Skip to main content

Advertisement

Log in

Adjuvant chemotherapy reduces the incidence of abdominal hypertrophic scarring following immediate TRAM breast reconstruction

  • Clinical Trial
  • Published:
Breast Cancer Research and Treatment Aims and scope Submit manuscript

Abstract

Among the many factors that affect the degree of completion and satisfaction of breast reconstruction, the scarring is one issue that a surgeon cannot completely control. We hypothesized that the administration of cytotoxic drugs following the immediate breast reconstruction using transverse rectus abdominis musculocutaneous (TRAM) flap might affect the process of scarring, thus resulting in reduced incidence of hypertrophic scarring at the donor site. Data have been collected from 1,000 consecutive patients between July 2001 and December 2009. The relationship between the adjuvant chemotherapy and the incidence of hypertrophic scarring was studied, and the influence of other presumed risk factors was analyzed. The incidence of hypertrophic scarring was 18.6 % (75 of 404) in the non-CTX group and 3.8 % (20 of 530) in the CTX group. Univariate analysis using logistic regression modeling confirmed the statistical significance of the reducing effect of chemotherapy on the incidence of hypertrophic scarring (p < 0.001; OR: 0.172). The incidence of donor-site hypertrophic scarring following immediate TRAM breast reconstruction was found in nearly 20 % of the patients without chemotherapy, showing a significant difference from the patients with chemotherapy. We believe that Asian patients who undergo immediate TRAM breast reconstruction without chemotherapy are a high-risk group that is prone to hypertrophic scarring, requiring active preventive measures.

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

Similar content being viewed by others

References

  1. Li-Tsang CW, Lau JC, Chan CC (2005) Prevalence of hypertrophic scar formation and its characteristics among the Chinese population. Burns 31(5):610–616

    Article  PubMed  Google Scholar 

  2. Alhady SM, Sivanantharajah K (1969) Keloids in various races. A review of 175 cases. Plast Reconstr Surg 44(6):564–566

    Article  PubMed  CAS  Google Scholar 

  3. Elliot D, Cory-Pearce R, Rees GM (1985) The behaviour of presternal scars in a fair-skinned population. Ann R Coll Surg Engl 67(4):238–240

    PubMed  CAS  Google Scholar 

  4. Yan XQ, Yang HY, Zhao YM, You L, Xu J (2007) Deep inferior epigastric perforator flap for breast reconstruction: experience with 43 flaps. Chin Med J (Engl) 120(5):380–384

    Google Scholar 

  5. Gangemi EN, Gregori D, Berchialla P, Zingarelli E, Cairo M, Bollero D et al (2008) Epidemiology and risk factors for pathologic scarring after burn wounds. Arch Facial Plast Surg 10(2):93–102

    Article  PubMed  Google Scholar 

  6. Wolfram D, Tzankov A, Pulzl P, Piza-Katzer H (2009) Hypertrophic scars and keloids—a review of their pathophysiology, risk factors, and therapeutic management. Dermatol Surg 35(2):171–181

    Article  PubMed  CAS  Google Scholar 

  7. Chalmers RL (2011) The evidence for the role of transforming growth factor-beta in the formation of abnormal scarring. Int Wound J 8(3):218–223

    Article  PubMed  Google Scholar 

  8. Profyris C, Tziotzios C, Do Vale I (2012) Cutaneous scarring: pathophysiology, molecular mechanisms, and scar reduction therapeutics Part I. The molecular basis of scar formation. J Am Acad Dermatol 66(1):1–10; quiz 11–12

    Google Scholar 

  9. De Felice B, Garbi C, Santoriello M, Santillo A, Wilson RR (2009) Differential apoptosis markers in human keloids and hypertrophic scars fibroblasts. Mol Cell Biochem 327(1–2):191–201

    Article  PubMed  CAS  Google Scholar 

  10. Ogawa R, Akaishi S, Huang C, Dohi T, Aoki M, Omori Y et al (2011) Clinical applications of basic research that shows reducing skin tension could prevent and treat abnormal scarring: the importance of fascial/subcutaneous tensile reduction sutures and flap surgery for keloid and hypertrophic scar reconstruction. J Nippon Med Sch 78(2):68–76

    Article  PubMed  Google Scholar 

  11. Gurtner GC, Dauskardt RH, Wong VW, Bhatt KA, Wu K, Vial IN et al (2011) Improving cutaneous scar formation by controlling the mechanical environment: large animal and phase I studies. Ann Surg 254(2):217–225

    Article  PubMed  Google Scholar 

  12. Burgic M, Bruant Rodier C, Wilk A, Bodin F, Rifatbegovic A, Halilbasic E et al (2010) Complications following autologous latissimus flap breast reconstruction. Bosn J Basic Med Sci 10(1):65–67

    PubMed  Google Scholar 

  13. Chen JS, Liu WC, Yang KC, Chen LW, Huang JS, Chang HT (2005) Reconstruction with bilateral pedicled TRAM flap for paraffinoma breast. Plast Reconstr Surg 115(1):96–104

    PubMed  CAS  Google Scholar 

  14. Shridharani SM, Magarakis M, Manson PN, Singh NK, Basdag B, Rosson GD (2010) The emerging role of antineoplastic agents in the treatment of keloids and hypertrophic scars: a review. Ann Plast Surg 64(3):355–361

    Article  PubMed  CAS  Google Scholar 

  15. Wang XQ, Liu YK, Qing C, Lu SL (2009) A review of the effectiveness of antimitotic drug injections for hypertrophic scars and keloids. Ann Plast Surg 63(6):688–692

    Article  PubMed  CAS  Google Scholar 

  16. Bland KI, Palin WE, von Fraunhofer JA, Morris RR, Adcock RA, Tobin GR 2nd (1984) Experimental and clinical observations of the effects of cytotoxic chemotherapeutic drugs on wound healing. Ann Surg 199(6):782–790

    Article  PubMed  CAS  Google Scholar 

  17. Noh R, Karp GI, Devereux DF (1991) The effects of doxorubicin and mitoxantrone on wound healing. Cancer Chemother Pharmacol 29(2):141–144

    Article  PubMed  CAS  Google Scholar 

  18. Juckett G, Hartman-Adams H (2009) Management of keloids and hypertrophic scars. Am Fam Physician 80(3):253–260

    PubMed  Google Scholar 

  19. Demidova-Rice TN, Wolf L, Deckenback J, Hamblin MR, Herman IM (2012) Human platelet-rich plasma- and extracellular matrix-derived peptides promote impaired cutaneous wound healing in vivo. PLoS One 7(2):e32146

    Article  PubMed  CAS  Google Scholar 

  20. Ashraf A, Lee PH, Kim K, Zaporojan V, Bonassar L, Valentini R et al (2009) Effect of sustained-release PDGF and TGF-beta on cyclophosphamide-induced impaired wound healing. Plast Reconstr Surg 124(4):1118–1124

    Article  PubMed  CAS  Google Scholar 

  21. Huang J, Yang J, Maity B, Mayuzumi D, Fisher RA (2011) Regulator of G protein signaling 6 mediates doxorubicin-induced ATM and p53 activation by a reactive oxygen species-dependent mechanism. Cancer Res 71(20):6310–6319

    Article  PubMed  CAS  Google Scholar 

  22. Chatterjee K, Zhang J, Honbo N, Karliner JS (2010) Doxorubicin cardiomyopathy. Cardiology 115(2):155–162

    Article  PubMed  CAS  Google Scholar 

  23. Muszynska A, Palka J, Wolczynski S (1998) Doxorubicin-induced inhibition of prolidase activity in human skin fibroblasts and its implication to impaired collagen biosynthesis. Pol J Pharmacol 50(2):151–157

    PubMed  CAS  Google Scholar 

  24. Muszynska A, Wolczynski S, Palka J (2001) The mechanism for anthracycline-induced inhibition of collagen biosynthesis. Eur J Pharmacol 411(1–2):17–25

    Article  PubMed  CAS  Google Scholar 

  25. Sasaki T (1992) The effects of basic fibroblast growth factor and doxorubicin on cultured human skin fibroblasts: relevance to wound healing. J Dermatol 19(11):664–666

    PubMed  CAS  Google Scholar 

  26. Sasaki T, Holeyfield KC, Uitto J (1987) Doxorubicin-induced inhibition of prolyl hydroxylation during collagen biosynthesis in human skin fibroblast cultures. Relevance to imparied wound healing. J Clin Invest 80(6):1735–1741

    Article  PubMed  CAS  Google Scholar 

  27. Alagol H, Dinc S, Basgut B, Abacioglu N (2007) Temporal variation in the recovery from impairment in adriamycin-induced wound healing in rats. J Circadian Rhythms 5:6

    Article  PubMed  Google Scholar 

  28. Albayrak BS, Ismailoglu O, Ilbay K, Yaka U, Tanriover G, Gorgulu A et al (2010) Doxorubicin for prevention of epineurial fibrosis in a rat sciatic nerve model: outcome based on gross postsurgical, histopathological, and ultrastructural findings. J Neurosurg Spine 12(3):327–333

    Article  PubMed  Google Scholar 

  29. Atkinson JA, McKenna KT, Barnett AG, McGrath DJ, Rudd M (2005) A randomized, controlled trial to determine the efficacy of paper tape in preventing hypertrophic scar formation in surgical incisions that traverse Langer’s skin tension lines. Plast Reconstr Surg 116(6):1648–1656; discussion 1657–1648

    Google Scholar 

Download references

Acknowledgments

Neither of the authors has any commercial associations or financial disclosures to declare.

Conflict of interest

None reported.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Eun Key Kim.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lee, T.J., Jeong, W.S., Eom, J.S. et al. Adjuvant chemotherapy reduces the incidence of abdominal hypertrophic scarring following immediate TRAM breast reconstruction. Breast Cancer Res Treat 137, 767–771 (2013). https://doi.org/10.1007/s10549-012-2394-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10549-012-2394-9

Keywords

Navigation