IMPACT OF RADICAL SYSTEMATIC MEDIASTINAL LYMPHADENECTOMY ON TUMOR STAGING IN LUNG-CANCER

Citation
Jr. Izbicki et al., IMPACT OF RADICAL SYSTEMATIC MEDIASTINAL LYMPHADENECTOMY ON TUMOR STAGING IN LUNG-CANCER, The Annals of thoracic surgery, 59(1), 1995, pp. 209-214
Citations number
18
Categorie Soggetti
Surgery
ISSN journal
00034975
Volume
59
Issue
1
Year of publication
1995
Pages
209 - 214
Database
ISI
SICI code
0003-4975(1995)59:1<209:IORSML>2.0.ZU;2-5
Abstract
The extent of lymphadenectomy in the treatment of non-small cell lung cancer is still a matter of controversy. While some centers perform me diastinal lymph node sampling with resection of only suspicious lymph nodes, others recommend a radical, systematic mediastinal lymphadenect omy (LA) to improve survival and achieve a better staging. Herein we r eport on the impact of LA on tumor staging in a controlled, prospectiv e, randomized clinical trial comparing lymph node sampling and LA in a total of 182 patients with operable non-small cell lung cancer. Regar dless of the type of lymphadenectomy performed, the percentage of pati ents with pathologic N1 or N2 (sampling: n = 23, 23.0%; LA: n = 22, 26 .8%) disease was very similar in both groups, indicating that systemat ic radical lymphadenectomy is not an essential prerequisite to determi ne the N stage of a patient. In contrast the number of patients detect ed to have lymph node involvement at multiple levels was significantly increased by LA. In the lymph node sampling group only 4 of 23 patien ts (17.4%) with N2 disease were found to have more than one lymph node level involved, whereas LA results in the detection of excessive N2 d isease in 12 of 21 patients (57.2%; p = 0.007), which was associated w ith a shorter distant metastases-free (p = 0.021) and overall survival . In conclusion, LA is not essential to determine the N stage of a pat ient, but results in a more detailed staging of the N2 region, which i s of prognostic significance. Therefore, it might be useful to identif y patients with a higher risk for tumor relapse.