Poumeaud François, Jaffrelot Marion, Gomez-Roca Carlos, Korakis Iphigénie, Leonardi Giulia, Joly Marine, Mazières Julien, Guimbaud Rosine, Fares Nadim, Alouani Emily
Department of Medical Oncology, Oncopole Claudius Regaud, Toulouse, France.
Department of Digestive Oncology, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
Front Med (Lausanne). 2024 Jul 30;11:1402902. doi: 10.3389/fmed.2024.1402902. eCollection 2024.
Selective rearranged during transfection (RET) tyrosine kinase inhibitor, pralsetinib, demonstrated clinical efficacy and was well tolerated in lung and thyroid cancers with gene mutations or fusions in clinical trials. While the latter focused on the risk of pneumonitis, there is a lack of data regarding other types of infectious risks associated with pralsetinib. Herein, we report the case of a 53-year-old patient with a fusion neuroendocrine tumor, who achieved a partial response with pralsetinib as the fifth-line therapy. Of particular note, during pralsetinib therapy, the clinical course was complicated by five severe infectious events, namely, two oxygen-requiring pneumonias, two distinct spondylodiscitis, and one pneumocystis. Our study highlights the increased risk of any type of opportunistic infectious event with pralsetinib, but not selpercatinib, which is probably caused by off-target JAK1/2 inhibition.
转染期间选择性重排(RET)酪氨酸激酶抑制剂普拉替尼在临床试验中对具有基因突变或融合的肺癌和甲状腺癌显示出临床疗效且耐受性良好。虽然后者关注的是肺炎风险,但缺乏关于普拉替尼相关其他类型感染风险的数据。在此,我们报告一例53岁患有RET融合神经内分泌肿瘤的患者,其接受普拉替尼作为五线治疗后获得部分缓解。特别值得注意的是,在普拉替尼治疗期间,临床病程因五次严重感染事件而复杂化,即两次需氧性肺炎、两次不同的脊椎椎间盘炎和一次肺孢子菌感染。我们的研究强调了普拉替尼而非塞尔帕替尼会增加任何类型机会性感染事件的风险,这可能是由脱靶的JAK1/2抑制引起的。