Research Group MOVANT, Department of Rehabilitation Sciences and Physiotherapy (REVAKI), University of Antwerp, Wilrijk, Belgium; Pain in Motion International Research Group, www.paininmotion.be, Belgium.
Research Group MOVANT, Department of Rehabilitation Sciences and Physiotherapy (REVAKI), University of Antwerp, Wilrijk, Belgium; Pain in Motion International Research Group, www.paininmotion.be, Belgium; Department of Radiology, Antwerp University Hospital, Antwerp, Belgium.
Pain Physician. 2024 Feb;27(2):E207-E220.
Chronic cancer-related pain remains underdiagnosed and undertreated, although it affects 40% of cancer survivors. Recent insights suggest that cytokine signaling between immune, neuro, and glial cells contributes to chronic pain.
This study systematically reviewed cytokine levels and their relation to chronic cancer-related pain and, additionally, investigated differences in cytokine levels between cancer survivors with and without chronic pain.
Systematic review.
This systematic review was conducted and reported following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis guidelines (PRISMA). The study conducted a systematic literature search in the databases PubMed, Web of Science, and Embase for articles examining cytokine levels and pain experience at a time point of a minimum of 3 months post-cancer diagnosis. Pain experience was categorized into a total pain score, pain intensity, and pain interference. The risk of bias was assessed using the Newcastle Ottawa Scale.
Eight articles were included, investigating 6 cancer types and 30 cytokines. Moderate evidence was found for pro-inflammatory cytokine IL-6 to be correlated with pain intensity, of which higher levels are observed in cancer survivors experiencing chronic pain compared to pain-free survivors. Moderate evidence was found for TNF-alpha to be not correlated with any pain experience, which is similar for anti-inflammatory cytokines IL-8 and IL-10 with pain intensity. For the remaining 26 cytokines and pain outcomes, only limited evidence was found for an association or alteration.
The number of included studies was small. Overall, studies showed a moderate risk of bias, except one indicated a high risk of bias.
More standardized post-cancer treatment studies are warranted to confirm these results and explore associations and alterations of other cytokines. Nonetheless, moderate evidence suggests that elevated levels of IL-6, in contrast with TNF-alpha levels, are correlated with pain intensity in cancer survivors experiencing chronic pain compared to pain-free survivors.
尽管慢性癌症相关疼痛影响了 40%的癌症幸存者,但这种疼痛仍然存在诊断不足和治疗不足的情况。最近的研究表明,免疫细胞、神经细胞和神经胶质细胞之间的细胞因子信号传递与慢性疼痛有关。
本研究系统地回顾了细胞因子水平及其与慢性癌症相关疼痛的关系,并进一步研究了癌症幸存者中伴有和不伴有慢性疼痛的细胞因子水平差异。
系统综述。
本系统综述按照系统评价和荟萃分析的首选报告项目(PRISMA)的指南进行和报告。研究在 PubMed、Web of Science 和 Embase 数据库中进行了系统的文献检索,以查找至少在癌症诊断后 3 个月时检查细胞因子水平和疼痛体验的文章。疼痛体验分为总疼痛评分、疼痛强度和疼痛干扰。使用纽卡斯尔渥太华量表评估偏倚风险。
共纳入 8 篇文章,涉及 6 种癌症类型和 30 种细胞因子。有中度证据表明促炎细胞因子 IL-6 与疼痛强度相关,患有慢性疼痛的癌症幸存者的水平高于无疼痛幸存者。有中度证据表明 TNF-alpha 与任何疼痛体验均不相关,抗炎细胞因子 IL-8 和 IL-10 与疼痛强度也相似。对于其余 26 种细胞因子和疼痛结局,仅发现了有限的关联或改变证据。
纳入研究的数量较少。总体而言,除一项研究表明存在高偏倚风险外,大多数研究显示存在中度偏倚风险。
需要更多标准化的癌症治疗后研究来证实这些结果,并探讨其他细胞因子的关联和改变。尽管如此,中度证据表明,与 TNF-alpha 水平相比,患有慢性疼痛的癌症幸存者中 IL-6 水平升高与疼痛强度相关,而无疼痛幸存者则没有。