Lowenbraun S, Fox N, Cunitz D
Cancer. 1987 Jul 1;60(1):14-7. doi: 10.1002/1097-0142(19870701)60:1<14::aid-cncr2820600104>3.0.co;2-f.
Although the semisynthetic broad-spectrum acylureido-penicillin, azlocillin has been demonstrated to have significant antibiotic activity in leukemic patients, its role in combination therapy of febrile granulocytopenic patients with chemotherapy-treated solid tumors has not been clearly delineated. Thirty-five solid tumor patients with chemotherapy-induced absolute granulocytopenia (less than 1000 granulocytes/ml) associated with fever (greater than 38.3 degrees C) were treated on a prospective study with a combination of azlocillin 4 g intravenously (IV) every 6 hours, cephalothin 2 g IV every 6 hours, and tobramycin 80 to 100 mg IV every 8 to 12 hours. Prior chemotherapy included doxorubicin combinations in 18 patients and other combinations in 17 patients. Granulocyte counts preantibiotic therapy were greater than 100 granulocyte/ml in 14 patients, 100 to 499 in nine patients, and 500 to 1000 in 12 patients. Granulocyte nadirs were less than 100 in 20 patients, 100 to 499 in nine patients, and 500 to 1000 in six patients. Times for granulocytes to rise towards normal were 1 to 3 days in eight patients, 4 to 6 days in 18 patients, and 7 or more days in nine patients. Tobramycin levels were primarily in the peak range of 3 to 6 micrograms/ml and trough range of 0 to 1.9 micrograms/ml. The site and pathogen were identified in nine patients, the infection site clinically documented without isolated pathogen in three patients, and no site or pathogen identified in 23 patients. Of the 35 patients, 34 had good responses to the antibiotic combination (complete disappearance of fever and other evidence of infection). Serum creatinine rose 0.4 to 0.6 mg/dl in nine patients, 0.7 to 1.5 in four patients, and 1.5 in one patient (obstructive uropathy). The only other noted antibiotic-related side effect was hypokalemia. This antibiotic combination had little toxicity with marked efficacy.
虽然半合成广谱酰脲基青霉素阿洛西林已被证明在白血病患者中具有显著的抗生素活性,但其在化疗治疗实体瘤的发热性粒细胞减少患者联合治疗中的作用尚未明确界定。35例实体瘤患者因化疗导致绝对粒细胞减少(低于1000个粒细胞/毫升)并伴有发热(高于38.3摄氏度),接受了一项前瞻性研究,联合使用阿洛西林4克静脉注射(IV)每6小时一次、头孢噻吩2克IV每6小时一次以及妥布霉素80至100毫克IV每8至12小时一次。先前的化疗包括18例患者使用阿霉素联合化疗,17例患者使用其他联合化疗。抗生素治疗前粒细胞计数大于100个粒细胞/毫升的有14例患者,100至499个的有9例患者,500至1000个的有12例患者。粒细胞最低点低于100的有20例患者,100至499的有9例患者,500至1000的有6例患者。粒细胞升至正常水平的时间,8例患者为1至3天,18例患者为4至6天,9例患者为7天或更长时间。妥布霉素水平主要在峰值范围3至6微克/毫升和谷值范围0至1.9微克/毫升。9例患者确定了感染部位和病原体,3例患者临床上记录了感染部位但未分离出病原体,23例患者未确定感染部位或病原体。35例患者中,34例对联合抗生素治疗反应良好(发热和其他感染证据完全消失)。9例患者血清肌酐升高0.4至0.6毫克/分升,4例患者升高0.7至1.5毫克/分升,1例患者升高1.5毫克/分升(梗阻性尿路病)。唯一其他注意到的与抗生素相关的副作用是低钾血症。这种联合抗生素毒性小且疗效显著。