Literature DB >> 27621395

PANCREOX: A Randomized Phase III Study of Fluorouracil/Leucovorin With or Without Oxaliplatin for Second-Line Advanced Pancreatic Cancer in Patients Who Have Received Gemcitabine-Based Chemotherapy.

Sharlene Gill1, Yoo-Joung Ko1, Christine Cripps1, Annie Beaudoin1, Sukhbinder Dhesy-Thind1, Muhammad Zulfiqar1, Pawel Zalewski1, Thuan Do1, Pablo Cano1, Wendy Yin Han Lam1, Scot Dowden1, Helene Grassin1, John Stewart1, Malcolm Moore1.   

Abstract

Purpose The standard of care for second-line therapy in patients with advanced pancreatic cancer after gemcitabine-based therapy is not clearly defined. The CONKO-003 phase III study reported a survival benefit with second-line fluorouracil (FU) and oxaliplatin using the oxaliplatin, folinic acid, and FU (OFF) regimen. 1 PANCREOX was a phase III multicenter trial to evaluate the benefit of FU and oxaliplatin administered as modified FOLFOX6 (mFOLFOX6; infusional fluorouracil, leucovorin, and oxaliplatin) versus infusional FU/leucovorin (LV) in this setting. Patients and Methods Patients with confirmed advanced pancreatic cancer who were previously treated with gemcitabine therapy and with an Eastern Cooperative Oncology Group performance status of 0-2 were eligible. A total of 108 patients were randomly assigned to receive biweekly mFOLFOX6 or infusional FU/LV until progression. Progression-free survival (PFS) was the primary end point. Results Baseline patient characteristics were similar in both arms. No difference was observed in PFS (median, 3.1 months v 2.9 months; P = .99). Overall survival (OS) was inferior in patients assigned to mFOLFOX6 (median, 6.1 months v 9.9 months; P = .02). Increased toxicity was observed with the addition of oxaliplatin, with grade 3/4 adverse events occurring in 63% of patients who received mFOLFOX6 and 11% of those who received FU/LV. More patients in the mFOLFOX6 arm withdrew from study due to adverse events than in the FU/LV arm (20% v 2%), whereas the use of postprogression therapy was significantly higher in the FU/LV arm (25% v 7%; P = .015). No significant differences were observed in time to deterioration on the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 global health scale. Conclusion No benefit was observed with the addition of oxaliplatin, administered as mFOLFOX6, versus infusional FU/LV in patients with advanced pancreatic cancer previously treated with first-line gemcitabine.

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Year:  2016        PMID: 27621395     DOI: 10.1200/JCO.2016.68.5776

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  68 in total

1.  Metastatic Pancreatic Cancer: ASCO Clinical Practice Guideline Update.

Authors:  Davendra P S Sohal; Erin B Kennedy; Alok Khorana; Mehmet S Copur; Christopher H Crane; Ignacio Garrido-Laguna; Smitha Krishnamurthi; Cassadie Moravek; Eileen M O'Reilly; Philip A Philip; Ramesh K Ramanathan; Joseph T Ruggiero; Manish A Shah; Susan Urba; Hope E Uronis; Michelle W Lau; Daniel Laheru
Journal:  J Clin Oncol       Date:  2018-05-23       Impact factor: 44.544

Review 2.  [Pancreatic ductal adenocarcinoma].

Authors:  E Gallmeier; T M Gress
Journal:  Internist (Berl)       Date:  2018-08       Impact factor: 0.743

Review 3.  Second-line therapy in advanced upper gastrointestinal cancers: current status and new prospects.

Authors:  Piercarlo Saletti; Alberto Zaniboni
Journal:  J Gastrointest Oncol       Date:  2018-04

4.  Post-progression survival following second-line chemotherapy in patients with advanced pancreatic cancer previously treated with gemcitabine: a meta-analysis.

Authors:  Akiyoshi Kasuga; Yasuo Hamamoto; Ayano Takeuchi; Naohiro Okano; Kazuhiro Togasaki; Yu Aoki; Takeshi Suzuki; Kenta Kawasaki; Kenro Hirata; Yasutaka Sukawa; Takanori Kanai; Hiromasa Takaishi
Journal:  Invest New Drugs       Date:  2018-03-23       Impact factor: 3.850

5.  Time to deterioration in cancer randomized clinical trials for patient-reported outcomes data: a systematic review.

Authors:  E Charton; B Cuer; F Cottone; F Efficace; C Touraine; Z Hamidou; F Fiteni; F Bonnetain; M-C Woronoff-Lemsi; C Bascoul-Mollevi; A Anota
Journal:  Qual Life Res       Date:  2019-11-27       Impact factor: 4.147

6.  The underreporting of phase III chemo-therapeutic clinical trial data of older patients with cancer: A systematic review.

Authors:  Karlynn BrintzenhofeSzoc; Jessica L Krok-Schoen; Beverly Canin; Ira Parker; Amy R MacKenzie; Thuy Koll; Ritika Vankina; Christine D Hsu; Brian Jang; Kathy Pan; Jennifer L Lund; Edith Starbuck; Armin Shahrokni
Journal:  J Geriatr Oncol       Date:  2020-01-10       Impact factor: 3.599

Review 7.  Current status on the place of FOLFIRINOX in metastatic pancreatic cancer and future directions.

Authors:  Aurélien Lambert; Céline Gavoille; Thierry Conroy
Journal:  Therap Adv Gastroenterol       Date:  2017-06-27       Impact factor: 4.409

Review 8.  Towards an optimal treatment algorithm for metastatic pancreatic ductal adenocarcinoma (PDA).

Authors:  M Uccello; M Moschetta; G Mak; T Alam; C Murias Henriquez; H-T Arkenau
Journal:  Curr Oncol       Date:  2018-02-28       Impact factor: 3.677

9.  Immune Checkpoint Blockade in Combination with Stereotactic Body Radiotherapy in Patients with Metastatic Pancreatic Ductal Adenocarcinoma.

Authors:  Changqing Xie; Austin G Duffy; Gagandeep Brar; Suzanne Fioravanti; Donna Mabry-Hrones; Melissa Walker; Cecilia Monge Bonilla; Bradford J Wood; Deborah E Citrin; Elizabeth M Gil Ramirez; Freddy E Escorcia; Bernadette Redd; Jonathan M Hernandez; Jeremy L Davis; Billel Gasmi; David Kleiner; Seth M Steinberg; Jennifer C Jones; Tim F Greten
Journal:  Clin Cancer Res       Date:  2020-01-29       Impact factor: 12.531

10.  Second-Line Treatment for Advanced Pancreatic Adenocarcinoma: Is There a Role for Gemcitabine?

Authors:  Daniel M Girardi; Luiza Dib B B Faria; Marcela C Teixeira; Frederico P Costa; Paulo Marcelo G Hoff; Gustavo S Fernandes
Journal:  J Gastrointest Cancer       Date:  2019-12
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