Bloomberg-Kimmel Institute, Sidney Kimmel Comprehensive Cancer Center, and The Skip Viragh Center for Pancreatic Cancer Research and Clinical Care, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Cancer Res Commun. 2022 Nov 11;2(11):1418-1425. doi: 10.1158/2767-9764.CRC-22-0343. eCollection 2022 Nov.
The treatment of metastatic pancreatic ductal adenocarcinoma (PDAC) is frequently characterized by significant toxicity and rapid development of resistance to current approved therapies. More reliable biomarkers of response are needed to guide clinical decision making. We evaluated cell-free DNA (cfDNA) using a tumor-agnostic platform and traditional biomarkers (CEA and CA19-9) levels in 12 patients treated at Johns Hopkins University on NCT02324543 "Study of Gemcitabine/Nab-Paclitaxel/Xeloda (GAX) in Combination With Cisplatin and Irinotecan in Subjects With Metastatic Pancreatic Cancer." The pretreatment values, levels after 2 months of treatment, and change in biomarker levels with treatment were compared with clinical outcomes to determine their predictive value. The variant allele frequency (VAF) of and mutations in cfDNA after 2 months of treatment was predictive of progression-free survival (PFS) and overall survival (OS). In particular, patients with a lower-than-average VAF after 2 months of treatment had a substantially longer PFS than patients with higher posttreatment VAF (20.96 vs. 4.39 months). Changes in CEA and CA19-9 after 2 months of treatment were also good predictors of PFS. Comparison via concordance index demonstrated or VAF after 2 months of treatment to be better predictors of PFS and OS than CA19-9 or CEA. This pilot study requires validation but suggests cfDNA measurement is a useful adjunct to traditional protein biomarkers and imaging evaluation and could distinguish between patients who are likely to achieve prolonged responses versus those that will have early progression and may benefit from a change in treatment approach.
We report on the association of cfDNA with response durability for patients undergoing treatment with a novel metronomic chemotherapy regimen (gemcitabine, nab-paclitaxel, capecitabine, cisplatin, irinotecan; GAX-CI) for metastatic PDAC. This investigation offers encouraging evidence that cfDNA may prove to be a valuable diagnostic tool to guide clinical management.
转移性胰腺导管腺癌(PDAC)的治疗常表现为显著的毒性和对当前批准的治疗方法迅速产生耐药性。需要更可靠的反应生物标志物来指导临床决策。我们在约翰霍普金斯大学的 NCT02324543 号“吉西他滨/ Nab-紫杉醇/卡培他滨(GAX)联合顺铂和伊立替康治疗转移性胰腺癌患者的研究”中评估了 12 名患者的无细胞 DNA(cfDNA),并使用肿瘤agnostic 平台和传统生物标志物(CEA 和 CA19-9)水平。将预处理值、治疗 2 个月后的水平以及与治疗相关的生物标志物水平的变化与临床结果进行比较,以确定其预测价值。治疗后 2 个月时 cfDNA 中 和 突变的变异等位基因频率(VAF)可预测无进展生存期(PFS)和总生存期(OS)。特别是,治疗后 2 个月 VAF 低于平均水平的患者的 PFS 明显长于 VAF 较高的患者(20.96 与 4.39 个月)。治疗后 2 个月 CEA 和 CA19-9 的变化也是 PFS 的良好预测指标。通过一致性指数的比较表明,治疗后 2 个月时 或 VAF 比 CA19-9 或 CEA 更能预测 PFS 和 OS。这项初步研究需要验证,但表明 cfDNA 测量是传统蛋白质生物标志物和影像学评估的有用辅助手段,可以区分可能获得长期缓解的患者与那些将早期进展的患者,并可能受益于治疗方法的改变。
我们报告了 cfDNA 与接受新型节拍化疗方案(吉西他滨、nab-紫杉醇、卡培他滨、顺铂、伊立替康;GAX-CI)治疗转移性 PDAC 的患者的反应持久性之间的关联。这项研究提供了令人鼓舞的证据,表明 cfDNA 可能成为一种有价值的诊断工具,用于指导临床管理。