免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Ketamine as a Novel Solution for Opioid-Refractory Pain in Radiation Necrosis.
Ketamine as a Novel Solution for Opioid-Refractory Pain in Radiation Necrosis.
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我们报告一例36岁女性复发性转移性黑色素瘤患者,并发左大腿远端肌肉组织放射性坏死,在完成局部放疗约七个月后出现难以忍受、使人衰弱的疼痛。姑息医学科受邀协助疼痛管理。入院前,患者对递增剂量的口服羟考酮和透皮芬太尼无反应,这些药物与包括对乙酰氨基酚、巴氯芬、塞来昔布、度洛西汀和普瑞巴林在内的多模式方案联合使用。就在就诊前,患者刚完成泼尼松逐渐减量治疗免疫检查点抑制剂结肠炎,怀疑类固醇可能在停药前掩盖或部分治疗了疼痛。由于即将计划进行TIL(肿瘤浸润淋巴细胞)治疗,她不适合重新开始使用类固醇。尽管阿片类药物剂量不断升级(高达口服吗啡等效剂量(OME)598.75 mg),我们的患者仍持续经历未控制的疼痛,并伴有进行性镇静。
我们开始给予她氯胺酮0.1 mg/kg/hr,并在接下来24小时内滴定至最终剂量0.3 mg/kg/hr,随后再持续给药48小时。在完成三天氯胺酮输注后,患者的OME降低了45%,降至327.5 mg。出院后的几个月内,患者随后逐渐停用长效阿片类药物,并能够恢复到其基线功能状态。此前尚无关于使用氯胺酮治疗继发于放射性坏死的阿片类药物难治性疼痛的病例报告。在本病例中,我们证明了氯胺酮输注作为一种成功的治疗策略,可减少患者的阿片类药物需求量,优化疼痛控制,并有助于改善功能状态和生活质量。
We present the case of a 36-year-old female with recurrent metastatic melanoma, complicated by radiation necrosis of the left distal thigh musculature, who presented with intractable, debilitating pain approximately seven months following completion of local radiation therapy. Palliative Medicine was consulted for assistance with pain management. Prior to admission, the patient had failed to respond to escalating doses of oral oxycodone and transdermal fentanyl, given in conjunction with a multimodal regimen including acetaminophen, baclofen, celecoxib, duloxetine, and pregabalin.
Just before presentation, the patient completed a prednisone taper for treatment of immune checkpoint inhibitor colitis, with suspicion that steroids were likely masking or partially treating pain before discontinuation. She was not a candidate for steroid re-initiation due to upcoming plans for tumor-infiltrating lymphocyte therapy. Despite escalating opioid dosing (up to oral morphine equivalent (OME) 598. 75 mg), our patient continued to experience uncontrolled pain along with progressive sedation.
We started her on ketamine 0. 1 mg/kg/hr and titrated this over the next 24 hours to a final dose of 0. 3 mg/kg/hr, which was then continued for 48 additional hours. Following completion of a three-day ketamine infusion, the patient's OME was reduced by 45% to 327. 5 mg. In the months following hospital discharge, the patient was subsequently weaned off long-acting opioids and was able to return to her baseline functional status.
No previous cases have been reported of the use of ketamine for the treatment of opioid-refractory pain secondary to radiation necrosis. In this case, we have demonstrated ketamine infusion as a successful treatment strategy for reducing our patient's opioid requirement, optimizing pain control, and helping to improve functional status and quality of life.
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