Abstract | BACKGROUND: METHODS: Patients with metastatic RCC were enrolled in a Phase I dose escalation trial. Patients received fixed dose rate gemcitabine on Days 1, 8, and 15 in combination with capecitabine, an oral 5-FU analog, given on Days 1-21 of a 28-day cycle. RESULTS: Nine patients were enrolled at one of two dose levels. The initial dose level produced dose-limiting toxicity (DLT), including prominent palmar-plantar erythrodysesthesia ( hand-foot syndrome). A modified second dose level also resulted in DLT, precluding further study. No central nervous system (CNS) toxicity was observed in three patients with CNS metastases. Two patients demonstrated an objective partial response. CONCLUSIONS: Fixed dose rate gemcitabine in combination with capecitabine produced unacceptable toxicity in patients with advanced RCC. Further development of this schedule in RCC cannot be recommended.
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Authors | Brian I Rini, Vivian Weinberg, Eric J Small |
Journal | Cancer
(Cancer)
Vol. 103
Issue 3
Pg. 553-8
(Feb 01 2005)
ISSN: 0008-543X [Print] United States |
PMID | 15612026
(Publication Type: Clinical Trial, Clinical Trial, Phase I, Journal Article)
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Copyright | (c) 2004 American Cancer Society |
Chemical References |
- Antimetabolites, Antineoplastic
- Deoxycytidine
- Capecitabine
- Fluorouracil
- Gemcitabine
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Topics |
- Adult
- Aged
- Antimetabolites, Antineoplastic
(administration & dosage, adverse effects)
- Antineoplastic Combined Chemotherapy Protocols
(administration & dosage, adverse effects)
- Capecitabine
- Carcinoma, Renal Cell
(drug therapy, secondary)
- Deoxycytidine
(administration & dosage, adverse effects, analogs & derivatives)
- Drug Administration Schedule
- Female
- Fluorouracil
(analogs & derivatives)
- Foot Dermatoses
(chemically induced)
- Hand Dermatoses
(chemically induced)
- Hematologic Diseases
(chemically induced)
- Humans
- Infusions, Intravenous
- Kidney Neoplasms
(drug therapy, pathology)
- Male
- Middle Aged
- Neoplasm Staging
- Severity of Illness Index
- Treatment Outcome
- Gemcitabine
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