Laser assisted pulmonary metastasectomy promises a low local recurrence rate.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
12 Mar 2024
Historique:
received: 12 11 2023
accepted: 08 03 2024
medline: 13 3 2024
pubmed: 13 3 2024
entrez: 13 3 2024
Statut: epublish

Résumé

Pulmonary metastasectomy (PM) is consensually performed in a parenchyma-sparing manner to preserve functionally healthy lung tissue. However, this may increase the risk of local recurrence at the surgical margin. Laser assisted pulmonary metastasectomy (LPM) is a relatively recent innovation that is especially useful to resect multiple metastatic pulmonary nodules. In this study we investigated the rate of local recurrence after LPM and evaluated the influence of various clinical and pathological factors on local recurrence. Retrospectively, a total of 280 metastatic nodules with different histopathological entities were studied LPM from 2010 till 2018. All nodules were resected via diode-pumped neodymium: yttrium-aluminum-garnet (Nd:YAG) 1,318 nm laser maintaining a safety margin of 5 mm. Patients included were observed on average for 44 ± 17 months postoperatively. Local recurrence at the surgical margin following LPM was found in 9 nodules out of 280 nodules (3.21%). Local recurrence at the surgical margin occurred after 20 ± 8.5 months post operation. Incomplete resection (p =  < 0.01) and size of the nodule (p = < 0.01) were associated with significantly increased risk of local recurrence at the surgical margin. Histology of the primary disease showed no impact on local recurrence. Three and five-year survival rates were 84% and 49% respectively. Following LPM, the rate of local recurrence is low. This is influenced by the size of the metastatic nodules and completeness of the resection. Obtaining a safety margin of 5 mm seems to be sufficient, larger nodules require larger safety margins.

Identifiants

pubmed: 38472291
doi: 10.1038/s41598-024-56566-5
pii: 10.1038/s41598-024-56566-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5988

Informations de copyright

© 2024. The Author(s).

Références

Panagiotopoulos, N., Patrini, D., Lawrence, D., Scarci, M. & Mitsos, S. Pulmonary metastasectomy and laser-assisted resection. J. Thorac. Dis. 10(Suppl 17), S1930–S1933. https://doi.org/10.21037/jtd.2018.05.08 (2018).
doi: 10.21037/jtd.2018.05.08 pubmed: 30023083 pmcid: 6036023
Lievens, Y. et al. Defining oligometastatic disease from a radiation oncology perspective: an ESTRO-ASTRO consensus document. Radiother. Oncol. 148, 157–166 (2020).
doi: 10.1016/j.radonc.2020.04.003 pubmed: 32388150
Shiono, S. et al. Histopathologic prognostic factors in resected colorectal lung metastases. Ann. Thorac. Surg. 79(1), 278–282. https://doi.org/10.1016/j.athoracsur.2004.06.096 (2005).
doi: 10.1016/j.athoracsur.2004.06.096 pubmed: 15620957
Lussier, Y. A. et al. Oligo-and polymetastatic progression in lung metastasis (es) patients is associated with specific microRNAs. PLoS One 7(12), e50141 (2012).
doi: 10.1371/journal.pone.0050141 pubmed: 23251360 pmcid: 3518475
Sawabata, N. et al. Optimal distance of malignant negative margin in excision of nonsmall cell lung cancer: A multicenter prospective study. Ann. Thorac. Surg. 77(2), 415–420 (2004).
doi: 10.1016/S0003-4975(03)01511-X pubmed: 14759408
Hermanek, P. & Wittekind, C. The pathologist and the residual tumor (R) classification. Pathol. Pract. 190(2), 115–123 (1994).
doi: 10.1016/S0344-0338(11)80700-4
Handy, J. R. et al. Expert consensus document on pulmonary metastasectomy. Ann. Thorac. Surg. 107(2), 631–649. https://doi.org/10.1016/j.athoracsur.2018.10.028 (2019).
doi: 10.1016/j.athoracsur.2018.10.028 pubmed: 30476477
Shiono, S. et al. Predictive factors for local recurrence of resected colorectal lung metastases. Ann. Thorac. Surg. 80(3), 1040–1045. https://doi.org/10.1016/j.athoracsur.2004.12.033 (2005).
doi: 10.1016/j.athoracsur.2004.12.033 pubmed: 16122482
Pastorino, U. et al. Long-term results of lung metastasectomy: Prognostic analyses based on 5206 cases. J. Thorac. Cardiovasc. Surg. 113(1), 37–49. https://doi.org/10.1016/S0022-5223(97)70397-0 (1997).
doi: 10.1016/S0022-5223(97)70397-0 pubmed: 9011700
Higashiyama, M. et al. Pulmonary metastasectomy: outcomes and issues according to the type of surgical resection. Gen. Thorac. Cardiovasc. Surg. 63(6), 320–330. https://doi.org/10.1007/s11748-015-0544-9 (2015).
doi: 10.1007/s11748-015-0544-9 pubmed: 25836329
Welter, S. et al. Safety distance in the resection of colorectal lung metastases: A prospective evaluation of satellite tumor cells with immunohistochemistry. J. Thorac. Cardiovasc. Surg. 141(5), 1218–1222. https://doi.org/10.1016/j.jtcvs.2010.08.089 (2011).
doi: 10.1016/j.jtcvs.2010.08.089 pubmed: 21163502
Higashiyama, M. et al. Intraoperative lavage cytologic analysis of surgical margins as a predictor of local recurrence in pulmonary metastasectomy. Arch. Surg. 137(4), 469–474. https://doi.org/10.1001/archsurg.137.4.469 (2002).
doi: 10.1001/archsurg.137.4.469 pubmed: 11926957
Welter, S. et al. Growth patterns of pulmonary metastases: Should we adjust resection techniques to primary histology and size?. Eur. J. Cardio-Thoracic Surg. 52(1), 39–46. https://doi.org/10.1093/ejcts/ezx063 (2017).
doi: 10.1093/ejcts/ezx063
Kim, S. et al. Pulmonary resection of metastatic sarcoma: prognostic factors associated with improved outcomes. Ann. Thorac. Surg. 92(5), 1780–1787 (2011).
doi: 10.1016/j.athoracsur.2011.05.081 pubmed: 22051274
Franzke, K. et al. Pulmonary metastasectomy – A retrospective comparison of surgical outcomes after laser-assisted and conventional resection. Eur. J. Surg. Oncol. 43(7), 1357–1364. https://doi.org/10.1016/j.ejso.2016.09.001 (2017).
doi: 10.1016/j.ejso.2016.09.001 pubmed: 27771210
Kirschbaum, A., Palade, E., Kayser, G. & Passlick, B. Local effects of high-powered neodymium-doped yttrium aluminium garnet laser systems on the pulmonary parenchyma: An experimental study on the isolated perfused pig lung lobe. Interact. Cardiovasc. Thorac. Surg. 15(2), 191–193. https://doi.org/10.1093/icvts/ivs140 (2012).
doi: 10.1093/icvts/ivs140 pubmed: 22535543 pmcid: 3397735
Rolle, A., Pereszlenyi, A., Koch, R., Bis, B. & Baier, B. Laser resection technique and results of multiple lung metastasectomies using a new 1,318 nm Nd:YAG laser system. Lasers Surg. Med. 38(1), 26–32. https://doi.org/10.1002/lsm.20259 (2006).
doi: 10.1002/lsm.20259 pubmed: 16444696
Welter, S., Jacobs, J., Krbek, T., Poettgen, C. & Stamatis, G. Prognostic impact of lymph node involvement in pulmonary metastases from colorectal cancer. Eur. J. Cardio-Thoracic Surg. 31(2), 167–172 (2007).
doi: 10.1016/j.ejcts.2006.11.004
Rolle, A. & Kozłowski, M. Laser resection of lung parenchyma–a new technical and clinical approach. Rocz. Akad. Med. Bialymst. 50, 193–196 (2005).
pubmed: 16358964
Rolle, A., Pereszlenyi, A., Koch, R., Richard, M. & Baier, B. Is surgery for multiple lung metastases reasonable? A total of 328 consecutive patients with multiple-laser metastasectomies with a new 1318-nm Nd:YAG laser. J. Thorac. Cardiovasc. Surg. 131(6), 1236–1242. https://doi.org/10.1016/j.jtcvs.2005.11.053 (2006).
doi: 10.1016/j.jtcvs.2005.11.053 pubmed: 16733151
A. Rolle, A. Pereszlenyi, Laser resection of lung metastasis. Multimed. Man. Cardiothorac. Surg. MMCTS, 2005(628), 2004, 2005.
Osei-Agyemang, T. et al. Pulmonary metastasectomy: an analysis of technical and oncological outcomes in 301 patients with a focus on laser resection. Zentralbl. Chir. 138, S45-51 (2013).
pubmed: 24150855
Shiono, S. et al. Outcomes of segmentectomy and wedge resection for pulmonary metastases from colorectal cancer. Eur. J. Cardio-Thoracic Surg. 51(3), 504–510 (2017).
Chung, J. H. et al. Impact of resection margin length and tumor depth on the local recurrence after thoracoscopic pulmonary wedge resection of a single colorectal metastasis. J. Thorac. Dis. 11(5), 1879 (2019).
doi: 10.21037/jtd.2019.05.12 pubmed: 31285880 pmcid: 6588790
Macherey, S., Doerr, F., Wahlers, T. & Hekmat, K. Role of laser resection in pulmonary metastasectomy. Pneumologie 71(7), 475–479 (2017).
pubmed: 28346958
Y. Kawaguchi et al., Locoregional recurrence via mucus- mediated extension following lung resection for mucinous tumors, pp. 1–10, 2021.
Okumura, S. et al. Pulmonary resection for metastatic colorectal cancer: experiences with 159 patients. J. Thorac. Cardiovasc. Surg. 112(4), 867–874 (1996).
doi: 10.1016/S0022-5223(96)70085-5 pubmed: 8873711
Nelson, D. B. et al. Surgical margins and risk of local recurrence after wedge resection of colorectal pulmonary metastases. J. Thorac. Cardiovasc. Surg. 157(4), 1648–1655 (2019).
doi: 10.1016/j.jtcvs.2018.10.156 pubmed: 30635188
Jaklitsch, M. T. et al. Sequential thoracic metastasectomy prolongs survival by re-establishing local control within the chest. J. Thorac. Cardiovasc. Surg. 121(4), 657–667 (2001).
doi: 10.1067/mtc.2001.112822 pubmed: 11279405
Ojanguren, A., Karenovics, W., Dackam, S., Demarchi, M. & Triponez, F. Laser pulmonary metastasectomy by video-assisted thoracic surgery. J. Vis. Surg. 5(2), 40–40. https://doi.org/10.21037/jovs.2019.03.06 (2019).
doi: 10.21037/jovs.2019.03.06

Auteurs

Ahmad Shalabi (A)

Thoracic and Vascular Surgery Department, SLK Lung Medical Center Löwenstein, Löwenstein, Germany. ahmadfshalabi@gmail.com.

Ahmed Ehab (A)

Pulmonary Medicine Department, SLK Lung Medical Center Löwenstein, Löwenstein, Germany.
Pulmonary Medicine Department, Mansoura University, Mansoura, Egypt.

Sundus F Shalabi (SF)

Faculty of Medicine, Arab American University, Jenin, Palestine.

Gudrun Kugler (G)

Thoracic and Vascular Surgery Department, SLK Lung Medical Center Löwenstein, Löwenstein, Germany.

H-J Schäfers (HJ)

Cardiovascular and Thoracic Surgery Department, Saarland University Medical Center, Homburg/Saar, Germany.

Thomas Graeter (T)

Thoracic and Vascular Surgery Department, SLK Lung Medical Center Löwenstein, Löwenstein, Germany.

Classifications MeSH