Analgesic effectiveness and tolerability of oral oxycodone/naloxone and pregabalin in patients with lung cancer and neuropathic pain: an observational analysis

被引:12
作者
De Santis, Stefano [1 ]
Borghesi, Cristina [1 ]
Ricciardi, Serena [2 ]
Giovannoni, Daniele [1 ]
Fulvi, Alberto [2 ]
Migliorino, Maria Rita [2 ]
Marcassa, Claudio [3 ]
机构
[1] San Camillo Forlanini Hosp, Palliat Care & Canc Pain Serv, Oncol Pulm Unit, Circonvallazione Gianicolense 87, I-00151 Rome, Italy
[2] San Camillo Forlanini Hosp, Oncol Pulm Unit, Rome, Italy
[3] Cardiol Fdn Maugeri IRCCS, Novara, Italy
来源
ONCOTARGETS AND THERAPY | 2016年 / 9卷
关键词
oxycodone/naloxone; opioids; pregabalin; neuropathic cancer pain; non-small-cell lung cancer; breakthrough cancer pain; OPIOID-INDUCED CONSTIPATION; PROLONGED-RELEASE OXYCODONE; DEPRESSION SCALE; HOSPITAL ANXIETY; PALLIATIVE CARE; OPEN-LABEL; MANAGEMENT; PREVALENCE; QUALITY; GUIDELINES;
D O I
10.2147/OTT.S108144
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Cancer-related pain has a severe negative impact on quality of life. Combination analgesic therapy with oxycodone and pregabalin is effective for treating neuropathic cancer pain. We investigated the efficacy and tolerability of a dose-escalation combination therapy with prolonged-release oxycodone/naloxone (OXN-PR) and pregabalin in patients with nonsmall- cell lung cancer and severe neuropathic pain. Methods: This was a 4-week, open-label, observational study. Patients were treated with OXN-PR and pregabalin. Average pain intensity ([ API] measured on a 0-10 numerical rating scale) and neuropathic pain (Douleur Neuropathique 4) were assessed at study entry and at follow-up visits. The primary endpoint was response to treatment, defined as a reduction of API at T28. 30% from baseline. Secondary endpoints included other efficacy measures, as well as patient satisfaction and quality of life (Brief Pain Inventory Short Form), Hospital Anxiety and Depression Scale, and Symptom Distress Scale; bowel function was also assessed. Results: A total of 56 patients were enrolled. API at baseline was 8.0 +/- 0.9, and decreased after 4 weeks by 48% (4.2 +/- 1.9; P<0.0001 vs baseline); 46 (82.1%) patients responded to treatment. Significant improvements were also reported in number/severity of breakthrough cancer pain episodes (P=0.001), Brief Pain Inventory Short Form (P=0.0002), Symptom Distress Scale (P<0.0001), Hospital Anxiety and Depression Scale depression (P=0.0006) and anxiety (P<0.0001) subscales, and bowel function (P=0.0003). At study end, 37 (66.0%) patients were satisfied/very satisfied with the new analgesic treatment. Combination therapy had a good safety profile. Conclusion: OXN-PR and pregabalin were safe and highly effective in a real-world setting of severe neuropathic cancer pain, with a high rate of satisfaction, without interference on bowel function.
引用
收藏
页码:4043 / 4052
页数:10
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