Hepatocellular Carcinoma Clinical Trial
Official title:
Pilot Phase 2 Study of Graviola (Guanabana) Leaves for The Treatment of Patients With Relapsed or Refractory Gastric Adenocarcinoma, Adenocarcinoma of Gastroesophageal Junction, Hepatocellular Carcinoma, Pancreatic Adenocarcinoma, Low Grade Lymphomas and Colorectal Adenocarcinoma
Guanabana, known also as Graviola or Annona muricata is a tropical fruit which has been commonly used as complimentary/alternative medicine in Latin American countries. The main compounds in Graviola are the annonaceous acetogenins. These acetogenins have been shown to be selective and toxic against various types of cancer cells in-vitro and in-vivo experimental animal models. In spite of this evidence of anti tumor activity of Graviola, no prospective clinical studies have been carried out to determine if it also has clinical activity.The Investigator have observed two patients at Auxilio Mutuo Cancer Center who experienced significant tumor shrinkage while taking a tea made of Graviola leaves. Neither of these patients were taking any other treatment for their cancer. The investigator propose to conduct a study using guanabana leaves extract in patients with Gastroesophageal junction(GEJ) adenocarcinoma, as well as in Gastric adenocarcinoma, Hepatocellular carcinoma, Pancreatic adenocarcinoma, Low Grade Lymphomas and Colorectal adenocarcinoma.
Status | Recruiting |
Enrollment | 54 |
Est. completion date | November 2023 |
Est. primary completion date | November 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Understand and voluntarily sign an informed consent form. - Age > 18 years at the time of signing the informed consent form. - Willing and able to adhere to the study visit schedule and other protocol requirements. - Must have measurable or evaluable disease. - All previous cancer therapy, including radiation, hormonal therapy and surgery, must have been discontinued at least 2 weeks prior to treatment in this study. - Performance status of = 2 on the Eastern Cooperative Oncology Group (ECOG) scale at study entry. Exclusion Criteria: - Patients actively taking guanabana or guanabana tea daily or who have used it at some point after their diagnosis of cancer. - Patients with Parkinson's disease. - Serum Total Bilirubin = 3.0 mg/dL - Serum Creatinine level = 3.0 mg/dL - Central Nervous System (CNS) involvement. - Known human immunodeficiency virus (HIV) infection; Known active hepatitis B or hepatitis C infection. - Females who are pregnant (positive urine test) or breast-feeding females. - Any history of a medical condition or a concomitant medical condition that, in the opinion of the investigator, would compromise the subject's ability to safely complete the study. |
Country | Name | City | State |
---|---|---|---|
Puerto Rico | Auxilio Mutuo Cancer Center | San Juan |
Lead Sponsor | Collaborator |
---|---|
Auxilio Mutuo Cancer Center |
Puerto Rico,
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | RECIST criteria | RECIST criteria will be used to measure response in solid tumors. | Through study completion, an average of 3 years. | |
Primary | Cheson criteria | Cheson criteria will be used for lymphomas. | Through study completion, an average of 3 years. | |
Primary | Blood Counts | Cases with Chronic Lymphocytic Leukemia will have their Complete Blood Counts monitored and the Absolute lymphocyte count will be followed for response. | Through study completion, an average of 3 years. |
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