Neoadjuvant chemoradiation for non-metastatic pancreatic cancer increases margin-negative and node-negative rates at resection

J Dig Dis. 2017 Nov;18(11):642-649. doi: 10.1111/1751-2980.12551.

Abstract

Objective: To compare neoadjuvant to adjuvant chemoradiation in non-metastatic pancreatic cancer patients.

Methods: Single-institution data were obtained for patients with non-metastatic pancreatic cancer treated with concurrent chemoradiation from 2011 to 2014. Univariate analyses were performed to evaluate clinical and pathological outcomes.

Results: Fifty-two well-matched patients were enrolled (21 underwent neoadjuvant chemoradiation, 11 with adjuvant chemoradiation and 20 in the definitive group). Median tumor size was 2.6 cm pretreatment and 2.5 cm after neoadjuvant chemoradiation but 3.2 cm on pathology, with a treatment effect in 95.2% of specimens. Clinical node positivity at diagnosis for neoadjuvant and adjuvant chemoradiation groups was similar (28.6% vs 27.3%, P = 0.12). Of the 36 neoadjuvant patients, 21 (58.3%) underwent complete resection. In the neoadjuvant vs adjuvant chemoradiation groups, positive margins were decreased (4.8% vs 63.6%, P < 0.001), as was pathological nodal positivity (23.8% vs 90.9%, P < 0.001). After a median follow-up of 13.3 months, locoregional control for neoadjuvant and adjuvant chemoradiation was 7.7 and 7.2 months, respectively (P = 0.12) and the definitive group was 1.2 months (P = 0.014 compared with the surgical cohort). One-year overall survival was better with neoadjuvant than with adjuvant chemoradiation but this was not significant (94% vs 82%, P = 0.20); 1-year survival for the definitive group was 59% (P = 0.03 compared with the surgical cohort).

Conclusions: Neoadjuvant chemoradiation remains a promising approach for non-metastatic pancreatic cancer for improving resectability and pathological and clinical findings. Computed tomography may not fully demonstrate the effectiveness of neoadjuvant treatment.

Keywords: borderline resectable; chemoradiotherapy; downstaging; neoadjuvant therapy; pancreatic neoplasms.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antimetabolites, Antineoplastic / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Chemoradiotherapy, Adjuvant
  • Deoxycytidine / administration & dosage
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / therapeutic use
  • Dose Fractionation, Radiation
  • Drug Combinations
  • Female
  • Fluorouracil / administration & dosage
  • Fluorouracil / therapeutic use*
  • Gemcitabine
  • Humans
  • Irinotecan
  • Leucovorin / therapeutic use
  • Lymph Node Excision
  • Lymph Nodes / pathology*
  • Lymph Nodes / surgery
  • Lymphatic Metastasis
  • Male
  • Margins of Excision
  • Middle Aged
  • Neoadjuvant Therapy
  • Neoplasm, Residual
  • Organometallic Compounds / therapeutic use
  • Organoplatinum Compounds / therapeutic use
  • Oxaliplatin
  • Pancreatectomy
  • Pancreatic Neoplasms / diagnostic imaging
  • Pancreatic Neoplasms / pathology*
  • Pancreatic Neoplasms / therapy*
  • Radiotherapy, Intensity-Modulated
  • Retrospective Studies
  • Survival Rate
  • Tomography, X-Ray Computed
  • Tumor Burden / drug effects
  • Tumor Burden / radiation effects

Substances

  • Antimetabolites, Antineoplastic
  • Drug Combinations
  • Organometallic Compounds
  • Organoplatinum Compounds
  • folfirinox
  • Oxaliplatin
  • Deoxycytidine
  • Irinotecan
  • Leucovorin
  • Fluorouracil
  • Gemcitabine

Supplementary concepts

  • Folfox protocol