Ablative 5-Fraction Stereotactic MRI-Guided Adaptive Radiotherapy for Oligometastatic Pancreatic Adenocarcinoma

Author:

Webking Samantha1ORCID,Sandoval Maria L.2,Chuong Michael D.3,Ucar Antonio4,Aparo Santiago4,De Zarraga Fernando4,Sahin Ibrahim5,Biachi Tiago6,Kim Dae W.6,Hoffe Sarah E.2,Frakes Jessica M.2,Palm Russell F.2ORCID

Affiliation:

1. American University of the Caribbean, Dutch Sint Maarten, Cupecoy

2. Department of Radiation Oncology, Moffitt Cancer Center, Tampa, FL, USA

3. Department of Radiation Oncology, Miami Cancer Institute, Miami, FL, USA

4. Department of Medical Oncology, Miami Cancer Institute, Miami, FL, USA

5. Department of Hematology and Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA

6. Department of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL, USA

Abstract

Introduction Metastatic pancreatic ductal adenocarcinoma (PDAC) carries a poor prognosis and significant morbidity from local tumor progression. We investigated outcomes among oligometastatic PDAC patients treated with stereotactic magnetic resonance image-guided ablative radiotherapy (SMART) to primary disease. Methods We performed a retrospective multi-institutional analysis of oligometastatic PDAC at diagnosis or with metachronous oligoprogression during induction chemotherapy treated with primary tumor SMART. Outcomes of interest included overall survival (OS), progression-free survival (PFS), freedom from locoregional failure (FFLRF), and freedom from distant failure (FFDF). Acute and late toxicity were reported and in exploratory analyses patients were stratified by the number of metastases, SMART indication, and addition of metastasis-directed therapy. Results From 2019 to 2021, 22 patients with oligometastatic PDAC (range: 1–6 metastases) received SMART to the primary tumor with a median follow-up of 11.2 months from SMART. Nineteen patients had de novo synchronous metastatic disease and three had metachronous oligoprogression. Metastasis location most commonly was liver only (40.9%), multiple organs (27.3%), lungs only (13.6%), or abdominal/pelvic nodes (13.6%). All patients received either FOLFIRINOX (64%) or gemcitabine/nab-paclitaxel (36%) followed by SMART (median 50 Gy, 5 fractions) for local control (77%), pain control (14%), or local progression (9%). Additionally, 41% of patients received other metastasis-directed treatments. The median OS from diagnosis and SMART was 23.9 months and 11.6 months, respectively. Calculated from SMART, the median PFS was 2.4 months with 91% of patients having distant progression, and 1-year local control was 68. Two patients (9%) experienced grade 3 toxicities, gastric outlet obstruction, and gastrointestinal bleed without grade 4 or 5 toxicity. Conclusion There was minimal morbidity of local disease progression after SMART in this cohort of oligometastatic PDAC. As systemic therapy options improve, additional strategies to identify patients who may derive benefits from local consolidation or metastasis-directed therapy are needed.

Publisher

SAGE Publications

Subject

Oncology,Hematology,General Medicine

Reference22 articles.

1. Fernandez-del Castillo C. Clinical manifestations, diagnosis, and staging of exocrine pancreatic cancer. In: TW Post, ed. UpToDate. Wolters Kluwer; 2023. Accessed 2022. https://www.uptodate.com/contents/clinical-manifestations-diagnosis-and-staging-of-exocrine-pancreatic-cancer?search=Clinicalmanifestations,diagnosis,andstagingofexocrinepancreaticcancer-UpToDate&source=search_result&selectedTitle=1%E2%88%BC150&usage_type=default&display_rank=12.

2. Pancreatic Cancer - Statistics. Cancer.net. Published June 25, 2012. Accessed November 29, 2023. https://www.cancer.net/cancer-types/pancreatic-cancer/statistics#:

3. Five-Fraction Stereotactic Body Radiation Therapy (SBRT) and Chemotherapy for the Local Management of Metastatic Pancreatic Cancer

4. The Impact of Local Disease Progression in Pancreatic Cancer at the End of Life

5. Oligometastases.

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