High-Selenium Brassica Juncea, Irinotecan, and Capecitabine in Treating Patients With Advanced Cancer
Клучни зборови
Апстракт
Опис
OBJECTIVES:
Primary
- To determine the maximum tolerated dose of high-selenium Brassica juncea (BJ-Se) and capecitabine when administered in combination with irinotecan hydrochloride in patients with advanced malignancies.
- To determine the effects of BJ-Se on the pharmacokinetics of irinotecan hydrochloride and capecitabine.
Secondary
- To determine the effect of BJ-Se on the serum selenium and protein profile.
- To correlate response and tolerance to this regimen with expression of key enzymes involved as targets or with the metabolism of the components of treatment, including thymidylate synthase and dihydropyrimidine dehydrogenase.
- To evaluate changes to potential selenium related parameters.
OUTLINE: This is a multicenter, dose-escalation study of high-selenium Brassica juncea (BJ-Se) and capecitabine. The dose of capecitabine is escalated first, followed by dose escalation of BJ-Se.
Patients receive oral BJ-Se on days -7 to 21 in course 1 and on days 1-21 in all other courses. Patients also receive irinotecan IV on days 1 and 8 and oral capecitabine twice daily on days 1-14. Treatment repeats every 21 days in the absence of unacceptable toxicity or disease progression.
After the maximum tolerated dose (MTD) of capecitabine and BJ-Se are determined, additional patients are accrued and receive treatment at the MTD. Blood is collected from these patients during course 1 for pharmacokinetic studies.
Датуми
| Последен пат проверено: | 10/31/2015 |
| Прво доставено: | 10/18/2007 |
| Поднесено е проценето запишување: | 10/18/2007 |
| Прво објавено: | 10/21/2007 |
| Последното ажурирање е доставено: | 11/03/2015 |
| Последно ажурирање објавено: | 11/05/2015 |
| Крај на датумот на започнување на студијата: | 03/31/2006 |
| Проценет датум на примарно завршување: | 07/31/2012 |
| Проценет датум на завршување на студијата: | 07/31/2012 |
Состојба или болест
Интервенција / третман
Dietary Supplement: Treatment (high-selenium therapy and chemotherapy)
Drug: Treatment (high-selenium therapy and chemotherapy)
Drug: Treatment (high-selenium therapy and chemotherapy)
Фаза
Групи за раце
| Рака | Интервенција / третман |
|---|---|
| Experimental: Treatment (high-selenium therapy and chemotherapy) | Dietary Supplement: Treatment (high-selenium therapy and chemotherapy) Dose Level A: 3200 mcg orally day -7 through duration of treatment. Dose Level B: 4800 mcg orally day -7 through duration of treatment. Dose Level C: 6400 mcg orally day -7 through duration of treatment. Dose Level D: 7200 mcg orally day -7 through duration of treatment. Dose Level E: 8000 mcg orally day -7 through duration of treatment. |
Критериуми за подобност
| Возраст подобни за студии | 18 Years До 18 Years |
| Полови квалификувани за студии | All |
| Прифаќа здрави волонтери | Да |
| Критериуми | Inclusion Criteria: - Patients with advanced, biopsy-proven cancer for which there is no standard curative therapy - Karnofsky Performance status >= 60 - Prior therapy completed at least 3 weeks before protocol treatment initiation with recovery from any side-effects - Prior capecitabine and/or irinotecan are allowed if subject did not progress while on treatment or within 6 months of treatment with these medications either alone or in combination - Prior radiation therapy allowed if < 30% of marrow treated - Alanine aminotransferase (ALT) and alkaline phosphatase with 3x upper limit of normal - Serum bilirubin within normal limits - Absolute neutrophil count >= 15000/ul - Platelet count >= 100,000/ul - Hemoglobin >= 10 gm/dl - transfusion allowed to achieve this - Serum creatinine within 1.5 x upper limit of normal - Ability to understand and sign an IRB approved informed consent - Ability to use appropriate contraception and no evidence of pregnancy in female patients of reproductive potential Exclusion Criteria: - No significant medical or psychiatric condition that would make treatment unsafe - No active brain metastases (patients who have treated brain metastases and are stable off of steroids are eligible) - Nursing women - Patients must be able to comply with protocol related studies and follow-up - Patients who are UGT1a1 7/7 positive will be excluded from the dose escalation portion of the trial, but may participate in the cohort of patients treated at the MTD |
Исход
Мерки на примарниот исход
1. Maximum tolerated dose of high-selenium Brassica juncea, irinotecan hydrochloride and capecitabine [After two 21 day cycles of treatment]
2. Toxicity [After two 21 day cycles of treatment]
3. Pharmacokinetics [For patients treated at the MTD only at the end of cycle one of treatment]
Секундарни мерки на исходот
1. Serum selenium and protein profile [21 days after the start of the last cycle of treatment]
