Sertraline Compared With Hypericum Perforatum (St.John's Wort) in Treating Depression

Inclusion Criteria

• •Mild or moderate depression as determined by the following criteria (see Section 7.1 and 8.0)
• •Mild : HRSD score 10-14; moderate: HRSD score 15-19 (Appendix IV)
• •At least 2 of nine symptoms of depression on the PHQ (Appendix V)
• •At least one of the nine PHQ symptoms must be either depressed/irritable mood or anhedonia
• •Histologically or cytologically documented solid tumor, lymphoma, or primary or metastatic brain tumor \> 6 months from radiation with stable disease or no evidence of disease.
• •Concurrent cancer chemotherapy with sertraline or St. John's wort is not allowed, therefore patients must have no plan for chemotherapy for 4 months
• •Prior chemotherapy is allowed, but patients must be \>4 weeks from prior chemotherapy except \>6 weeks from prior mitomycin-C or nitrosourea
• •Patients receiving Rituxin, Herceptin, Erbitux, Interferon, etc. are eligibile for this study while under treatment.
• •Prior or concurrent radiation is allowed except brain irradiation for brain metastases or primary brain tumor. Must be \> 6 months from radiation with stable disease or no evidence of disease.
• •Age \> 18 years
• •ECOG performance status 0 -1 (Appendix III)
• •Life expectancy \>4 months
• •Required initial laboratory values (within 3 days of registration): hemoglobin \>10 g/dl and bilirubin \<1.5 mg/dl, negative pregnancy test
• •Signed protocol specific informed consent prior to registration
• •Patient recruitment this study will be done through the out patient clinic. The research PI or designee including clinic physician, resident, research nurse or research assistant will review medical information to determine or verify protocol eligibility either at the time the patient is being seen in the clinic for a routine visit/consult or prior to the patient's clinic visit.