Hematologic Malignancies, Solid Tumors
Conditions
Brief summary
To collect and analyze specimens that will correlate with clinical outcomes such as acute and late toxicities, quality of life, local control, and survival of patients treated with photon/proton therapy.
Interventions
None listed
Sponsors
Mayo Clinic
Study design
Observational model
OTHER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
1. Treated with photon/proton at Mayo Clinic Rochester in Radiation Oncology 2. Radiation therapy for curative intent
Exclusion criteria
None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| analyze acute and late toxicities using CTCAE 4.03 | Patients will be followed for the duration of their life, an expected average of 20 years |
| analyze quality of life using LASA-3 and FACT-E | Patients will be followed for the duration of their life, an expected average of 20 years |
Secondary
| Measure | Time frame |
|---|---|
| analyze local control through tumor assessments | Patients will be followed for the duration of their life, an expected average of 20 years |
| analyze survival by contacting patient and EMR (electronic medical record) review | Patients will be followed for the duration of their life, an expected average of 20 years |
Countries
United States
Contacts
CONTACTClinical Trials Referral Office
PRINCIPAL_INVESTIGATORNadia N. Laack, MD
Mayo Clinic
Outcome results
None listed