Doubling Recruitment of Pediatric Low-grade Glioma within Two Decades does not change Outcome – Report from the German LGG Studies

Author:

Gnekow Astrid Katharina1,Kandels Daniela1,Pietsch Torsten2,Bison Brigitte3,Warmuth-Metz Monika3,Thomale Ulrich W.4,Kortmann Rolf-D.5,Timmermann Beate6,Driever Pablo Hernàiz7,Witt Olaf89,Schmidt René10,Spix Claudia11

Affiliation:

1. Faculty of Medicine, Swabian Children’s Cancer Center, University Hospital Augsburg, Augsburg, Germany

2. Institute of Neuropathology, DGNN Brain Tumor Reference Center, University Bonn, Bonn, Germany

3. Institute of Diagnostic and Interventional Neuroradiology, University Hospital Wuerzburg, Wuerzburg, Germany

4. Department of Pediatric Neuro-Surgery, Charité Berlin, Berlin, Germany

5. Referenzzentrum für Hirntumoren (Radioonkologie), Universitätsklinikum Leipzig AöR, Leipzig, Germany

6. Westgerman Proton Therapy Center Essen, University Essen, Essen, Germany

7. Pediatric Oncology and Hematology, Charité-Universitätsmedizin Berlin, Berlin, Germany

8. Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg University Hospital, Heidelberg, Germany

9. German Cancer Research Center (DKFZ), Heidelberg, Germany

10. Institute of Biostatistics and Clinical Research, University of Muenster, Muenster, Germany

11. Division of Childhood Cancer Epidemiology, Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Centre of the Johannes Gutenberg University Mainz, Mainz, Germany

Abstract

Abstract Background Successive multicenter studies for pediatric low-grade glioma (LGG) in Germany were accompanied by a doubling of annual recruitment over 2 decades. We investigated whether this increase conveyed a change of epidemiologic characteristics or survival. Methods and results Participating centers reported 4634 patients with the radiologic/histologic diagnosis of LGG (1996–2018), rising from 109 to 278/year. Relating these numbers to all pediatric CNS tumors registered at the German Childhood Cancer Registry, the LGG fraction and annual crude incidence rates increased (32% to 51%; 0.94 to 2.12/100,000 children/adolescents<15 years). The consecutive LGG studies recruited 899 (HIT-LGG 1996), 1592 (SIOP-LGG 2004), and 1836 (LGG-registry) patients with similar distribution of tumor-sites, histology, and dissemination. 5-year overall survival was 96%-98% at median observation time of 8.1 years. Acknowledging unequal follow-up periods, 589/899 (66%), 1089/1582 (69%), and 1387/1836 (76%) patients remained under observation, while 1252/4317 received adjuvant treatment with decreasing frequency of front-line radiotherapy from 16% to 5%. Conclusion Pediatric LGG incidence rates in Germany are now comparable to other European countries. The rise in patient numbers followed implementation of standard-of-care treatment protocols, but did not result in relevant changes of epidemiologic or clinical parameters or survival. Shifts in patient distribution between treatment arms reflect growing acceptance of the LGG therapy algorithm.

Publisher

Georg Thieme Verlag KG

Subject

Pediatrics, Perinatology and Child Health

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