Skip to main content

EDITORIAL article

Front. Surg., 28 June 2022
Sec. Thoracic Surgery
This article is part of the Research Topic Real-World Surgical Treatment of Thoracic Cancer in the Era of Precision Medicine View all 12 articles

Editorial: Real-world surgical treatment of thoracic cancer in the era of precision medicine

\r\nGuobang WeiGuobang WeiYongbing Chen
\r\nYongbing Chen*
  • Department of Thoracic Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, China

Editorial on the Research Topic

Real-world surgical treatment of thoracic cancer in the era of precision medicine

Surgical resection has been the first choice for treatment of early-stage thoracic cancer, mainly including lung and esophageal malignancies. Nowadays, the advent of the era of precision medicine, has highlighted the significant roles of evidence-based practice, not only applicable for surgical procedures, but also for perioperative management (1). In this section of “Frontiers in Surgery”, several studies were included which might facilitate the perfection of real-world surgical treatment.

Conventionally, lobectomy and systematic lymphadenectomy is the standard of care for the management of early-stage non-small cell lung cancer (NSCLC) (2, 3). However, numerous factors might exert impacts on the prognosis of patients with stage IA NSCLC receiving lobectomy, such as tumor pathological type and extent of lymph node dissection. Previously, Long et al. (2021) proposed that the order of vascular processing in lobectomy might become a prognostic factor that should not be ignored. More specifically, although there was no significant difference in recurrence rate between the vein-first group and the artery-first group, the vein-first group had better overall survival (OS) and disease-free survival (DFS), especially in the squamous cell carcinoma (LUSC) subgroup and the stage I-II subgroup. Similarly, in the study by Wei et al. (4), the vein-first group exhibited significantly better outcomes than the artery-first group for 5-year OS (73.6% vs 57.6%; P = 0.002), DFS (63.6% vs 48.4%; P = 0.001), and lung cancer-specific survival (LCSS) (76.4% vs 59.9%; P = 0.002). In the context of pulmonary function reserved as an important indicator, sublobar resection, including segmentectomy and wedge resection, has captured increasing attention in recent years which has shown non-inferiority to lobectomy for patients with stage T1a-bN0M0 NSCLC (5, 6). In our section, Hao et al. (2021) suggested that tumor size should be taken as a critical factor for surgical decision-making. In their study, segmentectomy was associated with better OS in patients with NSCLC ≥10 mm and ≤20 mm than wedge resection. Nonetheless, segmentectomy did not exhibit advantages in survival compared with wedge resection in patients with NSCLC ≤10 mm. In addition, it was observed that small-sized (≤20 mm) LUSC was associated with worse OS but not LCSS compared with lung adenocarcinoma. In other word, their findings indicated that surgical procedures and intraoperative manipulation should be personalized based on histology and tumor size.

For patients on whom intentional lobectomy are performed, video-assisted thoracic surgery (VATS) and robotic-assisted surgery (RAS) are two prevalent surgical approaches which are increasingly being paid attention to by virtue of the advantages of perioperative recovery (7). Gallina et al. (2021) pointed out that compared with open surgery, VATS and RAS could effectively reduce the incidence of postoperative complications, while the lymph nodes could be effectively dissected as well. They also found that the percentage of mediastinal lymph node metastasis and the number of lymph nodes dissected in the RAS group were significantly higher than those in the VATS group. More interestingly, the ratio of the number of dissected lymph nodes to the number of metastatic lymph nodes was significantly lower in the VATS group and thoracotomy group compared with the RAS group. The limitation of surgical field and operation space of VATS might account for such a phenomenon. Notably, the aforementioned limitations of VATS did not convert to survival disadvantages, while RAS might bring additional financial burdens to patients (8). In a word, although RAS have been more and more popular and exhibiting advantages in intraoperative manipulation and postoperative recovery, VATS has remained irreplaceable in chest surgery nowadays. More studies should be launched to investigate the pros and cons of RAS.

With accumulating evidences, the advantages of VATS are not only reflected in improving survival expectations of tumor patients (9), but also in having a favorable impact on the postoperative recovery of patients. In our section, Aeschbacher et al. (2021) reported that blood loss >100 ml (P = 0.029, HR 2.70) and open surgery (P = 0.032, HR 2.37) are independent risk factors for surgical site infections (SSI). SSI occurred much more frequently in open surgery than in VATS approach, and SSI was positively associated with significantly longer hospital stay (10). Undeniably, thoracotomy is currently preferred in the case of intraoperative complications or emergent events with extremely low probabilities, including major vascular injury, calcified lymph nodes around the hilum and dense adhesions. In other word, the studies in our section consistently highlighted the predominant role of VATS in lung cancer surgery.

Hitherto, the treatment of advanced-stage NSCLC patients with distant metastasis has been complex and highly personalized. Previous studies have indicated that systemic chemotherapy or targeted therapy instead of surgery should be recommended for NSCLC patients with malignant pleural dissemination (PD) (11). Sawabata et al. (12) even suggested that tumor resection brought no obvious benefit to postoperative survival of patients who have developed PD. However, Fan et al. (2021) observed that patients who underwent surgical resection of primary tumors had longer progression-free survival (PFS) (19.0 vs. 10.0 months, P < 0.0001) and OS (48.0 vs. 33.0 months, P < 0.0001) than patients who underwent pleural biopsy alone, suggesting that NSCLC patients with pleural metastasis could still benefit from surgical resection of primary tumors. In addition, postoperative targeted therapy and tumor <3 cm were also favorable prognostic factors, and the survival rate of patients receiving targeted therapy was significantly higher than those without (13). In a large cohort analysis of lung cancer patients with brain metastases, He et al. (2021) proposed that patients who received brain therapy before surgery for primary lung tumors might have a better prognosis, irrespective of the treatment modality on the metastasis site. Furthermore, patients who received brain surgery plus radiotherapy followed by primary lung tumor resection had the best survival expectation. The aforementioned studies indeed shed light on the potential therapeutic scheme of NSCLC patients with M1 disease.

In addition, our section also included some reports on surgical techniques Chen et al. (2021). For instance, reconstruction of the right gastroepiploic vessel may solve the awkward situation of injury of the right gastroepiploic artery and vein during the esophagectomy. Chen et al. (2021) highlighted two key technical points as key resolutions: (1) Immediate reconstruction of the right gastroepiploic artery (RGEA) and right gastroepiploic vein (RGEV) and long-term maintenance of the blood flow effectively; (2) Effective tension reduction of gastric conduit anastomosis and vascular anastomosis.

In a word, this section is intended to be the beginning of a small step towards precision medicine in the field of thoracic cancer, which needs further real-world evidences as stepping stones.

Author Contributions

YC: concept and review GW: draft the manuscript. All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Laursen LO, Petersen RH, Hansen HJ, Jensen TK, Ravn J, Konge L. Video-assisted thoracoscopic surgery lobectomy for lung cancer is associated with a lower 30-day morbidity compared with lobectomy by thoracotomy. Eur J Cardiothorac Surg. (2016) 49: 870–5. doi: 10.1093/ejcts/ezv205.26088592

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Dai C, Shen J, Ren Y, Zhong S, Zheng H, He J, et al. Choice of surgical procedure for patients with non-small-cell lung cancer ≤1 cm or >1 to 2 cm among lobectomy, segmentectomy, and wedge resection: a population-based study. J Clin Oncol. (2016) 34(26): 3175–82. doi: 10.1200/JCO.2015.64.6729.27382092

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Eguchi T, Kameda K, Lu S, Bott MJ, Tan KS, Montecalvo J, et al. Lobectomy is associated with better outcomes than sublobar resection in spread through air spaces (STAS)-positive T1 lung adenocarcinoma: a propensity score-matched analysis. J Thorac Oncol. (2019) 14(1): 87–98. doi: 10.1016/j.jtho.2018.09.005.30244070

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Wei S, Guo C, He J, Tan Q, Mei J, Yang Z, et al. Effect of vein-first vs artery-first surgical technique on circulating tumor cells and survival in patients with non-small cell lung cancer: a randomized clinical trial and registry-based propensity score matching analysis. JAMA Surg. (2019) 154(7): e190972. doi: 10.1001/jamasurg.2019.0972.31042283

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Cao J, Yuan P, Wang Y, Xu J, Yuan X, Wang Z, et al. Survival rates after lobectomy, segmentectomy, and wedge resection for non-small cell lung cancer. Ann Thorac Surg. (2018) 105(5): 1483–91. doi: 10.1016/j.athoracsur.2018.01.032.29462591

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Saji H, Okada M, Tusboi M, Nakajima R, Suzuki K, Aokage K, et al. Segmentectomy versus lobectomy in small-sized peripheral non-small-cell lung cancer (JCOG0802/WJOG4607l): a multicentre, open-label, phase 3, randomised, controlled, non-inferiority trial. Lancet. (2022) 399(10335): 1607–17. doi: 10.1016/S0140-6736(21)02333-3.35461558

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Licht PB, Jørgensen OD, Ladegaard L, Jakobsen E. A national study of nodal upstaging after thoracoscopic versus open lobectomy for clinical stage I lung cancer. Ann Thorac Surg. (2013) 96: 943–50. doi: 10.1016/j.athoracsur.2013.04.011.23684159

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Mao J, Tang Z, Mi Y, Xu H, Li K, Liang Y, et al. Robotic and video-assisted lobectomy/segmentectomy for non-small cell lung cancer have similar perioperative outcomes: a systematic review and meta-analysis. Transl Cancer Res. (2021) 10(9): 3883–93. doi: 10.21037/tcr-21-646.35116688

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Yan TD, Cao C, D’Amico TA, Demmy TL, He J, Hansen H, et al. Video-assisted thoracoscopic surgery lobectomy at 20 years: a consensus statement. Eur J Cardiothorac Surg. (2014) 45(4): 633–9. doi: 10.1093/ejcts/ezt463.24130372

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Anderson DJ, Podgorny K, Berrios-Torres SI, Bratzler DW, Dellinger EP, Greene L, et al. Strategies to prevent surgical site infections in acute care hospitals: 2014 update. Infect Control Hosp Epidemiol. (2014) 35: 605–27. doi: 10.1086/676022.24799638

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Ettinger DS, Wood DE, Aggarwal C, Aisner DL, Akerley W, Bauman JR, et al. NCCN Guidelines insights: non-small cell lung cancer, version 1.2020. J Natl Compr Canc Netw. (2019) 17(12): 1464–72. doi: 10.6004/jnccn.2019.0059.31805526

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Sawabata N, Matsumura A, Motohiro A, Osaka Y, Gennga K, Fukai S, et al. Malignant minor pleural effusion detected on thoracotomy for patients with non-small cell lung cancer: is tumor resection beneficial for prognosis? Ann Thorac Surg. (2002) 73: 412–5. doi: 10.1016/S0003-4975(01)03426-9.11845851

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Lida T, Shiba M, Yoshino I, Miyaoka E, Asamura H, Date H, et al. Surgical intervention for non-small-cell lung cancer patients with pleural carcinomatosis: results from the Japanese lung cancer registry in 2004. J Thorac Oncol. (2015) 10: 1076–82. doi: 10.1097/JTO.0000000000000554.26134225

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: thoracic cancer, surgery, real-world evidence, evidence-based medicine, prognosis

Citation: Wei G and Chen Y (2022) Editorial: Real-world surgical treatment of thoracic cancer in the era of precision medicine. Front. Surg. 9:928131. doi: 10.3389/fsurg.2022.928131

Received: 25 April 2022; Accepted: 14 June 2022;
Published: 28 June 2022.

Edited By:

Marco Scarci, Hammersmith Hospital, United Kingdom

© 2022 Wei and Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yongbing Chen Y2hlbnRvbmd0QHNpbmEuY29t

Speciality Section This article was submitted to Thoracic Surgery, a section of the journal Frontiers in Surgery

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.