S. Yuasa, Megumi Kabeya, S. Hibi, Y. Shirokawa, Chiaki Tokoro, R. Furuta, S. Nagao, S. Kayukawa, Yoshiteru Tanaka, K. Ina
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引用次数: 0
摘要
表皮生长因子受体(EGFR)因其缓解疼痛的治疗潜力而受到广泛关注。用抗egfr抗体或酪氨酸激酶抑制剂治疗后神经性疼痛的缓解已有报道。然而,很少有报道调查癌症相关的痛觉性疼痛或慢性化学诱导的周围神经病变与EGFR抑制的镇痛作用的关系。因此,我们对191例接受化疗加分子靶向药物的结直肠癌患者进行了回顾性调查,以研究抗egfr抗体对癌性疼痛或奥沙利铂诱导的周围神经病变的镇痛作用。我们发现帕尼单抗和贝伐单抗治疗的患者在痛觉性疼痛的改善率上存在显著差异(100% vs 9.1%;P < 0.01),但奥沙利铂诱导的周围神经病变不存在。总之,帕尼珠单抗可能有效减少癌症相关的痛觉性疼痛。
Retrospective Evaluation of the Analgesic Effects of Molecular Target Agents Against Cancer Pain and Oxaliplatin-Induced Chronic Peripheral Neuropathy
Epidermal growth factor receptor (EGFR) has received significant attention for its therapeutic potential for pain relief. The relief of neuropathic pain after treatment with anti-EGFR antibodies or tyrosine kinase inhibitors has been previously described. However, few reports have investigated the association of cancer-related nociceptive pain or chronic chemical induced peripheral neuropathy with the analgesic effects of EGFR inhibition.
Therefore, we conducted a retrospective survey of 191 patients with colorectal cancer receiving chemotherapy plus molecular targeting drugs to examine the analgesic effects of anti-EGFR antibodies against either cancer pain or oxaliplatin-induced peripheral neuropathy. We identified a significant difference in the improvement rates of nociceptive pain between panitumumab- and bevacizumab-treated patients (100% vs. 9.1%; p < 0.01), but not oxaliplatin-induced peripheral neuropathy.
In conclusion, panitumumab may be effective at reducing cancer-related nociceptive pain.