Skip to main content
Log in

3D Specimen Scanning and Mapping in Musculoskeletal Oncology: A Feasibility Study

  • Sarcoma
  • Published:
Annals of Surgical Oncology Aims and scope Submit manuscript

Abstract

Background

Surgical resection is the primary treatment for bone and soft tissue tumors. Negative margin status is a key factor in prognosis. Given the three-dimensional (3D) anatomic complexity of musculoskeletal tumor specimens, communication of margin results between surgeons and pathologists is challenging. We sought to perform ex vivo 3D scanning of musculoskeletal oncology specimens to enhance communication between surgeons and pathologists.

Methods

Immediately after surgical resection, 3D scanning of the fresh specimen is performed prior to frozen section analysis. During pathologic grossing, whether frozen or permanent, margin sampling sites are annotated on the virtual 3D model using computer-aided design (CAD) software.

Results

3D scanning was performed in seven cases (six soft tissue, one bone), with specimen mapping on six cases. Intraoperative 3D scanning and mapping was performed in one case in which the location of margin sampling was shown virtually in real-time to the operating surgeon to help achieve a negative margin. In six cases, the 3D model was used to communicate final permanent section analysis. Soft tissue, cartilage, and bone (including lytic lesions within bone) showed acceptable resolution.

Conclusions

Virtual 3D scanning and specimen mapping is feasible and may allow for enhanced documentation and communication. This protocol provides useful information for anatomically complex musculoskeletal tumor specimens. Future studies will evaluate the effect of the protocol on positive margin rates, likelihood that a re-resection contains additional malignancy, and exploration of targeted adjuvant radiation protocols using a patient-specific 3D specimen map.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. He F, Zhang W, Shen Y, et al. Effects of resection margins on local recurrence of osteosarcoma in extremity and pelvis: systematic review and meta-analysis. Int J Surg. 2016;36(Pt A):283–92.

    Article  PubMed  Google Scholar 

  2. Sambri A, Caldari E, Fiore M, et al. Margin assessment in soft tissue sarcomas: review of the literature. Cancers (Basel). 2021;13(7):1687.

    Article  PubMed  Google Scholar 

  3. O’Donnell PW, Griffin AM, Eward WC, et al. The effect of the setting of a positive surgical margin in soft tissue sarcoma. Cancer. 2014;120(18):2866–75.

    Article  PubMed  Google Scholar 

  4. Liu CY, Yen CC, Chen WM, et al. Soft tissue sarcoma of extremities: the prognostic significance of adequate surgical margins in primary operation and reoperation after recurrence. Ann Surg Oncol. 2010;17(8):2102–11.

    Article  PubMed  Google Scholar 

  5. Traub F, Griffin AM, Wunder JS, Ferguson PC. Influence of unplanned excisions on the outcomes of patients with stage III extremity soft-tissue sarcoma. Cancer. 2018;124(19):3868–75.

    Article  PubMed  Google Scholar 

  6. Gadgeel SM, Harlan LC, Zeruto CA, Osswald M, Schwartz AG. Patterns of care in a population-based sample of soft tissue sarcoma patients in the United States. Cancer. 2009;115(12):2744–54.

    Article  PubMed  Google Scholar 

  7. Bertrand TE, Cruz A, Binitie O, Cheong D, Letson GD. Do surgical margins affect local recurrence and survival in extremity, nonmetastatic, high-grade osteosarcoma? Clin Orthopaed Relat Research. 2016;474(3):677–83.

    Article  Google Scholar 

  8. Ahmad R, Jacobson A, Hornicek F, et al. The width of the surgical margin does not influence outcomes in extremity and truncal soft tissue sarcoma treated with radiotherapy. Oncologist. 2016;21(10):1269–76.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Sharif KF, Prasad K, Miller A, et al. Enhanced intraoperative communication of tumor margins using 3D scanning and mapping: the computer-aided design margin. Laryngoscope. 2023;133(8):1914–8.

    Article  PubMed  Google Scholar 

  10. Miller A, Prasad K, Sharif KF, et al. Virtual 3D specimen mapping in head & neck oncologic surgery. Laryngoscope. Epub 19 Jul 2023. https://doi.org/10.1002/lary.30881.

  11. Sharif KF, Lewis JS Jr, Ely KA, et al. The computer-aided design margin: ex vivo 3D specimen mapping to improve communication between surgeons and pathologists. Head Neck. 2023;45(1):22–31.

    Article  PubMed  Google Scholar 

  12. Brouwer de Koning SG, Schaeffers A, Schats W, van den Brekel MWM, Ruers TJM, Karakullukcu MB. Assessment of the deep resection margin during oral cancer surgery: a systematic review. Eur J Surg Oncol. 2021;47(9):2220–32.

    Article  CAS  PubMed  Google Scholar 

  13. Boyd J, Jonard B, Weiner S. Desmoplastic fibroma in the distal humerus of a 14-year-old boy: a case report. JBJS Case Connect. 2019;9(4):e0155.

    Article  PubMed  Google Scholar 

  14. Tanwar YS, Kharbanda Y, Rastogi R, Singh R. Desmoplastic fibroma of bone: a case series and review of literature. Indian J Surg Oncol. 2018;9(4):585–91.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Evans S, Ramasamy A, Jeys L, Grimer R. Desmoplastic fibroma of bone: a rare bone tumour. J Bone Oncol. 2014;3(3–4):77–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Papke DJ, Hung YP, Schaefer IM, et al. Clinicopathologic characterization of malignant chondroblastoma: a neoplasm with locally aggressive behavior and metastatic potential that closely mimics chondroblastoma-like osteosarcoma. Mod Pathol. 2020;33(11):2295–306.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Visgauss JD, Lazarides A, Dickson B, et al. Treatment of chondroblastoma with denosumab: a case report with a correlative analysis of effect on the RANK signaling pathway. JBJS Case Connect. 2021;11(2):e20.

    Article  Google Scholar 

  18. Focaccia M, Gambarotti M, Hakim R, et al. Chondroblastoma’s lung metastases treated with denosumab in pediatric patient. Cancer Res Treat. 2021;53(1):279–82.

    Article  CAS  PubMed  Google Scholar 

  19. Suster DI, Kurzawa P, Neyaz A, et al. Chondroblastoma expresses RANKL by RNA in situ hybridization and may respond to denosumab therapy. Am J Surg Pathol. 2020;44(12):1581–90.

    Article  PubMed  Google Scholar 

  20. Gao RW, Teraphongphom NT, van den Berg NS, et al. Determination of tumor margins with surgical specimen mapping using near-infrared fluorescence. Cancer Res. 2018;78(17):5144–54.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Tummers WS, Warram JM, van den Berg NS, et al. Recommendations for reporting on emerging optical imaging agents to promote clinical approval. Theranostics. 2018;8(19):5336–47.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. VanKoevering KK, Hollister SJ, Green GE. Advances in 3-dimensional printing in otolaryngology: a review. JAMA Otolaryngol Head Neck Surg. 2017;143(2):178–83.

    Article  PubMed  Google Scholar 

  23. de Boer E, Moore LS, Warram JM, et al. On the horizon: Optical imaging for cutaneous squamous cell carcinoma. Head Neck. 2016;38(Suppl 1):E2204-2213.

    PubMed  Google Scholar 

  24. de Boer E, Harlaar NJ, Taruttis A, et al. Optical innovations in surgery. Br J Surg. 2015;102(2):e56-72.

    Article  PubMed  Google Scholar 

  25. Farahani N, Braun A, Jutt D, et al. Three-dimensional imaging and scanning: current and future applications for pathology. J Pathol Inform. 2017;8:36.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Harmsen S, Teraphongphom N, Tweedle MF, Basilion JP, Rosenthal EL. Optical surgical navigation for precision in tumor resections. Mol Imaging Biol. 2017;19(3):357–62.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Keshtgar MR, Chicken DW, Austwick MR, et al. Optical scanning for rapid intraoperative diagnosis of sentinel node metastases in breast cancer. Br J Surg. 2010;97(8):1232–9.

    Article  CAS  PubMed  Google Scholar 

  28. van Keulen S, Nishio N, Fakurnejad S, et al. the clinical application of fluorescence-guided surgery in head and neck cancer. J Nucl Med. 2019;60(6):758–63.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Nguyen JQ, Gowani ZS, O’Connor M, et al. Intraoperative Raman spectroscopy of soft tissue sarcomas. Lasers Surg Med. 2016;48(8):774–81.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Kerawala CJ, Ong TK. Relocating the site of frozen sections–is there room for improvement? Head Neck. 2001;23(3):230–2.

    Article  CAS  PubMed  Google Scholar 

  31. Coutu B, Ryan E, Christensen D, et al. Positive margins matter regardless of subsequent resection findings. Oral Oncol. 2022;128:105850.

    Article  PubMed  Google Scholar 

  32. Prasad K, Sharma R, Habib D, et al. How often is cancer present in oral cavity re-resections after initial positive margins? Laryngoscope. Epub 16 Aug 2023. https://doi.org/10.1002/lary.30959.

  33. Ettl T, El-Gindi A, Hautmann M, et al. Positive frozen section margins predict local recurrence in R0-resected squamous cell carcinoma of the head and neck. Oral Oncol. 2016;55:17–23.

    Article  PubMed  Google Scholar 

  34. Buchakjian MR, Ginader T, Tasche KK, Pagedar NA, Smith BJ, Sperry SM. Independent predictors of prognosis based on oral cavity squamous cell carcinoma surgical margins. Otolaryngol Head Neck Surg. 2018;159(4):675–82.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Priya SR, D’Cruz AK, Pai PS. Cut margins and disease control in oral cancers. J Cancer Res Therap. 2012;8(1):74–9.

    Article  CAS  Google Scholar 

  36. Haas RL, Delaney TF, O’Sullivan B, et al. Radiotherapy for management of extremity soft tissue sarcomas: why, when, and where? Int J Radiat Oncol Biol Phys. 2012;84(3):572–80.

    Article  PubMed  Google Scholar 

  37. Mills GL. CORR Insights®: ninety percent or greater tumor necrosis is associated with survival and social determinants of health in patients with osteosarcoma in the national cancer database. Clin Orthop Relat Res. 2023;481(3):523–5.

    Article  PubMed  Google Scholar 

  38. Richardson SM, Wurtz LD, Collier CD. Ninety percent or greater tumor necrosis is associated with survival and social determinants of health in patients with osteosarcoma in the national cancer database. Clin Orthop Relat Res. 2023;481(3):512–22.

    Article  PubMed  Google Scholar 

  39. Tsuda Y, Tsoi K, Parry MC, et al. Impact of chemotherapy-induced necrosis on event-free and overall survival after preoperative MAP chemotherapy in patients with primary high-grade localized osteosarcoma. Bone Joint J. 2020;102-B(6):795–803.

    Article  PubMed  Google Scholar 

  40. Simon MA, Hecht JD. Invasion of joints by primary bone sarcomas in adults. Cancer. 1982;50(8):1649–55.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgment

JMC is supported by the National Institute of General Medical Sciences (NIGMS) of the National Institutes of Health under award number T32GM007347. The content in this report is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Funding

This work was supported by a Vanderbilt Clinical Oncology Research Career Development Program (K12 NCI 2K12CA090625-22A1) and an ACS Institutional Research Grant (#IRG-19-139-60).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Michael C. Topf MD.

Ethics declarations

Disclosures

Kayvon Sharif: USPTO application number: 63/351,292. Patent application title: Three-Dimensional Models of Surgical Margins. Juan M. Colazo, Kavita Prasad, Alexis Miller, Marina Aweeda, Carly Fassler, Reena Singh, Herbert S. Schwartz, Joshua M. Lawrenz, Ginger E. Holt, and Michael C. Topf have no conflicts of interest to declare in relation to this work.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 5992 KB)

Supplementary file2 (MP4 1292 KB)

Supplementary file3 (MP4 9912 KB)

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Colazo, J.M., Prasad, K., Miller, A. et al. 3D Specimen Scanning and Mapping in Musculoskeletal Oncology: A Feasibility Study. Ann Surg Oncol 31, 2051–2060 (2024). https://doi.org/10.1245/s10434-023-14757-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1245/s10434-023-14757-w

Keywords

Navigation