1. Immunotherapy for the prevention of high-risk oral disorders malignant transformation: the IMPEDE trial.
- Author
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Gurizzan C, Lorini L, Paderno A, Tomasoni M, Zigliani G, Bozzola A, Ardighieri L, Battocchio S, Bignotti E, Ravaggi A, Romani C, De Cecco L, Serafini MS, Miceli R, Bardellini E, Majorana A, Piazza C, and Bossi P
- Subjects
- Adult, Antibodies, Monoclonal, Humanized adverse effects, B7-H1 Antigen antagonists & inhibitors, Clinical Trials, Phase II as Topic, Disease-Free Survival, Female, Follow-Up Studies, Humans, Immune Checkpoint Inhibitors adverse effects, Italy epidemiology, Loss of Heterozygosity, Male, Mouth Neoplasms genetics, Mouth Neoplasms immunology, Mouth Neoplasms prevention & control, Multicenter Studies as Topic, Precancerous Conditions genetics, Precancerous Conditions immunology, Precancerous Conditions mortality, Recurrence, Tumor Escape genetics, Tumor Escape immunology, Young Adult, Antibodies, Monoclonal, Humanized administration & dosage, Immune Checkpoint Inhibitors administration & dosage, Mouth Neoplasms epidemiology, Precancerous Conditions drug therapy, Tumor Escape drug effects
- Abstract
Background: Oral Potentially Malignant Disorders (OPMD) have a non-negligible malignant transformation rate of up to 8%. Loss of heterozygosity (LOH) in critical chromosomal loci has proven to be the most effective marker in defining the risk of transformation and it is found in about 28% of OPMD and may therefore identify patients carrying higher risk. To date, clinical management of OPMD is limited to surgical excision and clinical surveillance, which however do not fully prevent oral cancer development. Immune system has been shown to play a key role in transformation surveillance mechanism and an immunosuppressive imbalance may be responsible for progression to cancer. Given all these considerations, we designed a clinical trial with the aim to prevent OPMD neoplastic transformation and revert the LOH status., Methods: This is a phase II, open label, single arm, multicentric trial involving Italian referral centres and expected to enrol 80 patients out of a total of 175 screened. Patients who meet all inclusion criteria and test positive for LOH after an incisional biopsy of the OPMD will undergo a short course of immunotherapy with 4 administration of avelumab. After 6 months since treatment start, resection of the entire OPMD will be performed and LOH assessment will be repeated. The follow-up for malignant transformation and safety assessment will last 30 months from the end of treatment, for a total planned study duration of approximately 5.5 years., Discussion: Restoring the activity of immune system through checkpoint inhibitor may play a crucial role against malignant transformation of OPMD by reverting the balance in favour of immune control and preventing cancer occurrence., Trial Registration: This trial was prospectively registered in ClinicalTrials.gov as NCT04504552 on 7th August 2020.
- Published
- 2021
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