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Risk Adapted Ablative Radiotherapy After Intensive Chemotherapy for Locally Advanced Pancreatic Cancer.
Rossi, Gabriella; Simoni, Nicola; Paiella, Salvatore; Rossi, Roberto; Venezia, Martina; Micera, Renato; Malleo, Giuseppe; Salvia, Roberto; Giuliani, Tommaso; Di Gioia, Anthony; Auriemma, Alessandra; Milella, Michele; Guariglia, Stefania; Cavedon, Carlo; Bassi, Claudio; Mazzarotto, Renzo.
Afiliação
  • Rossi G; Department of Radiation Oncology, University of Verona Hospital Trust, Verona, Italy.
  • Simoni N; Department of Radiation Oncology, University of Verona Hospital Trust, Verona, Italy.
  • Paiella S; Department of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.
  • Rossi R; Department of Radiation Oncology, University of Verona Hospital Trust, Verona, Italy.
  • Venezia M; Department of Radiation Oncology, University of Verona Hospital Trust, Verona, Italy.
  • Micera R; Department of Radiation Oncology, University of Verona Hospital Trust, Verona, Italy.
  • Malleo G; Department of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.
  • Salvia R; Department of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.
  • Giuliani T; Department of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.
  • Di Gioia A; Department of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.
  • Auriemma A; Department of Oncology, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.
  • Milella M; Department of Oncology, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.
  • Guariglia S; Department of Medical Physics, University of Verona Hospital Trust, Verona, Italy.
  • Cavedon C; Department of Medical Physics, University of Verona Hospital Trust, Verona, Italy.
  • Bassi C; Department of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.
  • Mazzarotto R; Department of Radiation Oncology, University of Verona Hospital Trust, Verona, Italy.
Front Oncol ; 11: 662205, 2021.
Article em En | MEDLINE | ID: mdl-33959509
ABSTRACT
BACKGROUND AND

OBJECTIVE:

To assess the efficacy of a Risk-Adapted Ablative Radiotherapy (RAdAR) approach, after intensive induction chemotherapy, in patients with locally advanced pancreatic cancer (LAPC). MATERIAL AND

METHODS:

Patients with LAPC who received RAdAR following induction chemotherapy from January 2017 to December 2019 were included in this observational study. The RAdAR approach consisted of an anatomy- and simultaneous integrated boost (SIB)-based dose prescription strategy. RAdAR was delivered with stereotactic ablative radiation therapy (SAbR), administering 30 Gy in 5 fractions to the tumor volume (PTVt) and 50 Gy SIB (BED10 100 Gy) to the vascular involvement, or with (hypo-)fractionated ablative radiotherapy (HART) prescribing 50.4 Gy in 28 fractions to the PTVt, with a vascular SIB of 78.4 Gy (BED10 100 Gy). Primary end points were freedom from local progression (FFLP), overall survival (OS), and progression-free survival (PFS).

RESULTS:

Sixty-four LAPC patients were included. Induction chemotherapy consisted of gemcitabine/nab-paclitaxel in 60.9% and FOLFIRINOX in 39.1% of cases. SAbR was used in 52 (81.2%) patients, and HART in 12 (18.8%). After RAdAR, surgery was performed in 17 (26.6%) patients. Median follow-up was 16.1 months. Overall local control (LC) rate was 78.1%, with no difference between resected and non-resected patients (2-year FFLP 75.3% vs 56.4%; p = 0.112). Median OS and PFS were 29.7 months and 8.7 months, respectively, for the entire cohort. Resected patients had a better median OS (not reached versus 26.1 months; p = 0.0001) and PFS (19 versus 5.6 months; p < 0.0001) compared to non-resected patients. In non-resected patients, no significant difference was found between SAbR and HART for median FFLP (28.1 versus 18.5 months; p = 0.614), OS (27.4 versus 25.3 months; p = 0.624), and PFS (5.7 versus 4.3 months; p = 0.486). One patient (1.6%) experienced acute grade 4 gastro-intestinal bleeding. No other acute or late grade ≥ 3 toxicities were observed.

CONCLUSIONS:

The RAdAR approach, following intensive induction chemotherapy, is an effective radiation treatment strategy for selected LAPC patients, representing a promising therapeutic option in a multimodality treatment regimen.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article