In the treatment of highly malignant skin tumors postoperative radiotherapy may be indicated after wound closure. In the University Hospital Carl Gustav Carus Dresden, Germany, a retrospective study of 75 patients, who received postoperative radiotherapy after wound closure, was conducted. In all 75 patients (56 male, 19 female), radical doses of irradiation (40-70 Gy in 20–35 fractions) were administered. The median time interval between surgery and radiation therapy was 7 weeks (range 3-48 weeks). The incidence of wound healing complications (WHCs) increased after radiotherapy (p<0.001). Univariable analysis showed that WHCs were associated with immunosuppression (p=0.002), split thickness skin graft (p=0.007) lymphoma or leukemia (p=0.032) and diabetes mellitus (p=0.046). Multivariable logistic regression showed that independent risk factors for WHCs were split thickness skin transplantation (odds ratio: 3.85, 95% confidence interval (CI): 1.13–13.1, p=0.031) and immunosuppression (odds ratio: 4.69, 95% CI: 1.18–18.7, p=0.029). The authors observed no association between surgical site infections and WHCs (p=1.0). Univariable analysis showed that SSIs were associated with leukemia or lymphoma (p=0.019). Together, the results show an increased incidence of WHCs after radiotherapy. Other conditions associated with WHCs were leukemia or lymphoma and diabetes mellitus. Immunosuppression and split thickness skin transplantation were independent risk factors for WHCs.
Published in | Journal of Surgery (Volume 10, Issue 2) |
DOI | 10.11648/j.js.20221002.13 |
Page(s) | 67-74 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2022. Published by Science Publishing Group |
Non-melanoma Skin Cancer, Wound Healing Complications, Adjuvant Radiotherapy, Wound Closure Techniques, Diabetes Complications, Retrospective Studies
[1] | Artamonova I, Schmitt L, Yazdi AS, Megahed M, Felbert V von, Balakirski G. Postoperative complications in dermatological patients undergoing microscopically controlled surgery in inpatient setting (next-day surgery): A single-center epidemiological study. J Dtsch Dermatol Ges. 2020; 18 (12): 1437-1446. doi: 10.1111/ddg.14148. |
[2] | Bakkour W, Purssell H, Chinoy H, Griffiths CEM, Warren RB. The risk of post-operative complications in psoriasis and psoriatic arthritis patients on biologic therapy undergoing surgical procedures. J Eur Acad Dermatol Venereol. 2016; 30 (1): 86-91. doi: 10.1111/jdv.12997. |
[3] | Balakirski G, Kotliar K, Pauly KJ, et al. Surgical Site Infections After Dermatologic Surgery in Immunocompromised Patients: A Single-Center Experience. Dermatol Surg. 2018; 44 (12): 1525-1536. doi: 10.1097/DSS.0000000000001615. |
[4] | Crişan D, Colosi HA, Manea A, et al. Retrospective Analysis of Complication Rates Associated With Auricular Reconstruction After Skin Cancer Surgery. J Cutan Med Surg. 2020; 24 (2): 137-143. doi: 10.1177/1203475419890841. |
[5] | Futoryan T, Grande D. Postoperative wound infection rates in dermatologic surgery. Dermatol Surg. 1995; 21 (6): 509-514. doi: 10.1111/j.1524-4725.1995.tb00255.x. |
[6] | Lee DH, Kim SY, Nam SY, Choi S-H, Choi JW, Roh J-L. Risk factors of surgical site infection in patients undergoing major oncological surgery for head and neck cancer. Oral Oncol. 2011; 47 (6): 528-531. doi: 10.1016/j.oraloncology.2011.04.002. |
[7] | Lee YK, Park KY, Koo YT, et al. Analysis of multiple risk factors affecting the result of free flap transfer for necrotising soft tissue defects of the lower extremities in patients with type 2 diabetes mellitus. J Plast Reconstr Aesthet Surg. 2014; 67 (5): 624-628. doi: 10.1016/j.bjps.2014.01.047. |
[8] | Berking Carola, Garbe Claus, Leiter Ulrike, Heppt Markus, Steeb Theresa, Amaral Teresa, Noor Seema. S3-Leitlinie Aktinische Keratose und Plattenepithelkarzinom der Haut. https://www.leitlinienprogramm-onkologie.de/fileadmin/user_upload/Downloads/Leitlinien/Aktinische_Keratosen_und_PEK/LL_Aktinische_Keratosen_PEK_Langversion_1.1.pdf. |
[9] | Likhacheva A, Awan M, Barker CA, et al. Definitive and Postoperative Radiation Therapy for Basal and Squamous Cell Cancers of the Skin: Executive Summary of an American Society for Radiation Oncology Clinical Practice Guideline. Pract Radiat Oncol. 2020; 10 (1): 8-20. doi: 10.1016/j.prro.2019.10.014. |
[10] | Becker Jürgen C., Eigentler Thomas, Frerich Bernhard, Gambichler Thilo, Grabbe Stephan, Hölle Ulrike, Klumpp Bernhard, Loquai Carmen, Krause-Bergmann Albrecht, Müller-Richter Urs, Pföhler Claudia, Schneider-Burrus Sylke, Stang Andreas, Terheyden Patrick, Ugurel Selma, Veith Johannes, Mauch Cornelia. S2k -Leitlinie -Merkelzellkarzinom (MZK, MCC, neuroendokrines Karzinom der Haut) –Update 2018. https://www.awmf.org/uploads/tx_szleitlinien/032-023l_S2k_Merkelzellkarzinom_2018-12.pdf. |
[11] | Shinde A, Verma V, Jones BL, et al. The Effect of Time to Postoperative Radiation Therapy on Survival in Resected Merkel Cell Carcinoma. Am J Clin Oncol. 2019; 42 (8): 636-642. doi: 10.1097/COC.0000000000000565. |
[12] | Auerswald S, Schreml S, Meier R, et al. Wound monitoring of pH and oxygen in patients after radiation therapy. Radiat Oncol. 2019; 14 (1): 199. doi: 10.1186/s13014-019-1413-y. |
[13] | Dormand E-L, Banwell PE, Goodacre TEE. Radiotherapy and wound healing. Int Wound J. 2005; 2 (2): 112-127. doi: 10.1111/j.1742-4801.2005.00079.x. |
[14] | Gieringer M, Gosepath J, Naim R. Radiotherapy and wound healing: principles, management and prospects (review). Oncol Rep. 2011; 26 (2): 299-307. doi: 10.3892/or.2011.1319. |
[15] | Haubner F, Ohmann E, Pohl F, Strutz J, Gassner HG. Wound healing after radiation therapy: review of the literature. Radiat Oncol. 2012: 162. doi: 10.1186/1748-717X-7-162. |
[16] | Karalashvili L, Mardaleishvili K, Uhryn M, Chakhunashvili D, Kakabadze Z. CURRENT CONDITION AND CHALLENGES IN TREATMENT OF NON-HEALING WOUND AFTER RADIATION THERAPY (REVIEW). Georgian Med News. 2018; (280-281): 23-28. |
[17] | Koerdt S, Rohleder NH, Rommel N, et al. An expression analysis of markers of radiation-induced skin fibrosis and angiogenesis in wound healing disorders of the head and neck. Radiat Oncol. 2015; 10: 202. doi: 10.1186/s13014-015-0508-3. |
[18] | Tadjalli HE, Evans GR, Gürlek A, Beller TC, Ang KK, Stephens LC. Skin graft survival after external beam irradiation. Plast Reconstr Surg. 1999; 103 (7): 1902-1908. doi: 10.1097/00006534-199906000-00015. |
[19] | Tibbs MK. Wound healing following radiation therapy: a review. Radiother Oncol. 1997; 42 (2): 99-106. doi: 10.1016/s0167-8140(96)01880-4. |
[20] | Wang J, Boerma M, Fu Q, Hauer-Jensen M. Radiation responses in skin and connective tissues: effect on wound healing and surgical outcome. Hernia. 2006; 10 (6): 502-506. doi: 10.1007/s10029-006-0150-y. |
[21] | Wang Q, Dickson GR, Carr KE. The effect of graft-bed irradiation on the healing of rat skin grafts. J Invest Dermatol. 1996; 106 (5): 1053-1057. doi: 10.1111/1523-1747.ep12338649. |
[22] | Olascoaga A, Vilar-Compte D, Poitevin-Chacón A, Contreras-Ruiz J. Wound healing in radiated skin: pathophysiology and treatment options. Int Wound J. 2008; 5 (2): 246-257. doi: 10.1111/j.1742-481X.2008.00436.x. |
[23] | Rohleder NH, Flensberg S, Bauer F, et al. Can tissue spectrophotometry and laser Doppler flowmetry help to identify patients at risk for wound healing disorders after neck dissection? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014; 117 (3): 302-311. doi: 10.1016/j.oooo.2013.11.497. |
[24] | Sumi Y, Ueda M, Kaneda T, Eto K. Effects of irradiation on grafted skin. J Oral Maxillofac Surg. 1983; 41 (9): 586-591. doi: 10.1016/0278-2391(83)90161-1. |
[25] | Sumi Y, Ueda M, Oka T, Torii S. Effects of irradiation of skin flaps. J Oral Maxillofac Surg. 1984; 42 (7): 447-452. doi: 10.1016/0278-2391(84)90231-3. |
[26] | Bui DT, Chunilal A, Mehrara BJ, Disa JJ, Alektiar KM, Cordeiro PG. Outcome of split thickness skin grafts after external beam radiotherapy. Ann Plast Surg. 2004; 52 (6): 551-6; discussion 557. doi: 10.1097/01.sap.0000123353.71205.43. |
[27] | Lal ST, Banipal RPS, Bhatti DJ. Tolerance of skin grafts to postoperative radiotherapy. Int J Appl Basic Med Res. 2015; 5 (3): 187-189. doi: 10.4103/2229-516X.165382. |
[28] | Azad TD, Varshneya K, Herrick DB, et al. Timing of Adjuvant Radiation Therapy and Risk of Wound-Related Complications Among Patients With Spinal Metastatic Disease. Global Spine J. 2021; 11 (1): 44-49. doi: 10.1177/2192568219889363. |
[29] | Itshayek E, Yamada J, Bilsky M, et al. Timing of surgery and radiotherapy in the management of metastatic spine disease: a systematic review. Int J Oncol. 2010; 36 (3): 533-544. |
[30] | Kumar N, Madhu S, Bohra H, et al. Is there an optimal timing between radiotherapy and surgery to reduce wound complications in metastatic spine disease? A systematic review. Eur Spine J. 2020; 29 (12): 3080-3115. doi: 10.1007/s00586-020-06478-5. |
[31] | Isaacs JH, Stiles WA, Cassisi NJ, Million RR, Parsons JT. Postoperative radiation of open head and neck wounds--updated. Head Neck. 1997; 19 (3): 194-199. doi: 10.1002/(sici)1097-0347(199705)19:3<194:aid-hed5>3.0.co;2-y. |
[32] | Isaacs JH, Thompson WB, Cassisi NJ, Million RR. Postoperative radiation of open head and neck wounds. Laryngoscope. 1987; 97 (3 Pt 1): 267-270. |
[33] | Yusuf M, Gaskins J, Tennant P, Bumpous J, Dunlap N. Survival Impact of Time to Initiation of Adjuvant Radiation for Merkel Cell Carcinoma: An Analysis of the National Cancer Database. Pract Radiat Oncol. 2019; 9 (4): e372-e385. doi: 10.1016/j.prro.2019.03.004. |
[34] | Heal C, Buettner P, Browning S. Risk factors for wound infection after minor surgery in general practice. Med J Aust. 2006; 185 (5): 255-258. doi: 10.5694/j.1326-5377.2006.tb00555.x. |
[35] | Heal CF, Buettner PG, Drobetz H. Risk factors for surgical site infection after dermatological surgery. Int J Dermatol. 2012; 51 (7): 796-803. doi: 10.1111/j.1365-4632.2011.05189.x. |
[36] | El-Hussuna A, Theede K, Olaison G. Increased risk of post-operative complications in patients with Crohn's disease treated with anti-tumour necrosis factor α agents - a systematic review. Dan Med J. 2014; 61 (12): A4975. |
[37] | Ginestal R, Pérez-Köhler B, Pérez-López P, et al. Comparing the influence of two immunosuppressants (fingolimod, azathioprine) on wound healing in a rat model of primary and secondary intention wound closure. Wound Repair Regen. 2019; 27 (1): 59-68. doi: 10.1111/wrr.12685. |
[38] | Schäffer M, Schier R, Napirei M, Michalski S, Traska T, Viebahn R. Sirolimus impairs wound healing. Langenbecks Arch Surg. 2007; 392 (3): 297-303. doi: 10.1007/s00423-007-0174-5. |
[39] | Milosević DB. The different level of immunological recovery after chemotherapy in leukemia and lymphoma patients. J Exp Clin Cancer Res. 2001; 20 (4): 517-522. |
[40] | Parry HM, Stevens T, Oldreive C, et al. NK cell function is markedly impaired in patients with chronic lymphocytic leukaemia but is preserved in patients with small lymphocytic lymphoma. Oncotarget. 2016; 7 (42): 68513-68526. doi: 10.18632/oncotarget.12097. |
[41] | van Bruggen JAC, Martens AWJ, Fraietta JA, et al. Chronic lymphocytic leukemia cells impair mitochondrial fitness in CD8+ T cells and impede CAR T-cell efficacy. Blood. 2019; 134 (1): 44-58. doi: 10.1182/blood.2018885863. |
[42] | Fernandez-Pineda I, Sandoval JA, Jones RM, et al. Gastrostomy Complications in Pediatric Cancer Patients: A Retrospective Single-Institution Review. Pediatr Blood Cancer. 2016; 63 (7): 1250-1253. doi: 10.1002/pbc.25968. |
[43] | Baltzis D, Eleftheriadou I, Veves A. Pathogenesis and treatment of impaired wound healing in diabetes mellitus: new insights. Adv Ther. 2014; 31 (8): 817-836. doi: 10.1007/s12325-014-0140-x. |
[44] | Othman S, Azoury SC, Weber KL, Kovach SJ. Free flap reconstruction of sarcoma defects in the setting of radiation: a ten-year experience. J Plast Surg Hand Surg. 2020; 54 (6): 365-371. doi: 10.1080/2000656X.2020.1791893. |
[45] | Kassel L, Hutton A, Zumach G, Rand J. Systematic review of perioperative use of immunosuppressive agents in patients undergoing bariatric surgery. Surg Obes Relat Dis. 2020; 16 (1): 144-157. doi: 10.1016/j.soard.2019.10.002. |
[46] | Mangrulkar S, Khair PS. Comparison of healing of surgical wounds between diabetics and non-diabetics. J Indian Med Assoc. 2009; 107 (11): 765-770. |
[47] | Ramanujam CL, Han D, Fowler S, Kilpadi K, Zgonis T. Impact of diabetes and comorbidities on split thickness skin grafts for foot wounds. J Am Podiatr Med Assoc. 2013; 103 (3): 223-232. doi: 10.7547/1030223. |
[48] | Bedi M, King DM, DeVries J, Hackbarth DA, Neilson JC. Does Vacuum-assisted Closure Reduce the Risk of Wound Complications in Patients With Lower Extremity Sarcomas Treated with Preoperative Radiation? Clin Orthop Relat Res. 2019; 477 (4): 768-774. doi: 10.1097/CORR.0000000000000371. |
[49] | Singh D, Chopra K, Sabino J, Brown E. Practical Things You Should Know about Wound Healing and Vacuum-Assisted Closure Management. Plast Reconstr Surg. 2020; 145 (4): 839e-854e. doi: 10.1097/PRS.0000000000006652. |
[50] | Eisbruch A, Dawson L. Re-irradiation of head and neck tumors. Benefits and toxicities. Hematol Oncol Clin North Am. 1999; 13 (4): 825-836. doi: 10.1016/s0889-8588(05)70095-2. |
[51] | Panizzon RG. Radiotherapy of skin tumors. Recent Results Cancer Res. 2002; 160: 234-239. doi: 10.1007/978-3-642-59410-6_27. |
APA Style
Hobelsberger, S., Lohaus, F., Löck, S., Rönsch, H., Brütting, J., et al. (2022). Conditions Associated with Wound Healing Complications After Adjuvant Radiotherapy in Patients with Non-Melanoma Skin Cancer: A Retrospective Analysis. Journal of Surgery, 10(2), 67-74. https://doi.org/10.11648/j.js.20221002.13
ACS Style
Hobelsberger, S.; Lohaus, F.; Löck, S.; Rönsch, H.; Brütting, J., et al. Conditions Associated with Wound Healing Complications After Adjuvant Radiotherapy in Patients with Non-Melanoma Skin Cancer: A Retrospective Analysis. J. Surg. 2022, 10(2), 67-74. doi: 10.11648/j.js.20221002.13
@article{10.11648/j.js.20221002.13, author = {Sarah Hobelsberger and Fabian Lohaus and Steffen Löck and Henriette Rönsch and Julia Brütting and Friedegund Meier and Stefan Beissert and Jörg Laske}, title = {Conditions Associated with Wound Healing Complications After Adjuvant Radiotherapy in Patients with Non-Melanoma Skin Cancer: A Retrospective Analysis}, journal = {Journal of Surgery}, volume = {10}, number = {2}, pages = {67-74}, doi = {10.11648/j.js.20221002.13}, url = {https://doi.org/10.11648/j.js.20221002.13}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.js.20221002.13}, abstract = {In the treatment of highly malignant skin tumors postoperative radiotherapy may be indicated after wound closure. In the University Hospital Carl Gustav Carus Dresden, Germany, a retrospective study of 75 patients, who received postoperative radiotherapy after wound closure, was conducted. In all 75 patients (56 male, 19 female), radical doses of irradiation (40-70 Gy in 20–35 fractions) were administered. The median time interval between surgery and radiation therapy was 7 weeks (range 3-48 weeks). The incidence of wound healing complications (WHCs) increased after radiotherapy (p<0.001). Univariable analysis showed that WHCs were associated with immunosuppression (p=0.002), split thickness skin graft (p=0.007) lymphoma or leukemia (p=0.032) and diabetes mellitus (p=0.046). Multivariable logistic regression showed that independent risk factors for WHCs were split thickness skin transplantation (odds ratio: 3.85, 95% confidence interval (CI): 1.13–13.1, p=0.031) and immunosuppression (odds ratio: 4.69, 95% CI: 1.18–18.7, p=0.029). The authors observed no association between surgical site infections and WHCs (p=1.0). Univariable analysis showed that SSIs were associated with leukemia or lymphoma (p=0.019). Together, the results show an increased incidence of WHCs after radiotherapy. Other conditions associated with WHCs were leukemia or lymphoma and diabetes mellitus. Immunosuppression and split thickness skin transplantation were independent risk factors for WHCs.}, year = {2022} }
TY - JOUR T1 - Conditions Associated with Wound Healing Complications After Adjuvant Radiotherapy in Patients with Non-Melanoma Skin Cancer: A Retrospective Analysis AU - Sarah Hobelsberger AU - Fabian Lohaus AU - Steffen Löck AU - Henriette Rönsch AU - Julia Brütting AU - Friedegund Meier AU - Stefan Beissert AU - Jörg Laske Y1 - 2022/03/11 PY - 2022 N1 - https://doi.org/10.11648/j.js.20221002.13 DO - 10.11648/j.js.20221002.13 T2 - Journal of Surgery JF - Journal of Surgery JO - Journal of Surgery SP - 67 EP - 74 PB - Science Publishing Group SN - 2330-0930 UR - https://doi.org/10.11648/j.js.20221002.13 AB - In the treatment of highly malignant skin tumors postoperative radiotherapy may be indicated after wound closure. In the University Hospital Carl Gustav Carus Dresden, Germany, a retrospective study of 75 patients, who received postoperative radiotherapy after wound closure, was conducted. In all 75 patients (56 male, 19 female), radical doses of irradiation (40-70 Gy in 20–35 fractions) were administered. The median time interval between surgery and radiation therapy was 7 weeks (range 3-48 weeks). The incidence of wound healing complications (WHCs) increased after radiotherapy (p<0.001). Univariable analysis showed that WHCs were associated with immunosuppression (p=0.002), split thickness skin graft (p=0.007) lymphoma or leukemia (p=0.032) and diabetes mellitus (p=0.046). Multivariable logistic regression showed that independent risk factors for WHCs were split thickness skin transplantation (odds ratio: 3.85, 95% confidence interval (CI): 1.13–13.1, p=0.031) and immunosuppression (odds ratio: 4.69, 95% CI: 1.18–18.7, p=0.029). The authors observed no association between surgical site infections and WHCs (p=1.0). Univariable analysis showed that SSIs were associated with leukemia or lymphoma (p=0.019). Together, the results show an increased incidence of WHCs after radiotherapy. Other conditions associated with WHCs were leukemia or lymphoma and diabetes mellitus. Immunosuppression and split thickness skin transplantation were independent risk factors for WHCs. VL - 10 IS - 2 ER -