First-line nanoparticle polymeric micellar paclitaxel with gemcitabine in metastatic pancreatic cancer: a single-arm, prospective, and exploratory study.

IF 4.2 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Gastroenterology Report Pub Date : 2026-05-01 eCollection Date: 2026-02-01 DOI:10.1093/gastro/goag034
Nan Lyu, Qianqian Wang, Kuirong Jiang, Dong Xu, Yang Wu, Kai Zhang, Jishu Wei, Jianmin Chen, Feng Guo, Zipeng Lu, Bin Xiao, Guosheng Chen, Junli Wu, Wentao Gao, Yuqi Wang, Fufeng Wang, Min Tu
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引用次数: 0

Abstract

Background: Pancreatic cancer is one of the most lethal malignancies, with limited therapeutic options. In this exploratory trial, we aimed to evaluate the efficacy and safety of nanoparticle polymeric micellar paclitaxel (pm-Pac) combined with gemcitabine as first-line treatment for metastatic pancreatic cancer (mPC).

Methods: Twenty-one patients with histologically or cytologically confirmed mPC were enrolled in this study. The primary endpoint was progression-free survival (PFS). Meanwhile, the secondary endpoints included the objective response rate (ORR), overall survival, disease control rate (DCR), duration of response (DOR), and safety of combination therapy.

Results: The median PFS was 7.4 months (95% confidence interval [CI]: 5.4-9.4 months). The ORR and DCR were 52.4% (95% CI: 29.1%-75.7%) and 95.2% (95% CI: 85.3%-100%), respectively. Amongst patients who achieved partial response, the median DOR was 4.8 months (95% CI: 1.5-8.1 months). No treatment-related deaths were reported. Grade 3-4 adverse events (AEs) occurred in 81.0% of patients, with increased γ-glutamyltransferase levels (38.1%), neutropenia (33.3%), and leukocytopenia (28.6%) being the most frequent AEs. Low SERPINB3 and SERPINB4 expression was correlated with prolonged PFS, accompanied by the significant downregulation of gene sets involved in DNA replication, nonsense-mediated mRNA decay, and protein translation in long-PFS tumours. Tumour immune microenvironment analysis revealed that patients with short PFS had increased levels of common lymphoid progenitors and decreased populations of mature B and T lymphocytes.

Conclusions: The combination of pm-Pac and gemcitabine as first-line therapy for mPC exhibited favourable tolerability and clinical efficacy. However, larger randomized-controlled trials are needed to validate these preliminary findings.

Trial registration: www.chictr.org.cn, ChiCTR2300078861.

纳米颗粒聚合胶束紫杉醇联合吉西他滨治疗转移性胰腺癌:单臂、前瞻性和探索性研究
背景:胰腺癌是最致命的恶性肿瘤之一,治疗选择有限。在这项探索性试验中,我们旨在评估纳米颗粒聚合物胶束紫杉醇(pm-Pac)联合吉西他滨作为转移性胰腺癌(mPC)一线治疗的有效性和安全性。方法:21例经组织学或细胞学证实的mPC患者入选本研究。主要终点为无进展生存期(PFS)。同时,次要终点包括客观缓解率(ORR)、总生存期、疾病控制率(DCR)、缓解持续时间(DOR)和联合治疗的安全性。结果:中位PFS为7.4个月(95%置信区间[CI]: 5.4-9.4个月)。ORR和DCR分别为52.4% (95% CI: 29.1% ~ 75.7%)和95.2% (95% CI: 85.3% ~ 100%)。在获得部分缓解的患者中,中位DOR为4.8个月(95% CI: 1.5-8.1个月)。没有与治疗相关的死亡报告。81.0%的患者发生3-4级不良事件(ae),其中γ-谷氨酰转移酶水平升高(38.1%)、中性粒细胞减少(33.3%)和白细胞减少(28.6%)是最常见的ae。SERPINB3和SERPINB4的低表达与PFS的延长相关,并伴随着长期PFS肿瘤中参与DNA复制、无义介导的mRNA衰变和蛋白质翻译的基因组的显著下调。肿瘤免疫微环境分析显示,短PFS患者的普通淋巴样祖细胞水平升高,成熟B淋巴细胞和T淋巴细胞数量减少。结论:pm-Pac联合吉西他滨作为一线治疗mPC具有良好的耐受性和临床疗效。然而,需要更大规模的随机对照试验来验证这些初步发现。试验注册:www.chictr.org.cn, ChiCTR2300078861。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Gastroenterology Report
Gastroenterology Report Medicine-Gastroenterology
CiteScore
4.60
自引率
2.80%
发文量
63
审稿时长
8 weeks
期刊介绍: Gastroenterology Report is an international fully open access (OA) online only journal, covering all areas related to gastrointestinal sciences, including studies of the alimentary tract, liver, biliary, pancreas, enteral nutrition and related fields. The journal aims to publish high quality research articles on both basic and clinical gastroenterology, authoritative reviews that bring together new advances in the field, as well as commentaries and highlight pieces that provide expert analysis of topical issues.
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