Intravenous Honokiol in Drug-Resistant Cancer: Two Case Reports

Context: Long-term patient survival in cancer is affected by drug resistance. Honokiol (HNK) is a small-molecule polyphenol isolated from the bark and seed cones of Magnolia officinalis . HNK has been shown to enhance the effects of chemotherapy and inhibit drug resistance in preclinical models. HNK...

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Main Authors: Isaac Eliaz MD, MS, LAc, Elaine Weil NP
Format: Article
Language:English
Published: SAGE Publishing 2020-06-01
Series:Integrative Cancer Therapies
Online Access:https://doi.org/10.1177/1534735420922615
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spelling doaj-58bea0495e0d4c94b0da3f95e3a835d32020-11-25T03:50:06ZengSAGE PublishingIntegrative Cancer Therapies1534-73541552-695X2020-06-011910.1177/1534735420922615Intravenous Honokiol in Drug-Resistant Cancer: Two Case ReportsIsaac Eliaz MD, MS, LAc0Elaine Weil NP1Amitabha Medical Clinic and Healing Center, Santa Rosa, CA, USAAmitabha Medical Clinic and Healing Center, Santa Rosa, CA, USAContext: Long-term patient survival in cancer is affected by drug resistance. Honokiol (HNK) is a small-molecule polyphenol isolated from the bark and seed cones of Magnolia officinalis . HNK has been shown to enhance the effects of chemotherapy and inhibit drug resistance in preclinical models. HNK was well tolerated in multiple animal models when administered orally, intravenously (IV), and via intraperitoneal route. However, there are limited human data on the use of HNK in general, and specifically via IV (HNK-IV) in cancer. Objective: We aim to assess the efficacy, safety, and tolerability of HNK-IV in patients with drug-resistant tumors. Methods: This is a case study of 2 cancer patients who utilized HNK-IV as part of their cancer treatment regimen. The initial infusion of HNK was 10 mg/kg body weight, and subsequent treatments were increased up to 50 mg/kg according to individual tolerance, over 2 weeks. Results: Positive clinical response was achieved in both patients, including improved symptoms and quality of life. No serious adverse side effects occurred, and there were no adverse effects on laboratory parameters (complete blood count, kidney, and liver function). Transient sedation and minor nausea were noted and resolved postinfusion. Conclusions: This is the first report of HNK-IV in human patients. Given the positive clinical results, safety, and tolerability, the use of HNK-IV warrants further investigation regarding optimum formulation, and its use as adjunctive therapy in cancer patients.https://doi.org/10.1177/1534735420922615
collection DOAJ
language English
format Article
sources DOAJ
author Isaac Eliaz MD, MS, LAc
Elaine Weil NP
spellingShingle Isaac Eliaz MD, MS, LAc
Elaine Weil NP
Intravenous Honokiol in Drug-Resistant Cancer: Two Case Reports
Integrative Cancer Therapies
author_facet Isaac Eliaz MD, MS, LAc
Elaine Weil NP
author_sort Isaac Eliaz MD, MS, LAc
title Intravenous Honokiol in Drug-Resistant Cancer: Two Case Reports
title_short Intravenous Honokiol in Drug-Resistant Cancer: Two Case Reports
title_full Intravenous Honokiol in Drug-Resistant Cancer: Two Case Reports
title_fullStr Intravenous Honokiol in Drug-Resistant Cancer: Two Case Reports
title_full_unstemmed Intravenous Honokiol in Drug-Resistant Cancer: Two Case Reports
title_sort intravenous honokiol in drug-resistant cancer: two case reports
publisher SAGE Publishing
series Integrative Cancer Therapies
issn 1534-7354
1552-695X
publishDate 2020-06-01
description Context: Long-term patient survival in cancer is affected by drug resistance. Honokiol (HNK) is a small-molecule polyphenol isolated from the bark and seed cones of Magnolia officinalis . HNK has been shown to enhance the effects of chemotherapy and inhibit drug resistance in preclinical models. HNK was well tolerated in multiple animal models when administered orally, intravenously (IV), and via intraperitoneal route. However, there are limited human data on the use of HNK in general, and specifically via IV (HNK-IV) in cancer. Objective: We aim to assess the efficacy, safety, and tolerability of HNK-IV in patients with drug-resistant tumors. Methods: This is a case study of 2 cancer patients who utilized HNK-IV as part of their cancer treatment regimen. The initial infusion of HNK was 10 mg/kg body weight, and subsequent treatments were increased up to 50 mg/kg according to individual tolerance, over 2 weeks. Results: Positive clinical response was achieved in both patients, including improved symptoms and quality of life. No serious adverse side effects occurred, and there were no adverse effects on laboratory parameters (complete blood count, kidney, and liver function). Transient sedation and minor nausea were noted and resolved postinfusion. Conclusions: This is the first report of HNK-IV in human patients. Given the positive clinical results, safety, and tolerability, the use of HNK-IV warrants further investigation regarding optimum formulation, and its use as adjunctive therapy in cancer patients.
url https://doi.org/10.1177/1534735420922615
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