Lung Cancer

Cancer remains the main use of Vilac Plus over the world since the publication of 3 clinical trials : Brain Tumor and Lung Cancer in 2006, then Cervical Cancer in 2007. The antiradical effectiveness of Vilac Plus had already been proved In Vitro (KRL Test).

Dr. Pongsiri Prathnadi

This 15 minutes long interview was taken from a December 2006 movie by William Oroso.

Dr Pongsiri Prathnadi is shown in his office of the Department of Surgery, Faculty of Medicine, Chiang Mai University, Thailand.

He is the President of the Anti-Tuberculosis Association of Chiang Mai Province.

He also presides the Society of Gerontology in Thailand.

His team first experimented the Vilac Plus® herbal drink as an immune booster, for HIV, and then on patients with various advanced cancers.

He talks about their findings (effects on immunity and quality of life especialy), and about the clinical trial results on cancer stade IIIB & IV at Khon Kaen University. (more…)

Lung Cancer – Clinical Trials

Evaluation of the effectiveness of the product the Vilac Plus® Eubiotic Drink G716/45 on Cancers Stage IIIB and IV.

Palliative treatment of advanced lung cancer with radiotherapy and thai herbal medicine as supportive remedy

Clinical trials HE480745 conducted at Srinagarind Public Hospital, Faculty of Medicine, Khon Kaen University, Thailand. Published in The Asean Journal of Radiology, September – December 2006.

Abstract

Objective

To evaluate the supportive effect of Thai herbal medicine, Vilac Plus (G716/45) on standard palliative radiotherapy in advanced stage IIIB-IV lung cancer compare with history control from the literature reports.

Patients and Methods

Thirteen patients in advanced lung cancer stage IIIB-IV with poor performance status were treated by palliative radiotherapy in adjuvant with the Thai herbal tonic solution (Vilac Plus G716/45).

Results

Thirteen patients (8 male, 5 female) in advanced stages lung cancer with poor performance status, stage IIIB 11 cases, stage IV 2 cases. Median age 66 years (range 44.4-83 years). The pathological diagnosis were 5 cases of squamous cell carcinoma, 2 cases of adenocarcinoma and 4 cases of clinically advanced lung cancer as of evidenced by computed tomography chest scan/chest X-ray. The results of treatment 4-6 weeks after radiotherapy revealed 76.92% (10/13 cases) of clinically improvement and 23.08% (3/13 cases) of clinically stable. Overall response rate was 46,15% (6/13) of partial response and 53.85% (7/13 cases) had shown stable diseases. Patterns of failure were found to be locally progressing 46.15% (6/13 cases) at the primary site, 30.77% (4/13 cases) at the locoregional, 23.08% (3/13 cases) at the locoregional with distant metastases. Median follow-up time is 18 months (range 7-50 months). Clinical benefit rate, evaluated at ≤ 15 months was 72.72%. However the median survival period analysis required longer follow-up and more detail assessment.

Conclusion

The results of this study are promising in the aspect of good quality of life and preferable because of the cost effectiveness to be used as an adjuvant for radiotherapy.

Montien PESEE M.D, Wichit KIRDPON Ph.D, Anucha PUAPAIROJ M.D, Sukachart KIRDPON M.D and Pongsiri PRATHNADI M.D

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