scholarly journals Gemcitabine/nab-paclitaxel as second-line therapy following FOLFIRINOX in metastatic/advanced pancreatic cancer—retrospective analysis of response

2017 ◽  
Vol 8 (3) ◽  
pp. 556-565 ◽  
Author(s):  
Khanh T. Nguyen ◽  
Aparna Kalyan ◽  
H. Scott Beasley ◽  
Aatur D. Singhi ◽  
Weijing Sun ◽  
...  
Oncology ◽  
2009 ◽  
Vol 76 (4) ◽  
pp. 270-274 ◽  
Author(s):  
Joanna M. Brell ◽  
Khalid Matin ◽  
Terry Evans ◽  
Robert L. Volkin ◽  
Gauri J. Kiefer ◽  
...  

2013 ◽  
Vol 31 (4_suppl) ◽  
pp. 275-275
Author(s):  
Osama E. Rahma ◽  
David J. Liewehr ◽  
Seth M. Steinberg ◽  
Austin G. Duffy ◽  
Tim F Greten

275 Background: Pancreatic cancer is one of the deadliest cancers with an estimated 5 years survival rate of 5%. Until recently gemcitabine had been considered the first line treatment for locally advanced or metastatic disease. Although many chemotherapy regimens have been used there is no standard of care for second line therapy. The aim of this analysis was to identify superior regimen in the second line setting. Methods: We conducted a general search on PubMed for “second line therapy in advanced pancreatic cancer”. We limited our search to trials published in English from 2000 through 2012. Studies presented as abstracts in major meetings were also included. Trials that used targeted therapy other than erlotinib were excluded. We compared in an exploratory fashion the RR, PFS and OS of BSC and each of the following regimens to the rest of the treatments: 5FU+platinum, gemcitabine+platinum, taxol, erlotinib. In addition, we compared the combinations of platinum with either 5FU or gemcitabine. Finally, we explored the trend of these treatments outcomes over time. Results: Forty-four trialswere identified, of which 34 trials (T) met the inclusion criteria treating 1503 patients (N). There was a trend toward an improved overall survival with treatments (T: 33; N: 1269) compared to BSC (T: 2; N: 234) only (P= 0.013). The combination of gemcitabine and platinum (T: 5; N: 154) was the only regimen that showed a trend toward superior outcomes compared to the other regimens (T: 28; N: 1115) in terms of RR and PFS (P= 0.006 and 0.059, respectively). However, there was no difference in overall survival (P= 0.10). When compared to 5FU+platinum (T: 12; N: 450) the regimen of gemcitabine+platinum (T: 5; N: 154) showed only a trend toward significance in terms of improved RR (P= 0.030) with no difference in PFS or OS (P= 0.60 and 0.22, respectively). Overall, there was a trend toward a worse RR and PFS with no change in OS over the past 13 years. Conclusions: The combination of gemcitabine and platinum may provide a valid second line option in patients with locally advanced or metastatic pancreatic cancer who progress on gemcitabine.


2013 ◽  
Vol 36 (2) ◽  
pp. 151-156 ◽  
Author(s):  
Peter J. Hosein ◽  
Gilberto de Lima Lopes ◽  
Vitor H. Pastorini ◽  
Christina Gomez ◽  
Jessica Macintyre ◽  
...  

Tumor Biology ◽  
2010 ◽  
Vol 31 (4) ◽  
pp. 351-357 ◽  
Author(s):  
Michael Haas ◽  
Rüdiger P. Laubender ◽  
Petra Stieber ◽  
Stefan Holdenrieder ◽  
Christiane J. Bruns ◽  
...  

2020 ◽  
Vol 40 (7) ◽  
pp. 4011-4015
Author(s):  
JEAN-DAVID FUMET ◽  
JULIE VINCENT ◽  
LEILA BENGRINE ◽  
AUDREY HENNEQUIN ◽  
LAURA GRANCONATO ◽  
...  

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