抗生素治疗晚期非大体积惰性淋巴瘤的正面前瞻性试验。

C. Portlock, P. Hamlin, J. Gerecitano, A. Noy, M. Palomba, Janelle Walkley, S. Corcoran, Jocelyn C. Migliacci, H. Schoder, G. Papanicolaou, A. Markowitz
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引用次数: 3

摘要

背景:我们前瞻性地研究了三个月疗程的克拉霉素(在前两周大便幽门螺杆菌阳性时,用Prevpac®、兰索拉唑/阿莫西林/克拉霉素替代)治疗非体积大的晚期惰性淋巴瘤。这些患者通常是预期监测的候选者,正是在这一时期,可能存在识别和治疗相关感染的机会之窗。方法所有新诊断为无痛性淋巴瘤(FL和非FL)且符合GELF标准的患者均接受12周克拉霉素治疗。32例可评估患者,其中4例有粪便幽门螺杆菌。结果在抗生素治疗1个月后,32例患者中有7例(21.9%)出现淋巴瘤缓解。另外2例患者在随访期间有客观缓解(总缓解28.1%)。抗生素应答者的中位无治疗生存期为69.9个月,无应答者为30.6个月(p = 0.019)。结论注意到三种反应模式,可能提示免疫介导的反应——提示PET阴性;延迟PET阴性反应的天赋;并逐步不断改进。这项前瞻性研究看起来很有希望,可能是通过减少“抗原驱动”来开发淋巴瘤预防策略的一步,值得进一步的临床/生物学研究。http://clinicaltrials.gov/show/NCT00461084。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Positive Prospective Trial of Antibiotic Therapy in Advanced Stage, Non-Bulky Indolent Lymphoma.
BACKGROUND We have prospectively studied a three month course of clarithromycin (substituted by Prevpac®, lansoprazole/ amoxicillin/ clarithromycin, in the first two wks when stool H pylori+) for non-bulky, advanced stage indolent lymphoma. These patients are often candidates for expectant monitoring and it is during this period that a window of opportunity may exist to identify and treat associated infections. METHODS All previously untreated patients with a new diagnosis of indolent lymphoma (FL and non-FL) meeting GELF criteria were treated with 12 weeks of clarithromycin. There were 32 evaluable patients, 4 of whom had stool H pylori. RESULTS At one month post-antibiotic therapy, we have observed lymphoma responses in 7 of 32 patients (21.9%). Two additional patients had objective response during followup (28.1% overall response). The median treatment free survival for antibiotic responders is 69.9 months and for non-responders, 30.6 months (p = 0.019). CONCLUSION Three response patterns have been noted, perhaps suggestive of an immune-mediated response -- prompt PET negative; flair with delayed PET negative response; and gradual continuous improvement. This prospective study appears promising, may be a step toward developing a lymphoma prevention strategy by reducing "antigen drive," and deserves further clinical/biological study. http://clinicaltrials.gov/show/NCT00461084.
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