Tumor Response Dynamics of Advanced Non-small Cell Lung Cancer Patients Treated with PD-1 Inhibitors: Imaging Markers for Treatment Outcome

被引:60
|
作者
Nishino, Mizuki [1 ,2 ]
Dahlberg, Suzanne E. [3 ]
Adeni, Anika E. [4 ,5 ,6 ]
Lydon, Christine A. [4 ,5 ,6 ]
Hatabu, Hiroto [1 ,2 ]
Janne, Pasi A. [4 ,5 ,6 ]
Hodi, F. Stephen [4 ,5 ,6 ]
Awad, Mark M. [4 ,5 ,6 ]
机构
[1] Brigham & Womens Hosp, Dept Radiol, 75 Francis St, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Dept Biostat, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[5] Dana Farber Canc Inst, Dept Med, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, 450 Brookline Ave, Boston, MA 02115 USA
关键词
IMMUNE-RELATED RESPONSE; EVALUATION CRITERIA; EGFR MUTATIONS; NSCLC PATIENTS; THERAPY; PEMBROLIZUMAB; PROGRESSION; GUIDELINES; NIVOLUMAB; PSEUDOPROGRESSION;
D O I
10.1158/1078-0432.CCR-17-1434
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We evaluated tumor burden dynamics in patients with advanced non-small cell lung cancer (NSCLC) treated with commercial PD-1 inhibitors to identify imaging markers associated with improved overall survival (OS). Experimental Design: The study included 160 patients with advanced NSCLC treated with commercial nivolumab or pembrolizumab monotherapy as a part of clinical care. Tumor burden dynamics were studied for the association with OS. Results: Tumor burden change at best overall response (BOR) ranged from -100% to +278% (median, +3.5%). Response rate (RR) was 18% (29/160). Current and former smokers had a higher RR than never smokers (P = 0.04). Durable disease control for at least 6 months was noted in 26 patients (16%), which included 10 patients with stable disease as BOR. Using a landmark analysis, patients with < 20% tumor burden increase from baseline within 8 weeks of therapy had longer OS than patients with >= 20% increase (median OS, 12.4 vs. 4.6 months, P < 0.001). Patients with < 20% tumor burden increase throughout therapy had significantly reduced hazards of death (HR, 0.24; Cox P < 0.0001) after adjusting for smoking (HR, 0.86; P = 0.61) and baseline tumor burden (HR, 1.55; P = 0.062), even though some patients met criteria for RECIST progression while on therapy. One patient (0.6%) had atypical response pattern consistent with pseudoprogression. Conclusions: Objective response or durable disease control was noted in 24% of patients with advanced NSCLC treated with commercial PD-1 inhibitors. A tumor burden increase of < 20% from baseline during therapy was associated with longer OS, proposing a practical marker of treatment benefit. Pseudoprogression is rare in NSCLCs treated with PD-1 inhibitors. (C) 2017 AACR.
引用
收藏
页码:5737 / 5744
页数:8
相关论文
共 50 条
  • [1] Inflammatory Markers as Predictors of Treatment Response and Survival in Patients With Non-Small Cell Lung Cancer Treated with PD-1 Inhibitors
    Tourkantonis, I.
    Gkiozos, I.
    Grapsa, D.
    Charpidou, A.
    Gogas, H.
    Psyrri, D.
    Syrigos, K.
    JOURNAL OF THORACIC ONCOLOGY, 2021, 16 (10) : S1144 - S1145
  • [2] Patterns of disease progression in advanced non-small cell lung cancer patients treated with PD-1 inhibitors
    Qin, Angel
    Kalemkerian, Gregory Peter
    Schneider, Bryan J.
    Hassan, Khaled Aref
    Cease, Kemp Bailey
    Zhao, Lili
    Warren, Edus H.
    Ramnath, Nithya
    JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
  • [3] Peripheral blood markers predictive of outcome and immune-related adverse events in advanced non-small cell lung cancer treated with PD-1 inhibitors
    Peng, Lihong
    Wang, Yong
    Liu, Fen
    Qiu, Xiaotong
    Zhang, Xinwei
    Fang, Chen
    Qian, Xiaoyin
    Li, Yong
    CANCER IMMUNOLOGY IMMUNOTHERAPY, 2020, 69 (09) : 1813 - 1822
  • [4] Peripheral blood markers predictive of outcome and immune-related adverse events in advanced non-small cell lung cancer treated with PD-1 inhibitors
    Lihong Peng
    Yong Wang
    Fen Liu
    Xiaotong Qiu
    Xinwei Zhang
    Chen Fang
    Xiaoyin Qian
    Yong Li
    Cancer Immunology, Immunotherapy, 2020, 69 : 1813 - 1822
  • [5] Impact of sarcopenia in patients with advanced non-small cell lung cancer treated with PD-1 inhibitors: A preliminary retrospective study
    Shiroyama, Takayuki
    Nagatomo, Izumi
    Koyama, Shohei
    Hirata, Haruhiko
    Nishida, Sumiyuki
    Miyake, Kotaro
    Fukushima, Kiyoharu
    Shirai, Yuya
    Mitsui, Yuichi
    Takata, So
    Masuhiro, Kentaro
    Yaga, Moto
    Iwahori, Kota
    Takeda, Yoshito
    Kida, Hiroshi
    Kumanogoh, Atsushi
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [6] Tumor response dynamics of advanced non-small-cell lung cancer (NSCLC) patients (pts) treated with commercial PD-1 inhibitors in the clinical setting.
    Nishino, Mizuki
    Dahlberg, Suzanne Eleanor
    Adeni, Anika E.
    Lydon, Christine A.
    Hatabu, Hiroto
    Janne, Pasi A.
    Hodi, F. Stephen
    Awad, Mark M.
    JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
  • [7] Blood Biomarkers Correlate with Outcome in Advanced Non-Small Cell Lung Cancer Patients Treated with Anti PD-1 Antibodies
    Soyano, A.
    Dholaria, B.
    Marin, J.
    Diehl, N.
    Hodge, D.
    Luo, Y.
    Yang, L.
    Adjei, A.
    Knutson, K.
    Lou, Y.
    JOURNAL OF THORACIC ONCOLOGY, 2017, 12 (11) : S2010 - S2010
  • [8] Pre-Treatment Tumor Volume in Non-Small Cell Lung Cancer (NSCLC) as a Predictor of Response to PD-1 Inhibitors
    Nagasaka, M.
    Crosby, M.
    Thummala, N.
    Abrams, J.
    Sukari, A.
    JOURNAL OF THORACIC ONCOLOGY, 2017, 12 (11) : S2431 - S2431
  • [9] Peripheral blood-based biomarkers of prognosis and treatment response in patients with non-small cell lung cancer treated with PD-1 inhibitors
    Tourkantonis, I.
    Grapsa, D.
    Charpidou, A.
    Gkiozos, I.
    Gogas, H.
    Psyrri, D.
    Syrigos, K.
    ANNALS OF ONCOLOGY, 2020, 31 : S1419 - S1419
  • [10] iSEND is an algorithmic model specific for advanced non-small cell lung cancer patients treated with PD-1/PD-L1 inhibitors
    Park, Wungki
    Florou, Vaia
    Algaze, Sandra
    Saravia, Diana
    Kwon, Deukwoo
    Lopes, Gilberto
    JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2017, 5