In this article, we present a diaphragm-invaded NSCLC case operated using VATS due to its rarity.
On PET examination taken after neoadjuvant treatment, there was no lymph node involvement, and a decrease in the metabolic activity of the tumor was reported (SUVmax= 3 .4). N o m etastasis w as observed on cranial magnetic resonance imaging. In the respiratory function test, the forced expiratory volume in 1 sec (FEV1) value was 2.0 L (91%). In the preoperative examinations, although there was no lymph node involvement on PET, the tumor was T4N0M0 (Stage IIIA) according to clinical Tumor, Node, Metastasis (cTNM) staging system, and mediastinal staging was performed with endobronchial ultrasound (EBUS) biopsy. The lymph node stations of 4R, 4L, and 7 were biopsied. The patient, who was evaluated as N0 according to the EBUS, was operated on Day 21 after neoadjuvant therapy.
As the operative method, right-side VATS was performed using three ports. A utility incision was made where the fifth intercostal space intersected with the midaxillary line. The camera port was placed at the junction of the seventh intercostal space and the anterior axillary line. Finally, an assistance port was placed in the area where the posterior axillary line intersected with the eighth intercostal space. The tumor was observed to be in the lower lobe of the right lung as tightly adhered to the diaphragm. The adhesions were partially removed, but the tumor was thought to invade an area on the diaphragm (Figure 2a). Then, a diaphragm area of 3 cm in diameter was resected with the energy device in full-thickness (Figure 2b, 2c). Afterward, a standard right lower lobectomy was performed. The inferior pulmonary vein and the arterial branches of the lower lobe were dissected and cut using endoscopic staplers. The fissure was completed with endoscopic staplers and an energy device. Following the removal of the specimen from the thorax, the systemic mediastinal lymph node dissection was performed. The lymph node stations of 2R, 4R, 7, 8, 9, and 11 were dissected. The resulting diaphragm defect was primarily repaired with separated suturing using non-absorbable monofilament polypropylene sutures (Figure 2d). Since the defect was in a diameter of 3 cm, any reconstructive material was not used. The operation lasted 180 min, and blood loss was approximately 200 cc. The postoperative period was uneventful. The chest tube was removed on the postoperative fifth day, and the patient was discharged on the sixth day. The patient's histopathology report revealed that the tumor 3 cm in diameter invaded the diaphragm superficially but not in full-depth, with N0 status. There were fibrosis and necrosis zones within the tumor. The diagnosis was confirmed as a squamous cell carcinoma, and the immunohistochemical staining result was CK5/6 (+), TTF1 (-), and P63 (+). Since the patient had a T4N0M0 tumor (Stage IIIA), the patient was referred to the oncology department in the postoperative period and received adjuvant therapy. The patient's disease-free follow-up still continues in the ninth postoperative month.
Figure 3. The chest radiograph of patient at the postoperative third month.
The main factors affecting survival in NSCLC cases with diaphragm invasion are N status and invasion depth.[2] In the study performed by Galetta et al.,[2] the five-year survival of N0 patients with invasion to the diaphragm was 43%. In the aforementioned study, cases showing full-depth diaphragm invasion did not survive five years, but five-year survival in superficial invasions was 50%. In the study of Yokoi et al.,[7] five-year survival in N0 status was 28.3% in diaphragm-invasive NSCLC cases, while this rate was 18.1% in N1-2 patients. In the same study, five-year survival in full-depth invasion was 14.3% and 33% in superficial invasions.[7] Our case had an N0 tumor, and the diaphragm invasion was superficial. Disease-free follow-up continues in the ninth postoperative month.
In conclusion, the video-assisted thoracoscopic surgery method can be used safely in locally advanced non-small cell lung cancer patients with diaphragm invasion. The merits of video-assisted thoracoscopic surgery allow the continuity of the treatment by rapidly overcoming the operative trauma. The surgeon's correct surgical planning in line with his/her experience is the most critical issue in such cases.
Patient Consent for Publication: A written informed consent was obtained from patient.
Data Sharing Statement: The data that support the findings of this study are available from the corresponding author upon reasonable request.
Author Contributions: Conception and design of the study: A.A, K.C.C.; Literature review: A.A., H.M.; Writing the article: A.A.; Control/Supervision: K.C.C., N.Y.
Conflict of Interest: The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.
Funding: The authors received no financial support for the research and/or authorship of this article.
1) Fan J, Yao J, Wang Q, Chang Z. Safety and feasibility
of uniportal video-assisted thoracoscopic surgery for
locally advanced non-small cell lung cancer. J Thorac Dis
2016;8:3543-50. doi: 10.21037/jtd.2016.12.12.
2) Galetta D, Borri A, Casiraghi M, Gasparri R, Petrella F,
Tessitore A, et al. Outcome and prognostic factors of resected
non-small-cell lung cancer invading the diaphragm. Interact
Cardiovasc Thorac Surg 2014;19:632-6. doi: 10.1093/icvts/
ivu183.
3) Wang Z, Pang L, Tang J, Cheng J, Chen N, Zhou J, et al.
Video-assisted thoracoscopic surgery versus muscle-sparing
thoracotomy for non-small cell lung cancer: A systematic
review and meta-analysis. BMC Surg 2019;19:144. doi:10.1186/s12893-019-0618-1.
4) Hanna JM, Berry MF, D'Amico TA. Contraindications
of video-assisted thoracoscopic surgical lobectomy and
determinants of conversion to open. J Thorac Dis 2013;5
Suppl 3:S182-9. doi: 10.3978/j.issn.2072-1439.2013.07.08.
5) Fang L, Wang L, Wang Y, Lv W, Hu J. Video assisted
thoracic surgery vs. thoracotomy for locally advanced lung
squamous cell carcinoma after neoadjuvant chemotherapy.
J Cardiothorac Surg 2018;13:128. doi: 10.1186/s13019-018-
0813-7.