Egusa Hiroki, Masuda Takeshi, Yamaguchi Kakuhiro, Sakamoto Shinjiro, Horimasu Yasushi, Kushitani Kei, Nakashima Taku, Iwamoto Hiroshi, Hamada Hironobu, Hattori Noboru
Department of Respiratory Medicine, Hiroshima University Hospital, Hiroshima, Japan.
Department of Pathology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Case Rep Oncol. 2024 Oct 9;17(1):1115-1123. doi: 10.1159/000540935. eCollection 2024 Jan-Dec.
There have been only a few cases showing the efficacy of pembrolizumab on granulocyte-colonystimulating factor (G-CSF)-producing non-small-cell lung cancer (NSCLC) with high programmed cell death ligand 1 (PD-L1) expression. Herein, we report the first case showing the efficacy of pembrolizumab for G-CSF-producing NSCLC with high PD-L1 expression, although the patient had factors indicative of poor pembrolizumab efficacy, such as poor performance status (PS) due to the tumor-induced inflammation and corticosteroids administration.
A 77-year-old woman was diagnosed with G-CSF-producing NSCLC-not otherwise specified, classified as clinical stage IVB, T2N3M1c. She had fever and her PS was 3, and her C-reactive protein (CRP) was 6.47 mg/dL due to inflammation by a G-CSF-producing tumor. Thus, we initiated the administration of dexamethasone (3.3 mg/day). Her fever abated the next day, and CRP dropped to 3.22 mg/dL after 4 days. Driver mutations were negative, and PD-L1, tumor proportion score, was highly expressed at 100%. Thus, pembrolizumab was started. Subsequently, the white blood cell count decreased, and the tumor shrank, indicating a partial response. After three cycles of pembrolizumab therapy, the anorexia improved, and she was discharged. The patient developed sclerosing cholangitis after discharge. Therefore, the pembrolizumab treatment was discontinued. The primary lesion was enlarged, indicating progressive disease. However, the patient and her family did not want additional treatment. Finally, her progression-free survival and overall survival were 6 and 7 months, respectively.
Pembrolizumab may be effective against G-CSF-producing NSCLC with high PD-L1 expression. Corticosteroids seemed to inhibit inflammation induced by the tumor, and exert the efficacy of pembrolizumab.
仅有少数病例显示派姆单抗对程序性细胞死亡配体1(PD-L1)高表达的产生粒细胞集落刺激因子(G-CSF)的非小细胞肺癌(NSCLC)有效。在此,我们报告首例显示派姆单抗对PD-L1高表达的产生G-CSF的NSCLC有效的病例,尽管该患者具有一些提示派姆单抗疗效不佳的因素,如因肿瘤诱导的炎症和使用糖皮质激素导致的体能状态(PS)较差。
一名77岁女性被诊断为产生G-CSF的NSCLC,未作其他特殊说明,临床分期为IVB期,T2N3M1c。她发热,PS为3,由于产生G-CSF的肿瘤引起炎症,其C反应蛋白(CRP)为6.47mg/dL。因此,我们开始给予地塞米松(3.3mg/天)。第二天她的发热消退,4天后CRP降至3.22mg/dL。驱动基因突变呈阴性,PD-L1肿瘤比例分数高表达,为100%。于是开始使用派姆单抗。随后,白细胞计数下降,肿瘤缩小,提示部分缓解。经过三个周期的派姆单抗治疗后,食欲改善,患者出院。出院后患者发生了硬化性胆管炎。因此,停止派姆单抗治疗。原发灶增大,提示疾病进展。然而,患者及其家属不希望接受进一步治疗。最后,她的无进展生存期和总生存期分别为6个月和7个月。
派姆单抗可能对PD-L1高表达的产生G-CSF的NSCLC有效。糖皮质激素似乎抑制了肿瘤诱导的炎症,并发挥了派姆单抗的疗效。