Rapamycin in With High-Dose Etoposide and Cytarabine in Relapsed/Refractory Aggressive Lymphoid Malignancies
Status: | Terminated |
---|---|
Conditions: | Blood Cancer, Lymphoma |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 6/9/2016 |
Start Date: | January 2007 |
A Phase I/II, Open-label Single Institution Study Evaluating Rapamycin in Combination With High-dose Etoposide and Cytarabine in Relapsed or Refractory Aggressive Lymphoid Malignancies
Assess the safety, tolerability and efficacy of rapamycin in combination with HiVAC in
relapsed and refractory patients with aggressive lymphoid malignancies.
relapsed and refractory patients with aggressive lymphoid malignancies.
Inclusion Criteria:
- Advanced lymphoid leukemia (primary refractory ALL; Relapsed ALL; CML in lymphoid
accelerated phase or blast crisis; relapsed or refractory Burkitt's lymphoma;
relapsed or refractory T-cell adult leukemia/lymphoma; relapsed or refractory
lymphoblastic lymphoma
- >= 18 and <= 65 years of age ECOG performance status 0, 1 Life expectancy >= 4 weeks
Able to consume oral medication Required initial laboratory values: Creatinine <=
2.0mg/dL, total or direct bilirubin <= 1.5 mg/dL, SGPT(ALT) <=ULN, glucose < 200
mg/dL, negative pregnancy test for women with child bearing potential
Exclusion Criteria:
- Subjects must not be receiving any chemotherapy agents (except Hydroxyurea)
- Subjects must not have received high-dose Ara-C within 6 months of relapse
- Subjects must not be receiving growth factors, except for erythropoietin
- No currently active second malignancy other than non-melanoma skin cancers
- No subjects with uncontrolled high blood pressure, unstable angina, symptomatic
congestive heart failure, MI within the last 6 months or serious uncontrolled cardiac
arrhythmia
- Subjects taking Carbamazepine, Rifabutin, Rifampin, Rifapentine, St. John's wort,
Clarithromycin, Cyclosporine, Diltiazem, Erythromycin, Telithromycin, Verapamil,
Tacrolimus
- Known HIV positivity or AIDS-related illness
- Evidence of cerebellar dysfunction or prior history of cerebellar dysfunction with
Ara-C administration
- Pregnant or lactating
- Uncontrolled infection
- Taking fluconazole, voriconazole, itraconazole and ketoconazole currently or within
one week of study entry
We found this trial at
1
site
Click here to add this to my saved trials