Small Animal Hospital, University of Glasgow, Glasgow, UK.
J Feline Med Surg. 2024 Apr;26(4):1098612X241234614. doi: 10.1177/1098612X241234614.
The aim of this study was to determine response rates, median progression-free intervals (PFIs) and median survival times (MSTs) for cats with intermediate-large cell lymphoma treated with a vincristine, cyclophosphamide, mitoxantrone and prednisolone (CMOP) protocol. A secondary objective was to determine the tolerability of mitoxantrone used within this multiagent protocol.
The medical records of 31 cats treated at a single institution between 2009 and 2022 were reviewed to identify suitable cases. Cats were included in the study if they had a confirmed diagnosis of intermediate-large cell lymphoma, had received a CMOP protocol as first-line treatment and had completed at least one 4-week cycle of this protocol. Modifications allowed in the protocol included the use of l-asparaginase, vinblastine substitution for vincristine, chlorambucil substitution for cyclophosphamide and dexamethasone or methylprednisolone substitution for prednisolone.
The overall response rate was 74% (n = 23), with 45% (n = 14) achieving complete remission (CR), 29% (n = 9) achieving partial remission (PR) and 26% (n = 8) achieving stable disease (SD). The Kaplan-Meier median PFI and MST were 139 days and 206 days, respectively. Responders (CR or PR) had a significantly longer ( <0.001) median PFI and MST compared with non-responders (SD) (176 days vs 62 days, and 251 days vs 61 days, respectively). Cats that achieved CR had a significantly longer median PFI and MST ( <0.001) at 178 days and 1176 days, respectively. The 6-month and 1- and 2-year survival rates in cats with CR were 64%, 57% and 35%, respectively. Treatment with mitoxantrone was generally well tolerated, with no cats experiencing Veterinary Cooperative Oncology Group adverse effects above grade 2.
The CMOP protocol is an alternative and well-tolerated treatment for cats with intermediate-large cell lymphoma. As demonstrated with previous chemotherapy protocols, cats that respond to treatment, particularly those that achieve CR, are likely to have more durable responses.
本研究旨在确定接受长春新碱、环磷酰胺、米托蒽醌和泼尼松(CMOP)方案治疗的中大型细胞淋巴瘤猫的反应率、中位无进展间隔(PFI)和中位总生存时间(MST)。次要目标是确定多药方案中米托蒽醌的耐受性。
对 2009 年至 2022 年在一家机构接受治疗的 31 只猫的病历进行回顾性分析,以确定合适的病例。符合研究条件的猫必须满足以下标准:经确认患有中大型细胞淋巴瘤、接受 CMOP 方案作为一线治疗、且至少完成一个 4 周的 CMOP 方案周期。方案中允许的修改包括使用 L-门冬酰胺酶、长春新碱替代长春碱、环磷酰胺替代苯丁酸氮芥、泼尼松替代地塞米松或甲泼尼龙。
总反应率为 74%(n=23),完全缓解(CR)45%(n=14),部分缓解(PR)29%(n=9),疾病稳定(SD)26%(n=8)。Kaplan-Meier 中位 PFI 和 MST 分别为 139 天和 206 天。与无反应者(SD)相比,缓解者(CR 或 PR)的中位 PFI 和 MST 显著延长(<0.001)(176 天比 62 天,251 天比 61 天)。CR 猫的中位 PFI 和 MST 显著延长(<0.001),分别为 178 天和 1176 天。CR 猫的 6 个月、1 年和 2 年生存率分别为 64%、57%和 35%。米托蒽醌治疗总体耐受良好,无猫出现兽医合作肿瘤学组(VCOG)不良事件≥2 级。
CMOP 方案是中大型细胞淋巴瘤猫的另一种替代且耐受良好的治疗方法。与之前的化疗方案一样,对治疗有反应的猫,尤其是达到 CR 的猫,其反应可能更持久。