Table 2.
SBRT selection criteria for dose escalation
Suggested SBRT (5 Fractions) dose-escalation inclusion criteria |
Cytologic- and biopsy-confirmed adenocarcinoma |
Locally advanced, unresectable, or borderline (abutment of SMA, celiac axis, SMV, or PV involvement*) |
ECOG ≤2 |
Pancreatic tumor size ≤5 cm |
No regional adenopathy† |
No evidence of distant metastasis |
Metal stent in place if duodenal stent required |
Reproducible motion management (encompass tumor motion ≤5 mm) |
Adequate hematologic function (ANC ≥ 1500/mm3, Hgb ≥ 8 g/dL, PLT ≥ 100,000/mm3) |
Adequate renal function (creatinine ≤1.5 X ULN) |
Adequate liver function (total bilirubin ≤ 1.5 X ULN; AST, ALT, and ALP ≤ 2.5 X ULN) |
Exclusion criteria |
Prior overlapping abdominal radiation treatment |
Prior surgical resection of pancreatic tumor |
Active or uncontrolled gastric or duodenal ulcer |
Direct invasion of duodenum by tumor |
Residual or persistent grade 3 chemotherapy toxicity |
Therapeutic anticoagulation |
Abbreviations: ALP = alkaline phosphatase; ALT = alanine aminotransferase; ANC = absolute neutrophil count; AST = aspartate aminotransferase; ECOG = Eastern Coppoeative Oncology Group; PLT = platelet; PV = portal vein; SMA = superior mesenteric artery; SMV = superior mesenteric vein; SBRT = stereotactic body radiation therapy; ULN = upper limit of normal.
Involvement requiring vascular reconstruction.
SBRT may be possible for select patients with nodal disease.