Evaluation of Ifosfamide for Treatment of Various Canine Neoplasms
Male
Lymphoma
Records
Sarcoma
Survival Analysis
3. Good health
Dogs
Treatment Outcome
Massachusetts
Animals
Female
Dog Diseases
Ifosfamide
Antineoplastic Agents, Alkylating
Retrospective Studies
DOI:
10.1111/j.1939-1676.2000.tb01166.x
Publication Date:
2010-03-11T00:53:55Z
AUTHORS (6)
ABSTRACT
Ifosfamide (3‐[2‐chloroethyl]‐2[(2 chloroethyl)amino]tetrahydro‐2H‐1,3,2‐oxazaphosphorine 2‐oxide) is an alkylating agent with a broad spectrum of antitumor activity. The efficacy and toxicity of ifosfamide were evaluated in 72 dogs with spontaneously occurring tumors. Forty dogs (56%) had lymphoma, 31 (43%) had sarcomas, and 1 had a metastatic carcinoma. Five dogs received ifosfamide at dosages <350 mg/m2 IV. Neither toxicity nor response were observed, and the remaining dogs received ifosfamide at 350 mg/m2 (n = 18) and 375 mg/m2 body surface area IV (n = 49). Saline diuresis and the thiol compound mesna were used to prevent urothelial toxicity. Fifty‐two dogs had measurable tumors and could be evaluated for response. Complete responses were seen in 1 dog with metastatic leiomyosarcoma of the urinary bladder and in 1 dog with metastatic cutaneous hemangiosarcoma. One dog with lymphoma had a partial response for 112 days. Six dogs with splenic hemangiosarcoma received ifosfamide post‐splenectomy and their median survival time was 147 days. The acute dose‐limiting toxicity was neutropenia 7 days after administration of ifosfamide. The median and mean neutrophil counts 7 days after ifosfamide at 350 mg/m2 were 2,035 cells/μL and 4,773 cells/μL, respectively (n = 12). The median and mean neutrophil counts 7 days after ifosfamide at 375 mg/m2 were 2,500 cells/μL and 3,594 cells/μL, respectively (n = 37). No dog developed clinical or microscopic evidence of hemorrhagic cystitis. Ifosfamide appears safe to use in tumor‐bearing dogs, and the evaluation of combination chemotherapy protocols that include ifosfamide should be considered.
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CITATIONS (38)
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