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Annals of Oncology 27 (Supplement 6): vi207–vi242, 2016

doi:10.1093/annonc/mdw371.72

series the patients were evaluated and offered CRT (50.4 Gy/27F & capecitabine) if
gastrointestinal tumours, deemed potentially resectable. Resections were performed if deemed possible by the
non-colorectal MDT.
Results: Between August 2012 and present, 59 patients have been recruited with a
median observation time of 17.4 months. Median age was 65(range 38-75) years, with
40%/60% stage II/III distribution. Median CA19-9 was 268(range 1-13,432).
680P Chemotherapy for patients with non-resectable pancreatic Three-hundred-sixty-two courses of FOLFIRINOX have been given, with a median of
cancer with additional chemo-radiotherapy for patients with 6.0 per patient, with a median of 2 without dose modifications. Presently twenty-two
potentially resectable tumours: Final results patients have been treated with CRT. Six-teen patients have been resected, of which 8
received prior CRT. Median survival for all patients was 21.1 months (14-NR) with a
P. Pfeiffer1, M. Ladekarl2, M.B. Mortensen3, A-L. Fromm4, J.K. Bjerregaard1 1-year survival of 74% (58-85). For patients not resected the median survival was 14.1
1
Department of Oncology, Odense University Hospital, Odense, Denmark, months (10-16) for resected the median survival has not yet been reached. The
2
Department of Oncology, Aarhus University Hospital, Aarhus, Denmark, FOLFIRINOX was associated with adverse events similar to what is expected in
3
Department of Surgery, Odense University Hospital, Odense, Denmark, metastatic patients.
4
Department of Oncology, University Hospital Herlev, Herlev, Denmark Conclusions: FOLFIRINOX with or without CRT in patients with LAPC shows
promising efficacy in patients with both borderline and never-resectable tumors.
Background: Locally advanced pancreatic cancer (LAPC) is often a mix of borderline Unmodified FOLFIRINOX had acceptable toxicity, however dose reductions are often
and never-resectable tumors. Multimodality treatment might downstage these tumors needed. CRT following initial FOLFIRINOX was feasible and without unexpected

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to allow a potential radical resection, especially the borderline group. In this ongoing toxicity.
phase II study we examined the feasibility of FOLFIRINOX with or without CRT Clinical trial identification: NCT-01397019
followed by surgery for both borderline and never-resectable tumors (NCT-01397019).
Legal entity responsible for the study: N/A
Methods: Patients in performance status 0-1, with initially non-resectable stage II/III
pancreatic cancer were offered FOLFIRINOX (oxaliplatin 85 mg/m2, irinotecan 180 Funding: Danish Pancreatic Cancer Group
mg/m2, leucovorin 400 mg/m2, 5FU 400 mg/m2+ 2400 mg/m2) every 14 days. Every 4th Disclosure: All authors have declared no conflicts of interest.

abstracts

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