Adamczyk Kamil, Zuzda Konrad, Jankowski Miłosz, Świerczyński Rafał, Chudziński Kamil, Czapski Bartosz, Szułdrzyński Konstanty
Department of Anesthesiology and Intensive Care, National Medical Institute of the Ministry of the Interior and Administration, 02-507 Warsaw, Poland.
Department of Neurosurgery, National Medical Institute of the Ministry of the Interior and Administration, 02-507 Warsaw, Poland.
Cancers (Basel). 2025 Mar 3;17(5):863. doi: 10.3390/cancers17050863.
: Managing cancer-related pain presents complex challenges involving the interplay between analgesic efficacy, immune system responses, and patient outcomes. : Following the Scale for the Assessment of Narrative Review Articles (SANRA) criteria, we conducted a comprehensive literature search in Medline, Scopus, and Web of Science databases. The review synthesized evidence regarding opioid pain management modalities, genetic variations affecting pain perception, and associated drug metabolism. The literature reveals significant associations between opioid administration and immune function, with potential implications for cancer progression and survival. Genetic polymorphisms in key genes influence individual responses to pain opioid metabolism and, finally, pain management strategies. The immunosuppressive effects of opioids emerge as a critical consideration in cancer pain management, potentially influencing disease progression and treatment outcomes. Genetic variants influence analgesic efficacy, while the interaction between opioid-induced immunosuppression and genetic factors impacts both pain control and survival outcomes. This emphasizes the need for personalized treatment approaches considering individual genetic profiles and immune function.
管理癌症相关疼痛面临着复杂的挑战,涉及镇痛效果、免疫系统反应和患者预后之间的相互作用。按照叙事综述文章评估量表(SANRA)标准,我们在Medline、Scopus和科学网数据库中进行了全面的文献检索。该综述综合了有关阿片类药物疼痛管理模式、影响疼痛感知的基因变异以及相关药物代谢的证据。文献揭示了阿片类药物给药与免疫功能之间存在显著关联,这对癌症进展和生存具有潜在影响。关键基因中的遗传多态性影响个体对疼痛、阿片类药物代谢的反应,最终影响疼痛管理策略。阿片类药物的免疫抑制作用成为癌症疼痛管理中的一个关键考虑因素,可能影响疾病进展和治疗结果。基因变异影响镇痛效果,而阿片类药物诱导的免疫抑制与遗传因素之间的相互作用则影响疼痛控制和生存结果。这强调了需要考虑个体基因谱和免疫功能的个性化治疗方法。