Abstract
Purpose
The purpose of this study was to evaluate postoperative radiotherapy regarding outcome and toxicity in patients with thymic epithelial tumors (TET) after surgery.
Materials and methods
We retrospectively analyzed medical records of 41 patients with TET treated with postoperative radiotherapy at our institution between 1995 and 2012. The impact of prognostic factors (e.g., Masaoka stage, histological subtype) was investigated and radiation-related toxicity was assessed.
Results
Median age was 59.8 years and median follow-up was 61 months. In 24.4 %, TETs were associated with paraneoplastic syndromes. The 5-year overall survival (OS) was 89.5 % and the 5-year disease-free survival (DFS) was 88.9 %. Masaoka stage had a significant impact on OS (p = 0.007). Locally limited stages I + II had a 5-year OS of 100 % compared to 80 % for stage III and 66.7 % for stage IV. The 5-year DFS was excellent with 100 % for both WHO groups A/AB/B1 and B2, respectively, and significantly (p = 0.005) differed from B3/C-staged patients with a 5-year DFS of 63.6 %. Resection status, paraneoplastic association, radiation dose, or tumor size did not influence survival. There were no high-grade acute or late side effects caused by radiotherapy.
Conclusion
Masaoka stage has a significant impact on OS as WHO type has on DFS in patients with TETs after surgery and adjuvant irradiation. Postoperative radiotherapy with doses around 50 Gy is safe and not likely to cause high-grade toxicity. Further prospective trials are necessary to separate patient subgroups that benefit from radiotherapy from those that do not.
Zusammenfassung
Ziel
Die vorliegende Studie hatte zum Ziel, die postoperative Radiotherapie von Patienten nach Resektion einer Thymusneoplasie epithelialen Ursprungs (Thymom, Thymuskarzinom, „thymic epithelial tumors“, TET) hinsichtlich prognostischer Relevanz und Nebenwirkungsprofil zu beurteilen.
Material und methoden
Wir analysierten retrospektiv die medizinischen Krankenakten von 41 Patienten mit TET, die zwischen 1995 und 2012 eine postoperative Radiotherapie in unserer Einrichtung erhielten. Hierbei untersuchten wir insbesondere mögliche Prognosefaktoren wie Masaoka-Stadium, histologischen Subtyp sowie weitere und erfassten radiogene Nebenwirkungen.
Ergebnisse
Das mediane Alter betrug 59,8 Jahre, das mediane Follow-up lag bei 61 Monaten. Bei 24,4 % aller Patienten trat ein paraneoplastisches Syndrom auf. Das 5-Jahres-Gesamtüberleben lag bei 89,5 %, das krankheitsfreie 5-Jahres-Übeleben bei 88,9 %. Das Masaoka-Stadium hatte signifikanten Einfluss auf das Gesamtüberleben (p = 0,007). Die lokal begrenzten Stadien I + II hatten ein 5-Jahres-Gesamtüberleben von 100 % im Vergleich zu 80 % bei Masaoka III und 66,7 % bei Masaoka IV. Das krankheitsfreie 5-Jahres-Übeleben war mit jeweils 100 % in den WHO-Gruppen A/AB/B1 bzw. B2 exzellent und damit signifikant besser (p = 0,005) im Vergleich zu 63,6 % bei Patienten mit B3/C. Resektionsstatus, Paraneoplasien, Bestrahlungsdosis oder Tumorgröße hatten keinen Einfluss auf das Überleben. Es traten keine höhergradigen, radiogenen Akut- oder Spätnebenwirkungen auf.
Schlussfolgerung
Das Masaoka-Stadium hat signifikanten Einfluss auf das Gesamtüberleben und der WHO-Subtyp auf das krankheitsfreie Überleben bei Patienten mit postoperativer Radiotherapie nach Resektion eines TET. Eine Bestrahlungsdosis von ca. 50 Gy kann hierbei sicher und ohne besonderes Risiko für höhergradige Nebenwirkungen appliziert werden. Allerdings werden weitere, prospektive Studien benötigt, um zu differenzieren, welche Patientensubgruppen von einer adjuvanten Radiotherapie profitieren und welche nicht.
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M.F. Häfner, F. Roeder, F. Sterzing, D. Krug, S.A. Koerber, J. Kappes, H. Hoffmann, A. Slynko, J. Debus, and M. Bischof state that there are no conflicts of interest. All studies on patient data were carried out with approval of the institutional ethical review committee and in accordance with national law and the Helsinki Declaration of 1975 (in its current, revised form).
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Häfner, M., Roeder, F., Sterzing, F. et al. Postoperative radiotherapy of patients with thymic epithelial tumors (TET). Strahlenther Onkol 191, 133–140 (2015). https://doi.org/10.1007/s00066-014-0740-z
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DOI: https://doi.org/10.1007/s00066-014-0740-z