PRISM: Pre-Operative Radiotherapy and Immunotherapy for Sinonasal Melanoma

Trial Title: PRISM: Pre-Operative Radiotherapy and Immunotherapy for Sinonasal Melanoma

NCT ID: NCT05546827

Condition: Sinonasal Melanoma

Conditions: Official terms:
Melanoma

Study type: Interventional

Study phase: Phase 2

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Procedure
Intervention name: Surgical resection
Description: Surgical resection after receiving neodjuvant combination immunotherapy followed by radiation therapy.
Arm group label: Surgical resection

Summary: The goal of this clinical research study is to learn if pre-operative radiation therapy can help patients with sinonasal melanoma have better outcomes

Detailed description: To determine the rate of pathologic response (<50% viable tumor or >50% fibrosis) for non-metastatic sinonasal melanoma patients having surgical resection after receiving neoadjuvant combination immunotherapy followed by radiation therapy.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Patients must have histologically or cytologically confirmed melanoma involving the nasal cavity and/or paranasal sinuses. - Evidence of sinonasal tumor on clinical exam or imaging. - No evidence of distant metastasis - Patients must be evaluated by Head and Neck Surgery to establish surgical status as resectable, borderline resectable or unresectable. - Patients must be planned for combination immunotherapy (e.g. ipilimumab and nivolumab or nivolumab and relatlimab). - Patients must have a baseline skull base MRI unless contraindicated by medical or financial toxicity. - ECOG performance status ≤3. - Age ≥18 years because melanoma is extremely rare in patients <18 years of age and RT is considered high risk in this population due to risk of secondary malignancy and potentially growing tissues that may be adversely impacted by RT. - RT is a known teratogen. For this reason women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. (refer to MDA Policy CLN 1114) This includes all female patients, between the onset of menses and 55 years unless the patient presents with an applicable exclusionary factor which may be one of the following: • Postmenopausal (no menses in greater than or equal to 12 consecutive months). • History of hysterectomy or bilateral salpingo-oophorectomy. • Ovarian failure (Follicle Stimulating Hormone and Estradiol in menopausal range, who have received Whole Pelvic Radiation Therapy). • History of bilateral tubal ligation or another surgical sterilization procedure. Approved methods of birth control are as follows: Hormonal contraception (i.e. birth control pills, injection, implant, transdermal patch, vaginal ring), Intrauterine device (IUD), Tubal Ligation or hysterectomy, Subject/Partner post vasectomy, Implantable or injectable contraceptives, and condoms plus spermicide. Not engaging in sexual activity for the total duration of the trial and the drug washout period is an acceptable practice; however periodic abstinence, the rhythm method, and the withdrawal method are not acceptable methods of birth control. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. - Men treated or enrolled on this protocol must also agree to use adequate contraception prior to the study, for the duration of study participation, and 6 months after completion of RT. - Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with their ability to safely receive the study interventions are eligible for this trial. - Ability to understand and the willingness to sign a written informed consent document. Exclusion Criteria: - Previous radiation therapy to the sinonasal area. - Metastatic disease - Pregnant women are excluded from this study because RT is a known teratogen. - Patients who are less than 18 years of age because melanoma is extremely rare in this population and the treatment agent is a known carcinogen.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: M D Anderson Cancer Center

Address:
City: Houston
Zip: 77030
Country: United States

Status: Recruiting

Contact:
Last name: Devarati Mitra
Email: dmitra@mdanderson.org

Contact backup:
Last name: Devarati Mitra, MD

Start date: September 23, 2022

Completion date: July 31, 2026

Lead sponsor:
Agency: M.D. Anderson Cancer Center
Agency class: Other

Source: M.D. Anderson Cancer Center

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05546827
http://www.mdanderson.org