Croghan M K, Aickin M G, Meyskens F L
Department of Radiation Oncology, University of Arizona Cancer Center, Tucson 85724.
Am J Clin Oncol. 1991 Aug;14(4):331-5. doi: 10.1097/00000421-199108000-00012.
We assessed the ototoxicity associated with oral alpha-difluoromethylornithine (DFMO) administration in 58 patients with metastatic malignant melanoma. One hundred seventy-nine sequential audiograms obtained from patients treated with DFMO alone (16 patients) or in combination with alpha 2b-interferon (42 patients) were evaluated. DFMO doses ranged from 2 to 12 g/m2/d and were given over periods of 2 to 50 weeks. Total doses ranging from 60 g/m2 to 1390 g/m2 were correlated with clinical effects and pure tone audiometric changes. By regression analysis cumulative DFMO dose showed a consistent and statistically significant positive relationship to hearing loss at multiple frequencies (500, 1000, 2000, 4000, and 8000 Hz). Patients with normal (threshold less than 30 db) baseline audiograms demonstrated more hearing loss than those with abnormal (threshold greater than or equal to 30 db) baseline audiograms at the higher frequency levels. Of the patients with normal prestudy hearing thresholds 10% or less developed a demonstrable hearing deficit at cumulative DFMO doses below 150 g/m2. Conversely, up to 75% of the patients who received more than 250 g/m2 developed a clinically demonstrable hearing loss. Other factors which adversely affected hearing included age, male gender, and the concomitant use of alpha 2b-interferon. In summary, the risk of clinically significant hearing loss in patients treated with DFMO was primarily related to dose and the presence of a pre-existing hearing deficit.
我们评估了58例转移性恶性黑色素瘤患者口服α-二氟甲基鸟氨酸(DFMO)后的耳毒性。对单独接受DFMO治疗(16例患者)或联合α2b干扰素治疗(42例患者)的患者进行的179次连续听力图进行了评估。DFMO剂量范围为2至12 g/m²/天,给药时间为2至50周。总剂量范围为60 g/m²至1390 g/m²,与临床疗效和纯音听力测定变化相关。通过回归分析,累积DFMO剂量在多个频率(500、1000、2000、4000和8000 Hz)与听力损失呈一致且具有统计学意义的正相关。基线听力图正常(阈值小于30 dB)的患者在较高频率水平上比基线听力图异常(阈值大于或等于30 dB)的患者听力损失更多。在研究前听力阈值正常的患者中,累积DFMO剂量低于150 g/m²时,10%或更少的患者出现可证实的听力缺陷。相反,接受超过250 g/m²的患者中,高达75%出现临床上可证实的听力损失。其他对听力有不利影响的因素包括年龄、男性性别以及同时使用α2b干扰素。总之,接受DFMO治疗的患者出现具有临床意义的听力损失的风险主要与剂量和既往存在的听力缺陷有关。