Abstract
Background
Local recurrence of microinvasive sarcoma or benign aggressive pathologies can be limb- and life-threatening. Although frozen pathology is reliable, tumor microinvasion can be subtle or missed, having an impact on surgical margins and postoperative radiation planning. The authors’ service has begun to temporize the tumor bed after primary tumor excision with a wound vacuum-assisted closure (VAC) pending formal margin analysis, with coverage performed in the setting of final negative margins.
Methods
This retrospective analysis included all patients managed at a tertiary referral cancer center with VAC temporization after soft tissue sarcoma or benign aggressive tumor excision from 1 January 2000 to 1 January 2019 and at least 2 years of oncologic follow-up evaluation. The primary outcome was local recurrence. The secondary outcomes were distant recurrence, unplanned return to the operating room for wound/infectious indications, thromboembolic events, and tumor-related deaths.
Results
For 62 patients, VAC temporization was performed. The mean age of the patients was 62.2 ± 22.3 years (median 66.5 years; 95% confidence interval [CI] 61.7–72.5 years), and the mean age-adjusted Charlson Comorbidity Index was 5.3 ± 1.9. The most common tumor histology was myxofibrosarcoma (51.6%, 32/62). The mean volume was 124.8 ± 324.1 cm3, and 35.5% (22/62) of the cases were subfascial. Local recurrences occurred for 8.1% (5/62) of the patients. Three of these five patients had planned positive margins, and 17.7% (11/62) of the patients had an unplanned return to the operating room. No demographic or tumor factors were associated with unplanned surgery.
Conclusions
The findings showed that VAC-temporized management of microinvasive sarcoma and benign aggressive pathologies yields favorable local recurrence and unplanned operating room rates suggestive of oncologic and technical safety. These findings will need validation in a future randomized controlled trial.
Similar content being viewed by others
References
Trovik CS, Gustafson P, Bauer HCF, et al. Consequences of local recurrence of soft tissue sarcoma: 205 patients from the Scandinavian Sarcoma Group register. Acta Orthop Scand. 2000;71:488–95.
Sugiura H, Tsukushi S, Yoshida M, et al. What is the success of repeat surgical treatment of a local recurrence after initial wide resection of soft tissue sarcomas? Clin Orthop Relat Res. 2018;476:1791–800.
Zagars GK, Ballo MT, Pisters PWT, et al. Prognostic factors for patients with localized soft-tissue sarcoma treated with conservation surgery and radiation therapy: an analysis of 1225 patients. Cancer. 2003;97:2530–43.
Choy E. Sarcoma after 5 years of progression-free survival: lessons from the French Sarcoma Group. Cancer. 2014;120:2942–3.
Golouh R, Bracko M. Accuracy of frozen section diagnosis in soft tissue tumors. Mod Pathol. 1990;3:729–33.
Ma Z, Shou K, Li Z, et al. Negative-pressure wound therapy promotes vessel destabilization and maturation at various stages of wound healing and thus influences wound prognosis. Exp Ther Med. 2016;11:1307–17.
Senchenkov A, Petty PM, Knoetgen J, et al. Outcomes of skin graft reconstructions with the use of vacuum-assisted closure (VAC) dressing for irradiated extremity sarcoma defects. World J Surg Oncol. 2007;5:138. https://doi.org/10.1186/1477-7819-5-138.
Kopp J, Strnad V, Bach AD, et al. Vacuum application increases therapeutic safety and allows intensified local radiation treatment of malignant soft-tissue tumors. Strahlentherapie und Onkol. 2005;181:124–30.
Naghavi AO, Gonzalez RJ, Scott JG, et al. Staged reconstruction brachytherapy has lower overall cost in recurrent soft-tissue sarcoma. J Contemp Brachyther. 2017;9:20–9.
Lawrenz JM, Mesko NW, Marshall DC, et al. Immediate versus staged soft tissue reconstruction after soft tissue sarcoma resection has similar wound and oncologic outcomes. Ann Plast Surg. 2020;85:163–70.
Naghavi AO, Gonzalez RJ, Scott JG, et al. Implications of staged reconstruction and adjuvant brachytherapy in the treatment of recurrent soft tissue sarcoma. Brachytherapy. 2016;15:495–503.
Dougherty PJ, Andreatta P. CORR curriculum—orthopaedic education: competency-based medical education—how do we get there? Clin Orthop Relat Res. 2017;475:1557–60.
Chen Y, Xu SF, Xu M, et al. Use of negative-pressure wound therapy as an adjunct to the treatment of extremity soft-tissue sarcoma with ulceration or impending ulceration. Oncol Lett. 2016;12:757–63.
Siegel GW, Kuzon WM, Hasen JM, et al. Staged soft tissue reconstruction following sarcoma excision with anticipated large cutaneous defects: an oncologically safe alternative. Iowa Orthop J. 2016;36:104.
Nakamura T, Grimer R, Gaston C, et al. The value of C-reactive protein and comorbidity in predicting survival of patients with high-grade soft tissue sarcoma. Eur J Cancer. 2013;49:377–85.
Slump J, Bastiaannet E, Halka A, et al. Risk factors for postoperative wound complications after extremity soft tissue sarcoma resection: a systematic review and meta-analyses. J Plast Reconstr Aesthet Surg. 2019;72:1449–64.
Traub F, Griffin AM, Wunder JS, et al. Influence of unplanned excisions on the outcomes of patients with stage III extremity soft-tissue sarcoma. Cancer. 2018;124:3868–75.
Bianchi G, Sambri A, Cammelli S, et al. Impact of residual disease after “unplanned excision” of primary localized adult soft tissue sarcoma of the extremities: evaluation of 452 cases at a single institution. Musculoskelet Surg. 2017;101:243–8.
Odei B, Rwigema JC, Eilber FR, et al. Predictors of local recurrence in patients with myxofibrosarcoma. Am J Clin Oncol Cancer Clin Trials. 2018;41:827–31.
Look Hong NJ, Hornicek FJ, Raskin KA, et al. Prognostic factors and outcomes of patients with myxofibrosarcoma. Ann Surg Oncol. 2013;20:80–6.
Ghazala CG, Agni NR, Ragbir M, et al. Myxofibrosarcoma of the extremity and trunk a multidisciplinary approach leads to good local rates of local control. Bone Jt J. 2016;98-B:1682–8.
Chen S, Huang W, Luo P, et al. Undifferentiated pleomorphic sarcoma: long-term follow-up from a large institution. Cancer Manag Res. 2019;11:10001–9.
Winchester D, Lehman J, Tello T, et al. Undifferentiated pleomorphic sarcoma: factors predictive of adverse outcomes. J Am Acad Dermatol. 2018. https://doi.org/10.1016/j.jaad.2018.05.022.
Kim BJ, Kim H, Jin US, et al. Wide local excision for dermatofibrosarcoma protuberans: a single-center series of 90 patients. Biomed Res Int. 2015. https://doi.org/10.1155/2015/642549.
Miller SJ, Alam M, Andersen JS, et al. Dermatofibrosarcoma protuberans. JNCCN J Natl Compr Cancer Netw. 2012;10:312–8.
Paradisi A, Abeni D, Rusciani A, et al. Dermatofibrosarcoma protuberans: wide local excision versus Mohs micrographic surgery. Cancer Treat Rev. 2008;34:728–36.
Huang C, Leavitt T, Bayer LR, et al. Effect of negative-pressure wound therapy on wound healing. Curr Probl Surg. 2014. https://doi.org/10.1067/j.cpsurg.2014.04.001.
Nuutila K, Siltanen A, Peura M, et al. Gene expression profiling of negative-pressure-treated skin graft donor-site wounds. Burns. 2013. https://doi.org/10.1016/j.burns.2012.09.014.
Erba P, Ogawa R, Ackermann M, et al. Angiogenesis in wounds treated by microdeformational wound therapy. Ann Surg. 2011. https://doi.org/10.1097/SLA.0b013e31820563a8.
Kairinos N, Solomons M, Hudson DA. The paradox of negative-pressure wound therapy: in vitro studies. J Plast Reconstr Aesthet Surg. 2010. https://doi.org/10.1016/j.bjps.2008.08.037.
Ehnman M, Chaabane W, Haglund F, et al. The tumor microenvironment of pediatric sarcoma: mesenchymal mechanisms regulating cell migration and metastasis. Curr Oncol Rep. 2019. https://doi.org/10.1007/s11912-019-0839-6.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Disclosures
There are conflicts of interest.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Fourman, M.S., Ramsey, D.C., Newman, E.T. et al. Assessing the Safety and Utility of Wound VAC Temporization of the Sarcoma or Benign Aggressive Tumor Bed Until Final Margins Are Achieved. Ann Surg Oncol 29, 2290–2298 (2022). https://doi.org/10.1245/s10434-021-11023-9
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1245/s10434-021-11023-9