Prognosis of non‐small cell lung cancer with postoperative regional lymph node recurrence

Author:

Ohtaki Yoichi1ORCID,Nagashima Toshiteru1,Okano Naoko2,Kubo Nobuteru2,Ohtaka Takeru3,Sunaga Noriaki4ORCID,Sakurai Reiko4,Miura Yosuke4,Nakazawa Seshiru1,Kawatani Natsuko1,Yazawa Tomohiro1,Yoshikawa Ryohei1,Narusawa Eiji1,Shirabe Ken1

Affiliation:

1. Department of General Surgical Science, Gunma University Graduate School of Medicine, Division of General Thoracic Surgery Integrative Center of General Surgery, Gunma University Hospital Maebashi Japan

2. Gunma University Heavy Ion Medical Center Maebashi Japan

3. Department of Radiation Oncology Gunma University Graduate School of Medicine Maebashi Japan

4. Division of Allergy and Respiratory Medicine Integrative Center of Internal Medicine, Gunma University Hospital Maebashi Japan

Abstract

AbstractBackgroundRegional lymph node recurrence after radical surgery for non‐small cell lung cancer (NSCLC) is an oligo‐recurrent disease; however, no treatment strategy has been established. In the present study we aimed to determine the clinical outcomes of postoperative regional lymph node recurrence and identify prognostic predictors in the era of molecular‐targeted therapy.MethodsWe retrospectively analyzed data on clinical characteristics and outcomes of patients with regional lymph node recurrence after surgery who underwent treatment for NSCLC between 2002 and 2022.ResultsA total of 53 patients were included in this study. The median time between surgery and detection of recurrence was 1.21 years. Radiotherapy (RT) alone and chemoradiotherapy (CRT) were performed in 38 and six patients, respectively. Driver gene alterations were detected in eight patients (EGFR: 6, ROS1:1, and BRAF: 1) and programmed death‐ligand 1 (PD‐L1) expression was examined in 22 patients after 2016. Median progression‐free survival (PFS) and overall survival (OS) after lymph node recurrences were 1.32 and 4.34 years, respectively. Multiple lymph node recurrence was an independent prognostic factor for PFS, whereas driver gene alteration was the only prognostic factor for OS. There was no significant difference in the OS between patients stratified according to the initial treatment modality for lymph node recurrence.ConclusionOur results suggest that the number of tumor recurrences may correlate with PFS, while detection of driver gene alterations could guide decision‐making for the appropriate molecular‐targeted therapy to achieve longer OS.

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

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