Side Effects 15 Years After Lymph Node Irradiation in Breast Cancer: Randomized EORTC Trial 22922/10925

Author:

Poortmans Philip M12ORCID,Struikmans Henk3ORCID,De Brouwer Peter4,Weltens Caroline5ORCID,Fortpied Catherine6,Kirkove Carine7,Budach Volker8,Peignaux-Casasnovas Karine9,van der Leij Femke10,Vonk Ernest11ORCID,Valli Mariacarla12,vanTienhoven Geertjan13,Weidner Nicola14,Noel Georges15,Guckenberger Matthias16ORCID,Koiter Eveline17,vanLimbergen Erik5,Engelen Antoine4,Fourquet Alain18,Bartelink Harry19,

Affiliation:

1. Department of Radiation Oncology, Iridium Netwerk, Wilrijk-Antwerp, Belgium

2. Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk-Antwerp, Belgium

3. Department of Radiation Oncology, Leiden University Medical Centre, Leiden, the Netherlands

4. Department of Radiation Oncology, Institute Verbeeten, Tilburg, the Netherlands

5. Department of Radiation Oncology, University Hospital Leuven, KU Leuven Faculty of Medicine, Leuven, Belgium

6. European Organisation for Research and Treatment of Cancer (EORTC), Headquarters, Brussels, Belgium

7. Department of Radiation Oncology, University Hospital Saint Luc, Université Catholique de Louvain, Brussels, Belgium

8. Department of Radiation Oncology, Charité–Universitaetsmedizin Berlin, Free University Berlin, Humboldt-University Berlin, Berlin Institute of Health, Berlin, Germany

9. Department of Radiation Oncology, Centre Georges François Leclerc, Dijon, France

10. Department of Radiation Oncology, University Medical Centre Utrecht, Utrecht, the Netherlands

11. Institute for Radiation Oncology RISO, Deventer, the Netherlands

12. Department of Radiation Oncology, Sant Anna Hospital, Como, Italy

13. Department of Radiation Oncology, Cancer Center Amsterdam, Amsterdam UMC, University of Amsterdam, the Netherlands

14. Department of Radiation Oncology, University Hospital, Tübingen, Germany

15. Department of Radiation Oncology, Centre Paul Strauss, Strasbourg, France

16. Department of Radiation Oncology, University Hospital Zurich, University of Zurich, Zurich, Switzerland

17. Department of Radiation Oncology, Medisch Spectrum Twente, Enschede, the Netherlands

18. Department of Radiation Oncology, Institut Curie, Paris, France

19. Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands

Abstract

Abstract Background Uncertainty about the benefit–risk ratio of regional lymph node irradiation led to varying clinical protocols. We investigated long-term late side effects after internal mammary and medial supraclavicular (IM-MS) lymph node irradiation to improve shared decision making. Methods The multicenter European Organization for Research and Treatment of Cancer trial (ClinicalTrials.gov, NCT00002851) randomly assigned stage I-III breast cancer patients with involved axillary nodes and/or a medially located primary tumor. We analyzed late side effects both longitudinally at every follow-up and cross-sectionally at 5-year intervals. All statistical tests were 2-sided. Results Between 1996 and 2004, 46 departments from 13 countries accrued 4004 patients. Median follow-up was 15.7 years. Longitudinal follow-up data showed cumulative incidence rates at 15 years of 2.9% (95% confidence interval [CI] = 2.2% to 3.8%) vs 5.7% (95% CI = 4.7% to 6.9%) (P < .001) for lung fibrosis, 1.1% (95% CI = 0.7% to 1.7%) vs 1.9% (95% CI = 1.3% to 2.6%) (P = .07) for cardiac fibrosis, and 9.4% (95% CI = 8.0% to 10.8%) vs 11.1% (95% CI = 9.6% to 12.7%) (P = .04) for any cardiac disease when treated without or with IM-MS lymph node irradiation. There was no evidence for differences between left- and right-sided breast cancer (Wald χ2 test of treatment by breast side interaction, P = .33 and P = .35, for cardiac fibrosis and for any cardiac disease, respectively). The cumulative incidence probabilities of cross-sectionally reported side effects with a score of 2 or greater at 15 years were 0.1% (95% CI = 0.0% to 0.5%) vs 0.8% (95% CI = 0.4% to 1.4%) for pulmonary (P = .02), 1.8% (95% CI = 1.1% to 2.8%) vs 2.6% (95% CI = 1.8% to 3.7%) for cardiac (P = .15), and 0.0% (95% CI not evaluated) vs 0.1% (95% CI = 0.0% to 0.4%) for esophageal (P = .16), respectively. No difference was observed in the incidence of second malignancies, contralateral breast cancer, or cardiovascular deaths. Conclusions The incidence of late pulmonary side effects was statistically significantly higher after IM-MS lymph node irradiation, as were some of the cardiac events, without a difference between left- and right-sided treatments. Absolute rates and differences were very low, without increased non-breast cancer–related mortality, even before introducing heart-sparing techniques.

Funder

La Ligue nationale contre le cancer from France

KWF Kanker Bestrijding from the Netherlands

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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