scholarly journals Clinical Outcomes of Recurrent Ovarian Granulosa Cell Tumours Treated with Letrozole: a 10-Year Retrospective Case-Series of the Royal Marsden Hospital

2014 ◽  
Vol 25 ◽  
pp. iv305
Author(s):  
R. Canario ◽  
J.P. Lima ◽  
C. Migali ◽  
N. Tunariu ◽  
A. George ◽  
...  
Pain Practice ◽  
2020 ◽  
Author(s):  
Nafisseh S. Warner ◽  
Kalli K. Schaefer ◽  
Jason S. Eldrige ◽  
Tim J. Lamer ◽  
Matthew J. Pingree ◽  
...  

2018 ◽  
Vol 36 (4_suppl) ◽  
pp. 496-496 ◽  
Author(s):  
Swetha Kambhampati ◽  
Kelly Bauer ◽  
Jimmy Hwang ◽  
Andrea Grace Bocobo ◽  
John Dozier Gordan ◽  
...  

496 Background: HCC patients (pts) with Child Pugh B (CPB) cirrhosis have poor prognosis and limited treatment (Tx) options. Nivolumab demonstrated durable responses and acceptable safety in Child Pugh A (CPA) HCC in the CheckMate-040 trial with rates of hepatotoxicity similar to non-HCC populations. The safety and efficacy of nivolumab has not been established in pts with CPB cirrhosis. Methods: Design: Retrospective case series with IRB approval. Key eligibility: HCC with CPB cirrhosis; treated with nivolumab as standard Tx; enrolled in the UCSF Hepatobiliary Tissue Bank and Registry. Study endpoints: Safety during nivolumab Tx including all-cause grade(Gr) ≥ 3 adverse events (AE), serious AE (SAE), any grade immune-related (ir)AE, and systemic steroid (SS) requirement; clinical outcomes including time on Tx (TOT) with nivolumab and overall survival (OS). Results: Thirteen pts were included: male 77%; Asian 38%, white 54%; median age 66 (range: 26-86); HCV Ab+ 31%, HBsAg+ 23%; BCLC B/C 31%/69%; median Child-Pugh score 8; median prior systemic Tx 1 (range: 0-6); prior sorafenib 69%, median duration on prior sorafenib 137 days (range 10-341). The Table depicts safety outcomes on nivolumab. Median TOT on nivolumab: 44 days (95% CI: 32, 98) (range: 17-811+). Median OS from start of nivolumab: 119 days (95% CI: 40, 247) (range: 40-811+). Best response of at least stable disease occurred in 3/13 (23%) of patients, including prolonged stable disease (SD) for 6+ months and complete response (CR) for 24+ months on nivolumab (1 pt each). Conclusions: CPB HCC pts treated with nivolumab experienced high rates of all-cause Gr ≥ 3 AE and SAE and short OS, similar to prior studies in CPB HCC. Rates of irAE attributed to nivolumab were similar to rates reported in CheckMate-040 CPA population, without unexpected AE. A subset of pts experienced prolonged stable disease and CR. Nivolumab warrants further study in CPB HCC.[Table: see text]


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