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Efficacy and feasibility of stereotactic radiotherapy after folfirinox in patients with locally advanced pancreatic cancer (LAPC-1 trial)

Authors :
Suker, M. (Mustafa)
Nuyttens, J.J.M.E. (Joost)
Eskens, F.A.L.M. (Ferry)
Haberkorn, B. (Brigitte)
Coene, P-P. (Peter Paul)
Harst, E. (Erwin) van der
Bonsing, B.A. (Bert)
Vahrmeijer, A.L. (Alexander)
Mieog, J.S.D. (Sven)
Jan Swijnenburg, R. (Rutger)
Roos, D. (Daphne)
Groot Koerkamp, B. (Bas)
Eijck, C.H.J. (Casper) van
Suker, M. (Mustafa)
Nuyttens, J.J.M.E. (Joost)
Eskens, F.A.L.M. (Ferry)
Haberkorn, B. (Brigitte)
Coene, P-P. (Peter Paul)
Harst, E. (Erwin) van der
Bonsing, B.A. (Bert)
Vahrmeijer, A.L. (Alexander)
Mieog, J.S.D. (Sven)
Jan Swijnenburg, R. (Rutger)
Roos, D. (Daphne)
Groot Koerkamp, B. (Bas)
Eijck, C.H.J. (Casper) van
Publication Year :
2019

Abstract

Background: We conducted a multicentre phase II trial to investigate feasibility and antitumor activity of sequential FOLFIRINOX and Stereotactic Body Radiotherapy (SBRT) in patients with locally advanced pancreatic cancer (LAPC), (LAPC-1 trial). Methods: Patients with biopsy-proven LAPC treated in four hospitals in the Netherlands between December 2014 and June 2017. Patients received 8 cycles of FOLFIRINOX followed by SBRT (5 fractions/8 Gy) if no tumour progression after the FOLFIRINOX treatment was observed. Primary outcome was 1-year overall survival (OS). Secondary outcomes were median OS, 1-year progression-free survival (PFS), treatment-related toxicity, and resection rate. The study is registered with ClinicalTrials.gov, NCT02292745, and is completed. Findings: Fifty patients were included. Nineteen (38%) patients did not receive all 8 cycles of FOLFIRINOX, due to toxicity (n = 12), disease progression (n = 6), or patients’ preference (n = 1). Thirty-nine (78%) patients received the SBRT treatment. The 1-year OS and PFS were 64% (95% CI: 50%-76%) and 34

Details

Database :
OAIster
Notes :
application/pdf, EClinicalMedicine vol. 17, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1134975398
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.eclinm.2019.10.013