Du J, Qiu X, Ni J Y, Wang Q L, Tong F, Sha H Z, Zhu Y H, Qi L, Cai W, Gao C, Wei X W, Chen M B, Qian Z Y, Cai M H, Tao M, Wang C L, Zheng G C, Jiang H, Dai A W, Wu J, Zhao M H, Li X Q, Lu B, Wang C B, Liu B R
Department of Oncology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing210008, China Drum Tower Clinical College of Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing210008, China.
Department of Oncology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing210008, China.
Zhonghua Zhong Liu Za Zhi. 2024 Nov 23;46(11):1038-1048. doi: 10.3760/cma.j.cn112152-20231223-00383.
To observe and evaluate the clinical efficacy and safety of albumin-bound paclitaxel as first-line treatment for patients with advanced pancreatic cancer in China, and to explore the prognosis-related molecules in pancreatic cancer based on next-generation sequencing (NGS) of tumor tissues. From December 2018 to December 2020, patients with locally advanced or metastatic pancreatic cancer were recruited to accept albumin-bound paclitaxel as first-line treatment in the oncology departments of 24 hospitals in East China. The primary endpoints were overall survival (OS) and treatment related adverse events, and the secondary endpoint was progression-free survival (PFS). Adverse effects were graded using Common Terminology Criteria for Adverse Events 5.0 (CTCAE 5.0). NGS sequencing on the primary or metastatic tissue samples of pancreatic cancer obtained through surgical resection or biopsy was performed. This study recruited 229 patients, including 70 patients with locally advanced pancreatic cancer (LAPC) and 159 patients with metastatic pancreatic cancer (mPC). The disease control rate was 79.9% and the objective response rate is 36.3%.The common adverse effects during treatment were anaemia (159 cases), leucopenia (170 cases), neutropenia (169 cases), increased aminotransferases (110 cases), and thrombocytopenia (95 cases), and the incidence of grade 3-4 neutropenia is 12.2% (28/229). The median follow-up time was 21.2 months (95% : 18.5-23.1 months). The median PFS (mPFS) was 5.3 months (95% : 4.37-4.07 months) and the median OS (mOS) was 11.2 months (95% : 9.5-12.9 months). The mPFS of patients with LAPC was 7.4 months (95% : 6.6-11.2 months), and their mOS was 15.5 months (95% : 12.6-NA months). The mPFS of patients with mPC was 3.9 months (95% : 3.4-5.1 months), and their mOS was 9.3 months (95% : 8.0-10.8 months). Multivariate Cox regression analysis showed that clinical stage (=1.47, 95% : 1.06-2.04), primary tumor site (=0.64, 95% : 0.48-0.86), Eastern Cooperative Oncology Group Performance Status (ECOG PS) score (=2.66, 95% : 1.53-4.65), and whether to combine radiotherapy (=0.65, 95% : 0.42-1.00) were independent influencing factors for the PFS of these patients. The primary tumor site (=0.68, 95% : 0.48-0.95), ECOG score (=5.82, 95% : 3.14-10.82), and whether to combine radiotherapy (=0.58, 95% : 0.35-0.96) were independent influencing factors of the OS of these patients. The most frequent gene mutations in these advanced stage pancreatic patients were (89.66%), (77.01%), (32.18%), and (21.84%) by NGS of tumor tissues from 87 pancreatic cancer patients with sufficient specimens. Further analysis revealed that mutations in , , , and genes were significantly associated with an increased risk of death (<0.05). Albumin-bound paclitaxel as first-line treatment demonstrated feasible anti-tumor efficacy and manageable safety for patients with advanced pancreatic cancer in China.
观察和评估白蛋白结合型紫杉醇作为中国晚期胰腺癌患者一线治疗的临床疗效和安全性,并基于肿瘤组织的二代测序(NGS)探索胰腺癌的预后相关分子。2018年12月至2020年12月,招募局部晚期或转移性胰腺癌患者,在华东地区24家医院的肿瘤科接受白蛋白结合型紫杉醇作为一线治疗。主要终点为总生存期(OS)和治疗相关不良事件,次要终点为无进展生存期(PFS)。使用不良事件通用术语标准5.0(CTCAE 5.0)对不良反应进行分级。对通过手术切除或活检获得的胰腺癌原发或转移组织样本进行NGS测序。本研究共纳入229例患者,其中局部晚期胰腺癌(LAPC)患者70例,转移性胰腺癌(mPC)患者159例。疾病控制率为79.9%,客观缓解率为36.3%。治疗期间常见的不良反应为贫血(159例)、白细胞减少(170例)、中性粒细胞减少(169例)、转氨酶升高(110例)和血小板减少(95例),3-4级中性粒细胞减少的发生率为12.2%(28/229)。中位随访时间为21.2个月(95%:18.5 - 23.1个月)。中位PFS(mPFS)为5.3个月(95%:4.37 - 4.07个月),中位OS(mOS)为11.2个月(95%:9.5 - 12.9个月)。LAPC患者的mPFS为7.4个月(95%:6.6 - 11.2个月),mOS为15.5个月(95%:12.6 - NA个月)。mPC患者的mPFS为3.9个月(95%:3.4 - 5.1个月),mOS为9.3个月(95%:8.0 - 10.8个月)。多因素Cox回归分析显示,临床分期(=1.47,95%:1.06 - 2.04)、原发肿瘤部位(=0.64,95%:0.48 - 0.86)、东部肿瘤协作组体能状态(ECOG PS)评分(=2.66,95%:1.53 - 4.65)以及是否联合放疗(=0.65,95%:0.42 - 1.00)是这些患者PFS的独立影响因素。原发肿瘤部位(=0.68,95%:0.48 - 0.95)、ECOG评分(=5.82,95%:3.14 - 10.82)以及是否联合放疗(=0.58,95%:0.35 - 0.96)是这些患者OS的独立影响因素。通过对87例有足够标本的胰腺癌患者的肿瘤组织进行NGS检测,这些晚期胰腺癌患者中最常见的基因突变是(89.66%)、(77.01%)、(32.18%)和(21.84%)。进一步分析显示,、、和基因的突变与死亡风险增加显著相关(<0.05)。白蛋白结合型紫杉醇作为一线治疗对中国晚期胰腺癌患者显示出可行的抗肿瘤疗效和可控的安全性。