Abstract
Minimally invasive surgery (MIS) to resect primary and metastatic pediatric embryonal tumors offers the potential for reduced postoperative morbidity with smaller wounds, less pain, fewer surgical site infections, decreased blood loss, shorter hospital stays, and less disruption to treatment regimens. However, significant controversy surrounds the question of whether a high-fidelity oncologic resection of childhood embryonal tumors with gross total resection, negative margins, and appropriate lymph node sampling can be achieved through MIS. This review outlines the diverse applications of MIS to treat definitively pediatric embryonal malignancies, including this approach to metastatic deposits. It outlines specific patient populations and presentations that may be particularly amenable to the minimally invasive approach. This work further summarizes the current evidence supporting the efficacy of MIS to accomplish a definitive, oncologic resection without compromising relapse-free or overall survival. Finally, the review offers technical considerations to consider in order to achieve a safe and complete resection.
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Selby, L. V., DeMatteo, R. P., Tholey, R. M., Jarnagin, W. R., Garcia-Aguilar, J., Strombom, P. D., et al. (2017). Evolving application of minimally invasive cancer operations at a tertiary cancer center. Journal of Surgical Oncology, 115(4), 365–370. https://doi.org/10.1002/jso.24526.
Raoof, M., Nota, C., Melstrom, L. G., Warner, S. G., Woo, Y., Singh, G., & Fong, Y. (2018). Oncologic outcomes after robot-assisted versus laparoscopic distal pancreatectomy: analysis of the National Cancer Database. Journal of Surgical Oncology, 118(4), 651–656. https://doi.org/10.1002/jso.25170.
Ramirez, P. T., Frumovitz, M., Pareja, R., Lopez, A., Vieira, M., Ribeiro, R., Buda, A., Yan, X., Shuzhong, Y., Chetty, N., Isla, D., Tamura, M., Zhu, T., Robledo, K. P., Gebski, V., Asher, R., Behan, V., Nicklin, J. L., Coleman, R. L., & Obermair, A. (2018). Minimally invasive versus abdominal radical hysterectomy for cervical cancer. The New England Journal of Medicine, 379(20), 1895–1904. https://doi.org/10.1056/NEJMoa1806395.
Barr, E. K., & Applebaum, M. A. (2018). Genetic predisposition to neuroblastoma. Children (Basel), 5(9). https://doi.org/10.3390/children5090119.
Dome, J. S., & Huff, V. (1993). Wilms Tumor Predisposition. In M. P. Adam, H. H. Ardinger, R. A. Pagon, S. E. Wallace, L. J. H. Bean, K. Stephens, et al. (Eds.), GeneReviews((R)). Seattle (WA): University of Washington University of Washington, Seattle. GeneReviews is a registered trademark of the University of Washington, Seattle. All rights reserved.
Lupo, P. J., Danysh, H. E., Plon, S. E., Curtin, K., Malkin, D., Hettmer, S., et al. (2015). Family history of cancer and childhood rhabdomyosarcoma: a report from the Children’s Oncology Group and the Utah Population Database. Cancer Medicine, 4(5), 781–790. https://doi.org/10.1002/cam4.448.
von Allmen, D., Davidoff, A. M., London, W. B., Van Ryn, C., Haas-Kogan, D. A., Kreissman, S. G., et al. (2017). Impact of extent of resection on local control and survival in patients from the COG A3973 study with high-risk neuroblastoma. Journal of Clinical Oncology, 35(2), 208–216. https://doi.org/10.1200/JCO.2016.67.2642.
Phelps, H. M., Ayers, G. D., Ndolo, J. M., Dietrich, H. L., Watson, K. D., Hilmes, M. A., et al. (2018). Maintaining oncologic integrity with minimally invasive resection of pediatric embryonal tumors. Surgery, 164(2), 333–343. https://doi.org/10.1016/j.surg.2018.03.020.
Leclair, M. D., de Lagausie, P., Becmeur, F., Varlet, F., Thomas, C., Valla, J. S., et al. (2008). Laparoscopic resection of abdominal neuroblastoma. Annals of Surgical Oncology, 15(1), 117–124. https://doi.org/10.1245/s10434-007-9499-0.
Kelleher, C. M., Smithson, L., Nguyen, L. L., Casadiego, G., Nasr, A., Irwin, M. S., et al. (2013). Clinical outcomes in children with adrenal neuroblastoma undergoing open versus laparoscopic adrenalectomy. Journal of Pediatric Surgery, 48(8), 1727–1732. https://doi.org/10.1016/j.jpedsurg.2013.03.056.
Irtan, S., Brisse, H. J., Minard-Colin, V., Schleiermacher, G., Canale, S., & Sarnacki, S. (2015). Minimally invasive surgery of neuroblastic tumors in children: Indications depend on anatomical location and image-defined risk factors. Pediatric Blood & Cancer, 62(2), 257–261. https://doi.org/10.1002/pbc.25248.
Phelps, H. M., & Lovvorn 3rd, H. N. (2018). Minimally Invasive Surgery in Pediatric Surgical Oncology. Children (Basel), 5(12). https://doi.org/10.3390/children5120158.
Fraga, J. C., Rothenberg, S., Kiely, E., & Pierro, A. (2012). Video-assisted thoracic surgery resection for pediatric mediastinal neurogenic tumors. Journal of Pediatric Surgery, 47(7), 1349–1353. https://doi.org/10.1016/j.jpedsurg.2012.01.067.
Malek, M. M., Mollen, K. P., Kane, T. D., Shah, S. R., & Irwin, C. (2010). Thoracic neuroblastoma: a retrospective review of our institutional experience with comparison of the thoracoscopic and open approaches to resection. Journal of Pediatric Surgery, 45(8), 1622–1626. https://doi.org/10.1016/j.jpedsurg.2010.03.018.
Posner, J. B. (2004). Paraneoplastic syndromes in neuroblastoma. Journal of Pediatric Hematology/Oncology, 26(9), 553–554. https://doi.org/10.1097/01.mph.0000139454.22338.17.
Kieran, K., Anderson, J. R., Dome, J. S., Ehrlich, P. F., Ritchey, M. L., Shamberger, R. C., et al. (2012). Lymph node involvement in Wilms tumor: results from National Wilms Tumor Studies 4 and 5. Journal of Pediatric Surgery, 47(4), 700–706. https://doi.org/10.1016/j.jpedsurg.2011.08.017.
Rauth, T. P., Slone, J., Crane, G., Correa, H., Friedman, D. L., & Lovvorn 3rd, H. N. (2011). Laparoscopic nephron-sparing resection of synchronous Wilms tumors in a case of hyperplastic perilobar nephroblastomatosis. Journal of Pediatric Surgery, 46(5), 983–988. https://doi.org/10.1016/j.jpedsurg.2011.01.025.
Yadav, P., Mahajan, A., Kandpal, D. K., & Chowdhary, S. K. (2018). Nephron-sparing surgery for syndromic Wilms’ tumor: robotic approach. Urology, 116, 172–175. https://doi.org/10.1016/j.urology.2018.03.003.
Javid, P. J., Lendvay, T. S., Acierno, S., & Gow, K. W. (2011). Laparoscopic nephroureterectomy for Wilms' tumor: oncologic considerations. Journal of Pediatric Surgery, 46(5), 978–982. https://doi.org/10.1016/j.jpedsurg.2011.01.014.
Chui, C. H., & Lee, A. C. (2011). Peritoneal metastases after laparoscopic nephron-sparing surgery for localized Wilms tumor. Journal of Pediatric Surgery, 46(3), e19–e21. https://doi.org/10.1016/j.jpedsurg.2010.11.024.
Ehrlich, P., Chi, Y. Y., Chintagumpala, M. M., Hoffer, F. A., Perlman, E. J., Kalapurakal, J. A., et al. (2017). Results of the first prospective multi-institutional treatment study in children with bilateral Wilms tumor (AREN0534): a report from the Children’s Oncology Group. Annals of Surgery, 266(3), 470–478. https://doi.org/10.1097/SLA.0000000000002356.
Yada, K., Ishibashi, H., Mori, H., & Shimada, M. (2014). Laparoscopic resection of hepatoblastoma: report of a case. Asian Journal of Endoscopic Surgery, 7(3), 267–270. https://doi.org/10.1111/ases.12106.
Schultz, K. A. P., Williams, G. M., Kamihara, J., Stewart, D. R., Harris, A. K., Bauer, A. J., et al. (2018). DICER1 and Associated conditions: identification of at-risk individuals and recommended surveillance strategies. Clinical Cancer Research, 24(10), 2251–2261. https://doi.org/10.1158/1078-0432.CCR-17-3089.
Davidoff, A. M. (2012). Neuroblastoma. Seminars in Pediatric Surgery, 21(1), 2–14. https://doi.org/10.1053/j.sempedsurg.2011.10.009.
Hashii, Y., Kusafuka, T., Ohta, H., Yoneda, A., Osugi, Y., Kobayashi, Y., et al. (2008). A case series of children with high-risk metastatic neuroblastoma treated with a novel treatment strategy consisting of postponed primary surgery until the end of systemic chemotherapy including high-dose chemotherapy. Pediatric Hematology and Oncology, 25(5), 439–450. https://doi.org/10.1080/08880010802104601.
Hishiki, T., Fujino, A., Watanabe, T., Tahara, K., Ohno, M., Yamada, Y., et al. (2019). Definitive tumor resection after myeloablative high dose chemotherapy is a feasible and effective option in the multimodal treatment of high-risk neuroblastoma: a single institution experience. Journal of Pediatric Surgery. https://doi.org/10.1016/j.jpedsurg.2019.08.050.
Metzelder, M., Kuebler, J., Shimotakahara, A., Vieten, G., von Wasielewski, R., & Ure, B. M. (2008). CO(2) pneumoperitoneum increases systemic but not local tumor spread after intraperitoneal murine neuroblastoma spillage in mice. Surgical Endoscopy, 22(12), 2648–2653. https://doi.org/10.1007/s00464-008-9778-2.
Reismann, M., Wehrmann, F., Schukfeh, N., Kuebler, J. F., Ure, B., & Gluer, S. (2009). Carbon dioxide, hypoxia and low pH lead to overexpression of c-myc and HMGB-1 oncogenes in neuroblastoma cells. European Journal of Pediatric Surgery, 19(4), 224–227. https://doi.org/10.1055/s-0029-1202778.
Warmann, S. W., Godzinski, J., van Tinteren, H., Heij, H., Powis, M., Sandstedt, B., et al. (2014). Minimally invasive nephrectomy for Wilms tumors in children - data from SIOP 2001. Journal of Pediatric Surgery, 49(11), 1544–1548. https://doi.org/10.1016/j.jpedsurg.2014.06.005.
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The authors would like to acknowledge the support of the Surgical Outcomes Center for Kids of Monroe Carrell, Jr. Children’s Hospital.
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Portions of this manuscript (specifically “Pearls and Pitfalls” and Table 1) are adapted from work previously published in the November 2018 issue of Children [12]. Appropriate citations are provided in accordance with the journal’s open access copyright policy, which can be found at https://www.mdpi.com/authors/rights.
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Phelps, H.M., Lovvorn, H.N. Minimally invasive surgery to treat embryonal tumors of childhood. Cancer Metastasis Rev 38, 695–708 (2019). https://doi.org/10.1007/s10555-019-09830-4
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DOI: https://doi.org/10.1007/s10555-019-09830-4