A phase II evaluation of pembrolizumab in recurrent microsatellite instability-high (MSI-H) endometrial cancer patients with Lynch-like versus MLH-1 methylated characteristics (NCT02899793)

Author(s):  
S. Bellone ◽  
D.M. Roque ◽  
E.R. Siegel ◽  
N. Buza ◽  
P. Hui ◽  
...  
Medicina ◽  
2014 ◽  
Vol 50 (4) ◽  
pp. 216-221 ◽  
Author(s):  
Daiva Kanopienė ◽  
Giedrė Smailytė ◽  
Jolanta Vidugirienė ◽  
Jeff Bacher

2014 ◽  
Vol 132 (1) ◽  
pp. 50-54 ◽  
Author(s):  
Lisa M. Landrum ◽  
Elizabeth K. Nugent ◽  
Rosemary E. Zuna ◽  
Elizabeth Syzek ◽  
Robert S. Mannel ◽  
...  

2021 ◽  
Vol 39 (15_suppl) ◽  
pp. 5523-5523
Author(s):  
Dana M Roque ◽  
Stefania Bellone ◽  
Eric R. Siegel ◽  
Natalia Buza ◽  
Elena Bonazzoli ◽  
...  

5523 Background: Microsatellite instability (MSI-H) is a biomarker for response to immune-checkpoint inhibitors (ICIs); however, these neoplasms are heterogenous including Lynch (germline), Lynch-like (somatic) and sporadic ( MLH1-methylated) tumors. Whether mechanisms underlying MSI alter responses to ICIs is unclear. We report data from a phase II pilot study (NCT02899793) of pembrolizumab in recurrent MSI-H endometrial cancer (EC) patients and potential mechanisms of primary/secondary ICI resistance. Methods: Patients with measurable, MSI-H EC confirmed by immunohistochemistry and polymerase chain reaction were evaluated by next-generation sequencing and received pembrolizumab 200 mg intravenously every 3 weeks for up to 2 years. The primary end point was objective response rate (ORR) per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. Results: Twenty-five patients (24 evaluable) were treated. Six (25%) patients harbored Lynch/Lynch-like tumors while 18 (75%) had sporadic EC. Tumor mutational burden (TMB) was higher in Lynch-like (median 2939, IQR:867-5108) versus sporadic tumors (median 604, IQR:411-798) ( P= 0.0076). Median follow-up was 25.8 months with an ORR of 58% (95% CI, 36.6-77.9%). ORR was 100% in Lynch/Lynch-like patients but only 44% in sporadic patients ( P= 0.024). The 3-year progression-free (PFS) and overall survival (OS) proportions were 100% versus 30% ( P= 0.017) and 100% versus 43% ( P= 0.043), respectively. Grade 3/4 treatment-related adverse events (6.8%) occurred in 12 patients. Defective antigen processing/presentation and deranged induction in interferon responses served as mechanisms of resistance in sporadic MSI-H EC. Conclusions: Our study demonstrated prognostic significance of Lynch-like versus sporadic MSI-H EC on ORR, PFS and OS when treated with pembrolizumab. Clinical studies evaluating separate subtypes of MSI-H EC treated with ICIs are warranted. Clinical trial information: NCT02899793.


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