局部晚期、复发性或转移性食管鳞状细胞癌患者接受紫杉醇加铂 (TP) 化疗联合延迟使用 PD-1 抑制剂的临床疗效:一项回顾性研究

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL Drug Design, Development and Therapy Pub Date : 2024-07-03 DOI:10.2147/dddt.s455248
Lin Shen, Zixuan Chen, Zhi Zhang, Yunjiang Wu, Yue Ren, Ying Li, Yue Li, Xudong Yin, Fang Han, Yong Chen
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引用次数: 0

摘要

目的:免疫检查点抑制剂(ICIs)联合化疗已成为局部晚期或转移性食管鳞状细胞癌(ESCC)的一线标准治疗方法。有证据表明,化疗与延迟给药 ICIs 联用可提高化疗的协同效应。在这项研究中,我们对ESCC患者接受紫杉醇加铂(TP)化疗联合PD-1抑制剂延迟给药的疗效进行了回顾性调查:回顾性研究了2019年1月至2023年4月期间作为一线治疗在TP化疗后3-5天接受PD-1抑制剂治疗的ESCC患者的临床数据。分析了临床结果和治疗安全性。研究了中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)、单核细胞与淋巴细胞比值(MLR)和泛免疫炎症值(PIV)的潜在作用:共有34例局部晚期、复发或转移性ESCC患者在TP化疗后3-5天接受了PD-1抑制剂治疗。客观反应率(ORR)和疾病控制率(DCR)分别为85.3%和97.1%。中位无进展生存期(PFS)和总生存期(OS)分别为13.2个月和19.1个月。7名患者接受了根治性手术,1名患者获得了病理完全反应(pCR),3名患者获得了主要病理反应(MPR)。在未接受手术的27名患者中,中位生存期(PFS)和生存期(OS)分别为9.7个月和19.1个月。预后较好与免疫化疗第3和第4周期时NLR小于3有关。其他参数(PLR、MLR和PIV)与预后无明显相关性。共有22名患者出现了3-4级毒性事件:结论:在TP化疗后3-5天使用PD-1抑制剂作为ESCC一线治疗的优化序列显示出良好的疗效。关键词:免疫检查点抑制剂;化疗;合理顺序;食管鳞状细胞癌;外周血参数
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Clinical Efficacy of Taxol Plus Platinum (TP) Chemotherapy Combined with Delayed Administration of PD-1 Inhibitors in Patients with Locally Advanced, Recurrent or Metastatic Esophageal Squamous Cell Carcinoma: A Retrospective Study
Purpose: Immune checkpoint inhibitors (ICIs) combined with chemotherapy have become the first-line standard treatment for locally advanced or metastatic esophageal squamous cell carcinoma (ESCC). The evidence also demonstrates improved synergistic effects of chemotherapy when combined with delayed administration of ICIs. In this study, we conducted a retrospective investigation into the treatment efficacy of taxol plus platinum (TP) chemotherapy combined with delayed administration of PD-1 inhibitors for ESCC patients.
Patients and Methods: Clinical data of ESCC patients who received PD-1 inhibitors 3– 5 days after TP chemotherapy as first-line treatment was retrospectively reviewed between January 2019 and April 2023. Clinical outcomes and treatment safety were analyzed. The potential roles of neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR), and pan-immune-inflammation value (PIV) were investigated.
Results: A total of 34 locally advanced, recurrent or metastatic ESCC patients received PD-1 inhibitors 3– 5 days following TP chemotherapy were included. The objective response rate (ORR) and disease control rate (DCR) were 85.3% and 97.1% respectively. The median progression-free survival (PFS) and overall survival (OS) were 13.2 and 19.1 month respectively. Seven patients received radical surgery, 1 patient achieved pathologic complete response (pCR) and 3 patients achieved major pathologic response (MPR). Among the 27 patients without surgery, the median PFS and OS were 9.7 and 19.1 month respectively. A more favorable prognosis was correlated with NLR less than 3 at the 3rd and 4th cycle of immunochemotherapy. No significant correlations between other parameters (PLR, MLR and PIV) and prognosis were observed. A total of 22 patients developed grade 3– 4 toxicity events.
Conclusion: The optimized sequence of PD-1 inhibitors administered 3– 5 days after TP chemotherapy as the first-line treatment of ESCC demonstrated favorable treatment efficacy. Pretreatment NLR of less than 3 at the 3rd and 4th cycle of immunochemotherapy is associated with a better prognosis.

Keywords: immune checkpoint inhibitors, chemotherapy, rational sequence, esophageal squamous cell carcinoma, peripheral blood parameters
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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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