自体骨髓移植大规模治疗伯基特淋巴瘤的作用

T. Philip, R. Pinkerton, O. Hartmann, C. Patte, I. Philip, P. Biron, M. Favrot
{"title":"自体骨髓移植大规模治疗伯基特淋巴瘤的作用","authors":"T. Philip,&nbsp;R. Pinkerton,&nbsp;O. Hartmann,&nbsp;C. Patte,&nbsp;I. Philip,&nbsp;P. Biron,&nbsp;M. Favrot","doi":"10.1016/S0308-2261(86)80012-1","DOIUrl":null,"url":null,"abstract":"<div><p>Burkitt's lymphoma has proved to be a very useful model for the evaluation of both massive therapy regimens and purging techniques. Results from several centres now confirm a number of general principles in relation to the use of ABMT procedures in this tumour. Patients in whom conventional chemotherapy has failed can be cured by massive therapy but this should be limited to those who have responded to salvage regimens or have only achieved first PR. Chemoresistant relapse is unlikely to be cured and the high probability of a transient response does not justify the procedure in such cases. Important ongoing clinical studies include the use of ABMT in first CR for CNS disease or B-cell ALL. Results in allogeneic grafts suggest that current massive therapy regimens are curative in only 20–50% of patients (Appelbaum and Thomas, 1983) and new combinations are, therefore, still required. Phase I and II studies in patients with ‘resistant relapse’ are investigating the use of sequential high-dose alkylating agents and role of TBI.</p><p>It is of particular importance to develop effective conventional ‘salvage’ regimens. Recent experience indicates that the combination of high-dose cisplatin and VP 16 is useful; other possibilities include high-dose interferon and high-dose cytarabine. Purging techniques in BL are now at an advanced stage and the combination of immunological and chemical treatments, once of prove efficacy in individual patients at a laboratory level, should be the subject of randomized studies.</p></div>","PeriodicalId":75718,"journal":{"name":"Clinics in haematology","volume":"15 1","pages":"Pages 205-217"},"PeriodicalIF":0.0000,"publicationDate":"1986-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"32","resultStr":"{\"title\":\"The role of massive therapy with autologous bone marrow transplantation in Burkitt's lymphoma\",\"authors\":\"T. Philip,&nbsp;R. Pinkerton,&nbsp;O. Hartmann,&nbsp;C. Patte,&nbsp;I. Philip,&nbsp;P. Biron,&nbsp;M. Favrot\",\"doi\":\"10.1016/S0308-2261(86)80012-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Burkitt's lymphoma has proved to be a very useful model for the evaluation of both massive therapy regimens and purging techniques. Results from several centres now confirm a number of general principles in relation to the use of ABMT procedures in this tumour. Patients in whom conventional chemotherapy has failed can be cured by massive therapy but this should be limited to those who have responded to salvage regimens or have only achieved first PR. Chemoresistant relapse is unlikely to be cured and the high probability of a transient response does not justify the procedure in such cases. Important ongoing clinical studies include the use of ABMT in first CR for CNS disease or B-cell ALL. Results in allogeneic grafts suggest that current massive therapy regimens are curative in only 20–50% of patients (Appelbaum and Thomas, 1983) and new combinations are, therefore, still required. Phase I and II studies in patients with ‘resistant relapse’ are investigating the use of sequential high-dose alkylating agents and role of TBI.</p><p>It is of particular importance to develop effective conventional ‘salvage’ regimens. Recent experience indicates that the combination of high-dose cisplatin and VP 16 is useful; other possibilities include high-dose interferon and high-dose cytarabine. Purging techniques in BL are now at an advanced stage and the combination of immunological and chemical treatments, once of prove efficacy in individual patients at a laboratory level, should be the subject of randomized studies.</p></div>\",\"PeriodicalId\":75718,\"journal\":{\"name\":\"Clinics in haematology\",\"volume\":\"15 1\",\"pages\":\"Pages 205-217\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1986-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"32\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinics in haematology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0308226186800121\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinics in haematology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0308226186800121","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 32

摘要

伯基特淋巴瘤已被证明是一种非常有用的模型,用于评估大规模治疗方案和清除技术。来自几个中心的结果现在证实了一些关于在这种肿瘤中使用ABMT手术的一般原则。常规化疗失败的患者可以通过大规模治疗治愈,但这应限于那些对挽救方案有反应或仅达到首次PR的患者。化疗耐药复发不太可能治愈,短暂反应的高概率并不能证明在这种情况下进行治疗是合理的。正在进行的重要临床研究包括在首次CR中使用ABMT治疗中枢神经系统疾病或b细胞ALL。同种异体移植的结果表明,目前的大规模治疗方案仅对20-50%的患者有效(Appelbaum和Thomas, 1983),因此仍需要新的联合治疗方案。“耐药复发”患者的I期和II期研究正在调查序贯大剂量烷基化剂的使用和TBI的作用。制定有效的常规“救助”制度特别重要。最近的经验表明,大剂量顺铂和VP 16联合使用是有用的;其他可能包括高剂量干扰素和高剂量阿糖胞苷。目前,清除技术在BL中的应用已进入晚期阶段,免疫和化学联合治疗一旦在实验室水平上证明对个体患者有效,就应该成为随机研究的主题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of massive therapy with autologous bone marrow transplantation in Burkitt's lymphoma

Burkitt's lymphoma has proved to be a very useful model for the evaluation of both massive therapy regimens and purging techniques. Results from several centres now confirm a number of general principles in relation to the use of ABMT procedures in this tumour. Patients in whom conventional chemotherapy has failed can be cured by massive therapy but this should be limited to those who have responded to salvage regimens or have only achieved first PR. Chemoresistant relapse is unlikely to be cured and the high probability of a transient response does not justify the procedure in such cases. Important ongoing clinical studies include the use of ABMT in first CR for CNS disease or B-cell ALL. Results in allogeneic grafts suggest that current massive therapy regimens are curative in only 20–50% of patients (Appelbaum and Thomas, 1983) and new combinations are, therefore, still required. Phase I and II studies in patients with ‘resistant relapse’ are investigating the use of sequential high-dose alkylating agents and role of TBI.

It is of particular importance to develop effective conventional ‘salvage’ regimens. Recent experience indicates that the combination of high-dose cisplatin and VP 16 is useful; other possibilities include high-dose interferon and high-dose cytarabine. Purging techniques in BL are now at an advanced stage and the combination of immunological and chemical treatments, once of prove efficacy in individual patients at a laboratory level, should be the subject of randomized studies.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信