Literature DB >> 2439668

Neoadjuvant chemotherapy for newly diagnosed germ-cell tumors of the central nervous system.

J C Allen, J H Kim, R J Packer.   

Abstract

A neoadjuvant (preradiotherapy) chemotherapy regimen consisting of either cyclophosphamide alone (60 to 80 mg/kg) or a modified multidrug regimen (vinblastine, bleomycin, cyclophosphamide, and cisplatin) was administered to 15 newly diagnosed patients with histologically confirmed, fully staged, primary germ-cell tumors (GCT's) of the central nervous system (CNS). There were 11 patients with germinomas and four with non-germinoma malignant GCT's. There were six females and nine males, whose median age was 13 years (range 4 months to 24 years). Seven germinoma patients (64%) had disseminated disease. For the germinoma patients, the subsequent radiotherapy dose was modified based on the response to the neoadjuvant chemotherapy, and craniospinal radiotherapy was given only to those with disseminated CNS disease at diagnosis. Ten of the 11 germinoma patients had complete disappearance of all evaluable disease after two courses of chemotherapy (cyclophosphamide in eight and multidrug in three) and one had a partial response. The planned dose of radiotherapy to the primary tumor was reduced from 5500 to 3000 rads, and the craniospinal dose was lowered from 3600 to 2000 rads. Ten patients remain in continuous disease-free remission 20+ to 89+ months after diagnosis (median follow-up period 47 months). All four patients with non-germinoma GCT's received the multidrug regimen, and two fo three patients with evaluable disease had a partial response. High-dose regional and craniospinal radiotherapy was administered thereafter, but only two patients remain in their first remission. Previously untreated germinoma is a highly chemosensitive disease and the neoadjuvant treatment strategy permits the identification of active chemotherapy regimens in newly diagnosed patients. Patients who have complete responses to neoadjuvant chemotherapy tolerate a significant radiotherapy dose reduction without compromising long-term survival, thereby allowing a reduction of some of the late effects of therapeutic radiation. Germinomas tend to disseminate early in the course of the disease and a pre-therapy staging evaluation permits individualized radiotherapy treatment planning.

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Year:  1987        PMID: 2439668     DOI: 10.3171/jns.1987.67.1.0065

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  30 in total

1.  Treatment of malignant intracranial germ cell tumours.

Authors:  S Senan
Journal:  BMJ       Date:  1992-07-04

2.  Descriptive epidemiology of central nervous system germ cell tumors: nonpineal analysis.

Authors:  J Lee Villano; Irim Y Virk; Vanessa Ramirez; Jennifer M Propp; Herbert H Engelhard; Bridget J McCarthy
Journal:  Neuro Oncol       Date:  2009-12-21       Impact factor: 12.300

3.  Improved prognosis of intracranial non-germinoma germ cell tumors with multimodality therapy.

Authors:  P L Robertson; R C DaRosso; J C Allen
Journal:  J Neurooncol       Date:  1997-03       Impact factor: 4.130

4.  Complete disappearance of giant intracranial germinoma after irradiation.

Authors:  N G Rainov; H J Holzhausen; W Burkert
Journal:  Neurosurg Rev       Date:  1995       Impact factor: 3.042

5.  Intracranial germ-cell tumours--treatment results and residuals.

Authors:  C Haupt; U Ancker; M Muller; H D Herrmann; F J Schulte
Journal:  Eur J Pediatr       Date:  1996-03       Impact factor: 3.183

6.  Cisplatin-based chemotherapy in primary central nervous system germ cell tumors.

Authors:  S R Patel; J C Buckner; W A Smithson; B W Scheithauer; R V Groover
Journal:  J Neurooncol       Date:  1992-01       Impact factor: 4.130

Review 7.  Current advances in the diagnosis and management of intracranial germ cell tumors.

Authors:  Casilda Balmaceda; Jonathan Finlay
Journal:  Curr Neurol Neurosci Rep       Date:  2004-05       Impact factor: 5.081

8.  Germ cell tumor in the hypothalamo-neurohypophysial region: clinical features and treatment.

Authors:  S Nishio; T Inamura; I Takeshita; M Fukui; K Kamikaseda
Journal:  Neurosurg Rev       Date:  1993       Impact factor: 3.042

9.  Treatment strategy for intracranial primary pure germinoma.

Authors:  Kyu-Won Shim; Eun Kyung Park; Yoon-Ho Lee; Chang-Ok Suh; Jaeho Cho; Joong-Uhn Choi; Dong-Seok Kim
Journal:  Childs Nerv Syst       Date:  2012-09-11       Impact factor: 1.475

10.  High-dose chemotherapy with autologous peripheral blood stem cell support for recurrent primary AFP-producing intracranial germinoma.

Authors:  Carsten Ziske; Jörg Mezger; Carlos Jiménez; Rolf Kleinschmidt; Hendrik Pels; Uwe Schlegel; Ingo G H Schmidt-Wolf
Journal:  Ger Med Sci       Date:  2003-07-01
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