Ryan W Soussa, Suzie Jaderberg, Tim L Williams, Jane M Dobson
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Measured outcomes included the type, frequency, and severity of hematological and other more general toxicities.</p><p><strong>Results: </strong>24 of 30 dogs experienced at least 1 hematological toxicity, 6 experienced gastrointestinal toxicity, and 4 experienced lethargy. The most common toxicity was anemia (15/30 [50%]), with 93.3% (14/15 dogs) classified as Veterinary Cooperative Oncology Group-Common Terminology Criteria for Adverse Events grade I and 6.6% (1/15) classified as grade II. The second most common toxicity was neutropenia (14/30 [46.6%]), with 71.4% (10/14) classified as grade I and 28.6% (4/14) as grade III. The least common hematological toxicity was thrombocytopenia (4/30 [13%]), all grade I. Neutropenia mainly occurred during weeks 2 and 3; however, there was no significant decrease in neutrophil count relative to baseline. Neutrophil count increased and Hct decreased during weeks 6 to 12 of treatment when compared to baseline. No change in platelet count was observed.</p><p><strong>Clinical relevance: </strong>Vinblastine/prednisolone chemotherapy leads to hematological toxicity; however, this was mostly low-grade and did not require major intervention. Vinblastine/prednisolone chemotherapy is well tolerated in dogs bearing high-grade or metastatic MCTs.</p>","PeriodicalId":14658,"journal":{"name":"Javma-journal of The American Veterinary Medical Association","volume":null,"pages":null},"PeriodicalIF":1.6000,"publicationDate":"2024-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Vinblastine/prednisolone chemotherapy leads to hematological toxicity in dogs with high-grade or metastatic mast cell tumors.\",\"authors\":\"Ryan W Soussa, Suzie Jaderberg, Tim L Williams, Jane M Dobson\",\"doi\":\"10.2460/javma.24.03.0214\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To determine the myelosuppressive effects/hematological toxicities, other general toxicities, and when these occur during vinblastine/prednisolone chemotherapy in dogs bearing high-grade or metastatic cutaneous/subcutaneous mast cell tumors (MCTs).</p><p><strong>Methods: </strong>Medical records were retrospectively reviewed between November 1, 2016, and March 1, 2023. 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The second most common toxicity was neutropenia (14/30 [46.6%]), with 71.4% (10/14) classified as grade I and 28.6% (4/14) as grade III. The least common hematological toxicity was thrombocytopenia (4/30 [13%]), all grade I. Neutropenia mainly occurred during weeks 2 and 3; however, there was no significant decrease in neutrophil count relative to baseline. Neutrophil count increased and Hct decreased during weeks 6 to 12 of treatment when compared to baseline. No change in platelet count was observed.</p><p><strong>Clinical relevance: </strong>Vinblastine/prednisolone chemotherapy leads to hematological toxicity; however, this was mostly low-grade and did not require major intervention. 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引用次数: 0
摘要
目的确定患有高级别或转移性切面/皮下肥大细胞瘤(MCTs)的犬在接受长春新碱/泼尼松龙化疗期间的骨髓抑制作用/血液毒性、其他一般毒性以及这些毒性发生的时间:对2016年11月1日至2023年3月1日期间的病历进行回顾性审查。纳入了30只经组织病理学确诊为皮肤高级别肥大细胞瘤/转移性皮下肥大细胞瘤并随后完成了为期12周的长春新碱/强的松龙化疗方案的客户饲养犬。化疗开始前和每次长春新碱治疗前都要进行血液学评估。评估了每次治疗对血液学数值的影响。测量结果包括血液学和其他一般毒性的类型、频率和严重程度。结果:30 只狗中有 24 只至少出现过一种血液学毒性,6 只出现过胃肠道毒性,4 只出现过嗜睡。最常见的毒性是贫血(15/30 [50%]),93.3%(14/15 只狗)被列为兽医合作肿瘤组织-不良事件通用术语标准 I 级,6.6%(1/15 只)被列为 II 级。第二种最常见的毒性是中性粒细胞减少症(14/30 [46.6%]),71.4%(10/14)为 I 级,28.6%(4/14)为 III 级。最不常见的血液毒性是血小板减少(4/30 [13%]),均为 I 级。中性粒细胞减少主要发生在第 2 周和第 3 周,但中性粒细胞计数与基线相比没有显著下降。与基线相比,中性粒细胞计数在治疗的第6周至第12周期间有所增加,血清白蛋白(Hct)有所下降。血小板计数未见变化:临床相关性:长春新碱/泼尼松龙化疗会导致血液学毒性,但这种毒性大多较低,无需进行重大干预。患有高级别或转移性MCT的狗对长春新碱/强的松龙化疗的耐受性良好。
Vinblastine/prednisolone chemotherapy leads to hematological toxicity in dogs with high-grade or metastatic mast cell tumors.
Objective: To determine the myelosuppressive effects/hematological toxicities, other general toxicities, and when these occur during vinblastine/prednisolone chemotherapy in dogs bearing high-grade or metastatic cutaneous/subcutaneous mast cell tumors (MCTs).
Methods: Medical records were retrospectively reviewed between November 1, 2016, and March 1, 2023. Thirty client-owned dogs with histopathologically confirmed cutaneous high-grade MCTs/metastatic subcutaneous MCTs and that subsequently completed a 12-week vinblastine/prednisolone chemotherapy protocol were included. Hematology was assessed before commencing chemotherapy and before each vinblastine treatment. The effect of each treatment upon hematological values was evaluated. Measured outcomes included the type, frequency, and severity of hematological and other more general toxicities.
Results: 24 of 30 dogs experienced at least 1 hematological toxicity, 6 experienced gastrointestinal toxicity, and 4 experienced lethargy. The most common toxicity was anemia (15/30 [50%]), with 93.3% (14/15 dogs) classified as Veterinary Cooperative Oncology Group-Common Terminology Criteria for Adverse Events grade I and 6.6% (1/15) classified as grade II. The second most common toxicity was neutropenia (14/30 [46.6%]), with 71.4% (10/14) classified as grade I and 28.6% (4/14) as grade III. The least common hematological toxicity was thrombocytopenia (4/30 [13%]), all grade I. Neutropenia mainly occurred during weeks 2 and 3; however, there was no significant decrease in neutrophil count relative to baseline. Neutrophil count increased and Hct decreased during weeks 6 to 12 of treatment when compared to baseline. No change in platelet count was observed.
Clinical relevance: Vinblastine/prednisolone chemotherapy leads to hematological toxicity; however, this was mostly low-grade and did not require major intervention. Vinblastine/prednisolone chemotherapy is well tolerated in dogs bearing high-grade or metastatic MCTs.
期刊介绍:
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