Long-term outcomes of endoscopic argon plasma coagulation (APC) therapy for early esophageal cancer and precancerous lesions.
- Author:
Guo-qing WANG
1
;
Chang-qing HAO
;
Wen-qiang WEI
;
Lin ZHAO
Author Information
- Publication Type:Journal Article
- MeSH: Argon Plasma Coagulation; methods; statistics & numerical data; Carcinoma, Squamous Cell; surgery; Endoscopy; Esophageal Neoplasms; surgery; Esophagoscopy; Follow-Up Studies; Humans; Precancerous Conditions; surgery; Survival Rate
- From: Chinese Journal of Oncology 2013;35(6):456-458
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo evaluate the long-term outcomes of endoscopic argon plasma coagulation (APC) therapy for early esophageal cancer and precancerous lesions.
METHODSOne-hundred and seventy-one cases with early esophageal cancer (intramucosal carcinoma) and precancerous lesions were treated by APC from 1994 to 2005, and all the cases were followed up. One-hundred and sixty-eight (98.2%) cases were follow-up by endoscopic examination for several times. On average, each patient was endoscopically examined 2.8 times. The follow-up rate was 100%.
RESULTSThe precancerous lesion group had 160 patients. They were followed up for 5 years. 11 patients died of causes unrelated to cancer. The lesions developed into esophageal squamous cell carcinoma in five patients ( 2 died and 3 underwent esophagectomy). The remaining 144 cases survived without cancer. In this group, the esophageal cancer incidence rate is only 3.1% (5/160). The early cancer (i.e. intramucosal cancer) group had 11 patients. During the 5-year follow-up period, two patients died of causes unrelated to cancer,six patients had recurrence (4 patients died and 2 patients underwent esophagectomy), and only 3 patients survived without cancer. Therefore, the 5-year survival rate was only 27.3% (3/11).
CONCLUSIONSThe APC therapy for precancerous lesions of the esophagus is effective and successful. Indications should be carefully considered when treating early esophageal cancer such as intramucosal carcinoma by APC therapy.