia, Sunil; Knoll, Gregory; Lam, Ngan; Mydlarski, Paule R; Ponzo, Marisa G; Rao, Jaggi; Sapir-Pichhadze, Ruth; Singer, Lianne G; Tomlinson, George A |
| Institution: | Women's College Hospital (Toronto) |
| CIHR Institute: | Musculoskeletal Health and Arthritis |
| Program: | |
| Peer Review Committee: | Randomized Controlled Trials 2 |
| Competition Year: | 2021 |
| Term: | 5 yrs 0 mth |
Abstract Summary
As patients live longer after receiving an organ transplant, there is a need to reduce the long-term side effects of the drugs used to prevent organ rejection. In particular, long-term use of these drugs increases the risk of skin cancer. Skin cancer is now a leading cause of illness and disfigurement after kidney, liver, heart, and lung transplantation. Given the increased risk and burden of skin cancer in transplant recipients, prevention is critical. Nicotinamide is a form of Vitamin B3 that has been shown to protect against skin cancer in the general population. However, it is unclear whether nicotinamide is safe and effective among immune-suppressed transplant recipients. We will conduct a clinical trial involving multiple transplant centres in Canada to evaluate whether oral nicotinamide (500 mg twice daily) is effective and safe for preventing skin cancer. We will recruit 396 high-risk adult kidney, liver, heart, and lung transplant patients who have previously had at least one skin cancer. Patients will receive nicotinamide or sham tablets for at least 2 years. The results will inform efforts to improve the long-term health of transplant recipients.
No special research characteristics identified
This project does not include any of the advanced research characteristics tracked in our database.