Zylla D, Kuskowski M A, Gupta K, Gupta P
Division of Hematology/Oncology/Transplantation, Department of Medicine, University of Minnesota, Minneapolis, MN, USA Hematology/Oncology Section, Department of Medicine and Present address: Park Nicollet Health Services, Oncology Research, St Louis Park, MN, USA.
Geriatric Research and Education Clinical Center, Minneapolis VA Health Care System, Minneapolis, MN, USA.
Br J Anaesth. 2014 Jul 1;113(Suppl 1):i109-i116. doi: 10.1093/bja/aeu351. Epub 2014 Oct 10.
Pain is associated with shorter survival in non-small cell lung cancer (NSCLC). Lung cancer cells express opioid receptors. Opioids promote angiogenesis, tumour growth, and metastases, and shorten survival in animal models.
We examined retrospectively if long-term opioid requirement, independently of chronic pain, is associated with reduced survival in 209 patients with stage IIIB/IV NSCLC. Opioid doses were converted to average oral morphine equivalents (OME). Patients were stratified by proportion of time they reported severe pain, and required <5 or ≥5 mg day OME. Effects of pain, opioid requirement, and known prognostic variables on overall survival were analysed.
Severe pain before chemotherapy initiation was associated with shorter survival (hazards ratio 1.39, 95% confidence interval, 1.02-1.87, P=0.035). The magnitude of pain and opioid requirement during first 90 days of chemotherapy were predictive of shorter survival: patients with no/mild pain and requiring <5 mg day OME had 12 months longer median survival compared with those requiring more opioids, experiencing more pain, or both (18 compared with 4.2-7.7 months, P≤0.002). Survival differences (16 compared with 5.5-7.8 months, P<0.001) were similar when chronic pain and opioid requirement were assessed until death or last follow-up. In multivariable models, opioid requirement and chronic pain remained independent predictors of survival, after adjustment for age, stage, and performance status.
The severity of chronic cancer-related pain or greater opioid requirement is associated with shorter survival in advanced NSCLC, independently of known prognostic factors. While pain adversely influences prognosis, controlling it with opioids does not improve survival. Prospective studies should determine if pain control using equi-analgesic opioid-sparing approaches can improve outcomes.
疼痛与非小细胞肺癌(NSCLC)患者较短的生存期相关。肺癌细胞表达阿片受体。阿片类药物可促进血管生成、肿瘤生长和转移,并缩短动物模型的生存期。
我们回顾性研究了209例IIIB/IV期NSCLC患者中,与慢性疼痛无关的长期阿片类药物需求是否与生存期缩短相关。将阿片类药物剂量换算为平均口服吗啡等效剂量(OME)。根据患者报告严重疼痛的时间比例以及每日所需OME<5或≥5mg进行分层。分析疼痛、阿片类药物需求以及已知预后变量对总生存期的影响。
化疗开始前的严重疼痛与较短的生存期相关(风险比1.39,95%置信区间1.02 - 1.87,P = 0.035)。化疗前90天内疼痛的程度和阿片类药物需求可预测生存期较短:与那些需要更多阿片类药物、经历更多疼痛或两者皆有的人相比,无/轻度疼痛且每日所需OME <5mg的患者中位生存期长12个月(分别为18个月与4.2 - 7.7个月,P≤0.002)。在评估直至死亡或最后随访的慢性疼痛和阿片类药物需求时,生存期差异(16个月与5.5 - 7.8个月,P <0.001)相似。在多变量模型中,在调整年龄、分期和体能状态后,阿片类药物需求和慢性疼痛仍然是生存期的独立预测因素。
晚期NSCLC患者中,慢性癌症相关疼痛的严重程度或更高的阿片类药物需求与较短的生存期相关,且独立于已知的预后因素。虽然疼痛对预后有不利影响,但使用阿片类药物控制疼痛并不能改善生存期。前瞻性研究应确定使用等效镇痛的阿片类药物节省方法控制疼痛是否能改善预后。