• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于剂量强化、无需维持的 CHOP 方案治疗犬淋巴瘤的疗效和毒性:130 例病例。

Outcome and toxicity associated with a dose-intensified, maintenance-free CHOP-based chemotherapy protocol in canine lymphoma: 130 cases.

机构信息

Department of Clinical Studies, School of Veterinary Medicine of the University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Vet Comp Oncol. 2010 Sep;8(3):196-208. doi: 10.1111/j.1476-5829.2010.00222.x.

DOI:10.1111/j.1476-5829.2010.00222.x
PMID:20691027
Abstract

A dose-intensified/dose-dense chemotherapy protocol for canine lymphoma was designed and implemented at the Veterinary Hospital of the University of Pennsylvania. In this study, we describe the clinical characteristics, prognostic factors, efficacy and toxicity in 130 dogs treated with this protocol. The majority of the dogs had advanced stage disease (63.1% stage V) and sub-stage b (58.5%). The median time to progression (TTP) and lymphoma-specific survival were 219 and 323 days, respectively. These results are similar to previous less dose-intense protocols. Sub-stage was a significant negative prognostic factor for survival. The incidence of toxicity was high; 53.9 and 45% of the dogs needed dose reductions and treatment delays, respectively. Dogs that required dose reductions and treatment delays had significantly longer TTP and lymphoma-specific survival times. These results suggest that dose density is important, but likely relative, and needs to be adjusted according to the individual patient's toxicity for optimal outcome.

摘要

宾夕法尼亚大学兽医院设计并实施了一种犬淋巴瘤的强化/密集化疗方案。在这项研究中,我们描述了 130 只接受该方案治疗的犬的临床特征、预后因素、疗效和毒性。大多数犬患有晚期疾病(63.1%为 V 期)和亚期 b(58.5%)。进展时间(TTP)和淋巴瘤特异性生存中位数分别为 219 天和 323 天。这些结果与以前剂量不那么密集的方案相似。亚期是生存的一个显著负预后因素。毒性发生率较高;53.9%和 45%的犬分别需要减少剂量和治疗延迟。需要减少剂量和治疗延迟的犬 TTP 和淋巴瘤特异性生存时间明显更长。这些结果表明,剂量密度很重要,但可能是相对的,需要根据个体患者的毒性进行调整,以达到最佳疗效。

相似文献

1
Outcome and toxicity associated with a dose-intensified, maintenance-free CHOP-based chemotherapy protocol in canine lymphoma: 130 cases.基于剂量强化、无需维持的 CHOP 方案治疗犬淋巴瘤的疗效和毒性:130 例病例。
Vet Comp Oncol. 2010 Sep;8(3):196-208. doi: 10.1111/j.1476-5829.2010.00222.x.
2
Doxorubicin alone or in combination with asparaginase, followed by cyclophosphamide, vincristine, and prednisone for treatment of multicentric lymphoma in dogs: 121 cases (1987-1995).单独使用阿霉素或联合使用天冬酰胺酶,随后使用环磷酰胺、长春新碱和强的松治疗犬多中心淋巴瘤:121例(1987 - 1995年)
J Am Vet Med Assoc. 1997 Feb 15;210(4):512-6.
3
Evaluation of a multidrug chemotherapy protocol with mitoxantrone based maintenance (CHOP-MA) for the treatment of canine lymphoma.评价米托蒽醌维持的多药化疗方案(CHOP-MA)治疗犬淋巴瘤的效果。
Vet Comp Oncol. 2010 Mar;8(1):11-22. doi: 10.1111/j.1476-5829.2009.00199.x.
4
CHOP chemotherapy for the treatment of canine multicentric T-cell lymphoma.CHOP 化疗治疗犬多中心 T 细胞淋巴瘤。
Vet Comp Oncol. 2011 Mar;9(1):38-44. doi: 10.1111/j.1476-5829.2010.00230.x.
5
Efficacy of a continuous, multiagent chemotherapeutic protocol versus a short-term single-agent protocol in dogs with lymphoma.连续多药化疗方案与短期单药化疗方案治疗犬淋巴瘤的疗效比较
J Am Vet Med Assoc. 2008 Mar 15;232(6):879-85. doi: 10.2460/javma.232.6.879.
6
Evaluation of a 15-week CHOP protocol for the treatment of canine multicentric lymphoma.评价 15 周 CHOP 方案治疗犬多中心淋巴瘤的效果。
Vet Comp Oncol. 2013 Dec;11(4):306-15. doi: 10.1111/j.1476-5829.2012.00324.x. Epub 2012 May 2.
7
Evaluation of factors associated with second remission in dogs with lymphoma undergoing retreatment with a cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy protocol: 95 cases (2000-2007).对采用环磷酰胺、阿霉素、长春新碱和强的松化疗方案进行再治疗的淋巴瘤犬第二次缓解相关因素的评估:95例病例(2000 - 2007年)
J Am Vet Med Assoc. 2011 Feb 15;238(4):501-6. doi: 10.2460/javma.238.4.501.
8
Immunochemotherapy with rituximab and cyclophosphamide, doxorubicin, vincristine, and prednisone significantly improves response and time to treatment failure, but not long-term outcome in patients with previously untreated mantle cell lymphoma: results of a prospective randomized trial of the German Low Grade Lymphoma Study Group (GLSG).利妥昔单抗联合环磷酰胺、阿霉素、长春新碱及泼尼松进行免疫化疗可显著提高反应率并延长至治疗失败时间,但对既往未治疗的套细胞淋巴瘤患者的长期预后无改善:德国低度淋巴瘤研究组(GLSG)一项前瞻性随机试验的结果
J Clin Oncol. 2005 Mar 20;23(9):1984-92. doi: 10.1200/JCO.2005.08.133. Epub 2005 Jan 24.
9
Comparison of a second-generation combination chemotherapeutic regimen (m-BACOD) with a standard regimen (CHOP) for advanced diffuse non-Hodgkin's lymphoma.第二代联合化疗方案(m-BACOD)与标准方案(CHOP)治疗晚期弥漫性非霍奇金淋巴瘤的比较。
N Engl J Med. 1992 Nov 5;327(19):1342-9. doi: 10.1056/NEJM199211053271903.
10
Cytosine arabinoside in addition to VCAA-based protocols for the treatment of canine lymphoma with bone marrow involvement: does it make the difference?除基于VCAA方案外,阿糖胞苷用于治疗伴有骨髓受累的犬淋巴瘤:会有不同效果吗?
Vet Comp Oncol. 2008 Jun;6(2):80-9. doi: 10.1111/j.1476-5829.2007.00141.x.

引用本文的文献

1
Efficacy of formula against canine lymphoma chemotherapy-induced myelosuppression.配方对犬淋巴瘤化疗引起的骨髓抑制的疗效。
Front Vet Sci. 2025 Aug 12;12:1635504. doi: 10.3389/fvets.2025.1635504. eCollection 2025.
2
Half-Body Radiation Therapy Results in a Prolonged Progression-Free Interval in Canine High-Grade Lymphoma After First Remission.半身放射治疗可延长犬高级别淋巴瘤首次缓解后的无进展间期。
Vet Comp Oncol. 2025 Jun;23(2):236-245. doi: 10.1111/vco.13050. Epub 2025 Mar 15.
3
Clinical Outcome of Multicentric Lymphoma Treated with Cyclophosphamide, Doxorubicin, Vincristine, and Prednisolone (CHOP) in Small Breed Dogs.
小型犬多中心淋巴瘤采用环磷酰胺、阿霉素、长春新碱和强的松龙(CHOP方案)治疗的临床结果
Animals (Basel). 2024 Oct 17;14(20):2994. doi: 10.3390/ani14202994.
4
Early progression during or after cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy indicates poor outcome with rescue protocols in dogs with multicentric lymphoma.在接受环磷酰胺、多柔比星、长春新碱和泼尼松化疗期间或之后早期进展的多中心淋巴瘤犬采用挽救方案预后不良。
J Vet Intern Med. 2024 Jul-Aug;38(4):2282-2292. doi: 10.1111/jvim.17139. Epub 2024 Jul 3.
5
Stage Migration in Canine Multicentric Lymphoma: Impact of Diagnostic Techniques on Assessing Disease Extent.犬多中心性淋巴瘤的分期迁移:诊断技术对评估疾病范围的影响。
In Vivo. 2024 May-Jun;38(3):1429-1435. doi: 10.21873/invivo.13585.
6
Evaluation of a multiagent chemotherapy protocol combining vincristine, cyclophosphamide, mitoxantrone and prednisolone (CMOP) for treatment of feline intermediate-large cell lymphoma.评估一种包含长春新碱、环磷酰胺、米托蒽醌和泼尼松龙的联合化疗方案(CMOP)治疗猫中间大细胞淋巴瘤的效果。
J Feline Med Surg. 2024 Apr;26(4):1098612X241234614. doi: 10.1177/1098612X241234614.
7
Use of genome-wide DNA methylation analysis to identify prognostic CpG site markers associated with longer survival time in dogs with multicentric high-grade B-cell lymphoma.利用全基因组 DNA 甲基化分析鉴定与多中心高级别 B 细胞淋巴瘤犬生存时间延长相关的预后 CpG 位点标志物。
J Vet Intern Med. 2024 Jan-Feb;38(1):316-325. doi: 10.1111/jvim.16931. Epub 2023 Dec 19.
8
Individualized chemotherapy drug dose escalation in dogs with multicentric lymphoma.在患有多中心淋巴瘤的犬中进行个体化化疗药物剂量递增。
J Vet Intern Med. 2023 Nov-Dec;37(6):2402-2409. doi: 10.1111/jvim.16875. Epub 2023 Oct 3.
9
Review of Canine Lymphoma Treated with Chemotherapy-Outcomes and Prognostic Factors.犬淋巴瘤化疗治疗的回顾——结果与预后因素
Vet Sci. 2023 May 11;10(5):342. doi: 10.3390/vetsci10050342.
10
Efficacy and tolerability of a 12-week combination chemotherapy followed by lomustine consolidation treatment in canine B- and T-cell lymphoma.12 周联合化疗后洛莫司汀巩固治疗对犬 B 细胞和 T 细胞淋巴瘤的疗效和耐受性。
Acta Vet Scand. 2022 Dec 12;64(1):36. doi: 10.1186/s13028-022-00660-z.