Intralesional Nivolumab for the Treatment of High-Risk Premalignant Oral Lesions
This phase I trial tests the safety, side effects, and best dose of intralesional nivolumab in treating high-risk premalignant oral lesions. Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving nivolumab directly into oral lesions that are at high-risk of becoming cancerous may help treat them and prevent oral cancer.
Inclusion Criteria
- Presence of a treatment naive, biopsy proven, intraoral premalignant lesion visible from oral cavity
- Be willing and able to provide written informed consent for the trial. In the event that non-English speaking participants are eligible for this study, a short form (if applicable) or an informed consent document (ICD) in their language, will be utilized and completed in accordance with the MD Anderson Cancer Center (MDACC) "Policy for Consenting Non-English Speaking Participants"
- Be >= 18 years of age on day of signing informed consent
- Be willing to provide tissue, either archive or from a newly obtained oral biopsy
- Have a performance status of 0-2 on the Eastern Cooperative Oncology Group (ECOG) performance scale
- Absolute neutrophil count (ANC) >= 1,000/mcL
- Platelets >= 75,000/mcL
- Serum total bilirubin =< 1.5 x upper limit of normal (ULN) OR direct bilirubin =< ULN for subjects with total bilirubin levels > 1.5 ULN
- Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 2.5 x ULN
- Female subject of childbearing potential should have a negative urine or serum pregnancy test within 72 hours prior to receiving the first dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
- Female subjects of childbearing potential should be willing to use 2 methods of birth control or be surgically sterile or abstain from heterosexual activity for the course of study therapy through 120 days after the last dose of nivolumab. Subjects of childbearing potential are those who have not been surgically sterilized or have not been free from menses for > 1 year
- Male subjects should agree to use an adequate method of contraception starting with the first dose of study therapy through 120 days after the last dose of study therapy
Exclusion Criteria
- Is currently participating and receiving study therapy with potential anti-neoplastic activity or has participated in a study of an investigational agent and received study therapy with potential anti-neoplastic activity within 4 weeks of the first dose of treatment
- Has a known history of active TB (Bacillus tuberculosis)
- Hypersensitivity to nivolumab or any of its excipients
- Has had a prior anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study day 1 or who has not recovered (i.e., =< grade 2 or at baseline) from adverse events due to agents administered more than 4 weeks earlier
- Has had prior chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to study day 1 or who has not recovered (i.e., =< grade 2 or at baseline) from adverse events due to a previously administered agent
- Has a known additional malignancy that is progressing or requires active treatment other than adjuvant hormonal therapy. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin or in situ cervical cancer
- Has known history of, or any evidence of active, non-infectious pneumonitis
- Has an active infection requiring systemic therapy
- Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject’s participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
- Is pregnant or breastfeeding or expecting to conceive or father children within the projected duration of treatment with nivolumab, starting with the pre-screening or screening visit through 120 days after the last dose of trial treatment.
- Has received a live vaccine within 30 days of planned start of study therapy. * Note: Seasonal influenza vaccines for injection are generally inactivated flu vaccines and are allowed; however intranasal influenza vaccines (e.g., Flu-Mist) are live attenuated vaccines, and are not allowed
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05327270.
PRIMARY OBJECTIVE:
I. To characterize the safety and tolerability of nivolumab injected intralesionally in patients with high-risk oral premalignant lesions.
SECONDARY OBJECTIVES:
I. To describe the objective response rate (ORR) in index lesions following intralesional injections of nivolumab in patients with high-risk oral premalignant lesions, according to modified World Health Organization (WHO) criteria.
II. To describe the pathologic complete response (CR) rate in index lesions following intralesional injections of nivolumab in patients with high-risk oral premalignant lesions.
III. To describe the major pathologic response rate in index lesions following intralesional injections of nivolumab in patients with high-risk oral premalignant lesions.
IV. To evaluate systemic exposure of nivolumab following intralesional injections of nivolumab in patients with high-risk oral premalignant lesions.
V. To assess the immunogenicity of nivolumab in patients with high-risk oral premalignant lesions.
VI. To establish a recommended dose of intralesional nivolumab for further study in patients with high-risk oral premalignant lesions.
OUTLINE: This is a dose-escalation study followed by a dose-expansion study.
Patients receive nivolumab intralesionally every 3 weeks (Q3W) for up to 10 weeks in the absence of disease progression or unacceptable toxicity. Patients also undergo biopsy and collection of blood samples throughout the study.
After completion of study treatment, patients are followed up for 90 days.
Trial PhasePhase I
Trial Typetreatment
Lead OrganizationM D Anderson Cancer Center
Principal InvestigatorMoran Amit
- Primary ID2021-1011
- Secondary IDsNCI-2022-02940
- ClinicalTrials.gov IDNCT05327270