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ASO Author Reflections: Survival Outcomes between Patients with Hypermetabolic Non-small Cell Lung Cancer Undergoing Systematic and Lobe-Specific Mediastinal Lymph Node Dissection

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A S O A U T H O R R E F L E C T I O N S

ASO Author Reflections: Survival Outcomes between Patients with Hypermetabolic Non-small Cell Lung Cancer Undergoing Systematic and Lobe-Specific Mediastinal Lymph Node Dissection

Yoshinori Handa, MD, PhD, Yasuhiro Tsutani, MD, PhD, and Morihito Okada, MD, PhD

Department of Surgical Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan

Complete systematic lymph node dissection (LND) has long been performed as standard surgical treatment. However, several previous studies have demonstrated detailed nodal spread patterns in surgically resected non-small cell lung cancer (NSCLC), and lobe-specific mediastinal LND is being widely recognized and performed more frequently, aiming for surgery with less burden on patients.1–3The prospective ran- domized clinical trial by the Japanese Clinical Oncology Group (JCOG1413) is ongoing based on these previous reports.4However, the optimal extent of LND for hyperme- tabolic tumors, which are associated with high rates of nodal disease, recurrence, or mortality, has not been elucidated.

The present study analyzed postoperative and survival outcomes between patients with high maximum standard uptake value (SUVmax) NSCLC undergoing systematic mediastinal LND and lobe-specific mediastinal LND, using a multicenter database and adjusted for preoperative factors to minimize patient selection bias.5We showed that, in the propensity-score-matched cohort (101 pairs), systematic LND dissected significantly more lymph nodes (20.0 vs.

16.0 nodes,P = 0.0057) and detected lymph node metas- tasis more frequently (53.5% versus 33.7%, P = 0.0069).

Six (5.9%) patients in the systematic LND group had a metastatic N2 lymph node ‘‘in the systematic LND field’’

that lobe-specific LND could not dissect. The systematic

LND group tended to have better prognosis than the lobe- specific LND group (5-year CSS rates, 82.6% versus 69.6%; 5-year RFI rates, 56.6% versus 47.3%).

Our study suggests that systematic LND could harvest more metastatic lymph nodes and provide better oncological outcome than lobe-specific LND in a cohort of hyperme- tabolic NSCLC patients. Systematic mediastinal LND should not be proscribed for patients with hypermetabolic NSCLC. Further investigations on the appropriate extent of lymphadenectomy for treatment of NSCLC are still needed.

DISCLOSURE This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

REFERENCES

1. Asamura H, Nakayama H, Kondo H, et al. Lobe-specific extent of systematic lymph node dissection for non-small cell lung carci- nomas according to a retrospective study of metastasis and prognosis.J Thorac Cardiovasc Surg. 1999;117:1102–11.

2. Okada M, Sakamoto T, Yuki T, et al. Selective mediastinal lymphadenectomy for clinico-surgical stage I non-small cell lung cancer.Ann Thorac Surg. 2006;81:1028–32.

3. Okada M, Tsubota N, Yoshimura M, et al. Proposal for reasonable mediastinal lymphadenectomy in bronchogenic carcinomas: role of subcarinal nodes in selective dissection.J Thorac Cardiovasc Surg. 1998;116(6):949–53.

4. Hishida T, Saji H, Watanabe S, et al. A randomized Phase III trial of lobe-specific vs. systematic nodal dissection for clinical stage I–

II non-small cell lung cancer (JCOG1413). Jpn J Clin Oncol.

2018;48:190–4.

5. Handa Y, Tsutani Y, Okada M, et al. Systematic versus lobe-specific mediastinal lymphadenectomy for hypermetabolic lung cancer. Ann Surg Oncol. 2021.https://doi.org/10.1245/s10434-021-10020-2.

Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

ÓSociety of Surgical Oncology 2021 First Received: 18 March 2021 Accepted: 18 March 2021;

Published Online: 3 September 2021 M. Okada, MD, PhD

e-mail: morihito@hiroshima-u.ac.jp Ann Surg Oncol (2021) 28:7172

https://doi.org/10.1245/s10434-021-10037-7

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