pentostatin has been researched along with Kidney-Failure--Chronic* in 2 studies
1 review(s) available for pentostatin and Kidney-Failure--Chronic
Article | Year |
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The management of myelomatosis.
Topics: Amyloidosis; Antineoplastic Combined Chemotherapy Protocols; Bacterial Infections; Bone Marrow Transplantation; Clinical Trials as Topic; Coformycin; Combined Modality Therapy; Humans; Interferons; Kidney Failure, Chronic; Leukemia, Myeloid, Acute; Multiple Myeloma; Neoplasm Recurrence, Local; Neoplasms, Multiple Primary; Palliative Care; Pentostatin | 1987 |
1 trial(s) available for pentostatin and Kidney-Failure--Chronic
Article | Year |
---|---|
The management of myelomatosis.
Topics: Amyloidosis; Antineoplastic Combined Chemotherapy Protocols; Bacterial Infections; Bone Marrow Transplantation; Clinical Trials as Topic; Coformycin; Combined Modality Therapy; Humans; Interferons; Kidney Failure, Chronic; Leukemia, Myeloid, Acute; Multiple Myeloma; Neoplasm Recurrence, Local; Neoplasms, Multiple Primary; Palliative Care; Pentostatin | 1987 |
1 other study(ies) available for pentostatin and Kidney-Failure--Chronic
Article | Year |
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[Pentostatin treatment for a patient with chronic type adult T-cell leukemia undergoing hemodialysis].
This is a preliminary feasibility study to assess the pharmacokinetics and efficacy of pentostatin in a patient undergoing dialysis. Pentostatin is a safe and well-tolerated medication, but a dose reduction is required for patients with renal insufficiency. We present a patient with chronic adult T-cell leukemia, whose white blood cell count exceeded 100 X 10(9)/l, and end-stage renal disease, receiving long-term thrice-weekly dialysis. The initial treatment with oral cyclophosphamide or with oral etoposide resulted in no response. After informed consent was obtained, pentostatin (1, 2, or 3mg/m2) was administered. 1 or 2 hours after injection, the patient received hemodialysis over 4 hours to remove any of the drug remaining in his system. Plasma concentrations of pentostatin were calculated with the known pharmacokinetics parameters. The differential equations describing a 2-compartment open-infusion pharmacokinetic model were fitted to the measured concentration-time data. Tumor lysis syndrome occurred 4 days after the course of the highest dose (3mg/m2), and the patient achieved complete remission. Anorexia, graded as 2 according to the NCI-CTC classification system, occurred and continued for four weeks. Pentostatin therapy consisting of the decreased dose (2mg/m2) was then administered every other week and provided a transient partial response with mild anorexia. Consequently, pentostatin can be considered as one of the chemotherapeutic regimens available for a patient undergoing dialysis. Topics: Antibiotics, Antineoplastic; Chronic Disease; Dose-Response Relationship, Drug; Feasibility Studies; Female; Humans; Kidney Failure, Chronic; Leukemia-Lymphoma, Adult T-Cell; Middle Aged; Models, Biological; Pentostatin; Remission Induction; Renal Dialysis | 2005 |