Klin Padiatr 2014; 226(03): 161-168
DOI: 10.1055/s-0034-1368785
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Childhood Craniopharyngioma – Changes of Treatment Strategies in the Trials KRANIOPHARYNGEOM 2000/2007

Kraniopharyngeom im Kindes- und Jugendalter – Änderungen der Behandlungsstrategien im Rahmen der multizentrischen Studien KRANIOPHARYNGEOM 2000/2007
A. Hoffmann
1   Klinikum Oldenburg, Department of Pediatrics, Oldenburg, Germany
,
M. Warmth-Metz
2   Department of Neuroradiology, University Hospital Wuerzburg, ­Wuerzburg, Germany
,
U. Gebhardt
1   Klinikum Oldenburg, Department of Pediatrics, Oldenburg, Germany
,
T. Pietsch
3   Institute of Neuropathology, University of Bonn, Bonn, Germany
,
F. Pohl
4   Department of Radiooncology, University Hospital Regensburg, ­Regensburg, Germany
,
R.-D. Kortmann
5   Department of Radiooncology, University Hospital Leipzig, Leipzig, ­Germany
,
G. Calaminus
6   Department of Pediatric Oncology, University Hospital Muenster, ­Muenster, Germany
,
H. L. Müller
1   Klinikum Oldenburg, Department of Pediatrics, Oldenburg, Germany
› Author Affiliations
Further Information

Publication History

Publication Date:
12 May 2014 (online)

Abstract

Background: Prognosis in childhood cranio­pharyngioma, is frequently impaired due to sequelae. Radical surgery was the treatment of choice for decades. Even at experienced facilities radical surgery can result in hypothalamic disorders such as severe obesity.

Objective: We analyzed, whether treatment strategies for childhood craniopharyngioma patients recruited in GPOH studies have changed during the last 12 years.

Materials and methods: We compared the grade of pre-surgical hypothalamic involvement, treatment, degree of resection and grade of surgical hypothalamic lesions between patients recruited in KRANIOPHARYNGEOM 2000 (n=120; 2001–2007) and KRANIOPHARYNGEOM 2007 (n=106; 2007–2012).

Results: The grade of initial hypothalamic involvement was similar in patients treated 2001–2007 and 2007–2012. The realized treatment was more radical (p=0.01) in patients recruited 2001–2007 (38%) when compared with patients treated 2007–2012 (18%). In patients with pre-surgical involvement of anterior/posterior hypothalamic areas, the rate of hypothalamus-sparing operations resulting in no (further) hypothalamic lesions was higher (p=0.005) in patients treated 2007–2012 (35%) in comparison with the 2001–2007 cohort (13%). Event-free-survival rates were similar in both cohorts.

Conclusions: A trend towards less radical surgical approaches is observed, which was accompanied by a reduced rate of severe hypothalamic lesions. Radical surgery is not an appropriate treatment strategy in patients with hypothalamic involvement. Despite previous recommendations to centralize treatment at specialized centers, a trend towards further decentralization was seen.

Zusammenfassung

Hintergrund: Die Prognose von Kindern und Jugendlichen mit Kraniopharyngeom wird durch Spätfolgen beeinträchtigt. Die radikale Resektion galt über Jahrzehnte als Therapie der Wahl. ­Allerdings drohen selbst bei Operation durch erfahrene neurochirurgische Teams hypothalami­sche Läsionen.

Fragestellung: Untersucht wurde, ob sich im Verlauf der Studien KRANIOPHARYNGEOM 2000/2007 Änderungen hinsichtlich der Behandlungs­strategie ergaben.

Patienten und Methoden: Verglichen wurden der Grad präoperativer hypothalamischer Beteiligung, operative Strategien, Resektionsgrad und Grad chirurgischer hypothalamischer Läsionen zwischen den Patientenkollektiven in KRANIO­PHARYNGEOM 2000 [n=120; 2001–2007) und KRANIOPHARYNGEOM 2007 (n=106; 2007–2012).

Ergebnisse: Es bestanden keine Unterschiede hinsichtlich der präoperativen hypothala­mischen Beteiligung zwischen beiden Studienkollektiven. Die Anzahl der radikalen Resektionen war höher (p=0.01) bei Patienten, die 2001–2007 rekrutiert wurden (38%), im Vergleich zum Rekrutierungs­zeitraum 2007–2012 (18%). Bei Risikopatienten mit präoperativer Beteiligung anteriorer/poste­riorer hypothalamischer Areale resultierte im Rekrutierungszeitraum 2007–2012 eine scho­nendere operative Vorgehendweise in einer höheren Rate von Patienten ohne operative Läsionen (35%) im Vergleich zum Rekrutierungs­zeitraum 2001–2007 (13%). Die ereignisfreie Überlebensrate war in beiden Studien gleich.

Schlussfolgerungen: Im Vergleich der Studien zeigt sich in den letzten 12 Jahren ein Trend hin zu weniger radikalen chirurgischen Behandlungsstrategien mit Reduktion schwerer hypo­tha­lamischer Läsionen. Bei Kraniopharyngeomen mit hypothalamischer Beteiligung erscheint die radikale Resektion nicht empfeh­­lenswert.

 
  • References

  • 1 Cohen M, Bartels U, Branson H et al. Trends in treatment and outcomes of pediatric craniopharyngioma, 1975-2011. Neuro Oncol 2013; 15: 767-774
  • 2 Deutsche Gesellschaft für Kinder- und Jugendmedizin (DGKJ) published by Gesellschaft für Pädiatrische Onkologie und Hämatologie (GPOH). Clinical guideline: Kraniopharyngeom im Kindes- und Jugendalter – http://www.awmf.org/leitlinien/detail/ll/025-026.html (last update: June 2013)
  • 3 Elowe-Gruau E, Beltrand J, Brauner R et al. Childhood craniopharyngioma: hypothalamus-sparing surgery decreases the risk of obesity. J Clin Endocrinol Metab 2013; 98: 2376-2382
  • 4 Fjalldal S, Holmer H, Rylander L et al. Hypothalamic Involvement Predicts Cognitive Performance and Psychosocial Health in Long-term Survivors of Childhood Craniopharyngioma. J Clin Endocrinol Metab 2013; 98: 3253-3262
  • 5 Flitsch J, Muller HL, Burkhardt T. Surgical strategies in childhood craniopharyngioma. Front Endocrinol (Lausanne) 2011; 2: 96
  • 6 Garre ML, Cama A. Craniopharyngioma: modern concepts in pathogenesis and treatment. Curr Opin Pediatr 2007; 19: 471-479
  • 7 Gobel U, Korholz D, Bernig T et al. Treatment of children and adolecents with cancer after the application of the guide lines for good clinical practice in 2004 and the evaluation of new measurements. Klin Padiatr 2012; 224: 335-338
  • 8 Holmer H, Ekman B, Bjork J et al. Hypothalamic involvement predicts cardiovascular risk in adults with childhood onset craniopharyngioma on long-term GH therapy. Eur J Endocrinol 2009; 161: 671-679
  • 9 Karavitaki N, Cudlip S, Adams CB et al. Craniopharyngiomas. Endocr Rev 2006; 27: 371-397
  • 10 Kortmann RD. Different approaches in radiation therapy of craniopharyngioma. Front Endocrinol (Lausanne) 2011; 2: 100
  • 11 Koustenis E, Pfitzer C, Balcerek M et al. Impact of Cranial Irradiation and Brain Tumor Location on Fertility: a Survey. Klin Padiatr 2013; 225: 320-324
  • 12 Mallucci C, Pizer B, Blair J et al. Management of craniopharyngioma: the Liverpool experience following the introduction of the CCLG guidelines. Introducing a new risk assessment grading system. Childs Nerv Syst 2012; 28: 1181-1192
  • 13 Muller HL. Childhood craniopharyngioma–current concepts in diagnosis, therapy and follow-up. Nat Rev Endocrinol 2010; 6: 609-618
  • 14 Muller HL. Consequences of craniopharyngioma surgery in children. J Clin Endocrinol Metab 2011; 96: 1981-1991
  • 15 Muller HL. Paediatrics: Surgical strategy and quality of life in craniopharyngioma. Nat Rev Endocrinol 2013; 9: 447-449
  • 16 Muller HL, Bruhnken G, Emser A et al. Longitudinal study on quality of life in 102 survivors of childhood craniopharyngioma. Childs Nerv Syst 2005; 21: 975-980
  • 17 Muller HL, Bueb K, Bartels U et al. Obesity after childhood craniopharyngioma–German multicenter study on pre-operative risk factors and quality of life. Klin Padiatr 2001; 213: 244-249
  • 18 Muller HL, Faldum A, Etavard-Gorris N et al. Functional capacity, obesity and hypothalamic involvement: cross-sectional study on 212 patients with childhood craniopharyngioma. Klin Padiatr 2003; 215: 310-314
  • 19 Muller HL, Gebhardt U, Faldum A et al. Xanthogranuloma, Rathke's cyst, and childhood craniopharyngioma: results of prospective multinational studies of children and adolescents with rare sellar malformations. J Clin Endocrinol Metab 2012; 97: 3935-3943
  • 20 Muller HL, Gebhardt U, Maroske J et al. Long-term follow-up of morbidly obese patients with childhood craniopharyngioma after laparoscopic adjustable gastric banding (LAGB). Klin Padiatr 2011; 223: 372-373
  • 21 Muller HL, Gebhardt U, Schroder S et al. Analyses of treatment variables for patients with childhood craniopharyngioma–results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up. Horm Res Paediatr 2010; 73: 175-180
  • 22 Muller HL, Gebhardt U, Teske C et al. Post-operative hypothalamic lesions and obesity in childhood craniopharyngioma: results of the multinational prospective trial KRANIOPHARYNGEOM 2000 after 3-year follow-up. Eur J Endocrinol 2011; 165: 17-24
  • 23 Puget S, Garnett M, Wray A et al. Pediatric craniopharyngiomas: classification and treatment according to the degree of hypothalamic involvement. J Neurosurg 2007; 106: 3-12
  • 24 Rajan B, Ashley S, Gorman C et al. Craniopharyngioma–a long-term results following limited surgery and radiotherapy. Radiother Oncol 1993; 26: 1-10
  • 25 Regine WF, Kramer S. Pediatric craniopharyngiomas: long term results of combined treatment with surgery and radiation. Int J Radiat Oncol Biol Phys 1992; 24: 611-617
  • 26 Sainte-Rose C, Puget S, Wray A et al. Craniopharyngioma: the pendulum of surgical management. Childs Nerv Syst 2005; 21: 691-695
  • 27 Sanford RA. Craniopharyngioma: results of survey of the American Society of Pediatric Neurosurgery. Pediatr Neurosurg 1994; 21 (Suppl. 01) 39-43
  • 28 Spoudeas HA, Saran F, Pizer B. A multimodality approach to the treatment of craniopharyngiomas avoiding hypothalamic morbidity: a UK perspective. J Pediatr Endocrinol Metab 2006; 19 (Suppl. 01) 447-451
  • 29 Stripp DC, Maity A, Janss AJ et al. Surgery with or without radiation therapy in the management of craniopharyngiomas in children and young adults. Int J Radiat Oncol Biol Phys 2004; 58: 714-720
  • 30 Tomita T, Bowman RM. Craniopharyngiomas in children: surgical experience at Children’s Memorial Hospital. Childs Nerv Syst 2005; 21: 729-746