TY - JOUR
T1 - Results of a planned interim toxicity analysis with trimodality therapy, including carboplatin AUC = 4, paclitaxel, 5-fluorouracil, amifostine, and radiation for locally advanced esophageal cancer
T2 - Preliminary analyses and treatment recommendations from the North Central Cancer Treatment Group
AU - Jatoi, Aminah
AU - Martenson, James
AU - Mahoney, Michelle R.
AU - Lair, Bradley S.
AU - Brindle, Jeffrey S.
AU - Nichols, Frank
AU - Caron, Normand
AU - Rowland, Kendrith
AU - Tschetter, Loren
AU - Alberts, Steven
PY - 2004/11/8
Y1 - 2004/11/8
N2 - Purpose: An aggressive trimodality approach from the Minnie Pearl Cancer Research Network [carboplatin AUC = 6, days 1 and 22; 5-fluorouracil 225 mg/m2 continuous infusion, days 1-42, paclitaxel 200 mg/m2, days 1 and 22; 45 Gy] has resulted in remarkable pathologic response rates but notable toxicity. This trial was designed to mitigate this toxicity by starting with a lower carboplatin dose, AUC = 4, and by adding subcutaneous amifostine. Methods: This phase II trial included patients with locally advanced, potentially resectable esophageal cancer. All were to receive the above regimen with modifications of carboplatin AUC = 4 and amifostine 500 mg subcutaneously before radiation. All were then to undergo an esophagectomy. A planned interim toxicity analysis after the first 10 patients was to determine whether the carboplatin dose should escalate to AUC = 6. Results: Ten patients were enrolled, and all required dose reductions/omissions during neoadjuvant therapy. One patient died from paclitaxel anaphylaxis. Six patients manifested a complete pathologic response. Conclusion: With this regimen, carboplatin AUC = 4 for patients with locally advanced esophageal cancer is appropriate.
AB - Purpose: An aggressive trimodality approach from the Minnie Pearl Cancer Research Network [carboplatin AUC = 6, days 1 and 22; 5-fluorouracil 225 mg/m2 continuous infusion, days 1-42, paclitaxel 200 mg/m2, days 1 and 22; 45 Gy] has resulted in remarkable pathologic response rates but notable toxicity. This trial was designed to mitigate this toxicity by starting with a lower carboplatin dose, AUC = 4, and by adding subcutaneous amifostine. Methods: This phase II trial included patients with locally advanced, potentially resectable esophageal cancer. All were to receive the above regimen with modifications of carboplatin AUC = 4 and amifostine 500 mg subcutaneously before radiation. All were then to undergo an esophagectomy. A planned interim toxicity analysis after the first 10 patients was to determine whether the carboplatin dose should escalate to AUC = 6. Results: Ten patients were enrolled, and all required dose reductions/omissions during neoadjuvant therapy. One patient died from paclitaxel anaphylaxis. Six patients manifested a complete pathologic response. Conclusion: With this regimen, carboplatin AUC = 4 for patients with locally advanced esophageal cancer is appropriate.
UR - http://www.scopus.com/inward/record.url?scp=18244409873&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=18244409873&partnerID=8YFLogxK
U2 - 10.1186/1477-7800-1-9
DO - 10.1186/1477-7800-1-9
M3 - Article
C2 - 15533252
AN - SCOPUS:18244409873
SN - 1477-7800
VL - 1
JO - International Seminars in Surgical Oncology
JF - International Seminars in Surgical Oncology
ER -