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A Multi-Institutional Phase 2 Trial of Ablative 5-Fraction Stereotactic Magnetic Resonance-Guided On-Table Adaptive Radiation Therapy for Borderline Resectable and Locally Advanced Pancreatic Cancer

  • Parag Jitendra Parikh
  • , Percy Lee
  • , Daniel A. Low
  • , Joshua Kim
  • , Kathryn E. Mittauer
  • , Michael F. Bassetti
  • , Carri K. Glide-Hurst
  • , Ann C. Raldow
  • , Yingli Yang
  • , Lorraine Portelance
  • , Kyle R. Padgett
  • , Bassem Zaki
  • , Rongxiao Zhang
  • , Hyun Kim
  • , Lauren E. Henke
  • , Alex T. Price
  • , Joseph D. Mancias
  • , Christopher L. Williams
  • , John Ng
  • , Ryan Pennell
  • M. Raphael Pfeffer, Daphne Levin, Adam C. Mueller, Karen E. Mooney, Patrick Kelly, Amish P. Shah, Luca Boldrini, Lorenzo Placidi, Martin Fuss, Michael D. Chuong
  • Henry Ford Health - Cancer
  • City of Hope National Med Center
  • University of California at Los Angeles
  • Baptist Hospital Miami
  • University of Wisconsin-Madison
  • University of Miami
  • Dartmouth-Hitchcock Medical Center
  • Washington University St. Louis
  • Harvard University
  • Cornell University
  • Assuta Medical Center
  • Thomas Jefferson University
  • Orlando Regional Medical Center
  • Inc

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

Purpose: Magnetic resonance (MR) image guidance may facilitate safe ultrahypofractionated radiation dose escalation for inoperable pancreatic ductal adenocarcinoma. We conducted a prospective study evaluating the safety of 5-fraction Stereotactic MR-guided on-table Adaptive Radiation Therapy (SMART) for locally advanced (LAPC) and borderline resectable pancreatic cancer (BRPC). Methods and Materials: Patients with LAPC or BRPC were eligible for this multi-institutional, single-arm, phase 2 trial after ≥3 months of systemic therapy without evidence of distant progression. Fifty gray in 5 fractions was prescribed on a 0.35T MR-guided radiation delivery system. The primary endpoint was acute grade ≥3 gastrointestinal (GI) toxicity definitely attributed to SMART. Results: One hundred thirty-six patients (LAPC 56.6%, BRPC 43.4%) were enrolled between January 2019 and January 2022. Mean age was 65.7 (36-85) years. Head of pancreas lesions were most common (66.9%). Induction chemotherapy mostly consisted of (modified)FOLFIRINOX (65.4%) or gemcitabine/nab-paclitaxel (16.9%). Mean CA19-9 after induction chemotherapy and before SMART was 71.7 U/mL (0-468). On-table adaptive replanning was performed for 93.1% of all delivered fractions. Median follow-up from diagnosis and SMART was 16.4 and 8.8 months, respectively. The incidence of acute grade ≥3 GI toxicity possibly or probably attributed to SMART was 8.8%, including 2 postoperative deaths that were possibly related to SMART in patients who had surgery. There was no acute grade ≥3 GI toxicity definitely related to SMART. One-year overall survival from SMART was 65.0%. Conclusions: The primary endpoint of this study was met with no acute grade ≥3 GI toxicity definitely attributed to ablative 5-fraction SMART. Although it is unclear whether SMART contributed to postoperative toxicity, we recommend caution when pursuing surgery, especially with vascular resection after SMART. Additional follow-up is ongoing to evaluate late toxicity, quality of life, and long-term efficacy.
Lingua originaleInglese
pagine (da-a)799-808
Numero di pagine10
RivistaInternational Journal of Radiation Oncology Biology Physics
Volume117
DOI
Stato di pubblicazionePubblicato - 2023

OSS delle Nazioni Unite

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  1. SDG 3 - Salute e benessere
    SDG 3 Salute e benessere

Keywords

  • Pancreatic Neoplasms

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