A Phase I/II Trial of Intensity Modulated Radiation (IMRT) Dose Escalation With Concurrent Fixed-dose Rate Gemcitabine (FDR-G) in Patients With Unresectable Pancreatic Cancer

• Published in: International journal of radiation oncology, biology, physics Vol. 84; no. 5; pp. 1166 - 1171
• Main Authors: Ben-Josef, Edgar, MD, Schipper, Mathew, PhD, Francis, Isaac R., MD, Hadley, Scott, PhD, Ten-Haken, Randall, PhD, Lawrence, Theodore, MD, PhD, Normolle, Daniel, PhD, Simeone, Diane M., MD, Sonnenday, Christopher, MD, Abrams, Ross, MD, Leslie, William, MD, Khan, Gazala, MD, Zalupski, Mark M., MD
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01-12-2012; Elsevier
• Subjects: Adenocarcinoma; Adenocarcinoma - mortality; Adenocarcinoma - pathology; Adenocarcinoma - radiotherapy; Aged; Aged, 80 and over; ALANINES; ANOREXIA; BILIRUBIN; Biological and medical sciences; CARCINOMAS; Cause of Death; CREATININE; DEATH; DEHYDRATION; Deoxycytidine - administration & dosage; Deoxycytidine - adverse effects; Deoxycytidine - analogs & derivatives; Disease Progression; Dose Fractionation; DOSE RATES; FAILURES; Female; FEVER; Gastroenterology. Liver. Pancreas. Abdomen; Gastrointestinal Tract - radiation effects; Hematology, Oncology and Palliative Medicine; Humans; Liver. Biliary tract. Portal circulation. Exocrine pancreas; Male; Maximum Tolerated Dose; Medical sciences; Middle Aged; NAUSEA; Neutropenia - etiology; NEUTROPHILS; Organs at Risk - radiation effects; PANCREAS; Pancreatic Neoplasms - mortality; Pancreatic Neoplasms - pathology; Pancreatic Neoplasms - radiotherapy; PATIENTS; PERFORATION; RADIATION DOSES; Radiation-Sensitizing Agents - administration & dosage; Radiation-Sensitizing Agents - adverse effects; Radiology; RADIOLOGY AND NUCLEAR MEDICINE; RADIOTHERAPY; Radiotherapy, Intensity-Modulated - adverse effects; Radiotherapy, Intensity-Modulated - methods; Thrombocytopenia - chemically induced; Time Factors; TOXICITY; Tumors; VOMITING; Antineoplastic agent; Human; Gemcitabine; Concurrent; Malignant tumor; Dose rate; Increasing dose; Intensity modulated radiotherapy; Cancerology; Treatment; Antimetabolic; Pancreas cancer; Phase II trial; Phase I trial; Unresectable; Pyrimidine derivatives; Digestive diseases; Fluorine Organic compounds; Pyrimidine nucleoside; Cancer; Pancreatic disease
• ISSN: 0360-3016; 1879-355X
• DOI: 10.1016/j.ijrobp.2012.02.051

Purpose Local failure in unresectable pancreatic cancer may contribute to death. We hypothesized that intensification of local therapy would improve local control and survival. The objectives were to determine the maximum tolerated radiation dose delivered by intensity modulated radiation with fixed-dose rate gemcitabine (FDR-G), freedom from local progression (FFLP), and overall survival (OS). Methods and Materials Eligibility included pathologic confirmation of adenocarcinoma, radiographically unresectable, performance status of 0-2, absolute neutrophil count of ≥1500/mm3 , platelets ≥100,000/mm3 , creatinine <2 mg/dL, bilirubin <3 mg/dL, and alanine aminotransferase/aspartate aminotransferase ≤2.5 × upper limit of normal. FDR-G (1000 mg/m2 /100 min intravenously) was given on days −22 and −15, 1, 8, 22, and 29. Intensity modulated radiation started on day 1. Dose levels were escalated from 50-60 Gy in 25 fractions. Dose-limiting toxicity was defined as gastrointestinal toxicity grade (G) ≥3, neutropenic fever, or deterioration in performance status to ≥3 between day 1 and 126. Dose level was assigned using TITE-CRM (Time-to-Event Continual Reassessment Method) with the target dose-limiting toxicity (DLT) rate set to 0.25. Results Fifty patients were accrued. DLTs were observed in 11 patients: G3/4 anorexia, nausea, vomiting, and/or dehydration (7); duodenal bleed (3); duodenal perforation (1). The recommended dose is 55 Gy, producing a probability of DLT of 0.24. The 2-year FFLP is 59% (95% confidence interval [CI]: 32-79). Median and 2-year overall survival are 14.8 months (95% CI: 12.6-22.2) and 30% (95% CI 17-45). Twelve patients underwent resection (10 R0, 2 R1) and survived a median of 32 months. Conclusions High-dose radiation therapy with concurrent FDR-G can be delivered safely. The encouraging efficacy data suggest that outcome may be improved in unresectable patients through intensification of local therapy.