Clinical Trial Finder

Inclusion Criteria:

• - Age ≥ 18 years.

• - Diagnosis of glioma and intention to treat with either new or ongoing systemic therapy for at least 6 months.

• - NOTE: Patient may be enrolled following completion of surgery and/or radiation therapy for newly diagnosed or recurrent tumor.

• - NOTE: Any number of prior recurrences is permitted.

• - Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2, AND Karnofsky performance status (KPS) of ≥ 60.

• - Expected survival ≥ 6 months in the opinion of treatment team.

• - Willing and able to adhere with the protocol for the duration of the study including undergoing treatment, and attending scheduled visits, and examinations.

• - Negative pregnancy test ≤ 8 days prior to registration for persons of childbearing potential only.

• - Provide written informed consent.

• - Ability to complete assessments and questionnaires by themselves or with assistance.

Exclusion Criteria:

• - Pregnant or nursing, imprisoned, or lacking capacity for understanding.

- Uncontrolled and/or intercurrent illness or other condition which limits safety of or compliance with study proceedings

PRIMARY OBJECTIVE:

• I. Determine the feasibility of the remote chemotherapy management and patient monitoring platform glioma home-based sequential therapy (GHoST) protocol among patients with glioma undergoing systemic therapy.

SECONDARY OBJECTIVES:

• I. Evaluate compliance, adherence, and feasibility in terms of the adherence to systemic therapy monitored remotely.

• II. Determine progression free survival (PFS) for each therapeutic evaluated for newly diagnosed or recurrent glioma, stratified by tumor type.

• III. Determine objective response rate (ORR) for each therapeutic evaluated for newly diagnosed or recurrent glioma, stratified by tumor type.

• IV. Assess the safety and tolerability of remote chemotherapy management and patient monitoring among patients with glioma undergoing systemic therapy.

EXPLORATORY OBJECTIVES:

• I. Assess the acceptance or satisfaction of patients with the remote monitoring in this trial and how these may differ between newly diagnosed and recurrent glioma.

• II. Investigate PFS based on therapeutic sequence administered.

• III. Explore potential differences in compliance, adherence, and satisfaction measures and how they may correspond to health disparities and social determinants of health.

• IV. Compare access to neuro-oncology care at Mayo Clinic among patients with low socioeconomic status assessed based on the Mayo Clinic Housing-Based Socioeconomic Status (HOUSES) Index during the two years following study activation compared to historical utilization data.

• V. Compare access to neuro-oncology care at Mayo Clinic among patients with increased distance from academic centers assessed by geospatial index during the two years following study activation compared to historical utilization data.

OUTLINE: Patients receive access to the remote chemotherapy management and patient monitoring platform to watch educational videos, report when medication is taken or missed, and report any symptoms related to cancer or medication side effects on study. Patients also receive standard of care chemotherapy as assigned by their treating physician as part of the platform on study. Upon completion of standard of care chemotherapy, if there is no disease progression, patients transition to surveillance for up to 1 year. Patients who experience disease progression during treatment or surveillance may rejoin the platform and/or be assigned by their treating physician to a different chemotherapy agent as part of the platform. Patients also undergo magnetic resonance imaging (MRI) or computed tomography (CT) throughout the study.

Arms

Experimental: Supportive Care (remote chemotherapy management)

Patients receive access to the remote chemotherapy management and patient monitoring platform to watch educational videos, report when medication is taken or missed, and report any symptoms related to cancer or medication side effects on study. Patients also receive standard of care chemotherapy as assigned by their treating physician as part of the platform on study. Upon completion of standard of care chemotherapy, if there is no disease progression, patients transition to surveillance for up to 1 year. Patients who experience disease progression during treatment or surveillance may rejoin the platform and/or be assigned by their treating physician to a different chemotherapy agent as part of the platform. Patients also undergo MRI or CT throughout the study.

Interventions

Drug: - Chemotherapy

Receive standard of care chemotherapy

Procedure: - Computed Tomography

Undergo CT

Other: - Internet-Based Intervention

Receive access to the remote chemotherapy management and patient monitoring platform

Procedure: - Magnetic Resonance Imaging

Undergo MRI

Procedure: - Neurologic Examination

Ancillary studies

Other: - Questionnaire Administration

Ancillary studies

Behavioral: - Surveillance

Undergo surveillance