Pancreas Centre BC, Vancouver, BC, Canada.
Division of Medical Oncology, BC Cancer, Vancouver, BC, Canada.
Nat Commun. 2022 Aug 26;13(1):5020. doi: 10.1038/s41467-022-32591-8.
Immunotherapy-based monotherapy treatment in metastatic pancreatic ductal adenocarcinoma (mPDAC) has shown limited benefit outside of the mismatch repair deficiency setting, while safety and efficacy of combining dual-checkpoint inhibitor immunotherapy with chemotherapy remains uncertain. Here, we present results from the CCTG PA.7 study (NCT02879318), a randomized phase II trial comparing gemcitabine and nab-paclitaxel with and without immune checkpoint inhibitors durvalumab and tremelimumab in 180 patients with mPDAC. The primary endpoint was overall survival. Secondary endpoints included progression-free survival and objective response rate. Results of the trial were negative as combination immunotherapy did not improve survival among the unselected patient population (p = 0.72) and toxicity was limited to elevation of lymphocytes in the combination immunotherapy group (p = 0.02). Exploratory baseline circulating tumor DNA (ctDNA) sequencing revealed increased survival for patients with KRAS wildtype tumors in both the combination immunotherapy (p = 0.001) and chemotherapy (p = 0.004) groups. These data support the utility of ctDNA analysis in PDAC and the prognostic value of ctDNA-based KRAS mutation status.
基于免疫疗法的单药治疗在错配修复缺陷以外的转移性胰腺导管腺癌(mPDAC)中的疗效有限,而联合双重检查点抑制剂免疫疗法与化疗的安全性和疗效仍不确定。在这里,我们展示了 CCTG PA.7 研究(NCT02879318)的结果,这是一项随机的 II 期试验,比较了在 180 名 mPDAC 患者中使用吉西他滨和 nab-紫杉醇联合或不联合免疫检查点抑制剂 durvalumab 和 tremelimumab 的效果。主要终点是总生存期。次要终点包括无进展生存期和客观缓解率。试验结果为阴性,因为联合免疫疗法并没有改善未选择的患者人群的生存(p=0.72),并且毒性仅限于联合免疫疗法组淋巴细胞升高(p=0.02)。探索性的基线循环肿瘤 DNA(ctDNA)测序显示,在联合免疫疗法(p=0.001)和化疗(p=0.004)组中,KRAS 野生型肿瘤患者的生存时间延长。这些数据支持 ctDNA 分析在 PDAC 中的实用性以及基于 ctDNA 的 KRAS 突变状态的预后价值。