Immune-Related Adverse Events and Corticosteroid Use for Cancer-Related Symptoms Are Associated With Efficacy in Patients With Non-small Cell Lung Cancer Receiving Anti-PD-(L)1 Blockade Agents

被引:44
作者
Riudavets, Mariona [1 ,2 ]
Mosquera, Joaquin [3 ]
Garcia-Campelo, Rosario [3 ]
Serra, Jorgina [1 ]
Anguera, Georgia [1 ]
Gallardo, Pablo [1 ]
Sullivan, Ivana [1 ]
Barba, Andres [1 ]
del Carpio, Luis [1 ]
Barnadas, Agusti [1 ]
Gich, Ignasi [4 ,5 ,6 ]
Majem, Margarita [1 ]
机构
[1] Hosp Santa Creu & Sant Pau, Dept Med Oncol, Barcelona, Spain
[2] Univ Autonoma Barcelona UAB, Dept Med, Barcelona, Spain
[3] Hosp Univ A Coruna, Dept Med Oncol, La Coruna, Spain
[4] Hosp Santa Creu & Sant Pau, Dept Clin Epidemiol & Publ Hlth, Barcelona, Spain
[5] CIBER Epidemiol & Salud Publ CIBERESP, Madrid, Spain
[6] St Pau Biomed Res Inst IIB St Pau, Barcelona, Spain
来源
FRONTIERS IN ONCOLOGY | 2020年 / 10卷
关键词
immune-related adverse events; immunotherapy; advanced NSCLC; corticosteroids; efficacy; OPEN-LABEL; NIVOLUMAB; DOCETAXEL; PEMBROLIZUMAB;
D O I
10.3389/fonc.2020.01677
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background:Immune-related adverse events (irAEs) have been associated with improved efficacy in advanced non-small cell lung cancer (NSCLC) patients receiving anti-PD-(L)1 blockade agents, while the concurrent use of corticosteroids seems to worsen it. We evaluated outcomes in advanced NSCLC patients treated with anti-PD-(L)1 blockade agents in relation to the presence of irAEs and the reasons for using corticosteroids: whether for palliative cancer-related reasons or for the management of irAEs. Methods:Clinical outcomes in advanced NSCLC patients treated with anti-PD-(L)1 blockade agents were calculated with regard to the presence of irAEs and the use of corticosteroids. A landmark analysis was performed to avoid immortal time bias due to the time-dependent nature of irAEs. Results:Out of a total of 267 patients, the 56.9% of patients who experienced irAEs had significantly improved outcomes. In the landmark analysis, median progression-free survival (PFS) was 12.4 months for patients with irAEs vs. 4.1 months for patients without irAEs (p< 0.001), while median overall survival (OS) was 28.2 vs. 12.5 months, respectively (p< 0.001). Likewise, objective response and disease control rates were significantly higher in patients experiencing irAEs: 48.6 vs. 22.8% and 77.1 vs. 39.6% (p< 0.001), respectively. Median OS was significantly shorter for patients receiving >= 10 mg of prednisone equivalent daily for cancer-related symptoms than for the rest of patients (<10 mg prednisone equivalent daily or for management of irAEs): 6 vs. 15.9 months (p< 0.001). Conclusions:IrAEs were associated with improved efficacy in advanced NSCLC patients when a landmark analysis was applied. Patients receiving corticosteroids had significantly poorer outcomes when they were used for cancer-related symptoms.
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页数:11
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共 35 条
  • [1] Analysis of survival by tumor response and other comparisons of time-to-event by outcome variables
    Anderson, James R.
    Cain, Kevin C.
    Gelber, Richard D.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (24) : 3913 - 3915
  • [2] [Anonymous], 2009, COMM TERM CRIT ADV E
  • [3] Impact of Baseline Steroids on Efficacy of Programmed Cell Death-1 and Programmed Death-Ligand 1 Blockade in Patients With Non-Small-Cell Lung Cancer
    Arbour, Kathryn C.
    Mezquita, Laura
    Long, Niamh
    Rizvi, Hira
    Auclin, Edouard
    Ni, Andy
    Martinez-Bernal, Gala
    Ferrara, Roberto
    Lai, W. Victoria
    Hendriks, Lizza E. L.
    Sabari, Joshua K.
    Caramella, Caroline
    Plodkowski, Andrew J.
    Halpenny, Darragh
    Chaft, Jamie E.
    Planchard, David
    Riely, Gregory J.
    Besse, Benjamin
    Hellmann, Matthew D.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (28) : 2872 - +
  • [4] Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer
    Borghaei, H.
    Paz-Ares, L.
    Horn, L.
    Spigel, D. R.
    Steins, M.
    Ready, N. E.
    Chow, L. Q.
    Vokes, E. E.
    Felip, E.
    Holgado, E.
    Barlesi, F.
    Kohlhaeufl, M.
    Arrieta, O.
    Burgio, M. A.
    Fayette, J.
    Lena, H.
    Poddubskaya, E.
    Gerber, D. E.
    Gettinger, S. N.
    Rudin, C. M.
    Rizvi, N.
    Crino, L.
    Blumenschein, G. R.
    Antonia, S. J.
    Dorange, C.
    Harbison, C. T.
    Finckenstein, F. Graf
    Brahmer, J. R.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (17) : 1627 - 1639
  • [5] Molecular analysis of the RET and NTRK1 gene rearrangements in papillary thyroid carcinoma in the Polish population
    Brzezianska, Ewa
    Karbownik, Malgorzata
    Migdalska-Sek, Monika
    Pastuszak-Lewandoska, Dorota
    Wloch, Jan
    Lewinski, Andrzej
    [J]. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2006, 599 (1-2) : 26 - 35
  • [6] Management of immune checkpoint blockade dysimmune toxicities: a collaborative position paper
    Champiat, S.
    Lambotte, O.
    Barreau, E.
    Belkhir, R.
    Berdelou, A.
    Carbonnel, F.
    Cauquil, C.
    Chanson, P.
    Collins, M.
    Durrbach, A.
    Ederhy, S.
    Feuillet, S.
    Francois, H.
    Lazarovici, J.
    Le Pavec, J.
    De Martin, E.
    Mateus, C.
    Michot, J. -M.
    Samuel, D.
    Soria, J. -C.
    Robert, C.
    Eggermont, A.
    Marabelle, A.
    [J]. ANNALS OF ONCOLOGY, 2016, 27 (04) : 559 - 574
  • [7] Endocrine Toxicity of Cancer Immunotherapy Targeting Immune Checkpoints
    Chang, Lee-Shing
    Barroso-Sousa, Romualdo
    Tolaney, Sara M.
    Hodi, F. Stephen
    Kaiser, Ursula B.
    Min, Le
    [J]. ENDOCRINE REVIEWS, 2019, 40 (01) : 17 - 65
  • [8] Oncology Meets Immunology: The Cancer-Immunity Cycle
    Chen, Daniel S.
    Mellman, Ira
    [J]. IMMUNITY, 2013, 39 (01) : 1 - 10
  • [9] Landmark Analysis at the 25-Year Landmark Point
    Dafni, Urania
    [J]. CIRCULATION-CARDIOVASCULAR QUALITY AND OUTCOMES, 2011, 4 (03) : 363 - U216
  • [10] New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1)
    Eisenhauer, E. A.
    Therasse, P.
    Bogaerts, J.
    Schwartz, L. H.
    Sargent, D.
    Ford, R.
    Dancey, J.
    Arbuck, S.
    Gwyther, S.
    Mooney, M.
    Rubinstein, L.
    Shankar, L.
    Dodd, L.
    Kaplan, R.
    Lacombe, D.
    Verweij, J.
    [J]. EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) : 228 - 247