Hook Edward W, Dionne Jodie A, Workowski Kimberly, McNeil Candice J, Taylor Stephanie N, Batteiger Teresa A, Dombrowski Julia C, Mayer Kenneth H, Seña Arlene C, Hamill Matthew M, Wiesenfeld Harold C, Zhu Chunming, Perlowski Charlotte, Mejia-Galvis Jorge E, Newman Lori M
Department of Medicine, University of Alabama at Birmingham, Birmingham.
Department of Medicine, Emory University, Atlanta.
N Engl J Med. 2025 Sep 4;393(9):869-878. doi: 10.1056/NEJMoa2401802.
Controversy persists regarding the appropriate duration of therapy with benzathine penicillin G in persons with early (i.e., primary, secondary, or early latent) syphilis ( infection).
In a multicenter, randomized, controlled, noninferiority trial, we assigned persons who had early syphilis, with or without human immunodeficiency virus (HIV) infection, to receive intramuscular injections of benzathine penicillin G in a one-time dose of 2.4 million units or in doses of 2.4 million units administered at three successive weekly intervals. The primary end point was seroreversion to nonreactive status or a decrease in the rapid plasma reagin titer by two or more dilutions at 6 months, referred to here as a serologic response (noninferiority margin, 10 percentage points). A key secondary end point was a serologic response within subgroups defined according to HIV status, also assessed in a noninferiority analysis.
A total of 249 persons with early syphilis were enrolled. Most participants were men (97%), 62% were Black, and 153 (61%) were living with HIV infection. The distribution according to syphilis stage was 19% with primary syphilis, 47% with secondary syphilis, and 33% with early latent syphilis. The percentage of participants with a serologic response at 6 months was 76% (95% confidence interval [CI], 68 to 82) in the single-dose group and 70% (95% CI, 61 to 77) in the three-dose group (difference, -6 percentage points; 90% CI, -15 to 3, indicating noninferiority). No clinical relapse or treatment failure occurred in either group. In the one-dose group, a serologic response at 6 months was observed in 76% of participants who had HIV infection and 76% of those who did not, and in the three-dose group, a serologic response at 6 months was observed in 71% of participants who had HIV infection and 70% of those who did not. Most participants in each group had local injection-site pain and tenderness with treatment (76% with a single dose and 85% with three doses).
Treatment with one dose of 2.4 million units of benzathine penicillin G was noninferior to treatment with three doses with regard to serologic response 6 months after treatment. (Funded by the National Institute of Allergy and Infectious Diseases; ClinicalTrials.gov number, NCT03637660.).
关于苄星青霉素G治疗早期(即一期、二期或早期潜伏)梅毒感染患者的合适疗程仍存在争议。
在一项多中心、随机、对照、非劣效性试验中,我们将患有早期梅毒、无论是否感染人类免疫缺陷病毒(HIV)的患者,分配至接受单次肌肉注射240万单位苄星青霉素G或连续3周每周注射240万单位苄星青霉素G。主要终点为在6个月时血清学转为非反应性状态或快速血浆反应素滴度降低两个或更多稀释度,在此称为血清学反应(非劣效性界值为10个百分点)。一个关键次要终点是在根据HIV状态定义的亚组内的血清学反应,也在非劣效性分析中进行评估。
共纳入249例早期梅毒患者。大多数参与者为男性(97%),62%为黑人,153例(61%)感染HIV。梅毒分期分布为一期梅毒占19%,二期梅毒占47%,早期潜伏梅毒占33%。单剂量组在6个月时出现血清学反应的参与者百分比为76%(95%置信区间[CI],68%至82%),三剂量组为70%(95%CI,61%至77%)(差异为-6个百分点;90%CI,-15至3,表明非劣效性)。两组均未发生临床复发或治疗失败。在单剂量组中,感染HIV的参与者中有76%在6个月时出现血清学反应,未感染HIV的参与者中有76%出现该反应;在三剂量组中,感染HIV的参与者中有71%在6个月时出现血清学反应,未感染HIV的参与者中有70%出现该反应。每组中的大多数参与者在治疗时出现局部注射部位疼痛和压痛(单剂量组为76%,三剂量组为85%)。
就治疗后6个月的血清学反应而言,单次注射240万单位苄星青霉素G的治疗效果不劣于三次注射。(由美国国立过敏与传染病研究所资助;ClinicalTrials.gov编号,NCT03637660。)