약물

메벤다졸 - 알벤다졸 투여량

unicircle 2021. 9. 26. 01:55

Table 1

Antitumorigenicity of benzimidazole anthelmintics in clinical aspects

StageCancer typePurposeMethodsResults and ongoingRef.

Phase 1 36 patients with refractory solid tumors Maximum-tolerated dose Albendazole: p.o. on a day 1–14 of a 3-weekly cycle, from 400 mg b.d. to 1,200 mg b.d. 2,400 mg/day from 1,200 mg b.d. (95)
Decreased plasma VEGF
Patients (16%) had a tumor marker response with a fall of at least 50%
Adverse effects: myelosuppression, fatigue and mild gastrointestinal upset
Case report 74-year-old man with metastatic colon cancer Treatment for significant progression in the lungs and abdominal lymph nodes with new partly, poorly defined liver metastases Mebendazole: 100 mg b.d. for 6 wk Near complete remission of the metastases in the lungs and lymph nodes and a good partial remission in the liver (96)
48-year-old man with adrenocortical carcinoma Treatment for failure or intolerance to conventional treatments with mitotane, 5-fluorouracil, streptozotocin, bevacizumab, and radiation therapy Mebendazole: 100 mg b.d. for 19 months Regression of hepatic metastatic lesions and subsequently remained stable for 19 months, but progressed after 24 months (97)
No clinically adverse effects; quality of life was satisfactory
Phase 1 A patient with hepatocellular carcinoma with metastasis Evaluation of albendazole Albendazole: 10 mg/kg/day, p.o. in 2 divided doses for 28 days Stabilization of the disease, but because of neutropenia, treatment was stopped on day 19 (98)
8 patients with colorectal cancer with metastasis Decreased carcinoembryonic antigen (CEA) in 2 patients and stabilized in 3 patients, an initial stabilization (5–10 days) in 2 patients (98)
No significant changes in liver and kidney function tests, but neutropenia in 2 patients
Phase 1 24 high-grade glioma Mebendazole in newly diagnosed high-grade glioma patients receiving temozolomide Mebendazole: 500 mg chewable tablets with meals, p.o. 3 times every day on 28-day cycle Study period: April 4, 2013 to September 2025  
NCT01729260 Location: The Johns Hopkins Hospital, Baltimore, Maryland, United States
NCT02644291 21 high-grade glioma Phase I study of mebendazole therapy for recurrent/progressive pediatric brain tumors Mebendazole: 500 mg chewable tablets, 3 divided doses with meals Study period: May 2016 to June 2022  
Location: Johns Hopkins All Children's Hospital
Saint Petersburg, Florida, United States
Johns Hopkins University School of Medicine
Baltimore, Maryland, United States
Phases 1/2 36 low- and high-grade glioma A phase I study of mebendazole for the treatment of pediatric gliomas Mebendazole: 50, 100, and 200 mg/kg/day, p.o. and b.d. for 70 wk for low-grade glioma patients and 48 wk for high-grade glioma patients Study period: October 22, 2013 to April 2020  
NCT01837862 Location: Cohen Children's Medical Center of New York, New Hyde Park, New York, United States
Phase 2 250 patients with malignant disease that is considered untreatable, progressive and fatal Clinical evaluation of a new form of cancer therapy based on the principles of atavistic metamorphosis (atavistic chemotherapy) Anti-bacterial, anti-fungal, anti-protozoal agents: anti-cancer properties of albendazole and mebendazole Study period: July 2011 to December 31, 2023  
NCT02366884 Location: Dr. Frank Arguello Cancer Clinic
San Jose del Cabo, Baja California Sur, Mexico
Instituto de Ciencia y Medicina Genomica
Torreon, Coahuila, Mexico
Phase 3 40 patients with stage 4 colorectal cancer Mebendazole as adjuvant treatment for colon cancer Mebendazole Study period: April 1, 2019 to December 2028  
NCT03925662 Location: Sherief Abd-Elsalam, Cairo, Egypt
NCT02201381 207 participants with cancer Study of the safety, tolerability and efficacy of metabolic combination treatments on cancer (METRICS) Mebendazole: 100 mg, p.o. and u.i.d. for study duration Study period: May 22, 2017 to May 22, 2022  
Location: Care Oncology Clinic, London, United Kingdom

b.d., twice daily; p.o., oral administration; u.i.d., once daily dosage.

 

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458798/