Author/Authors :
Salek, Roham Cancer Research Center - Faculty of Medicine - Mashhad University of Medical Sciences , Anvari, Kazem Cancer Research Center - Faculty of Medicine - Mashhad University of Medical Sciences , Aledavood, Seyed Amir Cancer Research Center - Faculty of Medicine - Mashhad University of Medical Sciences , Seilanian Toussi,Mehdi Cancer Research Center - Faculty of Medicine - Mashhad University of Medical Sciences , Forghani, Mohammad Naser Cancer Research Center - Faculty of Medicine - Mashhad University of Medical Sciences , Mohtashami, Samira Cancer Research Center - Faculty of Medicine - Mashhad University of Medical Sciences , Homaee Shandiz, Fatemeh Cancer Research Center - Faculty of Medicine - Mashhad University of Medical Sciences , Nowferesti, Gholamhossein Cancer Research Center - Faculty of Medicine - Mashhad University of Medical Sciences , Rajabi, Mohammad Taghi Endoscopic and Minimally Invasive Surgery Research Center - Ghaem Hospital - Faculty of Medicine, Mashhad University of Medical Sciences , Nosrati, Fatemeh Omid Hospital - Radiation Oncology Specialist - Mashhad University of Medical Sciences, Mashhad
Abstract :
Background: Esophageal carcinoma is a common malignancy in the North East of Iran. Combined modality treatments have
been adopted to improve survival in patients with esophageal carcinoma. In this trial, we evaluated the effi cacy and toxicity of a
preoperative concurrent chemoradiotherapy protocol in the patients with locally advanced esophageal carcinoma. Materials and
Methods: Between 2006 and 2011, eligible patients with locally advanced esophageal carcinoma underwent concurrent radiotherapy
and chemotherapy and 3-4 weeks later, esophagectomy. Pathologic response, overall survival rate, toxicity, and feasibility were
evaluated. Results: One hundred ninety-seven patients with a median age of 59 (range: 27-70) entered the protocol. One hundred
ninety-four cases (98.5%) had esophageal squamous cell carcinoma. Grades 3-4 of toxicity in patients undergoing neoadjuvant
chemoradotherapy were as follows: Neutropenia in 21% and esophagitis in 2.5% of cases. Th ere were 11 (5.6%) early death probably
due to the treatment-related toxicities. One hundred twenty-seven patients underwent surgery with postsurgical mortality of 11%.
In these cases, the complete pathological response was shown in 38 cases (29.9%) with a 5-year overall survival rates of 48.2% and
median overall survival of 44 months (95% confi dence interval, 24.46-63.54). Conclusion: Th e pathological response rate and the
overall survival rate are promising in patients who completed the protocol as receiving at least one cycle of chemotherapy. However,
the treatment toxicities were relatively high.