Chakraborty Pinaki, Borgohain Mrinal
Department of Oncology, Gauhati Medical College and Hospital, Guwahati 781007, Assam, India.
Medical Affairs, MSN Laboratories, Hyderabad 500084, Telangāna, India.
World J Clin Oncol. 2025 Apr 24;16(4):104827. doi: 10.5306/wjco.v16.i4.104827.
Chronic neuropathic pain and depression are common and debilitating conditions in cancer patients, significantly impacting their quality of life. Pregabalin, an anticonvulsant medication, is used for neuropathic pain and may also influence depressive symptoms. This study evaluates the efficacy and safety of pregabalin on pain intensity, depression severity, and side effects in cancer patients with chronic neuropathic pain and depression.
To evaluate the impact of pregabalin on pain intensity, depression severity, and the safety profile in cancer patients with chronic neuropathic pain and depression.
This observational case series included 10 cancer patients experiencing chronic neuropathic pain and depression. Pregabalin was administered at a starting dose of 150 mg twice daily, with adjustments based on patient tolerance and pain response up to 300 mg twice daily. Pain intensity and depression severity were assessed using the brief pain inventory (BPI) and the Hamilton depression rating scale (HDRS) at baseline, 4 weeks, and 8 weeks. Side effects were monitored using a self-reported side effect questionnaire.
Pregabalin led to a significant reduction in pain intensity and depression severity. The mean BPI score decreased from 7.8 (SD = 1.2) at baseline to 5.2 (SD = 1.4) at 4 weeks and 4.1 (SD = 1.5) at 8 weeks, representing reductions of 33.3% and 47.4%, respectively. The mean HDRS score decreased from 18.5 (SD = 4.0) at baseline to 13.2 (SD = 4.1) at 4 weeks and 9.8 (SD = 3.6) at 8 weeks, showing reductions of 28.4% and 47.0%, respectively. Side effects included dizziness (50%), drowsiness (40%), weight gain (30%), and dry mouth (20%). No severe adverse effects were reported. All patients completed the study, with 30% requiring dose adjustments.
Pregabalin significantly alleviates both chronic neuropathic pain and depression in cancer patients with a manageable safety profile. These findings support the use of pregabalin in this patient population, though further research with larger samples and controlled designs is warranted.
慢性神经性疼痛和抑郁症在癌症患者中很常见且使人衰弱,严重影响他们的生活质量。普瑞巴林是一种抗惊厥药物,用于治疗神经性疼痛,也可能影响抑郁症状。本研究评估普瑞巴林对患有慢性神经性疼痛和抑郁症的癌症患者的疼痛强度、抑郁严重程度及副作用的疗效和安全性。
评估普瑞巴林对患有慢性神经性疼痛和抑郁症的癌症患者的疼痛强度、抑郁严重程度及安全性的影响。
本观察性病例系列纳入了10例患有慢性神经性疼痛和抑郁症的癌症患者。普瑞巴林起始剂量为每日两次,每次150毫克,根据患者耐受性和疼痛反应进行调整,最大剂量为每日两次,每次300毫克。在基线、4周和8周时,使用简明疼痛评估量表(BPI)和汉密尔顿抑郁评定量表(HDRS)评估疼痛强度和抑郁严重程度。使用自我报告的副作用问卷监测副作用。
普瑞巴林使疼痛强度和抑郁严重程度显著降低。BPI平均评分从基线时的7.8(标准差=1.2)降至4周时的5.2(标准差=1.4)和8周时的4.1(标准差=1.5),分别降低了33.3%和47.4%。HDRS平均评分从基线时的18.5(标准差=4.0)降至4周时的13.2(标准差=4.1)和8周时的9.8(标准差=3.6),分别降低了28.4%和47.0%。副作用包括头晕(50%)、嗜睡(40%)、体重增加(30%)和口干(20%)。未报告严重不良反应。所有患者均完成了研究,30%的患者需要调整剂量。
普瑞巴林可显著缓解患有慢性神经性疼痛和抑郁症的癌症患者的疼痛和抑郁症状,且安全性可控。这些发现支持在该患者群体中使用普瑞巴林,不过需要进一步开展更大样本量和对照设计的研究。