TY - JOUR
T1 - Long-Term Prognosis of Patients With Resected Adenocarcinoma In Situ and Minimally Invasive Adenocarcinoma of the Lung
AU - Yotsukura, Masaya
AU - Asamura, Hisao
AU - Motoi, Noriko
AU - Kashima, Jumpei
AU - Yoshida, Yukihiro
AU - Nakagawa, Kazuo
AU - Shiraishi, Kouya
AU - Kohno, Takashi
AU - Yatabe, Yasushi
AU - Watanabe, Shun ichi
N1 - Funding Information:
Disclosure: Dr. Asamura reports receiving unrestricted institutional funds from Eli Lilly Japan K.K., Pfizer Japan Inc., Shionogi & Co., Ltd., Ono Pharmaceutical Co., Ltd., Tsumura & Co., Taiho Pharmaceutical Co., Ltd., Meiji Seika Pharma Co., Ltd., Astellas Pharma Inc., and Covidien Japan Inc. Dr. Motoi reports receiving personal fees from AstraZeneca K. K., Chugai Pharmaceutical Co., Ltd., Merck Sharp & Dohme K. K., Novartis Pharma K. K., Becton Dickinson and Company, and Covidien Japan Inc., and institutional research funding from Roche Diagnostics K. K., Ono Pharmaceutical Co., Ltd., and NEC Corporation, outside of this work. Dr. Yatabe reports receiving personal fees from Merck Sharp & Dohme K. K., Chugai Pharmaceutical Co., Ltd., AstraZeneca K. K., Pfizer Japan Inc., from Roche/Ventana, Agilent/Dako, Thermo Fisher Scientific, ArcherCD, Novartis Pharma K. K., Eli Lilly Japan K.K., and Daiichi Sankyo, Inc., outside of this work. The remaining authors declare no conflict of interest.This work was supported in part by MEXT KAKENHI grant number 15K08373 (Dr. Motoi), 16KT0197 (Dr. Shiraishi), and 20H00545 (Dr. Kohno), and AMED grant number 19ck0106323h003 (Dr. Watanabe). The authors thank Professor Koji Tsuta at the Department of Clinical Sciences and Laboratory Medicine, Kansai Medical University, for contributing data. The authors also thank members of the Division of Biostatistics at the National Cancer Center for offering fruitful opinions and suggestions on the statistical methods.
Funding Information:
This work was supported in part by MEXT KAKENHI grant number 15K08373 (Dr. Motoi), 16KT0197 (Dr. Shiraishi), and 20H00545 (Dr. Kohno), and AMED grant number 19ck0106323h003 (Dr. Watanabe). The authors thank Professor Koji Tsuta at the Department of Clinical Sciences and Laboratory Medicine, Kansai Medical University, for contributing data. The authors also thank members of the Division of Biostatistics at the National Cancer Center for offering fruitful opinions and suggestions on the statistical methods.
Publisher Copyright:
© 2021 International Association for the Study of Lung Cancer
PY - 2021/8
Y1 - 2021/8
N2 - Introduction: The WHO classification of lung tumors defines adenocarcinoma in situ (AIS) and minimally invasive adenocarcinoma (MIA) as cancers with no or limited histologic invasive components. The probability of patients with AIS or MIA being recurrence free for 5 years postoperatively has been found to be 100%. This study aimed to analyze the prognosis of patients with AIS or MIA after more than 5 postoperative years. Methods: We reviewed the pathologic findings of 4768 patients who underwent resection for lung cancer between 1998 and 2010. Of these, 524 patients with curative resection for AIS (207 cases, 39.5%) and MIA (317 cases, 60.5%) were included. Postoperative recurrence, survival, and development of secondary primary lung cancer (SPLC) were analyzed. Results: Of the included patients, 342 (65.3%) were of female sex, 333 (63.5%) were nonsmokers, and 229 (43.7%) underwent sublobar resection. Average pathologic total tumor diameter was 15.2 plus or minus 5.5 mm. Median postoperative follow-up period was 100 months (range: 1–237). No recurrence of lung cancer was observed for either AIS or MIA cases. Estimated 10-year postoperative disease-specific survival rates were 100% and 100% (p = 0.72), and overall survival rates were 95.3% and 97.8% (p = 0.94) for AIS and MIA cases, respectively. Estimated incidence rates of metachronous SPLC at 10 years after surgery were 5.6% and 7.7% for AIS and MIA, respectively (p = 0.45), and these were not correlated with the EGFR mutation status. Conclusions: Although the development of metachronous SPLC should be noted, the risk of recurrence is quite low at more than 5 years after resection of AIS and MIA. This finding strengthens the clinical value of distinguishing AIS and MIA from other adenocarcinomas of the lung.
AB - Introduction: The WHO classification of lung tumors defines adenocarcinoma in situ (AIS) and minimally invasive adenocarcinoma (MIA) as cancers with no or limited histologic invasive components. The probability of patients with AIS or MIA being recurrence free for 5 years postoperatively has been found to be 100%. This study aimed to analyze the prognosis of patients with AIS or MIA after more than 5 postoperative years. Methods: We reviewed the pathologic findings of 4768 patients who underwent resection for lung cancer between 1998 and 2010. Of these, 524 patients with curative resection for AIS (207 cases, 39.5%) and MIA (317 cases, 60.5%) were included. Postoperative recurrence, survival, and development of secondary primary lung cancer (SPLC) were analyzed. Results: Of the included patients, 342 (65.3%) were of female sex, 333 (63.5%) were nonsmokers, and 229 (43.7%) underwent sublobar resection. Average pathologic total tumor diameter was 15.2 plus or minus 5.5 mm. Median postoperative follow-up period was 100 months (range: 1–237). No recurrence of lung cancer was observed for either AIS or MIA cases. Estimated 10-year postoperative disease-specific survival rates were 100% and 100% (p = 0.72), and overall survival rates were 95.3% and 97.8% (p = 0.94) for AIS and MIA cases, respectively. Estimated incidence rates of metachronous SPLC at 10 years after surgery were 5.6% and 7.7% for AIS and MIA, respectively (p = 0.45), and these were not correlated with the EGFR mutation status. Conclusions: Although the development of metachronous SPLC should be noted, the risk of recurrence is quite low at more than 5 years after resection of AIS and MIA. This finding strengthens the clinical value of distinguishing AIS and MIA from other adenocarcinomas of the lung.
KW - Adenocarcinoma in situ
KW - EGFR
KW - Lung adenocarcinoma
KW - Minimally invasive adenocarcinoma
KW - Prognosis
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U2 - 10.1016/j.jtho.2021.04.007
DO - 10.1016/j.jtho.2021.04.007
M3 - Article
C2 - 33915249
AN - SCOPUS:85106982744
SN - 1556-0864
VL - 16
SP - 1312
EP - 1320
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 8
ER -