Impact of First Line Antiangiogenic Therapy Duration on Nivolumab Outcome in Metastatic Renal Cell Carcinoma Patients Treated in the GETUG-AFU 26 NIVOREN

被引:0
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作者
Guilhem-Ducleon, Guillemette [1 ]
Dalban, Cecile [2 ]
Negrier, Sylvie [3 ]
Gravis, Gwenaelle [4 ]
Laguerre, Brigitte [5 ]
Chevreau, Christine [6 ]
Oudard, Stephane [7 ]
Barthelemy, Philippe [8 ]
Ladoire, Sylvain [9 ]
Boughalem, Elouen [10 ]
Borchiellini, Delphine [11 ]
Linassier, Claude [12 ,13 ]
Nenan, Soazig [14 ]
Flippot, Ronan [15 ]
Albiges, Laurence [15 ]
Goupil, Marine Gross [1 ,16 ]
机构
[1] Univ Hosp Bordeaux, Dept Med Oncol, Bordeaux, France
[2] Ctr Leon Berard, Ctr Lutte Canc, Dept Clin Res & Innovat, Lyon, France
[3] Univ Lyon 1, Ctr Leon Berard, Lyon, France
[4] Inst Paoli Calmettes, Dept Med Oncol, Marseille, France
[5] Ctr Eugene Marquis, Dept Med Oncol, Rennes, France
[6] Inst Univ Canc Toulouse Oncopole, Dept Med Oncol, Toulouse, France
[7] Univ Paris Cite, Hop Europeen Georges Pompidou, APHP Ctr, Dept Med Oncol,Inst Canc Paris CARPEM, Paris, France
[8] Inst Cancerol Strasbourg Europe, Dept Med Oncol, Strasbourg, France
[9] Ctr Georges Francois Leclerc, Dept Med Oncol, Dijon, France
[10] Inst Cancerol Ouest, Dept Med Oncol, F-49055 Angers, France
[11] Univ Cote Azur, Ctr Antoine Lacassagne, Dept Med Oncol, Nice, France
[12] CHU Bretonneau, Dept Med Oncol, Tours, France
[13] Univ Tours, Tours, France
[14] Unicancer, Paris, France
[15] Univ Paris Saclay, Dept Med Oncol, Gustave Roussy Canc Campus, Villejuif, France
[16] Univ Hosp Bordeaux, Dept Med Oncol, 1 Rue Jean Burguet, F-33000 Bordeaux, France
关键词
Advanced Renal Cell Carcinoma; Immune Checkpoint Inhibitor; Tyrosine Kinase Inhibitor; Survival analyses; Response; RANDOMIZED PHASE-3; TARGETED THERAPY; SUNITINIB; CABOZANTINIB; EVEROLIMUS; SURVIVAL;
D O I
10.1016/j.clgc.2023.07.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: In metastatic renal clear cell carcinoma (ccRCC), vascular endothelial growth factor receptor (VEGFR) and immune checkpoint are 2 main therapeutic targets. We investigated the impact of duration exposure to antiangiogenic on immunotherapy clinical outcomes in metastatic ccRCC.Methods: Patients from NIVOREN trial who received nivolumab after only 1 prior antiangiogenic therapy were included. Response rate, clinical benefit, progression free survival (PFS) and overall survival (OS) were prospectively analyzed depending on the duration of the first line (< 6 months, >= 6 months) and exploratory in patients with long first line exposure (>= 18 months). The circulating levels of 8 plasma proteins and cytokines at baseline were collected and compared according to first line antiangiogenic duration.Results: Among 354 patients, 127 (36%) and 227 (64%) patients had received first line antiangiogenic for < 6months and >= 6months respectively. Respective duration of first line therapy was not associated with objective response to nivolumab (20.5% vs. 23.9%, P = .50), or PFS (HR 0.92; P = .421). Median OS was respectively 16.6 and 31.3 months in the <6 and >= 6 months subgroups respectively. Adjusted on international metastatic renal cell carcinoma database consortium risk, age and metastatic site, OS was longer in patients with longer treatment duration in the first line setting (HR 0.73; P = .017). Duration of first line VEGFR TKI was independent from circulating levels of 8 proteins and cytokines at nivolumab baseline.Conclusion: Nivolumab activity in second line is independent from first-line duration of VEGFR TKI. However, first line VEGFR TKI duration >= 6 months is associated with longer OS.
引用
收藏
页码:643 / 652
页数:10
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