Mohammadianpanah Mohammad, Shirazi Mehdi, Mosalaei Ahmad, Omidvari Shapour, Ahmadloo Niloofar
Department of Radiation Oncology, Nemazee Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
Clin Ther. 2007 Jun;29(6):1161-5. doi: 10.1016/j.clinthera.2007.06.004.
Hemorrhagic cystitis is a potentially life-threatening complication in patients receiving cancer therapy. This urologic emergency is commonly associated with the chemotherapeutic use of oxazaphosphorine alkylating agents. This report describes a case of hemorrhagic cystitis associated with dacarbazine treatment.
A 63-year-old man with asymptomatic metastatic malignant melanoma received 3 cycles of dacarbazine (600-850 mg/m2) monochemotherapy, each 3 weeks apart. Two weeks after the third cycle, he presented with gross hematuria and mild dysuria. Physical examination revealed no significant finding. Hematuria was confirmed by urinalysis, and urinary infection was excluded by repeated urine cultures. Ultrasonography revealed diffuse bladder wall thickening with no discrete mass or ulceration. Cystoscopy findings revealed generalized inflammation and edema of the mucosa of the bladder, confirming the diagnosis of hemorrhagic cystitis. The patient's gross hematuria continued for 2 weeks and then completely resolved with supportive care. Two weeks after complete resolution, the patient experienced 2 transient episodes of gross hematuria that lasted a few hours and subsided spontaneously.
Dacarbazine is currently considered the standard first-line treatment in patients with advanced malignant melanoma. At standard prescribed doses (a single dose of 850-1000 mg/m2 or 250 mg/m2 for 5 days per cycle), dacarbazine is a reasonably well tolerated chemotherapeutic drug; nausea, vomiting, and myelosuppression are the most common adverse effects. Association of dacarbazine with hemorrhagic cystitis has not been reported previously (in a PubMed literature search from 1950-2006), and only 1 case report associates temozolomide (an analog of dacarbazine) with hemorrhagic cystitis. Based on the Naranjo adverse drug reactions probability scale, an objective assessment revealed dacarbazine to be a probable cause of hemorrhagic cystitis in this case.
This case report suggests that dacarbazine at conventional doses was a probable cause of hemorrhagic cystitis. Regular urinalysis and early intervention are recommended, as a means of detecting early hematuria and subsequently reducing or discontinuing dacarbazine treatment. Adequate hydration before, during, and after dacarbazine administration may be useful in preventing this complication.
出血性膀胱炎是接受癌症治疗患者中一种潜在的危及生命的并发症。这种泌尿系统急症通常与氮杂膦酸烷化剂的化疗使用有关。本报告描述了一例与达卡巴嗪治疗相关的出血性膀胱炎病例。
一名63岁无症状转移性恶性黑色素瘤男性接受了3个周期的达卡巴嗪(600 - 850 mg/m²)单药化疗,每3周进行一次。第三个周期后两周,他出现肉眼血尿和轻度尿痛。体格检查未发现明显异常。尿液分析证实有血尿,多次尿培养排除了泌尿系统感染。超声检查显示膀胱壁弥漫性增厚,无明显肿块或溃疡。膀胱镜检查结果显示膀胱黏膜普遍炎症和水肿,确诊为出血性膀胱炎。患者的肉眼血尿持续了2周,然后通过支持治疗完全缓解。完全缓解后两周,患者经历了2次短暂的肉眼血尿发作,持续数小时后自行消退。
达卡巴嗪目前被认为是晚期恶性黑色素瘤患者的标准一线治疗药物。在标准规定剂量(单次剂量850 - 1000 mg/m²或每周期250 mg/m²,连用5天)下,达卡巴嗪是一种耐受性较好的化疗药物;恶心、呕吐和骨髓抑制是最常见的不良反应。达卡巴嗪与出血性膀胱炎的关联此前未被报道(在1950 - 2006年的PubMed文献检索中),仅有1例病例报告将替莫唑胺(达卡巴嗪的类似物)与出血性膀胱炎相关联。根据Naranjo药物不良反应概率量表进行的客观评估显示,在本病例中达卡巴嗪可能是出血性膀胱炎的病因。
本病例报告表明,常规剂量的达卡巴嗪可能是出血性膀胱炎的病因。建议定期进行尿液分析并尽早干预,作为检测早期血尿并随后减少或停用达卡巴嗪治疗的一种手段。在达卡巴嗪给药前、给药期间和给药后充分水化可能有助于预防这种并发症。