Klin-Padiatr. 1998 Jul-Aug; 210(4): 227-33
Preradiation chemotherapy of children and young adults with malignant brain tumors:
results of the German pilot trial HIT'88/'89.
Kuhl-J; Muller-HL; Berthold-F; Kortmann-RD; Deinlein-F; Maass-E; Graf-N; Gnekow-A;
Scheurlen-W; Gobel-U; Wolff-JE; Bamberg-M; Kaatsch-P; Kleihues-P; Rating-D; Sorensen-N;
Wiestler-OD
Department of Pediatric Oncology University of Wurzburg.
BACKGROUND: Preradiation chemotherapy could be beneficial in malignant brain tumors,
because the blood-brain tumor-barrier is disrupted after surgery, bone marrow
recovery-essential for intense chemotherapy--is still intact, and CNS toxicity and
ototoxicity of active drugs are lower before irradiation of a child's brain.
PATIENTS AND METHODS: A neoadjuvant phase 2 and a single arm pilot trial were initiated
to investigate the efficacy and toxicity of an intense multidrug regimen before
radiotherapy in 147 patients aged between 3 and 29; 9 years with medulloblastoma (94),
malignant glioma (22), ependymoma (21), and stPNET (10). They were treated with one or
two cycles consisting of procarbazine, ifosfamide/mesna with etoposide, high dose
methotrexate/CF, and cisplatin with cytarabine.
RESULTS: Radiation therapy was delayed for 17-30 weeks (median 23 weeks) in 112 patients
who received two cycles. Chemotherapy was well tolerated. Serious infections were
observed in 20 patients, with one fatal fungal septicemia. In 69 high risk patients with
a residual tumor and/or solid CNS metastases an objective response (CR plus PR) was
achieved in 67% medulloblastoma, 57% stPNET, 55% anaplastic ependymoma and 25% malignant
glioma. Progression-free survival (PFS) at 5 years was 57% in 14 high risk patients with
medulloblastoma, who achieved a complete response (CR). After a less than CR the PFS was
20% (p = 0.01). Overall survival at 5 years was 57% in medulloblastoma, 62% in
ependymoma, 36% in malignant glioma and 30% in stPNET.
CONCLUSION: The HIT'88/'89 regimen was well tolerated and efficacious in regard to
response rates and early PSF particularly in medulloblastoma and anaplastic ependymoma.
Based on these results the prospectively randomized trial HIT'91 was designed to
investigate the optimal timing of chemotherapy. Preradiation chemotherapy according to
the HIT'88/'89 regimen was compared with the standard regimen using CCNU, cisplatin, and
vincristine after radiation therapy. Additionally, strict quality control of the three
treatment modalities was instituted to help improve the survival rates in both trial
arms.
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