Department of Medical Oncology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
BMC Cancer. 2023 Oct 10;23(1):958. doi: 10.1186/s12885-023-11464-3.
There are no standard third-line treatment options for metastatic pancreatic ductal adenocarcinoma (mPDAC). Trametinib in combination with hydroxychloroquine (HCQ) or CDK4/6 inhibitors for pancreatic adenocarcinoma showed promising efficacy in preclinical studies. However, the regimens have not been well examined in patients with mPDAC.
Patients with mPDAC who received the combination of trametinib and HCQ or CDK4/6 inhibitors as third- or later-line therapy were reviewed. The efficacy and prognosis were further analyzed.
A total of 13 mPDAC patients were enrolled, of whom 8 and 5 patients were treated with trametinib plus HCQ or a CDK4/6 inhibitor (palbociclib or abemaciclib), respectively. All enrolled patients had either KRAS G12D or G12V mutations and had received a median of 3 prior lines of therapy (range, 2-6). The median trametinib treatment duration was 1.4 months. Of the 10 patients with measurable disease, only 1 patient achieved stable disease, and the remaining patients had progressive disease. Moreover, in patients treated with trametinib plus HCQ and a CDK4/6 inhibitor, the median progression-free survival was 2.0 and 2.8 months, respectively, and the median overall survival was 4.2 and 4.7 months, respectively. Moreover, 5 (50%) patients experienced grade 3-4 adverse events in 10 patients with available safety data.
The combination of trametinib and HCQ or CDK4/6 inhibitors may not be an effective later-line treatment for mPDAC, and the current preliminary findings need to be confirmed by other studies with larger sample sizes.
转移性胰腺导管腺癌(mPDAC)尚无标准的三线治疗选择。曲美替尼联合羟氯喹(HCQ)或 CDK4/6 抑制剂治疗胰腺腺癌在临床前研究中显示出良好的疗效。然而,这些方案在 mPDAC 患者中尚未得到充分研究。
对接受曲美替尼联合 HCQ 或 CDK4/6 抑制剂作为三线或更后线治疗的 mPDAC 患者进行了回顾性分析。进一步分析了疗效和预后。
共纳入 13 例 mPDAC 患者,其中 8 例和 5 例患者分别接受了曲美替尼联合 HCQ 或 CDK4/6 抑制剂(帕博西尼或阿贝西利)治疗。所有入组患者均携带 KRAS G12D 或 G12V 突变,且接受了中位数为 3 线(范围为 2-6)的治疗。曲美替尼治疗的中位持续时间为 1.4 个月。在 10 例可测量疾病患者中,仅有 1 例患者达到疾病稳定,其余患者均为疾病进展。此外,在接受曲美替尼联合 HCQ 和 CDK4/6 抑制剂治疗的患者中,中位无进展生存期分别为 2.0 个月和 2.8 个月,中位总生存期分别为 4.2 个月和 4.7 个月。此外,在 10 例可获得安全性数据的患者中,有 5 例(50%)患者发生 3-4 级不良事件。
曲美替尼联合 HCQ 或 CDK4/6 抑制剂可能不是 mPDAC 的有效后线治疗选择,目前的初步发现需要更大样本量的其他研究来证实。