Center for Cancer Diagnosis and Treatment, The Second Affiliated Hospital of Soochow University, Suzhou 215000, Jiangsu Province, China.
Department of Radiotherapy & Oncology, The Second Affiliated Hospital of Soochow University, Suzhou 215000, Jiangsu Province, China.
World J Gastroenterol. 2024 Mar 7;30(9):1237-1249. doi: 10.3748/wjg.v30.i9.1237.
Pancreatic ductal adenocarcinoma (PDAC) is a highly fatal disease with limited effective treatment especially after first-line chemotherapy. The human epidermal growth factor receptor 2 (HER-2) immunohistochemistry (IHC) positive is associated with more aggressive clinical behavior and shorter overall survival in PDAC.
We present a case of multiple metastatic PDAC with IHC mismatch repair proficient but HER-2 IHC weakly positive at diagnosis that didn't have tumor regression after first-line nab-paclitaxel plus gemcitabine and PD-1 inhibitor treatment. A novel combination therapy PRaG 3.0 of RC48 (HER2-antibody-drug conjugate), radiotherapy, PD-1 inhibitor, granulocyte-macrophage colony-stimulating factor and interleukin-2 was then applied as second-line therapy and the patient had confirmed good partial response with progress-free-survival of 6.5 months and overall survival of 14.2 month. She had not developed any grade 2 or above treatment-related adverse events at any point. Percentage of peripheral CD8Temra and CD4Temra were increased during first two activation cycles of PRaG 3.0 treatment containing radiotherapy but deceased to the baseline during the maintenance cycles containing no radiotherapy.
PRaG 3.0 might be a novel strategy for HER2-positive metastatic PDAC patients who failed from previous first-line approach and even PD-1 immunotherapy but needs more data in prospective trials.
胰腺导管腺癌(PDAC)是一种高度致命的疾病,尤其是在一线化疗后,有效的治疗方法有限。人表皮生长因子受体 2(HER-2)免疫组化(IHC)阳性与 PDAC 更具侵袭性的临床行为和更短的总生存期相关。
我们报告了一例 IHC 错配修复有效的多转移 PDAC 病例,但 HER-2 IHC 在诊断时呈弱阳性,在一线纳武利尤单抗联合吉西他滨和 PD-1 抑制剂治疗后没有肿瘤退缩。一种新的二线治疗方案 PRaG 3.0(RC48[HER2 抗体药物偶联物]、放疗、PD-1 抑制剂、粒细胞-巨噬细胞集落刺激因子和白细胞介素-2)随后被应用,患者有明确的部分缓解,无进展生存期为 6.5 个月,总生存期为 14.2 个月。在任何时候,她都没有发生任何 2 级或以上的治疗相关不良事件。在包含放疗的 PRaG 3.0 治疗的前两个激活周期中,外周血 CD8Temra 和 CD4Temra 的比例增加,但在不包含放疗的维持周期中降至基线。
PRaG 3.0 可能是一种新的策略,适用于先前一线治疗甚至 PD-1 免疫治疗失败的 HER2 阳性转移性 PDAC 患者,但需要前瞻性试验的更多数据。