Pembrolizumab in soft-tissue sarcomas with tertiary lymphoid structures: a phase 2 PEMBROSARC trial cohort

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作者
A. Italiano
A. Bessede
M. Pulido
E. Bompas
S. Piperno-Neumann
C. Chevreau
N. Penel
F. Bertucci
M. Toulmonde
C. Bellera
J. P. Guegan
C. Rey
C. Sautès-Fridman
A. Bougoüin
C. Cantarel
M. Kind
M. Spalato
B. Dadone-Montaudie
F. Le Loarer
J. Y. Blay
W. H. Fridman
机构
[1] Institut Bergonié,Department of Medical Oncology
[2] Gustave Roussy,DITEP
[3] University of Bordeaux,Unité de Recherche et d’Epidémiologie Cliniques
[4] Explicyte,Department of Medical Oncology
[5] Institut Bergonié,Department of Medical Oncology
[6] INSERM CIC,Department of Medical Oncology
[7] Institut de Cancérologie de L’Ouest,Department of Medical Oncology
[8] Institut Curie,Department of Medical Oncology
[9] Oncopole Toulouse,Centre de Recherche des Cordeliers, INSERM
[10] Centre Oscar Lambret,Department of Imaging
[11] Institut Paoli Calmettes,Department of Pathology
[12] Sorbonne Université,Department of Pathology
[13] Université Paris Cité,Department of Medical Oncology
[14] Equipe Labellisée Ligue contre le Cancer,undefined
[15] Institut Bergonié,undefined
[16] University Hospital Centre of Nice,undefined
[17] Institut Bergonié,undefined
[18] Centre Léon Bérard,undefined
来源
Nature Medicine | 2022年 / 28卷
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摘要
Immune checkpoint inhibitors (ICIs) show limited clinical activity in patients with advanced soft-tissue sarcomas (STSs). Retrospective analysis suggests that intratumoral tertiary lymphoid structures (TLSs) are associated with improved outcome in these patients. PEMBROSARC is a multicohort phase 2 study of pembrolizumab combined with low-dose cyclophosphamide in patients with advanced STS (NCT02406781). The primary endpoint was the 6-month non-progression rate (NPR). Secondary endpoints included objective response rate (ORR), progression-free survival (PFS), overall survival (OS) and safety. The 6-month NPR and ORRs for cohorts in this trial enrolling all comers were previously reported; here, we report the results of a cohort enrolling patients selected based on the presence of TLSs (n = 30). The 6-month NPR was 40% (95% confidence interval (CI), 22.7–59.4), so the primary endpoint was met. The ORR was 30% (95% CI, 14.7–49.4). In comparison, the 6-month NPR and ORR were 4.9% (95% CI, 0.6–16.5) and 2.4% (95% CI, 0.1–12.9), respectively, in the all-comer cohorts. The most frequent toxicities were grade 1 or 2 fatigue, nausea, dysthyroidism, diarrhea and anemia. Exploratory analyses revealed that the abundance of intratumoral plasma cells (PCs) was significantly associated with improved outcome. These results suggest that TLS presence in advanced STS is a potential predictive biomarker to improve patients’ selection for pembrolizumab treatment.
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页码:1199 / 1206
页数:7
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