Second-generation inflammation-related scores are more effective than systemic inflammation ratios in predicting prognosis of patients with unresectable or metastatic pancreatic cancer receiving cytotoxic chemotherapy

2018 ◽  
Vol 35 (12) ◽  
Author(s):  
Giuseppe A. Colloca ◽  
Antonella Venturino ◽  
Domenico Guarneri
2017 ◽  
Vol 28 ◽  
pp. v30-v31
Author(s):  
V. Pacheco-Barcia ◽  
O. Donnay ◽  
R. Mondejar ◽  
J. Rogado ◽  
M.D. Fenor de la Maza ◽  
...  

Pancreatology ◽  
2020 ◽  
Vol 20 (2) ◽  
pp. 254-264 ◽  
Author(s):  
Vilma Pacheco-Barcia ◽  
Rebeca Mondéjar Solís ◽  
Talya France ◽  
Jamil Asselah ◽  
Olga Donnay ◽  
...  

Pancreas ◽  
2019 ◽  
Vol 48 (5) ◽  
pp. e45-e47 ◽  
Author(s):  
Vilma Pacheco-Barcia ◽  
Rebeca Mondéjar Solís ◽  
Talya France ◽  
Jamil Asselah ◽  
Olga Donnay ◽  
...  

2015 ◽  
Vol 33 (34) ◽  
pp. 4039-4047 ◽  
Author(s):  
Herbert I. Hurwitz ◽  
Nikhil Uppal ◽  
Stephanie A. Wagner ◽  
Johanna C. Bendell ◽  
J. Thaddeus Beck ◽  
...  

Purpose Patients with advanced pancreatic adenocarcinoma have a poor prognosis and limited second-line treatment options. Evidence suggests a role for the Janus kinase (JAK)/signal transducer and activator of transcription pathway in the pathogenesis and clinical course of pancreatic cancer. Patients and Methods In this double-blind, phase II study, patients with metastatic pancreatic cancer who had experienced treatment failure with gemcitabine were randomly assigned 1:1 to the JAK1/JAK2 inhibitor ruxolitinib (15 mg twice daily) plus capecitabine (1,000 mg/m2 twice daily) or placebo plus capecitabine. The primary end point was overall survival (OS); secondary end points included progression-free survival, clinical benefit response, objective response rate, and safety. Prespecified subgroup analyses evaluated treatment heterogeneity and efficacy in patients with evidence of inflammation. Results In the intent-to-treat population (ruxolitinib, n = 64; placebo, n = 63), the hazard ratio was 0.79 (95% CI, 0.53 to 1.18; P = .25) for OS and was 0.75 (95% CI, 0.52 to 1.10; P = .14) for progression-free survival. In a prespecified subgroup analysis of patients with inflammation, defined by serum C-reactive protein levels greater than the study population median (ie, 13 mg/L), OS was significantly greater with ruxolitinib than with placebo (hazard ratio, 0.47; 95% CI, 0.26 to 0.85; P = .011). Prolonged survival in this subgroup was supported by post hoc analyses of OS that categorized patients by the modified Glasgow Prognostic Score, a systemic inflammation–based prognostic system. Grade 3 or greater adverse events were observed with similar frequency in the ruxolitinib (74.6%) and placebo (81.7%) groups. Grade 3 or greater anemia was more frequent with ruxolitinib (15.3%; placebo, 1.7%). Conclusion Ruxolitinib plus capecitabine was generally well tolerated and may improve survival in patients with metastatic pancreatic cancer and evidence of systemic inflammation.


Sign in / Sign up

Export Citation Format

Share Document