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一线帕博利珠单抗联合化疗治疗晚期非小细胞肺癌:肿瘤缓解动力学作为生存标志物。

Advanced non-small-cell lung cancer treated with first-line pembrolizumab plus chemotherapy: tumor response dynamics as a marker for survival.

机构信息

Department of Radiology, Brigham and Women's Hospital and Department of Imaging, Dana-Farber Cancer Institute, 450 Brookline Ave., MA, 02215, Boston, USA.

Department of Environmental Health, Harvard T.H. Chan School of Public Health, 665 Huntington Avenue, Boston, MA, 02115, USA.

出版信息

Eur Radiol. 2023 Oct;33(10):7284-7293. doi: 10.1007/s00330-023-09658-1. Epub 2023 Apr 26.

Abstract

OBJECTIVES

The study investigated tumor burden dynamics on computed tomography (CT) scans in patients with advanced non-small-cell lung cancer (NSCLC) during first-line pembrolizumab plus chemotherapy, to provide imaging markers for overall survival (OS).

METHODS

The study included 133 patients treated with first-line pembrolizumab plus platinum-doublet chemotherapy. Serial CT scans during therapy were assessed for tumor burden dynamics during therapy, which were studied for the association with OS.

RESULTS

There were 67 responders, with overall response rate of 50%. The tumor burden change at the best overall response ranged from - 100.0% to + 132.1% (median of - 30%). Higher response rates were associated with younger age (p < 0.001) and higher programmed cell death-1 (PD-L1) expression levels (p = 0.01). Eighty-three patients (62%) showed tumor burden below the baseline burden throughout therapy. Using an 8-week landmark analysis, OS was longer in patients with tumor burden below the baseline burden in the first 8 weeks than in those who experienced ≥ 0% increase (median OS: 26.8 vs. 7.6 months, hazard ratio (HR): 0.36, p < 0.001). Tumor burden remained below their baseline throughout therapy was associated with significantly reduced hazards of death (HR: 0.72, p = 0.03) in the extended Cox models, after adjusting for other clinical variables. Pseudoprogression was noted in only one patient (0.8%).

CONCLUSIONS

Tumor burden staying below the baseline burden throughout the therapy was predictive of prolonged overall survival in patients with advanced NSCLC treated with first-line pembrolizumab plus chemotherapy, and may be used as a practical marker for therapeutic decisions in this widely used combination regimen.

CLINICAL RELEVANCE STATEMENT

The analysis of tumor burden dynamics on serial CT scans in reference to the baseline burden can provide an additional objective guide for treatment decision making in patients treated with first-line pembrolizumab plus chemotherapy for their advanced NSCLC.

KEY POINTS

• Tumor burden remaining below baseline burden during therapy predicted longer survival during first-line pembrolizumab plus chemotherapy. • Pseudoprogression was noted in 0.8%, demonstrating the rarity of the phenomenon. • Tumor burden dynamics may serve as an objective marker for treatment benefit to guide treatment decisions during first-line pembrolizumab plus chemotherapy.

摘要

目的

本研究旨在探讨一线帕博利珠单抗联合化疗治疗晚期非小细胞肺癌(NSCLC)患者的 CT 扫描肿瘤负荷变化,为总生存期(OS)提供影像学标志物。

方法

本研究纳入了 133 例接受一线帕博利珠单抗联合铂类双药化疗的患者。对治疗期间的连续 CT 扫描进行评估,以研究治疗期间肿瘤负荷的变化与 OS 的关系。

结果

共有 67 例患者为缓解者,总体缓解率为 50%。最佳总缓解时的肿瘤负荷变化范围为-100.0%至+132.1%(中位数为-30%)。较高的缓解率与年龄较小(p<0.001)和较高的程序性死亡配体-1(PD-L1)表达水平(p=0.01)相关。83 例(62%)患者在整个治疗过程中肿瘤负荷低于基线水平。采用 8 周时间点分析,前 8 周肿瘤负荷低于基线水平的患者 OS 长于肿瘤负荷增加≥0%的患者(中位 OS:26.8 与 7.6 个月,风险比(HR):0.36,p<0.001)。在扩展的 Cox 模型中,在调整其他临床变量后,整个治疗期间肿瘤负荷持续低于基线与死亡风险显著降低相关(HR:0.72,p=0.03)。仅 1 例(0.8%)患者出现假性进展。

结论

在接受一线帕博利珠单抗联合化疗治疗的晚期 NSCLC 患者中,肿瘤负荷在整个治疗期间保持低于基线水平与延长总生存期相关,并且可能作为该广泛应用联合方案治疗决策的实用标志物。

临床相关性声明

对参考基线的连续 CT 扫描上的肿瘤负荷动态变化进行分析,可以为接受一线帕博利珠单抗联合化疗治疗的晚期 NSCLC 患者的治疗决策提供额外的客观指导。

关键点

  1. 治疗期间肿瘤负荷保持低于基线水平预测一线帕博利珠单抗联合化疗的生存时间更长。

  2. 假性进展的发生率为 0.8%,表明该现象罕见。

  3. 肿瘤负荷动态变化可能成为指导一线帕博利珠单抗联合化疗治疗获益的客观标志物,以指导治疗决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9baf/10896107/8c6eb57a6f39/nihms-1966096-f0001.jpg

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Pembrolizumab plus Chemotherapy for Squamous Non-Small-Cell Lung Cancer.帕博利珠单抗联合化疗用于鳞状非小细胞肺癌。
N Engl J Med. 2018 Nov 22;379(21):2040-2051. doi: 10.1056/NEJMoa1810865. Epub 2018 Sep 25.

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