Prospective Evaluation of Hypoxia in Primary Melanoma

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

When controlling for tumor present in the Sentinel lymph node (SLN), intranodal hypoxia, as measured by Carbonic Anhydrase IX (CAIX IHC), is associated with worse PFS. This suggests that melanoma tumors may be utilizing deregulated metabolism as a means of propagating themselves to the next station of metastasis. This study aims to prospectively validate previous findings. Patients who are to undergo WLE and SLNB per standard of care (SOC) will be evaluable. It is hypothesized that SLN(s) with increased hypoxia, as measured by pimonidazole staining, will be associated with worse Progression-free Survival (PFS).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
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• Must be willing and able to provide written informed consent for the study.

• Must have histologically confirmed melanoma for which a Sentinel Lymph Node Biopsy (SLNB) is indicated per the treating physician.

• Cutaneous or mucosal melanoma is permitted.

• Female patients of childbearing potential must have a negative urine or serum pregnancy test within 7 days from the time of pimonidazole administration.

‣ Female subjects of childbearing potential must not be pregnant or breastfeeding. Female subjects will be considered of non-reproductive potential if they:

• are postmenopausal (defined as at least 12 months with no menses without an alternative medical cause; in women \< 45 years of age a high follicle stimulating hormone (FSH) level in the postmenopausal range may be used to confirm a post-menopausal state in women not using hormonal contraception or hormonal replacement therapy. In the absence of 12 months of amenorrhea, a single FSH measurement is insufficient.

∙ have had a hysterectomy and/or bilateral oophorectomy, bilateral salpingectomy or bilateral tubal ligation/occlusion, at least 6 weeks prior to screening.

∙ have a congenital or acquired condition that prevents childbearing.

⁃ Female and male subjects of reproductive potential must agree to avoid becoming pregnant or impregnating a partner, respectively, while receiving study drug and 1 week after the dose of study drug for females and 2 weeks for males by complying with one of the following:

• practice abstinence from heterosexual activity

∙ use (or have their partner use) acceptable contraception during heterosexual activity.

• Adequate hematologic function: white blood cells (WBC) ≥ 2,500/μL, platelet count ≥ 100,000/μL, hemoglobin ≥ 8.0 g/dL

• Adequate renal function: serum creatinine ≤ 2.0 mg/dL

• Adequate hepatic function: serum alkaline phosphatase, bilirubin, and ALT ≤ twice the institutional upper limit of normal

Locations
United States
Pennsylvania
UPMC Hillman Cancer Center
RECRUITING
Pittsburgh
Contact Information
Primary
Danielle L Bednarz, RN, BSN
bednarzdl@upmc.edu
4126231191
Backup
Amy Rose, RN, BSN
kennaj@upmc.edu
412-647-8587
Time Frame
Start Date: 2025-04-09
Estimated Completion Date: 2027-03-31
Participants
Target number of participants: 50
Treatments
Pimonidazole
Single dose of 0.5 gm/m\^2 of pimonidazole (approximately 13 mg/kg)
Related Therapeutic Areas
Sponsors
Leads: Yana Najjar
Collaborators: Hypoxyprobe

This content was sourced from clinicaltrials.gov