Casadei Riccardo, Di Marco Mariacristina, Ricci Claudio, Santini Donatella, Serra Carla, Calculli Lucia, D'Ambra Marielda, Guido Alessandra, Morselli-Labate Antonio Maria, Minni Francesco
Dipartimento di Scienze Mediche e Chirurgiche (DIMEC), Chirurgia Generale-Minni, Alma Mater Studiorum - University of Bologna, Policlinico S.Orsola-Malpighi, Via Massarenti n.9, 40138, Bologna, Italy.
Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale (DIMES), Oncologia Medica-Biasco, Alma Mater Studiorum - University of Bologna, Policlinico S.Orsola-Malpighi, Via Massarenti n.9, 40138, Bologna, Italy.
J Gastrointest Surg. 2015 Oct;19(10):1802-12. doi: 10.1007/s11605-015-2890-4. Epub 2015 Jul 30.
The objective of the study is to evaluate the usefulness of neoadjuvant chemoradiotherapy in resectable pancreatic cancer.
A single-center RCT of patients affected by resectable pancreatic adenocarcinoma which included arm A (surgery alone) and arm B (neoadjuvant chemoradiation and surgery). The primary endpoint was R0 resection; the secondary endpoints were toxicity; number of patients who completed the neoadjuvant therapy; radiological and pathological response after chemoradiation; and pTNM stage, postoperative morbidity, mortality, and overall and disease-free survival. A sample size of 32 patients was required for each group.
The study was terminated early, and 38 patients were randomized: 20 in arm A and 18 in arm B. There was no significant difference regarding R0 resection rate in the two groups (intention-to-treat, OR = 1.91, P = 0.489). Neoadjuvant chemoradiotherapy was completed in 14 out of 18 cases (77.8 %) and the radiological and pathological response was efficacious in 72.3 and 90.9 % of cases, respectively.
Neoadjuvant chemoradiation was feasible, safe, and efficacious, although non-significant results were obtained as a result of the underpowered data due to the difficulty in recruiting patients. Additional multicenter RCTs are needed in the future.
本研究的目的是评估新辅助放化疗在可切除胰腺癌中的作用。
一项针对可切除胰腺腺癌患者的单中心随机对照试验,包括A组(单纯手术)和B组(新辅助放化疗及手术)。主要终点是R0切除;次要终点是毒性;完成新辅助治疗的患者数量;放化疗后的影像学和病理学反应;以及pTNM分期、术后发病率、死亡率、总生存期和无病生存期。每组需要32例患者的样本量。
该研究提前终止,38例患者被随机分组:A组20例,B组18例。两组的R0切除率无显著差异(意向性分析,OR = 1.91,P = 0.489)。18例中有14例(77.8%)完成了新辅助放化疗,影像学和病理学反应分别在72.3%和90.9%的病例中有效。
新辅助放化疗是可行、安全且有效的,尽管由于招募患者困难导致数据量不足而未得出显著结果。未来需要更多的多中心随机对照试验。