Shin Zushi Clinic, Zushi, Kanagawa, Japan.
Int J Clin Oncol. 2010 Feb;15(1):46-51. doi: 10.1007/s10147-009-0009-1.
Neuropathic pain is regarded as one of the main causes of cancer pain refractory to standard opioid therapy in palliative care. The use of adjuvant analgesics for neuropathic cancer pain is largely empirical and the true efficacy of these adjuvant analgesics has been unknown. Gabapentin is one of the new promising anticonvulsant drugs as an adjuvant analgesic for neuropathic cancer pain.
The clinical usefulness of gabapentin in combination with opioids for Japanese patients with neuropathic cancer pain was assessed in an open-label, single-center, prospective study. Gabapentin was initiated in addition to the drugs currently being administered. The dose of gabapentin was titrated from 200 mg to a maximum dose of 2400 mg per day over 15 days, based on discussion with each patient. The primary endpoint variable was the numerical rating scale (NRS) of 0-10 measured using the brief pain inventory.
From February 2007 to December 2007, gabapentin was administered to 24 patients that were already receiving an opioid without sufficient analgesia. Administration of gabapentin statistically reduced the worst-NRS, the least-NRS, and the average-NRS (7.3 --> 5.8, 3.6 --> 3.0, 5.8 --> 4.5, respectively). Four patients (16.7%) were withdrawn from the study because of adverse events (headache, myoclonus, heartburn, bronchial asthma).
Although gabapentin might be regarded as a promising new adjuvant analgesic for neuropathic cancer pain, our results indicated that the decrease in pain score was of minimal clinical benefit. Controlled trials with other adjuvant analgesics are needed.
神经性疼痛被认为是姑息治疗中阿片类药物标准治疗难治性癌症疼痛的主要原因之一。辅助阿片类药物治疗神经性癌痛在很大程度上是经验性的,这些辅助阿片类药物的真正疗效尚不清楚。加巴喷丁是一种新的有前途的抗惊厥药物,作为神经性癌痛的辅助镇痛药。
在一项开放性、单中心、前瞻性研究中,评估了加巴喷丁联合阿片类药物治疗日本神经性癌痛患者的临床效果。加巴喷丁在目前正在使用的药物基础上加用。根据与每位患者的讨论,将加巴喷丁的剂量从 200mg 滴定至每天最大剂量 2400mg,分 15 天进行。主要终点变量是使用简明疼痛量表(BPI)测量的 0-10 数字评定量表(NRS)。
从 2007 年 2 月至 2007 年 12 月,24 例已接受阿片类药物治疗但镇痛效果不佳的患者接受了加巴喷丁治疗。加巴喷丁治疗可使最差 NRS、最小 NRS 和平均 NRS 显著降低(分别为 7.3 降至 5.8,3.6 降至 3.0,5.8 降至 4.5)。4 例(16.7%)患者因不良反应(头痛、肌阵挛、胃灼热、支气管哮喘)退出研究。
尽管加巴喷丁可能被认为是一种有前途的治疗神经性癌痛的新型辅助镇痛药,但我们的结果表明,疼痛评分的降低仅具有最小的临床获益。需要进行其他辅助镇痛药的对照试验。