Johnson John L, Hadad David Jamil, Dietze Reynaldo, Maciel Ethel Leonor Noia, Sewali Barrett, Gitta Phineas, Okwera Alphonse, Mugerwa Roy D, Alcaneses Mary Rose, Quelapio Maria Imelda, Tupasi Thelma E, Horter Libby, Debanne Sara M, Eisenach Kathleen D, Boom W Henry
Tuberculosis Research Unit, Department of Medicine, Case Western Reserve University School of Medicine and University Hospitals Case Medical Center, Cleveland, Ohio 44106-5083, USA.
Am J Respir Crit Care Med. 2009 Sep 15;180(6):558-63. doi: 10.1164/rccm.200904-0536OC. Epub 2009 Jun 19.
Cavitary disease and delayed culture conversion have been associated with relapse. Combining patient characteristics and measures of bacteriologic response might allow treatment shortening with current drugs in some patients.
To assess whether treatment could be shortened from 6 to 4 months in patients with noncavitary tuberculosis whose sputum cultures converted to negative after 2 months.
This study was a randomized, open-label equivalence trial. HIV-uninfected adults with noncavitary tuberculosis were treated daily with isoniazid, rifampin, pyrazinamide, and ethambutol for 2 months, followed by 2 months of isoniazid and rifampin. After 4 months, patients with drug-susceptible TB whose sputum cultures on solid media were negative after 8 weeks of treatment were randomly assigned to continue treatment for 2 more months or to stop treatment. Patients were followed for relapse for 30 months after beginning treatment.
Enrollment was stopped by the safety monitoring committee after 394 patients were enrolled due to apparent increased risk for relapse in the 4-month arm. A total of 370 patients were eligible for per protocol analysis. Thirteen patients in the 4-month arm relapsed, compared with three subjects in the 6-month arm (7.0 vs. 1.6%; risk difference, 0.054; 95% confidence interval with Hauck-Anderson correction, 0.01-0.10).
Shortening treatment from 6 to 4 months in adults with noncavitary disease and culture conversion after 2 months using current drugs resulted in a greater relapse rate. The combination of noncavitary disease and 2-month culture conversion was insufficient to identify patients with decreased risk for relapse.
空洞性疾病和培养转阴延迟与复发相关。结合患者特征和细菌学反应指标可能使部分患者使用现有药物缩短治疗疗程。
评估痰培养在2个月后转为阴性的非空洞性肺结核患者的治疗疗程能否从6个月缩短至4个月。
本研究为一项随机、开放标签的等效性试验。未感染HIV的非空洞性肺结核成年患者每日接受异烟肼、利福平、吡嗪酰胺和乙胺丁醇治疗2个月,随后接受异烟肼和利福平治疗2个月。4个月后,治疗8周后固体培养基痰培养阴性的药物敏感结核病患者被随机分配继续治疗2个月或停止治疗。开始治疗后对患者进行30个月的复发随访。
在纳入394例患者后,安全监测委员会因4个月治疗组明显增加的复发风险而停止入组。共有370例患者符合符合方案分析标准。4个月治疗组有13例患者复发,而6个月治疗组有3例(7.0%对1.6%;风险差异,0.054;采用Hauck-Anderson校正的95%置信区间,0.01 - 0.10)。
使用现有药物将非空洞性疾病且2个月后培养转阴的成年患者的治疗疗程从6个月缩短至4个月导致更高的复发率。非空洞性疾病和2个月培养转阴的组合不足以识别复发风险降低的患者。