Phase I study of the botanical formulation PHY906 with capecitabine in advanced pancreatic and other gastrointestinal malignancies

Saif, M. Wasif; Lansigan, F.; Ruta, S.; Lamb, L.; Mezes, M.; Elligers, K.; Grant, N.; Jiang, Z.-L.; Liu, S.H.; Cheng, Y.-C.

doi:10.1016/j.phymed.2009.12.016

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Volume 17, Issue 3 , Pages 161-169, March 2010

Phase I study of the botanical formulation PHY906 with capecitabine in advanced pancreatic and other gastrointestinal malignancies☆

M. Wasif Saif
- Yale University School of Medicine, Section of Medical Oncology, 333 Cedar Street, FMP 116 New Haven, CT 06520, USA
- Corresponding author. Tel.: +12037371875; fax: +12037853788.
F. Lansigan
- Yale University School of Medicine, Section of Medical Oncology, 333 Cedar Street, FMP 116 New Haven, CT 06520, USA
S. Ruta
- Yale University School of Medicine, Section of Medical Oncology, 333 Cedar Street, FMP 116 New Haven, CT 06520, USA
L. Lamb
- Yale University School of Medicine, Section of Medical Oncology, 333 Cedar Street, FMP 116 New Haven, CT 06520, USA
M. Mezes
- Yale University School of Medicine, Section of Medical Oncology, 333 Cedar Street, FMP 116 New Haven, CT 06520, USA
K. Elligers
- Yale University School of Medicine, Section of Medical Oncology, 333 Cedar Street, FMP 116 New Haven, CT 06520, USA
N. Grant
- Yale University School of Medicine, Section of Medical Oncology, 333 Cedar Street, FMP 116 New Haven, CT 06520, USA
Z.-L. Jiang
- Yale University School of Medicine, Section of Medical Oncology, 333 Cedar Street, FMP 116 New Haven, CT 06520, USA
S.H. Liu
- PhytoCeutica Inc., New Haven, CT, USA
Y.-C. Cheng
- Yale University School of Medicine, Section of Medical Oncology, 333 Cedar Street, FMP 116 New Haven, CT 06520, USA

published online 21 January 2010.

Abstract

Purpose

The botanical formulation, PHY906, has been used widely in Eastern countries to treat gastrointestinal symptoms including diarrhea, nausea and vomiting. PHY906 may also have anti-tumor properties and may potentiate the action of several chemotherapeutic agents based on pre-clinical studies. We conducted a Phase I study using PHY906 in combination with capecitabine in patients with advanced pancreatic and gastrointestinal malignancies to determine the maximum tolerated dose (MTD) of capecitabine in combination with PHY906.

Patients and Methods

This study was a single institution, open-label, Phase I study of PHY906 800mg BID on days 1-4 in combination with escalating doses of capecitabine (1000, 1250, 1500, and 1750mg/m²) orally twice daily on days 1-7 of a 14-day cycle (7/7 schedule). Capecitabine was increased until the appearance of dose limiting toxicities (DLTs). Measurements of efficacy included tumor response by Response Evaluation Criteria in Solid Tumors (RECIST).

Results

Twenty-four patients with a median age of 67 years (range 40-84) with pancreatic cancer (15), colon cancer (6), cholangiocarcinoma (1), esophageal cancer (1) and unknown primary (1) received a total of 116 cycles (median 5 cycles; range 1-17 cycles) over 4 dose levels of capecitabine. One DLT (Grade 4 AST/ALT, Grade 3 hyponatremia) was observed in the 1000mg/m² cohort of patients. No further DLT was observed in the subsequent cohorts and doses of capecitabine were escalated to 1750mg/m² BID. There were no DLTs at the maximum dose level of 1750mg/m², however, the delivered dose-intensity of capecitabine was similar at the 1750mg/m² dose level as the 1500mg/m² dose level. Therefore, the MTD was defined at 1500mg/m² of capecitabine in this dosing schedule with PHY906. One patient achieved a partial response, and 13 patients had stable disease that lasted more than six weeks.

Conclusion

The MTD of capecitabine was determined to be 1500mg/m² BID administered in a 7/7 schedule, in combination with PHY906 800mg BID on days 1-4. This combination was well tolerated and warrants further study.

Keywords: Capecitabine, PHY906, Herbal medicines, Diarrhea