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

被引:1
|
作者
Nishino, Mizuki [1 ,2 ]
Wang, Xinan [3 ]
Ricciuti, Biagio [4 ,5 ,6 ]
Tseng, Shu-Chi [1 ,2 ,7 ,8 ]
Park, Hyesun [1 ,2 ]
Alessi, Joao V. [4 ,5 ,6 ]
Vaz, Victor R. [4 ,5 ,6 ]
Hatabu, Hiroto [1 ,2 ]
Lin, Xihong [9 ]
Christiani, David C. [3 ,10 ]
Awad, Mark M. [4 ,5 ,6 ]
机构
[1] Brigham & Womens Hosp, Dept Radiol, 450 Brookline Ave, Boston, MA 02215 USA
[2] Dana Farber Canc Inst, Dept Imaging, 450 Brookline Ave, Boston, MA 02215 USA
[3] Harvard TH Chan Sch Publ Hlth, Dept Environm Hlth, 665 Huntington Ave, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Dept Med Oncol, 450 Brookline Ave, Boston, MA 02215 USA
[5] Dana Farber Canc Inst, Dept Med, 450 Brookline Ave, Boston, MA 02215 USA
[6] Brigham & Womens Hosp, 450 Brookline Ave, Boston, MA 02215 USA
[7] Chang Gung Mem Hosp Linkou, Dept Med Imaging & Intervent, Taoyuan, Taiwan
[8] Chang Gung Univ, Taoyuan, Taiwan
[9] Harvard TH Chan Sch Publ Hlth, Dept Biostat, 665 Huntington Ave, Boston, MA 02115 USA
[10] Massachusetts Gen Hosp, Dept Med, Pulm & Crit Care Div, Boston, MA 02115 USA
关键词
Immune checkpoint inhibitors; Carcinoma; Non-small-cell lung; Response Evaluation Criteria in Solid Tumors; Tumor burden; EVALUATION CRITERIA; CLINICAL BENEFIT; GUIDELINES; RECIST; PROGRESSION; SAFETY; IMMUNOTHERAPY; RADIOLOGISTS; DISEASE;
D O I
10.1007/s00330-023-09658-1
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
ObjectivesThe 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).MethodsThe 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.ResultsThere 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%).ConclusionsTumor 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.
引用
收藏
页码:7284 / 7293
页数:10
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