Impact of Intercurrent Introduction of Steroids on Clinical Outcomes in Advanced Non-Small-Cell Lung Cancer (NSCLC) Patients under Immune-Checkpoint Inhibitors (ICI)

被引:48
作者
De Giglio, Andrea [1 ,2 ]
Mezquita, Laura [1 ,3 ,4 ]
Auclin, Edouard [5 ]
Blanc-Durand, Felix [1 ]
Riudavets, Mariona [1 ]
Caramella, Caroline [6 ]
Martinez, Gala [1 ]
Benitez, Jose Carlos [1 ]
Martin-Romano, Patricia [7 ]
El-Amarti, Lamiae [1 ]
Hendriks, Lizza [1 ,8 ]
Ferrara, Roberto [1 ,9 ]
Naltet, Charles [1 ]
Lavaud, Pernelle [1 ]
Gazzah, Anas [7 ]
Adam, Julien [10 ]
Planchard, David [1 ]
Chaput, Nathalie [11 ,12 ,13 ,14 ]
Besse, Benjamin [1 ,15 ]
机构
[1] Gustave Roussy, Dept Canc Med, F-94805 Villejuif, France
[2] Alma Mater Studiorum Univ Bologna, S Orsola Malpighi Univ Hosp, Dept Specialized Expt & Diagnost Med, I-40126 Bologna, Italy
[3] Hosp Clin Barcelona, Dept Med Oncol, Barcelona 08036, Spain
[4] IDIBAPS, Lab Translat Genom & Targeted Therapies Solid Tum, Barcelona 08036, Spain
[5] Georges Pompidou Hosp, Med & Thorac Oncol Dept, F-75015 Paris, France
[6] Gustave Roussy, Dept Radiol, F-94805 Villejuif, France
[7] Gustave Roussy, Early Drug Dev Dept, F-94805 Villejuif, France
[8] Maastricht UMC, GROW Sch Oncol & Dev Biol, Dept Pulm Dis, NL-6229 Maastricht, Netherlands
[9] Med Oncol Dept Fdn IRCCS Ist Nazl Tumori Milano, Thorac Oncol Unit, I-20133 Milan, Italy
[10] Gustave Roussy, Dept Pathol, F-94805 Villejuif, France
[11] Gustave Roussy, Lab Immunomonitoring Oncol, F-94805 Villejuif, France
[12] Gustave Roussy, CNRS, UMS 3655, F-94805 Villejuif, France
[13] Gustave Roussy, INSERM, US23, F-94805 Villejuif, France
[14] Univ Paris Saclay, Fac Pharm, F-92296 Chatenay Malabry, France
[15] Univ Paris Saclay, Fac Med, F-94276 Le Kremlin Bicetre, France
关键词
non-small cell lung cancer; immunotherapy; steroids; PEMBROLIZUMAB; IMMUNOTHERAPY; ASSOCIATION; RISK;
D O I
10.3390/cancers12102827
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Recently, the introduction of immunotherapy radically changed the therapeutic algorithm of non-small-cell lung cancer as an upfront or secondary strategy. Unfortunately, the small amount of patient benefits from immune-checkpoint inhibitors (ICI) and the prognostic role of concomitant treatments are a burning open issue. The use of steroids was associated with poor outcomes during ICI. We investigated the impact of intercurrent steroids, according to clinical indication, which is actually unclear. Interestingly, the use of intercurrent steroids given for cancer-unrelated symptoms has no survival impact on our study cohort. Background: Baseline steroids before ICI have been associated with poor outcomes, particularly when introduced due to cancer symptoms. Methods: Retrospective analysis of advanced NSCLC patients treated with ICI. We collected the use of intercurrent steroids (>= 10 mg of prednisone-equivalent) within the first eight weeks of ICI. We correlated steroid use with patient outcomes according to the indications. Results: 413 patients received ICI, 299 were steroids-naive at baseline. A total of 49 patients received intercurrent steroids (16%), of whom 38 for cancer-related symptoms and 11 for other indications, such as immune-related events. Overall, median (m) progression-free survival (PFS) was 1.9 months (mo.) [95% CI, 1.8-2.4] and overall survival (OS) 10 mo. [95% CI, 8.1-12.9]. Intercurrent steroids under ICI correlated with a shorter PFS/OS (1.3 and 2.3 mo. respectively, both p < 0.0001). Intercurrent steroids for cancer-related symptoms correlated with poorest mPFS [1.1 mo.; 95% CI, 0.9-1.5] and mOS [1.9 mo.; 95%CI, 1.5-2.4; p < 0.0001)]. No mOS and mPFS differences were found between cancer-unrelated-steroid group and no-steroid group. Steroid use for cancer-related symptoms was an independent prognostic factor for poor PFS [HR 2.64; 95% CI, 1.2-5.6] and OS [HR 4.53; 95% CI, 1.8-11.1], both p < 0.0001. Conclusion: Intercurrent steroids during ICI had no detrimental prognostic impact if the indication was unrelated to cancer symptoms.
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页码:1 / 11
页数:11
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