CPT-SIOP-Register

автор: Dr. med. U. Kordes, Dr. rer. nat. S.Hartung, erstellt am: 2011/02/28, Последнее изменение: 2015/06/11

титул International CPT-SIOP-Registry
Формы рака Choroid-Plexus -Tumors
Вид исследования International Registry
Цель исследования

Choroid plexus tumors are very rare tumours. They arise from normal tissue in the brain which produces cerebral spinal fluid, the "choroid plexus". Choroid plexus tumors account for only 0.5% of all tumors in adults and children. Most of the tumors occur in infants, but they can occur at any age. In children the tumors account between 1% and 4%, in children younger than one year they account up to 13%. In Germany over the last years ca. 13 patients per year were registered.
There are three tumor types, occuring with the same frequency: choroid plexus papilloma (relatively benign), atypical choroid plexus papilloma (intermediate form) and choroid plexus carcinoma (malignant). In some choroid plexus carcinoma a Li-Fraumeni-syndrome can be found, a rare autosomal dominant cancer predisposition, where the gene p53 is dysfunctioned. In other patients can be found an increase of the expression and copynumber of a gene for PDGF-receptors.

After the end of the trial CPT-SIOP-2000, which is still to be analized finally, and before the opening of the next trial CPT-SIOP 2009 in germany and other countries, the registry is open for all patients. Given the rareness of the desease the collection of the data of all patients over the world is desirable.

Objectives

  • Epidemiological and clinical recruitment of all patients with Choroid-Plexus tumors into an international database
  • Structured reference expertise for pathology, radiology and radiotherapy
  • Scientific analysis of all collected data
  • Evaluation of survival rates
  • Evaluation of the signifincance of the surgery, radiotherapy and chemotherapy
Лечение

The registry is not a clinical trial. It provides advice on basis of the interim-analysis of the trial CPT-SIOP 2000. The CPT-SIOP 2000 shows that patients with a choroid plexus carcinoma profit from a maximal possible surgical resection and irradiation, at least in children old enough that it can be given.
The CPT-SIOP-2009 Study will address the question, which of four different chemotherapy protocols is superior. Until the opening of the new study, all patients should be registered in the registry. The responsible doctor of the clinic decides over the treatment plan.

Кого берут в протокол
  • Patients with a Choroid-Plexus tumor, proven by a reference pathologist (Neuropathology Münster or Bonn)
  • Written informed concense of the patient or guardian for the collection and transfer of data
Сколько пациентов должно пройти через исследование Ca. 30 / year worldwidet (ca. 10 / year in Germany)
Status 03/10 untill start of new trial
Руководитель протокола Dr. med. Uwe Kordes, International Investigator Prof. Johannes Wolff
E-Mail mailto:cpt@uke.de
URL http://www.uke.de/cpt
С кем можно связаться

National Coordinator

PD Dr. med. Uwe Richard Kordes
Universitätsklinikum Hamburg-Eppendorf
Klinik und Poliklinik f. Päd. Hämatologie u. Onkologie
Martinistraße 52
20246 Hamburg
Telefon +49 (40) 7410 59199
Fax +49 (40) 7410-57544
kordes@uke.de

Studienassistenz

Dr. rer. nat. Stefan Hartung
Universitätsklinikum Hamburg-Eppendorf
Klinik u. Poliklinik f.Pädiatrische Hämatologie u. Onkologie
Martinistraße 52
Hamburg 20246
Telefon +49 (40) 7410 57697
Fax +49 40 7410 57544

Внутренние ссылки Studienliteratur CPT
Dokumente zum CPT-Registry
Кто финансирует Deutsche Kinderkrebsstiftung