Docetaxel and St. John's Wort in Treating Patients With Solid Tumors That Cannot Be Removed By Surgery

Alliance for Clinical Trials in Oncology

Overview

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. St. John's wort may interfere with the effectiveness of chemotherapy. It is not yet known if chemotherapy is more effective with or without St. John's Wort in treating solid tumors. PURPOSE: Randomized phase III trial to compare the effectiveness of docetaxel with or without St. John's wort in treating patients who have solid tumors that cannot be removed by surgery.

OBJECTIVES: * Determine the effect of Hypericum perforatum (St. John's Wort) on the pharmacokinetic clearance of docetaxel in patients with unresectable solid tumors. * Determine the effect of Hypericum perforatum on the production and plasma concentrations of M4-C13-hydroxydocetaxel in these patients. * Determine the effects of this drug on the pharmacodynamics of docetaxel in these patients. * Determine the relationship between the effects of this drug on docetaxel metabolic clearance and CYP3A4/CYP3A5 genotype in these patients. * Determine the relationship between the effect of this drug on docetaxel metabolic clearance and p-glycoprotein genotype in these patients. * Determine the relationship between the effect of this drug on docetaxel clearance and pregnane receptor genotype in these patients. * Assess compliance with this drug in these patients. * Assess the steady state concentrations of hyperforin, one of the putative psychoactive components of Hypericum perforatum, in these patients. OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients who have not been receiving chronic Hypericum perforatum (St. John's Wort) are assigned to group A, while a cohort of 8 patients who have been receiving chronic Hypericum perforatum are assigned to group B. * Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive oral placebo three times daily on days 1-14 and docetaxel IV over 1 hour on day 15. * Arm II: Patients receive oral Hypericum perforatum three times daily on days 1-14 and docetaxel as in arm I. * Group B (non-randomized group): Patients receive docetaxel as in arm I and continue to receive their chronic regimen of Hypericum perforatum except on day 15. Treatment in both groups repeats every 21 days for 2 courses in the absence of disease progression or unacceptable toxicity. Patients are followed for new primaries and survival only. PROJECTED ACCRUAL: Approximately 92 patients will be accrued for this study.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Conditions

Adult Solid Tumor Breast Cancer Head and Neck Cancer Kidney and Urinary Cancer Male Reproductive Cancer Thorax and Respiratory Cancer

Interventions

Hypericum perforatumDRUG

docetaxelDRUG

placeboOTHER

Eligibility

Sex: ALLMin age: 18 YearsMax age: 120 Years

Medical Language ↔ Plain English

DISEASE CHARACTERISTICS: * Histologically confirmed unresectable solid tumor, including, but not limited to, the following: * Lung cancer * Breast cancer * Head and neck cancer * Bladder cancer * Prostate cancer * Must be suitable for treatment with single-agent docetaxel * Hormone receptor status: * Not specified PATIENT CHARACTERISTICS: Age: * 18 and over Sex: * Male or female Menopausal status: * Not specified Performance status: * CTC 0-2 Life expectancy: * Not specified Hematopoietic: * Granulocyte count at least 1,500/mm\^3 * Platelet count at least 100,000/mm\^3 Hepatic: * Bilirubin less than upper limit of normal (ULN) * Alkaline phosphatase less than 2.5 times ULN Renal: * Creatinine no greater than 1.5 times ULN * BUN no greater than 1.5 times ULN Other: * Not pregnant or nursing * Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: * No prior bone marrow transplantation * No concurrent filgrastim (G-CSF) or sargramostim (GM-CSF) Chemotherapy: * See Disease Characteristics * At least 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) * No prior docetaxel * No more than 2 prior chemotherapy regimens * No other concurrent chemotherapy Endocrine therapy: * No concurrent hormonal agents except steroids for adrenal failure or hormones for non-disease-related conditions (e.g., insulin for diabetes) Radiotherapy: * At least 3 weeks since prior radiotherapy * No concurrent palliative radiotherapy Surgery: * At least 4 weeks since prior major surgery Other: * At least 6 months since prior Hypericum perforatum (St. John's Wort) * At least 1 week since prior CYP3A enzyme inducers including: * Phenobarbital * Phenytoin * Carbamazepine * Lamotrigine * Rifampin * Rifabutin * Isoniazid * Sulfinpyrazone * Pioglitazone * Anti-HIV drugs such as efavirenz or nevirapine * At least 1 week since prior CYP3A enzyme inhibitors including: * Erythromycin * Clarithromycin * Azithromycin * Roxithromycin * Ketoconazole * Fluconazole * Itraconazole * Metronidazole * Chloramphenicol * Ritonavir * Saquinavir * Indinavir * Nelfinavir mesylate * Delavirdine * Amiodarone * Cyclosporine * Tacrolimus * Sirolimus * Nefazodone * Fluvoxamine * No concurrent CYP3A enzyme inducers * No concurrent CYP3A enzyme inhibitors * No ethanol (especially red wine), grape fruit juice, or seville orange juice (CYP3A enzyme inhibitor) within 3 days before or after receiving docetaxel

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.