Overview
The goal of this observational study is to assess gaps in education about exercise, sexual health, fertility, survivorship, financial issues, interpersonal relationships, and clinical trial participation among adolescents and young adults with cancer.
Participants will be asked to complete a series of questionnaires.
Description
This descriptive study aims to assess current needs of adolescents and young adults with cancer.
Participants who were diagnosed with cancer between the ages of of 15-39 will be asked to complete questionnaires to provide information on their cancer treatments and follow-up care, fertility preservation, clinical trial participation, emotional health and interpersonal relationships, financial burden, mental health and additional general information (health related, sexual orientation, perceived needs for support, resources, programs and activities).
Eligibility
Inclusion Criteria:
- A diagnosis of MCADD and molecular confirmation of at least one copy of the common c.985A\>G mutation.
- ≥4 years of age
- Able to perform and comply with study activities placement of a continuous glucose monitor, IV catheter, and all blood draws.
- Negative pregnancy test for all female subjects of childbearing age.
- Signed informed consent by the subject or parent/guardian of minors.
- All females of childbearing age and all sexually active males must agree to use an acceptable method of contraception throughout the study. Appropriate contraceptive methods include hormonal contraceptives (oral, injected, implanted, or transdermal), tubal ligation, intrauterine device, hysterectomy, vasectomy, or double barrier methods. Abstinence is an acceptable form of birth control, though appropriate contraception must be used if the subject becomes sexually active.
- Willing and able to adhere to requirements for maintaining continuous glucose monitoring.
Exclusion Criteria:
- Use of any investigational drug within 30 days of Day 1.
- Active infection (viral or bacterial) or any other intercurrent condition as reported by the subject or noted on physical exam at screening.
- Any clinical or laboratory abnormality of Grade 3 or greater severity according to the CTCAE v5.0, or Grade 3 elevations in liver enzymes, defined as levels 5-20 times ULN in alanine aminotransferase (ALT/SGPT), or aspartate aminotransferase (AST/SGOT) in a clinically stable subject.
- Any clinical or laboratory abnormality or medical condition that, at the discretion of the investigator, may put the subject at increased risk by participating in this study.
- Use of any medication known to significantly affect renal clearance (e.g., probenecid) or to increase protein catabolism (e.g., corticosteroids), or other medication known to increase ammonia levels (e.g., valproic acid or haloperidol), within the 48 hours prior to Day 1 and throughout the study.
- Subjects with renal insufficiency will be excluded from the study. Cutoff eGFR \<60 mL/min/1.73m2 (GFR categories G3a-G5) will be used as measure of renal insufficiency.
- Use of sodium benzoate within one week of Day 1.
- Known hypersensitivity to PAA or PBA.
- Breastfeeding or lactating females.
- Subjects at risk of hypokalemia due to pre-existing diagnosis or on medications that can cause hypokalemia.
- Subjects with type 1 or type 2 diabetes, or who take medications as part of their routine care that can cause hypoglycemia
- A positive urine drug screen at screening for drugs without a prescription
- Subjects who are taking medications in the antimetabolite drug class (e.g., hydroxyurea, 5-fluorouracil (5-FU), methotrexate) will be excluded; these medications can interfere with the DEXCOM sensor and cause inaccurate glucose readings
