Literature DB >> 9207872

[High-dose chemotherapy in relapse of medulloblastoma in young children].

S Dupuis-Girod1, O Hartmann, E Benhamou, F Doz, F Mechinaud, E Bouffet, C Coze, C Kalifa.   

Abstract

Craniospinal irradiation is the gold standard treatment used in non metastatic medulloblastoma as prophylaxis against central nervous system (CNS) metastases. However, given the severe late effects caused by this procedure in children under 3 years of age, most pediatric oncologists are currently treating these patients with conventional chemotherapy in order to postpone or even avoid irradiation. In the French Society of Pediatric Oncology (SFOP) this attitude has been adopted since 1990. Among the patients treated without radiotherapy, 20 relapsed while on conventional chemotherapy and were entered in a study of high-dose chemotherapy (HDC) followed by autologous bone marrow transplantation (ABMT). Their median age at diagnosis was 23 months (range: 5-71 months) and the relapse occurred at a median time of 6.3 months after the initiation of chemotherapy. Complete surgical removal of the local relapse was the first treatment in 4/20 patients who were not evaluable for response. Sixteen of the 20 patients had measurable disease at the primary site (9 patients), or at metastatic sites (3 patients) or both (4 patients). The conditioning regimen consisted of combination busulfan 600 mg/m2 over 4 days and thiotepa 900 mg/m2 over 3 days. After recovery from aplasia, patients with a local relapse received local radiotherapy limited to posterior fossa. Among the 16 patients with measurable disease, 6 complete responses, 6 partial responses, 3 non response, were observed following HDC (response rate 75%). One patient was not evaluable. For the 20 patients, the event free survival (EFS) is 50%. Among the surviving patients, the median follow-up is 39.5 months post BMT (range: 21-92 months). Ten patients who developed a local relapse or local progression are alive with non evidence of disease (NED) without craniospinal irradiation. Among the 7 patients who developed a metastases or progression of metastases, only 1 is alive. Toxicity was high but manageable. One complication-related death occurred 1 month post BMT. With a 75% response rate, this HDC proved to be very efficient in relapsed medulloblastoma. A longer follow-up is necessary to demonstrate whether, after a local relapse, HDC could replace craniospinal irradiation as prophylaxis against CNS metastases.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9207872

Source DB:  PubMed          Journal:  Bull Cancer        ISSN: 0007-4551            Impact factor:   1.276


  3 in total

1.  Tandem thiotepa with autologous hematopoietic cell rescue in patients with recurrent, refractory, or poor prognosis solid tumor malignancies.

Authors:  Diana S Osorio; Ira J Dunkel; Kelly Ann Cervone; Rakesh K Goyal; K M Steve Lo; Jonathan L Finlay; Sharon L Gardner
Journal:  Pediatr Blood Cancer       Date:  2017-09-14       Impact factor: 3.167

2.  Pseudoprogression after high-dose busulfan-thiotepa with autologous stem cell transplantation and radiation therapy in children with brain tumors: Impact on survival.

Authors:  Laura Negretti; Pierre Blanchard; Dominique Couanet; Virginie Kieffer; Gisele Goma; Jean Louis Habrand; Frédéric Dhermain; Dominique Valteau-Couanet; Jacques Grill; Christelle Dufour
Journal:  Neuro Oncol       Date:  2012-10-05       Impact factor: 12.300

3.  Treatment of recurrent primitive neuroectodermal tumors (PNET) in children and adolescents with high-dose chemotherapy (HDC) and stem cell support: results of the HITREZ 97 multicentre trial.

Authors:  U Bode; M Zimmermann; O Moser; S Rutkowski; M Warmuth-Metz; T Pietsch; R D Kortmann; A Faldum; G Fleischhack
Journal:  J Neurooncol       Date:  2014-09-02       Impact factor: 4.130

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.