Methylphenidate and Physical Activity to Reduce Cancer Related Fatigue Due to Anti PD1 Immunotherapy

• Status: Active, not recruiting
• Trial end date: 2022-12-31
• Target enrollment: 0
• Participant gender: All

Summary

This phase III trial studies how well methylphenidate and physical activity works in reducing cancer-related fatigue in patients who are receiving anti-PD1 immunotherapy for cancer that has spread to other places in the body. Central nervous systems stimulants, such as methylphenidate, may help to improve cognitive function. Physical activity uses techniques, such as aerobic and resistance exercises, which may help to improve quality of life. Giving methylphenidate and physical activity may help in reducing cancer-related fatigue in patients with metastatic cancer who receive anti-PD1 immunotherapy.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: M.D. Anderson Cancer Center
• Collaborator: National Cancer Institute (NCI)
• Treatments: Methylphenidate

Criteria

Inclusion Criteria:

• Part 1: have a diagnosis of metastatic or recurrent cancer and previously received anti PD1 immunotherapy provided that they received therapy up to 1 month prior to enrollment

• Part 1: be willing to engage in follow-up telephone calls with a research staff

• Part 1: have telephone access so they can be contacted by the research staff

• Part 1: hemoglobin level of >= 8 g/dL within 2 weeks of enrollment

• Packed red blood cell (PRBC) transfusions will be allowed to patients with hemoglobin < 8 g/dl

• Part 1: be able to understand the description of the study and give written informed consent

• Part 1: able to read, write and speak English

• Part 2: have a diagnosis of metastatic or recurrent cancer and previously received anti PD1 immunotherapy provided that they received therapy up to 1 month prior to enrollment

• Part 2: be willing to engage in follow-up telephone calls with a research staff

• Part 2: have telephone access so they can be contacted by the research staff

• Part 2: have a hemoglobin level of >=8 g/dL within 2 weeks of enrollment

• PRBC transfusions will be allowed to patients with hemoglobin < 8 g/dl

• Part 2: be able to understand the description of the study and give written or verbal informed consent

• Part 2: able to read, write and speak English

• Part 2: presence of fatigue as defined FACIT-F subscale of =< 34 on a 0 to 52 scale (in which 52 = no fatigue and 0 = worst possible fatigue)

• Part 2: not currently taking methylphenidate, or have taken it within the previous 10 days

• Part 2: able to complete the baseline assessment forms

• Part 2: able to understand the recommendations for participation in the study

• Part 2: can be enrolled directly to part 2 independent of part 1 if on immunotherapy and having a FACIT-F fatigue =< 34, and able to complete baseline assessment and bloodwork as detailed in Part 1 at baseline and day 14 +/-3 days. Treating Oncologist should agree for participation in the intervention trial

Exclusion Criteria:

• Part 1: patients will be excluded if (1) have clinical evidence of cognitive failure as evidenced by Memorial Delirium Assessment Scale score of >= 13 at baseline completed in person, by phone, or via video-conference

• Part 2: Patients will be excluded if (1) have clinical evidence of cognitive failure as evidenced by Memorial Delirium Assessment Scale score of >= 13 at baseline completed in person, by phone, or via video-conference

• Part 2: have a major contraindication to MP (e.g., allergy/hypersensitivity to study medications or their constituents), or conditions making adherence difficult as determined by the attending physician

• Part 2: on monoamine oxidase inhibitors, tricyclic antidepressants, or clonidine

• Part 2: history of glaucoma

• Part 2: history of have severe cardiac disease (New York Heart Association functional class III or IV)

• Part 2: tachycardia and/or uncontrolled hypertension

• Part 2: currently receiving anticoagulants, anticonvulsants (phenobarbital, diphenylhydantoin, primidone), phenylbutazone, and/or tricyclic drugs (imipramine, clomipramine, or desipramine)

• Part 2: patients with Cut Down, Annoyed, Guilty and Eye Opener-Adapted to Include Drugs (CAGE-AID) >= 2