Abstract
Background and purpose
The purpose of this work was to identify parameters influencing the risk of late radiation side effects, fair or poor cosmetic outcomes (COs) and pain in breast cancer patients after breast-conserving therapy (BCT) and three-dimensional conformal radiotherapy (3D-CRT).
Patients and methods
Between 2006 and 2013, 159 patients were treated at the Hannover Medical School. Physician-rated toxicity according to the LENT-SOMA criteria, CO and pain were assessed by multivariate analysis.
Results
LENT-SOMA grade 1–4 toxicity was observed as follows: fibrosis 10.7 %, telangiectasia 1.2 %, arm oedema 8.8 % and breast oedema 5.0 %. In addition, 15.1 % of patients reported moderate or severe breast pain, and 21.4 % complained about moderate or severe pain in the arm or shoulder. In multivariate analysis, axillary clearing (AC) was significantly associated with lymphoedema of the arm [odds ratio (OR) 4.37, p = 0.011, 95 % confidence interval (CI) 1.4–13.58]. Breast oedema was also highly associated with AC (OR 10.59, p = 0.004, 95 % CI 2.1–53.36), a ptosis grade 2/3 or pseudoptosis and a bra size ≥ cup C (OR 5.34, p = 0.029, 95 % CI 1.2–24.12). A ptosis grade 2/3 or pseudoptosis and a bra size ≥ cup C were the parameters significantly associated with an unfavourable CO (OR 3.19, p = 0.019, 95 % CI 1.2–8.4). Concerning chronic breast pain, we found a trend related to the prescribed radiation dose including boost (OR 1.077, p = 0.060, 95 % CI 0.997–1.164). Chronic shoulder or arm pain was statistically significantly associated with lymphoedema of the arm (OR 3.9, p = 0.027, 95 % CI 1.17–13.5).
Conclusion
Chronic arm and breast oedema were significantly influenced by the extent of surgery (AC). Ptotic and large breasts were significantly associated with unfavourable COs and chronic breast oedema. Late toxicities exclusive breast pain were not associated with radiotherapy parameters.
Zusammenfassung
Hintergrund und Ziel
Ziel dieser Arbeit war es, Parameter zu identifizieren, die Spätschäden nach Radiotherapie, ein ungünstiges kosmetisches Ergebnis (CO) und Schmerzen bei Brustkrebspatientinnen nach brusterhaltender Therapie (BCT) und dreidimensionaler konformaler Radiotherapie (3D-CRT) beeinflusst haben.
Patienten und Methoden
Zwischen 2006 und 2013 wurden an der Medizinischen Hochschule Hannover 159 Patientinnen behandelt. Die nach LENT-SOMA-Kriterien bewerteten Spätnebenwirkungen sowie das CO und Schmerzen wurden mittels multivariater Analyse ausgewertet.
Ergebnisse
Folgende Spätnebenwirkungen vom LENT-SOMA Grad 1–4 wurden beobachtet: Strahlenfibrose 10,7 %, Teleangiektasien 1,2 %, Lymphödem des Arms 8,8 % und Brustödem 5,0 %. Mäßigen bis schweren Schmerz in der Brust gaben 15,1 % an, mäßigen bis schweren Schmerz im Arm-Schulter-Bereich 21,4 %. In der multivariaten Analyse zeigte sich ein signifikanter Zusammenhang zwischen Axilladissektion und chronischem Lymphödem des Arms [Odds Ratio (OR) 4,37; p = 0,011; 95 %-Konfidenzintervall (KI) 1,4–13,58] und der Brust (OR 10,59; p = 0,04; 95 %-KI 2,1–53,36). Signifikanz bestand zwischen Ptosis vom Grad 2/3 oder einer Pseudoptosis bei einer Brustgröße ≥ C-Cup und einem chronischem Brustödem (OR 5,34; p = 0,029; 95 %-KI 1,2–24,12) sowie einem ungünstigen CO (OR 3,19; p = 0,019; 95 %-KI 1,2–8,4). Es zeigte sich ein Trend für die Gesamtstrahlendosis inklusive Boost und chronischem Brustschmerz (OR 1,077; p = 0,060; 95 %-KI 0,997–1,164). Chronischer Schulter- und Armschmerz war signifikant assoziiert mit einem chronischen Lymphödem des Arms (OR 3,9; p = 0,027; 95 %-KI 1,17–13,5).
Schlussfolgerung
Chronische Ödeme des Arms und der Brust zeigen eine signifikante Abhängigkeit vom Ausmaß der chirurgischen axillären Intervention. Ptotische und große Mammae hatten signifikant häufiger ein mäßiges CO und ein chronisches Brustödem. Mit Ausnahme vom chronischen Brustschmerz gab es keine Assoziation zwischen Spätnebenwirkungen und Strahlentherapieparametern.
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References
Veronesi U, Cascinelli N, Mariani L et al (2002) Twenty-year follow-up of a randomized study comparing breast-conserving surgery with radical mastectomy for early breast cancer. N Engl J Med 347:1227–1232. doi:10.1056/NEJMoa020989
Goffman TE, Laronga C, Wilson L et al (2004) Lymphedema of the arm and breast in irradiated breast cancer patients: risks in an era of dramatically changing axillary surgery. Breast J 10:405–411. doi:10.1111/j.1075-122X.2004.21411.x
Pusic AL, Cemal Y, Albornoz C et al (2013) Quality of life among breast cancer patients with lymphedema: a systematic review of patient-reported outcome instruments and outcomes. J Cancer Surviv 7:83–92. doi:10.1007/s11764-012-0247-5
Mansfield C (1979) Effects of radiation therapy on wound healing after mastectomy. Clin Plast Surg 6:19–26
Fajardo LF (1993) Basic mechanisms and general morphology of radiation injury. Semin Roentgenol 28:297–302
Mukesh MB, Barnett GC, Wilkinson JS et al (2013) Randomized controlled trial of intensity-modulated radiotherapy for early breast cancer: 5-year results confirm superior overall cosmesis. J Clin Oncol 31:4488–4495. doi:10.1200/JCO.2013.49.7842
Taylor ME, Perez CA, Halverson KJ et al (1995) Factors influencing cosmetic results after conservation therapy for breast cancer. Int J Radiat Oncol Biol Phys 31:753–764. doi:10.1016/0360-3016(94)00480-3
Vrieling C, Collette L, Fourquet A et al (2000) The influence of patient, tumor and treatment factors on the cosmetic results after breast-conserving therapy in the EORTC ‛boost vs. no boost’ trial. EORTC Radiotherapy and Breast Cancer Cooperative Groups. Radiother Oncol 55:219–232
Asgeirsson KS, Rasheed T, McCulley SJ et al (2005) Oncological and cosmetic outcomes of oncoplastic breast conserving surgery. Eur J Surg Oncol 31:817–823. doi:10.1016/j.ejso.2005.05.010
Rezai M, Nestle-Krämling C (1999) Oncoplastic surgical techniques in breast-conserving therapy for carcinoma of the breast. Gynäkologe 32:83–90. doi:10.1007/PL00003213
Hille-Betz U, Vaske B, Henseler H et al (2014) Dermoglandular rotation flaps for breast-conserving therapy: aesthetic results, patient satisfaction, and morbidity in comparison to standard segmentectomy. Int J Breast Cancer 2014:152451. doi:10.1155/2014/152451
Clough KB, Lewis JS, Couturaud B et al (2003) Oncoplastic techniques allow extensive resections for breast-conserving therapy of breast carcinomas. Ann Surg 237:26–34. doi:10.1097/01.SLA.0000041230.77663.22
International Commission on Radiation Units and Measurements (icru) ICRU Report 62. Bethesda: ICRU; 1999. Prescribing, Recording and Reporting Photon Beam Therapy [supplement to ICRU Report 50]
Regnault P (1976) Breast ptosis. Definition and treatment. Clin Plast Surg 3:193–203
Cardoso MJ, Cardoso J, Amaral N et al (2007) Turning subjective into objective: the BCCT.core software for evaluation of cosmetic results in breast cancer conservative treatment. Breast 16:456–461. doi:10.1016/j.breast.2007.05.002
Pavy JJ, Denekamp J, Letschert J et al (1995) EORTC Late Effects Working Group. Late effects toxicity scoring: the SOMA scale. Int J Radiat Oncol Biol Phys 31:1043–1047
Sprangers MA, Groenvold M, Arraras JI et al (1996) The European Organization for Research and Treatment of Cancer breast cancer-specific quality-of-life questionnaire module: first results from a three-country field study. J Clin Oncol 14:2756–2768
Kwan W, Jackson J, Weir LM et al (2002) Chronic arm morbidity after curative breast cancer treatment: prevalence and impact on quality of life. J Clin Oncol 20:4242–4248
Ahmed RL, Prizment A, Lazovich D et al (2008) Lymphedema and quality of life in breast cancer survivors: the Iowa Women’s Health Study. J Clin Oncol 26:5689–5696. doi:10.1200/JCO.2008.16.4731
Mansel RE, Fallowfield L, Kissin M et al (2006) Randomized multicenter trial of sentinel node biopsy versus standard axillary treatment in operable breast cancer: the ALMANAC Trial. J Natl Cancer Inst 98:599–609. doi:10.1093/jnci/djj158
Del Bianco P, Zavagno G, Burelli P et al (2008) Morbidity comparison of sentinel lymph node biopsy versus conventional axillary lymph node dissection for breast cancer patients: results of the sentinella-GIVOM Italian randomised clinical trial. Eur J Surg Oncol 34:508–513. doi:10.1016/j.ejso.2007.05.017
Lucci A, McCall LM, Beitsch PD et al (2007) Surgical complications associated with sentinel lymph node dissection (SLND) plus axillary lymph node dissection compared with SLND alone in the American College of Surgeons Oncology Group Trial Z0011. J Clin Oncol 25:3657–3663. doi:10.1200/JCO.2006.07.4062
Degnim AC, Miller J, Hoskin TL et al (2012) A prospective study of breast lymphedema: frequency, symptoms, and quality of life. Breast Cancer Res Treat 134:915–922. doi:10.1007/s10549-012-2004-x
Kelemen G, Varga Z, Lázár G et al (2012) Cosmetic outcome 1–5 years after breast conservative surgery, irradiation and systemic therapy. Pathol Oncol Res 18:421–427. doi:10.1007/s12253-011-9462-z
Chadha M, Vongtama D, Friedmann P et al (2012) Comparative acute toxicity from whole breast irradiation using 3-week accelerated schedule with concomitant boost and the 6.5-week conventional schedule with sequential boost for early-stage breast cancer. Clin Breast Cancer 12:57–62. doi:10.1016/j.clbc.2011.09.002
Barnett GC, Wilkinson JS, Moody AM et al (2011) The Cambridge Breast Intensity-modulated Radiotherapy Trial: patient- and treatment-related factors that influence late toxicity. Clinical Oncol (R Coll Radiol) 23:662–673. doi:10.1016/j.clon.2011.04.011
Mondry TE, Johnstone, Peter AS (2002) Manual lymphatic drainage for lymphedema limited to the breast. J Surg Oncol 81:101–104. doi:10.1002/jso.10154
Lilla C, Ambrosone CB, Kropp S et al (2007) Predictive factors for late normal tissue complications following radiotherapy for breast cancer. Breast Cancer Res Treat 106:143–150. doi:10.1007/s10549-006-9480-9
Bantema-Joppe EJ, Schilstra C, de Bock, Geertruida H et al (2012) Simultaneous integrated boost irradiation after breast-conserving surgery: physician-rated toxicity and cosmetic outcome at 30 months’ follow-up. Int J Radiat Oncol Biol Phys 83:e471–e477. doi:10.1016/j.ijrobp.2012.01.050
Johansson S, Svensson H, Denekamp J (2002) Dose response and latency for radiation-induced fibrosis, edema, and neuropathy in breast cancer atients. Int J Radiat Oncol Biol Phys 52:1207–1219
Ohsumi S, Shimozuma K, Kuroi K et al (2007) Quality of life of breast cancer patients and types of surgery for breast cancer—current status and unresolved issues. Breast Cancer 14:66–73
Clark RM (1983) Conservative surgery and radiation therapy in the treatment of operable breast cancer. Front Radiat Ther Oncol 17:91–101
Budach W, Matuschek C, Bolke E et al (2015) DEGRO practical guidelines for radiotherapy of breast cancer V. Therapy for locally advanced and inflammatory breast cancer, as well as local therapy in cases with synchronous distant metastases (DEGRO-Leitlinien fur die Radiotherapie des Mammakarzinoms V: Therapie des lokal fortgeschrittenen und inflammatorischen Mammakarzinoms sowie lokale Therapie bei Vorliegen synchroner Fernmetastasen). Strahlenther Onkol. doi:10.1007/s00066-015-0843-1
Bergom C, Kelly T, Morrow N et al (2012) Prone whole-breast irradiation using three-dimensional conformal radiotherapy in women undergoing breast conservation for early disease yields high rates of excellent to good cosmetic outcomes in patients with large and/or pendulous breasts. Int J Radiat Oncol Biol Phys 83:821–828. doi 10.1016/j.ijrobp.2011.08.020
Würschmidt F, Stoltenberg S, Kretschmer M et al (2014) Incidental dose to coronary arteries is higher in prone than in supine whole breast irradiation. A dosimetric comparison in adjuvant radiotherapy of early stage breast cancer. Strahlenther Onkol 190:563–568. doi:10.1007/s00066-014-0606-4
Meretoja TJ, Leidenius, Marjut H K, Tasmuth T et al (2014) Pain at 12 months after surgery for breast cancer. JAMA 311:90–92. doi:10.1001/jama.2013.278795
Hamilton CS, Nield JM, Adler GF et al (1990) Breast appearance and function after breast conserving surgery and radiotherapy. Acta Oncol 29:291–295
Poleshuck EL, Katz J, Andrus CH et al (2006) Risk factors for chronic pain following breast cancer surgery: a prospective study. J Pain 7:626–634. doi:10.1016/j.jpain.2006.02.007
Ishiyama H, Niino K, Hosoya T et al (2006) Results of a questionnaire survey for symptom of late complications caused by radiotherapy in breast conserving therapy. Breast Cancer 13:197–201
Mak KS, Chen Y, Catalano PJ et al (2014) Dosimetric inhomogeneity predicts for long-term breast pain after breast-conserving therapy. Int J Radiat Oncol Biol Phys. doi:10.1016/j.ijrobp.2014.05.021
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U. Hille-Betz, B. Vaske, M. Bremer, P. Soergel, S. Kundu, R. Klapdor, P. Hillemanns, and C. Henkenberens state that there are no conflict of interest.
This restrospective analysis was approved by the local ethics committee. Informed consent was obtained from all patients. Bernhard Vaske from the Institute of Medical Biometry and Informatics of the Hannover Medical School conducted the data management.
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Hille-Betz, U., Vaske, B., Bremer, M. et al. Late radiation side effects, cosmetic outcomes and pain in breast cancer patients after breast-conserving surgery and three-dimensional conformal radiotherapy. Strahlenther Onkol 192, 8–16 (2016). https://doi.org/10.1007/s00066-015-0899-y
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DOI: https://doi.org/10.1007/s00066-015-0899-y