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羟考酮纳洛酮缓释片获《中国慢性癌症相关性疼痛诊疗指南(2024版)》强推荐,用于治疗慢性内脏癌性疼痛

肿瘤医学组 绿医天地
2025年03月07日 07:59

指南背景

慢性癌症相关性疼痛(chronic cancer-related pain, CCRP)严重损害患者的身心健康,导致其机体生理功能进行性恶化,加剧肿瘤进展,同时引发治疗耐受性下降,甚至迫使患者中断抗肿瘤治疗进程,形成疼痛-功能障碍-治疗中断的恶性循环,缩短患者总体生存期并显著降低其生活质量[1]

当前国际癌痛管理领域虽存在多项指南,但基于《国际疾病分类-11》(ICD-11)框架的CCRP诊疗指南仍属空缺。为此,国内疼痛学科专家团队系统整合了近10年国内外高质量循证医学证据,特别针对中国临床实践特点,经严格论证与投票,形成《中国慢性癌症相关性疼痛诊疗指南(2024版)》推荐意见,为临床实践提供指导[2]


慢性癌症相关性疼痛(CCRP)概述 

1

定义

CCRP是由癌症本身或转移所致的疼痛以及癌症治疗引起的慢性疼痛[3-4]

2

流行病学

据统计,CCRP发生率呈现显著的病程相关性特征:初诊患者中约为25%,转移阶段骤增至75%,抗肿瘤治疗期间维持在59%,且1/3的患者在根治性治疗结束后仍存在持续性疼痛[5]。对于晚期癌症、临终的患者,CCRP发生率进一步攀升至66.0%,其中55.0%的患者为中至重度疼痛[3-4]

3

分类

CCRP可分为慢性癌性疼痛(CCP)和慢性癌症治疗后疼痛(CPCTP)。CCP主要包括慢性内脏癌性疼痛(CVCP)、慢性骨性癌性疼痛(CBCP)和慢性神经病理性癌痛(CNCP),分别由肿瘤对内脏器官、骨骼或神经系统的直接侵袭或转移引起。CPCTP则包括癌症药物治疗后的慢性疼痛(CPCMP)、慢性放射治疗后疼痛(CPRP)和慢性癌症术后疼痛(CPCSP),与抗癌药物、放疗或手术等治疗手段相关(如图1)[2]

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图1 CCRP分类

指南推荐 

1

推荐情况

阿片类药物(如吗啡或羟考酮)是中重度 CCRP 治疗的一线口服镇痛药物[6,7]。针对慢性内脏癌性疼痛(CVCP),指南推荐可选择羟考酮纳洛酮缓释片,证据质量:高质量(A),推荐强度: 强推荐(1)(如图2)[2]

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图2 镇痛药物循证医学证据质量分级及推荐强度


2

推荐依据

羟考酮纳洛酮缓释片的推荐来自国际多项关键临床试验,如表1[8-17]
表1 羟考酮纳洛酮缓释片推荐依据-临床试验汇总

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后续我们会总结其他指南/专家共识对羟考酮纳洛酮缓释片的推荐情况,敬请持续关注。


关于羟考酮纳洛酮缓释片


绿叶制药集团经多年研发的镇痛药——米美欣®(羟考酮纳洛酮缓释片)于2024年6月28日获得中国国家药品监督管理局的上市批准,适用于成人需阿片类镇痛药才能充分控制的重度疼痛。通过加入阿片受体拮抗剂纳洛酮,阻断羟考酮对肠道阿片受体的作用,有效减轻了阿片类药物常见的副作用便秘。


米美欣®是当前国内唯一能显著改善阿片类药物引起的肠功能障碍(OIBD),同时具有防滥用特性的国产强效镇痛药,其独特的“锁药”技术旨在防止药物被滥用。在确保有效疼痛管理的同时,米美欣®提供了可维持12小时的持续镇痛效果,简化患者的用药方案,改善其生活质量。


编译:张诗笛    审校:沈怡


参考文献

[1]ZYLLA D, STEELE G, GUPTA P. A systematic review of the impact of pain on overall survival in patients with cancer[J/OL]. Supportive Care in Cancer, 2017, 25(5): 1687-1698. DOI:10.1007/s00520-017-3614-y.

[2]中国慢性癌症相关性疼痛诊疗指南制订专家组,中国老年保健协会疼痛病学分会,程志祥,等. 中国慢性癌症相关性疼痛诊疗指南(2024版)[J]. 中华疼痛学杂志,2024,20(05):646-664.

[3]李小梅,袁文茜,曹伯旭,宋昱,宋学军,万有,樊碧发,韩济生,Bennett MI等.慢性癌症相关性疼痛[J].中国疼痛医学杂志,2021(03):161-165.

[4]BENNETT M I, KAASA S, BARKE A, et al. The IASP classification of chronic pain for ICD-11: Chronic cancer-related pain[J/OL]. Pain, 2019, 160(1): 38-44. DOI:10.1097/j.pain.0000000000001363.

[5]SCARBOROUGH B M, SMITH C B. Optimal pain management for patients with cancer in the modern era[J/OL]. CA: A Cancer Journal for Clinicians, 2018, 68(3): 182-196. DOI:10.3322/caac.21453.

[6]SCHMIDT-HANSEN M, BENNETT M I, ARNOLD S, et al. Oxycodone for cancer-related pain[J/OL]. The Cochrane Database of Systematic Reviews, 2022, 6(6): CD003870. DOI:10.1002/14651858.CD003870.pub7.

[7]WIFFEN P J, WEE B, MOORE R A. Oral morphine for cancer pain[J/OL]. The Cochrane Database of Systematic Reviews, 2016, 4(4): CD003868. DOI:10.1002/14651858.CD003868.pub4.

[8]DUPOIRON D, STACHOWIAK A, LOEWENSTEIN O, et al. A phase III randomized controlled study on the efficacy and improved bowel function of prolonged‐release (PR) oxycodone‐naloxone (up to 160/80 mg daily) vs oxycodone PR[J/OL]. European Journal of Pain, 2017, 21(9): 1528-1537. DOI:10.1002/ejp.1054.

[9]DUPOIRON D, STACHOWIAK A, LOEWENSTEIN O, et al. Long-term efficacy and safety of oxycodone-naloxone prolonged-release formulation (up to 180/90 mg daily) - results of the open-label extension phase of a phase III multicenter, multiple-dose, randomized, controlled study[J/OL]. European Journal of Pain (london, England), 2017, 21(9): 1485-1494. DOI:10.1002/ejp.1050.

[10]AHMEDZAI S H, NAUCK F, BAR-SELA G, et al. A randomized, double-blind, active-controlled, double-dummy, parallel-group study to determine the safety and efficacy of oxycodone/naloxone prolonged-release tablets in patients with moderate/severe, chronic cancer pain[J/OL]. Palliative Medicine, 2012, 26(1): 50-60. DOI:10.1177/0269216311418869.

[11]AHMEDZAI S H, LEPPERT W, JANECKI M, et al. Long-term safety and efficacy of oxycodone/naloxone prolonged-release tablets in patients with moderate-to-severe chronic cancer pain[J/OL]. Supportive Care in Cancer, 2015, 23(3): 823-830. DOI:10.1007/s00520-014-2435-5.

[12]SIMPSON K, LEYENDECKER P, HOPP M, et al. Fixed-ratio combination oxycodone/naloxone compared with oxycodone alone for the relief of opioid-induced constipation in moderate-to-severe noncancer pain[J/OL]. Current Medical Research and Opinion, 2008, 24(12): 3503-3512. DOI:10.1185/03007990802584454.

[13]LÖWENSTEIN O, LEYENDECKER P, HOPP M, et al. Combined prolonged-release oxycodone and naloxone improves bowel function in patients receiving opioids for moderate-to-severe non-malignant chronic pain: A randomised controlled trial[J/OL]. Expert Opinion on Pharmacotherapy, 2009, 10(4): 531-543. DOI:10.1517/14656560902796798.

[14]LÖWENSTEIN O, LEYENDECKER P, LUX E A, et al. Efficacy and safety of combined prolonged-release oxycodone and naloxone in the management of moderate/severe chronic non-malignant pain: Results of a prospectively designed pooled analysis of two randomised, double-blind clinical trials[J/OL]. BMC Clinical Pharmacology, 2010, 10: 12. DOI:10.1186/1472-6904-10-12.

[15]BLAGDEN M, HAFER J, DUERR H, et al. Long-term evaluation of combined prolonged-release oxycodone and naloxone in patients with moderate-to-severe chronic pain: Pooled analysis of extension phases of two phase III trials[J/OL]. Neurogastroenterology and Motility, 2014, 26(12): 1792-1801. DOI:10.1111/nmo.12463.

[16]KOOPMANS G, SIMPSON K, DE ANDRÉS J, et al. Fixed ratio (2:1) prolonged-release oxycodone/naloxone combination improves bowel function in patients with moderate-to-severe pain and opioid-induced constipation refractory to at least two classes of laxatives[J/OL]. Current Medical Research and Opinion, 2014, 30(11): 2389-2396. DOI:10.1185/03007995.2014.971355.

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*仅供医疗专业人士阅读


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