Open AccessContinuous Low‐Dose Oral Chemotherapy for Adjuvant Therapy of Splenic Hemangiosarcoma in Dogs
Author(s) -
Lana Susan,
U'ren Lance,
Plaza Susan,
Elmslie Robyn,
Gustafson Daniel,
Morley Paul,
Dow Steven
Publication year - 2007
Publication title -
journal of veterinary internal medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.356
H-Index - 103
eISSN - 1939-1676
pISSN - 0891-6640
DOI - 10.1111/j.1939-1676.2007.tb03019.x
Subject(s) - medicine , etoposide , adverse effect , chemotherapy , hemangiosarcoma , adjuvant , cyclophosphamide , gastroenterology , surgery , angiosarcoma
Background : Hemangiosarcoma (HSA) is a highly metastatic and often rapidly fatal tumor in dogs. At present, conventional adjuvant chemotherapy provides only a modest survival benefit for treated dogs. Continuous oral administration of low‐dose chemotherapy (LDC) has been suggested as an alternative to conventional chemotherapy protocols. Therefore, we evaluated the safety and effectiveness of LDC using a combination of cyclophosphamide, etoposide, and piroxicam as adjuvant therapy for dogs with stage II HSA. Hypothesis : We hypothesized that oral adjuvant therapy with LDC could be safely administered to dogs with HSA and that survival times would be comparable to those attained with conventional doxorubicin (DOX) chemotherapy. Animals : Nine dogs with stage II splenic HSA were enrolled in the LDC study. Treatment outcomes were also evaluated retrospectively for 24 dogs with stage II splenic HSA treated with DOX chemotherapy. Methods : Nine dogs with stage II splenic HSA were treated with LDC over a 6‐month period. Adverse effects and treatment outcomes were determined. The pharmacokinetics of orally administered etoposide were determined in 3 dogs. Overall survival times and disease‐free intervals were compared between the 9 LDC‐treated dogs and 24 DOX‐treated dogs. Results : Dogs treated with LDC did not develop severe adverse effects, and long‐term treatment over 6 months was well‐tolerated. Oral administration of etoposide resulted in detectable plasma concentrations that peaked between 30 and 60 minutes after dosing. Both the median overall survival time and the median disease‐free interval in dogs treated with LDC were 178 days. By comparison, the overall survival time and disease‐free interval in dogs treated with DOX were 133 and 126 days, respectively. Conclusions : Continuous orally administered LDC may be an effective alternative to conventional high‐dose chemotherapy for adjuvant therapy of dogs with HSA.