Analyze Diet
Veterinary sciences2026; 13(7); 691; doi: 10.3390/vetsci13070691

Electrochemotherapy Following Surgical Cytoreduction for the Treatment of Recurrent Equine Sarcoids: A Retrospective Study of 23 Lesions.

Abstract: Despite the wide range of therapeutic options currently available for equine sarcoids, recurrence of these lesions remains a major clinical challenge. Consequently, the identification of effective strategies for the management of recurrent sarcoids remains an important objective in equine oncology. The aim of this retrospective study was to evaluate the clinical outcome of surgical cytoreduction combined with intraoperative electrochemotherapy in horses affected by recurrent equine sarcoids. Medical records of horses treated between July 2018 and August 2025 at the Veterinary Teaching Hospital of the University of Bologna were retrospectively reviewed. Data collected included signalment, lesion location, clinical subtype, lesion size, chemotherapeutic agent used, recurrence status, and follow-up duration. Fourteen horses presenting 23 recurrent sarcoid lesions met the inclusion criteria. Recurrence was evaluated at both the lesion and horse levels. Local tumour control was achieved in 16 of 23 lesions (69.6%). Recurrence was observed in 7 lesions, corresponding to a lesion-based recurrence rate of 30.4%, and in 5 of 14 horses (35.7%). Malignant and fibroblastic lesions showed higher recurrence rates than other clinical subtypes, whereas larger lesions tended to recur more frequently than smaller lesions. No significant differences were identified between cisplatin- and carboplatin-treated lesions. Surgical cytoreduction combined with intraoperative electrochemotherapy provided encouraging local tumour control in a population composed exclusively of recurrent sarcoids. This treatment protocol may represent a valuable therapeutic option for horses with local recurrence of sarcoids, although larger prospective studies are required to further define prognostic factors and long-term outcomes.
Publication Date: 2026-07-16 PubMed ID: 42514702PubMed Central: PMC13418348DOI: 10.3390/vetsci13070691Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

Overview

  • This study analyzed the effectiveness of combining surgical removal and electrochemotherapy to treat recurrent equine sarcoids, a common skin tumor in horses, and found this approach resulted in good local control in the majority of treated lesions.

Background

  • Equine sarcoids are skin tumors in horses that often recur despite various available treatments.
  • Recurrent sarcoids are a significant clinical problem in equine oncology, necessitating improved management strategies.
  • Electrochemotherapy involves applying electrical pulses to tumors to increase chemotherapy drug uptake and improve treatment efficacy.
  • This study focused on evaluating surgical cytoreduction (removal of most tumor tissue) combined with intraoperative electrochemotherapy for recurrent sarcoids.

Study Design and Methods

  • This was a retrospective study reviewing medical records from July 2018 to August 2025 at the Veterinary Teaching Hospital of the University of Bologna.
  • Inclusion criteria: horses with recurrent sarcoids who underwent surgical cytoreduction followed by intraoperative electrochemotherapy.
  • Data collected included:
    • Horse signalment (age, breed, sex)
    • Lesion location on the horse
    • Clinical subtype of sarcoid (e.g., malignant, fibroblastic)
    • Size of lesions
    • Type of chemotherapy agent used (cisplatin or carboplatin)
    • Recurrence status during follow-up
    • Duration of follow-up
  • Recurrence was evaluated at both individual lesion and horse levels.

Results

  • 14 horses with 23 recurrent sarcoid lesions were included.
  • Local tumor control was achieved in 16 out of 23 lesions, indicating a 69.6% success rate.
  • Recurrence occurred in:
    • 7 lesions (30.4% lesion-level recurrence rate)
    • 5 horses (35.7% horse-level recurrence rate)
  • Higher recurrence rates were observed in malignant and fibroblastic sarcoid subtypes compared to other types.
  • Larger lesions tended to recur more often than smaller ones.
  • No statistically significant difference in recurrence was found between lesions treated with cisplatin versus carboplatin.

Conclusions and Implications

  • The combination of surgical cytoreduction and intraoperative electrochemotherapy showed encouraging local tumor control in recurrent equine sarcoids.
  • This treatment approach may be a valuable option for managing horses with locally recurrent sarcoids.
  • Because the study was retrospective and involved a relatively small number of cases, further larger prospective studies are needed.
  • Future research should focus on:
    • Confirming prognostic factors that influence treatment success
    • Evaluating long-term outcomes and recurrence rates over extended follow-up periods
    • Comparing the effectiveness of different chemotherapeutic agents in electrochemotherapy protocols
  • Overall, this study provides promising evidence that combining surgery with electrochemotherapy may improve treatment results in challenging recurrent equine sarcoids.

Cite This Article

APA
Spadari A, Meistro F, Tornago R, Facchetti C, D'Angelo P, Ralletti MV, Montemagno S, Rinnovati R. (2026). Electrochemotherapy Following Surgical Cytoreduction for the Treatment of Recurrent Equine Sarcoids: A Retrospective Study of 23 Lesions. Vet Sci, 13(7), 691. https://doi.org/10.3390/vetsci13070691

Publication

ISSN: 2306-7381
NlmUniqueID: 101680127
Country: Switzerland
Language: English
Volume: 13
Issue: 7
PII: 691

Researcher Affiliations

Spadari, Alessandro
  • Department of Veterinary Medical Sciences, University of Bologna, Ozzano dell'Emilia, 40064 Bologna, Italy.
Meistro, Federica
  • Department of Veterinary Medical Sciences, University of Bologna, Ozzano dell'Emilia, 40064 Bologna, Italy.
Tornago, Raimondo
  • Independent Researcher, 39012 Merano, Italy.
Facchetti, Cristian
  • Department of Veterinary Medical Sciences, University of Bologna, Ozzano dell'Emilia, 40064 Bologna, Italy.
D'Angelo, Paola
  • Department of Veterinary Medical Sciences, University of Bologna, Ozzano dell'Emilia, 40064 Bologna, Italy.
Ralletti, Maria Virginia
  • Department of Veterinary Medical Sciences, University of Bologna, Ozzano dell'Emilia, 40064 Bologna, Italy.
Montemagno, Salvatore
  • Department of Veterinary Medical Sciences, University of Bologna, Ozzano dell'Emilia, 40064 Bologna, Italy.
Rinnovati, Riccardo
  • Department of Veterinary Medical Sciences, University of Bologna, Ozzano dell'Emilia, 40064 Bologna, Italy.

Conflict of Interest Statement

The authors declare no conflicts of interest.

References

This article includes 48 references
  1. Taylor S, Haldorson G. A Review of Equine Sarcoid. Equine Vet. Educ. 2013;25:210–216.
  2. Knottenbelt DC. A Suggested Clinical Classification for the Equine Sarcoid. Clin. Tech. Equine Pract. 2005;4:278–295.
  3. Hollis AR. Management of Equine Sarcoids. Vet. J. 2023;291:105926.
    doi: 10.1016/j.tvjl.2022.105926pubmed: 36334801google scholar: lookup
  4. Parkinson NJ, Ward A, Malbon AJ, Reardon RJM, Kelly PG. Bovine Papillomavirus Gene Expression and Inflammatory Pathway Activation Vary between Equine Sarcoid Tumour Subtypes. Vet. Immunol. Immunopathol. 2024;277:110838.
    doi: 10.1016/J.VETIMM.2024.110838pubmed: 39357074google scholar: lookup
  5. Chambers G, Ellsmore VA, O’Brien PM, Reid SWJ, Love S, Campo MS, Nasir L. Association of Bovine Papillomavirus with the Equine Sarcoid. J. Gen. Virol. 2003;84:1055–1062.
    doi: 10.1099/VIR.0.18947-0pubmed: 12692268google scholar: lookup
  6. Haralambus R, Burgstaller J, Klukowska-Rötzler J, Steinborn R, Buchinger S, Gerber V, Brandt S. Intralesional Bovine Papillomavirus DNA Loads Reflect Severity of Equine Sarcoid Disease. Equine Vet. J. 2010;42:327–331.
  7. Yuan ZQ, Gault EA, Gobeil P, Nixon C, Campo MS, Nasir L. Establishment and Characterization of Equine Fibroblast Cell Lines Transformed in Vivo and in Vitro by BPV-1: Model Systems for Equine Sarcoids. Virology 2008;373:352–361.
    doi: 10.1016/j.virol.2007.11.037pubmed: 18191170google scholar: lookup
  8. Martens A, De Moor A, Demeulemeester J, Ducatelle R. Histopathological Characteristics of Five Clinical Types of Equine Sarcoid. Res. Vet. Sci. 2000;69:295–300.
    doi: 10.1053/rvsc.2000.0432pubmed: 11124103google scholar: lookup
  9. Martens A, De Moor A, Vlaminck L, Pille F, Steenhaut M. Evaluation of Excision, Cryosurgery and Local BCG Vaccination for the Treatment of Equine Sarcoids. Vet. Rec. 2001;149:665–669.
    doi: 10.1136/VR.149.22.665pubmed: 11765322google scholar: lookup
  10. Smith CH, Stewart HL, Stefanovski D, Levine DG. Outcomes Following Autologous Tumor Tissue Implantation with or without Concurrent Antineoplastic Therapies in the Treatment of Sarcoids in 50 Equids. Front. Vet. Sci. 2025;12:1559519.
    doi: 10.3389/fvets.2025.1559519pmc: PMC12098570pubmed: 40417356google scholar: lookup
  11. Galant L, Delverdier M, Lucas MN, Raymond-Letron I, Teissie J, Tamzali Y. Calcium Electroporation: The Bioelectrochemical Treatment of Spontaneous Equine Skin Tumors Results in a Local Necrosis. Bioelectrochemistry 2019;129:251–258.
  12. Karalus W, Subharat S, Orbell G, Vaatstra B, Munday JS. Equine Sarcoids: A Clinicopathologic Study of 49 Cases, with Mitotic Count and Clinical Type Predictive of Recurrence. Vet. Pathol. 2024;61:357–365.
    doi: 10.1177/03009858231209408pmc: PMC11067406pubmed: 37937724google scholar: lookup
  13. Ogłuszka M, Starzyński RR, Pierzchała M, Otrocka-Domagała I, Raś A. Equine Sarcoids—Causes, Molecular Changes, and Clinicopathologic Features: A Review. Vet. Pathol. 2021;58:472–482.
    doi: 10.1177/0300985820985114pubmed: 33461443google scholar: lookup
  14. . Macroscopical and Histopathological Changes in Regressing Primary and Recurrent Equine Sarcoids During Active Specific Bio-Immunotherapy—PubMed. .
    pubmed: 15999546
  15. Offer KS, Dixon CE, Sutton DGM. Treatment of Equine Sarcoids: A Systematic Review. Equine Vet. J. 2024;56:12–25.
    doi: 10.1111/EVJ.13935pubmed: 36917551google scholar: lookup
  16. Tellado M, Mir L.M, Maglietti F. Veterinary Guidelines for Electrochemotherapy of Superficial Tumors. Front. Vet. Sci. 2022;9:868989.
    doi: 10.3389/FVETS.2022.868989pmc: PMC9363792pubmed: 35968026google scholar: lookup
  17. Spugnini E.P., Baldi A. Electrochemotherapy in Veterinary Oncology: State-of-the-Art and Perspectives. Vet. Clin. N. Am. Small Anim. Pract. 2019;49:967–979.
    doi: 10.1016/j.cvsm.2019.04.006pubmed: 31176458google scholar: lookup
  18. Tamzali Y, Borde L, Rols M.P., Golzio M, Lyazrhi F, Teissie J. Successful Treatment of Equine Sarcoids with Cisplatin Electrochemotherapy: A Retrospective Study of 48 Cases. Equine Vet. J. 2012;44:214–220.
  19. Théon A.P., Wilson W.D., Magdesian K.G., Pusterla N., Snyder J.R., Galuppo L.D. Long-Term Outcome Associated with Intratumoral Chemotherapy with Cisplatin for Cutaneous Tumors in Equidae: 573 Cases (1995–2004). J. Am. Vet. Med. Assoc. 2007;230:1506–1513.
    doi: 10.2460/javma.230.10.1506pubmed: 17504043google scholar: lookup
  20. Tozon N, Kramaric P, Kos Kadunc V, Sersa G, Cemazar M. Electrochemotherapy as a Single or Adjuvant Treatment to Surgery of Cutaneous Sarcoid Tumours in Horses: A 31-Case Retrospective Study. Vet. Rec. 2016;179:627.
    doi: 10.1136/VR.103867pubmed: 27758950google scholar: lookup
  21. Igna C, Zaha C. REVIEW OF THERAPEUTICAL MANAGEMENT OF EQUINE SARCOID. Sci. Works Ser. C Vet. Med. 2021;LXVII:65–72.
  22. Finlay M, Yuan Z.Q., Burden F, Trawford A, Morgan I.M., Saveria Campo M, Nasir L. The Detection of Bovine Papillomavirus Type 1 DNA in Flies. Virus Res. 2009;144:315–317.
  23. Haspeslagh M, Vlaminck L, Martens A. The Possible Role of Stomoxys Calcitrans in Equine Sarcoid Transmission. Vet. J. 2018;231:8–12.
    doi: 10.1016/J.TVJL.2017.11.009pubmed: 29429489google scholar: lookup
  24. Funiciello B, Roccabianca P, Funiciello B, Roccabianca P. Equine Science. .
    doi: 10.5772/INTECHOPEN.91013google scholar: lookup
  25. Bogaert L, Martens A, Depoorter P, Gasthuys F. Equine Sarcoids—Part 2: Current Treatment Modalities. Vlaams Diergeneeskd. Tijdschr. 2008;77:62–67.
    doi: 10.21825/VDT.87196google scholar: lookup
  26. Knottenbelt D.C.. The Equine Sarcoid: Why Are There so Many Treatment Options?. Vet. Clin. N. Am. Equine Pract. 2019;35:243–262.
    doi: 10.1016/J.CVEQ.2019.03.006pubmed: 31097356google scholar: lookup
  27. Knottenbelt D.C., Kelly D.F.. The Diagnosis and Treatment of Periorbital Sarcoid in the Horse: 445 Cases from 1974 to 1999. Vet. Ophthalmol. 2000;3:169–191.
  28. Rashmir A.M., Hollis A., Knottenbelt D., Alfolter V.K., Unger L., Petersen A., Koch C. Equine Sarcoid Consensus Statement February 2026. .
  29. Goodrich L, Gerber H, Marti E, Antczak D.F.. Equine Sarcoids. Vet. Clin. N. Am. Equine Pract. 1998;14:607–623.
    doi: 10.1016/S0749-0739(17)30189-Xpubmed: 9891727google scholar: lookup
  30. Knottenbelt D.C.. Equine Wound Management: Are There Significant Differences in Healing at Different Sites on the Body?. Vet. Dermatol. 1997;8:273–290.
  31. Melinyshyn H. Multiple Excisions of an Equine Sarcoid and the Repercussions.. Can. Vet. J. 2019;60:1115.
    pmc: PMC6741832pubmed: 31597999
  32. Broström H. Equine Sarcoids. A Clinical and Epidemiological Study in Relation to Equine Leucocyte Antigens (ELA). Acta Vet. Scand. 1995;36:223.
    doi: 10.1186/BF03547691pmc: PMC8095413pubmed: 7484549google scholar: lookup
  33. Knottenbelt D.C., Schumacher J., Toth F. Equine Wound Management. 3rd ed. John Wiley & Sons; Hoboken, NJ, USA: 2016. Sarcoid Transformation at Wound Sites; pp. 490–507.. .
  34. Zhang C., Xu C., Gao X., Yao Q. Platinum-Based Drugs for Cancer Therapy and Anti-Tumor Strategies.. Theranostics 2022;12:2115.
    doi: 10.7150/THNO.69424pmc: PMC8899578pubmed: 35265202google scholar: lookup
  35. Vermorken J.B., Ten W.W., Huinink B., Eisenhauer E.A., Favalli G., Belpomme D., Conte P.F., Kaye S.B. Carboplatin versus Cisplatin.. Ann. Oncol. 1993;4:S41–S48.
    doi: 10.1093/annonc/4.suppl_4.S41pubmed: 8312200google scholar: lookup
  36. Fretz P.B., Barber S.M. Prospective Analysis Cryosurgery as the Sole Treatment for Equine Sarcoids.. Vet. Clin. N. Am. Small Anim. Pract. 1980;10:847–859.
    doi: 10.1016/S0195-5616(80)50085-9pubmed: 6972661google scholar: lookup
  37. Farris H.E., Fraunfelder F.T., Mason C.T. Cryotherapy of Equine Sarcoid and Other Lesions.. Vet. Med. Small Anim. Clin. 1976;71:325–329.
    pubmed: 1045702
  38. Curnow B., Rich A.F., Ireland J., Cubillos Correa D., Dunn J., Jenkins D., Carslake H., Ressel L. Histological Evidence of Superficial Inflammation Is Associated with Lower Recurrence of Equine Sarcoids Following Surgical Removal: A Follow-Up Study of 106 Tumours in 64 Horses.. Vet. J. 2023;292:105953.
    doi: 10.1016/j.tvjl.2023.105953pubmed: 36775186google scholar: lookup
  39. Monteiro M.M., de Castro E.L.A., Pereira A.J.M., Thiesen R., Thiesen R.M.C., Salvarani F.M. BCG Immunotherapy in Equine Sarcoid Treatment: Mechanisms, Clinical Efficacy, and Challenges in Veterinary Oncology.. Viruses 2025;17:1322.
    doi: 10.3390/v17101322pmc: PMC12567874pubmed: 41157593google scholar: lookup
  40. Caston S.S., Sponseller B.A., Dembek K.A., Hostetter J.M. Evaluation of Locally Injected Mycobacterium Cell Wall Fraction in Horses with Sarcoids.. J. Equine Vet. Sci. 2020;90:103102.
    doi: 10.1016/j.jevs.2020.103102pubmed: 32534762google scholar: lookup
  41. Studer U., Marti E., Stornetta D., Lazary S., Gerber H. The Therapy of Equine Sarcoid with a Non-Specific Immunostimulator--the Epidemiology and Spontaneous Regression of Sarcoids.. Schweiz. Arch. Tierheilkd. 1997;189:385–391.
    pubmed: 9411736
  42. Jindra C., Hainisch E.K., Brandt S. Immunotherapy of Equine Sarcoids—From Early Approaches to Innovative Vaccines.. Vaccines 2023;11:769.
    doi: 10.3390/VACCINES11040769pmc: PMC10145708pubmed: 37112681google scholar: lookup
  43. Pettersson C.M., Broström H., Humblot P., Bergvall K.E. Topical Treatment of Equine Sarcoids with Imiquimod 5% Cream or Sanguinaria Canadensis and Zinc Chloride—An Open Prospective Study.. Vet. Dermatol. 2020;31:471-e126.
    doi: 10.1111/VDE.12900pubmed: 33016520google scholar: lookup
  44. Stewart A.A., Rush B., Davis E. The Efficacy of Intratumoural 5-Fluorouracil for the Treatment of Equine Sarcoids.. Aust. Vet. J. 2006;84:101–106.
  45. Ribeiro G., Carvalho L., Borges J., Prazeres J. The Best Protocol to Treat Equine Skin Wounds by Second Intention Healing: A Scoping Review of the Literature.. Animals 2024;14:1500.
    doi: 10.3390/ANI14101500pmc: PMC11117370pubmed: 38791717google scholar: lookup
  46. Prpich CY, Santamaria AC, Simcock JO, Wong HK, Nimmo JS, Kuntz CA. Second Intention Healing after Wide Local Excision of Soft Tissue Sarcomas in the Distal Aspects of the Limbs in Dogs: 31 Cases (2005–2012). J. Am. Vet. Med. Assoc. 2014;244:187–194.
    doi: 10.2460/JAVMA.244.2.187pubmed: 24378028google scholar: lookup
  47. Laurenza C, Ansart L, Portier K. Risk Factors of Anesthesia-Related Mortality and Morbidity in One Equine Hospital: A Retrospective Study on 1,161 Cases Undergoing Elective or Emergency Surgeries. Front. Vet. Sci. 2020;6:514.
    doi: 10.3389/fvets.2019.00514pmc: PMC6990105pubmed: 32039253google scholar: lookup
  48. Kiernan M, Baiocchi MT. Casting New Light on Statistical Power: An Illuminating Analogy and Strategies to Avoid Underpowered Trials. Am. J. Epidemiol. 2022;191:1500.
    doi: 10.1093/AJE/KWAC019pmc: PMC9989344pubmed: 35292796google scholar: lookup

Citations

This article has been cited 0 times.