TY - JOUR
T1 - Feasibility of preoperative combined radiation therapy and chemotherapy with 5-fluorouracil and cisplatin in potentially resectable pancreatic adenocarcinoma
T2 - The French SFRO-FFCD 97-04 Phase II trial
AU - Mornex, Françoise
AU - Girard, Nicolas
AU - Scoazec, Jean Yves
AU - Bossard, Nadine
AU - Ychou, Marc
AU - Smith, Denis
AU - Seitz, Jean François
AU - Valette, Pierre Jean
AU - Roy, Pascal
AU - Rouanet, Philippe
AU - Ducreux, Michel
AU - Partensky, Christian
N1 - Funding Information:
Supported by the Ligue contre le cancer du Rhône, and by the Fondation de l’Avenir.
PY - 2006/8/1
Y1 - 2006/8/1
N2 - Purpose More than 80% of patients who undergo a potentially curative resection for pancreatic cancer develop local or distant recurrence. Neoadjuvant chemoradiotherapy might offer potential benefits regarding local and systemic control and survival. This multi-institutional Phase II trial explored the feasibility of preoperative chemoradiation in this situation. Methods and Materials Treatment consisted of concurrent radiotherapy (50 Gy within 5 weeks), and chemotherapy with 5-fluorouracil (300 mg/m2/day, 5 days/week, 5 consecutive weeks) and cisplatin (20 mg/m2/day, Days 1-5 and 29-33), followed by surgical resection of the pancreatic tumor in patients without progression. Results A total of 41 patients were enrolled. Of these, 38 (93%) received ≥47 Gy; 30 patients (73%) received ≥75% of the prescribed doses of chemotherapy. Surgical resection was performed in 26 patients (63%). Because of local or metastatic progression, 5 patients (12%) did not undergo surgery and 10 underwent surgery without resection of the pancreatic tumor. Operative mortality was 2.8%. Among 40 evaluable patients, 27 were successfully treated (67.5%; 95% CI, 50.9-81.4%). Conclusions Pancreatic cancer is chemo-radiosensitive. The proposed pre-operative scheme is feasible, does not prevent successful surgery, and must be tested on a Phase III setting. Yet, the large proportion of tumor progression during and after chemoradiation justifies the use of more efficient drugs such as Gemcitabine, and optimized radiotherapy including new techniques such as intensity-modulated radiation therapy.
AB - Purpose More than 80% of patients who undergo a potentially curative resection for pancreatic cancer develop local or distant recurrence. Neoadjuvant chemoradiotherapy might offer potential benefits regarding local and systemic control and survival. This multi-institutional Phase II trial explored the feasibility of preoperative chemoradiation in this situation. Methods and Materials Treatment consisted of concurrent radiotherapy (50 Gy within 5 weeks), and chemotherapy with 5-fluorouracil (300 mg/m2/day, 5 days/week, 5 consecutive weeks) and cisplatin (20 mg/m2/day, Days 1-5 and 29-33), followed by surgical resection of the pancreatic tumor in patients without progression. Results A total of 41 patients were enrolled. Of these, 38 (93%) received ≥47 Gy; 30 patients (73%) received ≥75% of the prescribed doses of chemotherapy. Surgical resection was performed in 26 patients (63%). Because of local or metastatic progression, 5 patients (12%) did not undergo surgery and 10 underwent surgery without resection of the pancreatic tumor. Operative mortality was 2.8%. Among 40 evaluable patients, 27 were successfully treated (67.5%; 95% CI, 50.9-81.4%). Conclusions Pancreatic cancer is chemo-radiosensitive. The proposed pre-operative scheme is feasible, does not prevent successful surgery, and must be tested on a Phase III setting. Yet, the large proportion of tumor progression during and after chemoradiation justifies the use of more efficient drugs such as Gemcitabine, and optimized radiotherapy including new techniques such as intensity-modulated radiation therapy.
KW - Chemoradiation
KW - Chemotherapy
KW - Neoadjuvant treatment
KW - Pancreatic adenocarcinoma
KW - Radiotherapy
KW - Surgery
UR - http://www.scopus.com/inward/record.url?scp=33746702065&partnerID=8YFLogxK
U2 - 10.1016/j.ijrobp.2006.02.054
DO - 10.1016/j.ijrobp.2006.02.054
M3 - Article
C2 - 16793214
AN - SCOPUS:33746702065
SN - 0360-3016
VL - 65
SP - 1471
EP - 1478
JO - International Journal of Radiation Oncology Biology Physics
JF - International Journal of Radiation Oncology Biology Physics
IS - 5
ER -