1993
DOI: 10.1002/1097-0142(19930901)72:5<1795::aid-cncr2820720546>3.0.co;2-n
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Response to neoadjuvant chemotherapy in children with pineoblastoma

Abstract: Background. The outlook of children with pineoblastoma treated with radiation therapy alone is extremely poor, but neoadjuvant chemotherapy has been tried only in a few cases of this rare childhood brain tumor with poor prognosis. Methods. Three consecutive children 3 to 7 years of age received neoadjuvant chemotherapy consisting of etoposide 100 mg/m2 days 1 to 3, cisplatin 100 mg/m2 day 1, and vincristine 1.5 mg/m2 day 1, repeated every 4 weeks. After four courses of chemotherapy, patients underwent craniosp… Show more

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Cited by 30 publications
(18 citation statements)
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“…12,15,26) Current agents used for PNETs include cyclophosphamide, cisplatin, carboplatin, vincristine, ifosmide, and etoposide. 2,17) While our study did not show any impact of chemotherapy on survival, the power of our analysis was limited by the small number of patients who received chemotherapy (n = 10, 29.4%) and the many different regimens used in these patients. Future studies should be directed towards the determination of the best chemotherapy regimen.…”
Section: Chemotherapymentioning
confidence: 65%
“…12,15,26) Current agents used for PNETs include cyclophosphamide, cisplatin, carboplatin, vincristine, ifosmide, and etoposide. 2,17) While our study did not show any impact of chemotherapy on survival, the power of our analysis was limited by the small number of patients who received chemotherapy (n = 10, 29.4%) and the many different regimens used in these patients. Future studies should be directed towards the determination of the best chemotherapy regimen.…”
Section: Chemotherapymentioning
confidence: 65%
“…Our search resulted in 109 publications 1, 3, 4, 7, 10, 17‐61. amounting to 299 nonduplicated, diaggregated patients who were treated for pineoblastoma (see Fig.…”
Section: Resultsmentioning
confidence: 99%
“…17 Phenytoin earlier was reported to inhibit microtubular polymerization, 33,34 an activity that has been postulated to be the cause of its teratogenic action. 16,18 Mareel and coworkers 36 demonstrated a fairly complete inhibition of invasion of malignant murine cells into embryonic chick heart fragments at 1 g VCR/ml. 17 The addition of a noncytostatic drug to a chemotherapeutic agent not only is an attractive concept, in terms of augmentation of the antiproliferative activity with fewer side effects, but also promises further insight into the functional mechanisms of tumor control.…”
Section: Vinca Alkaloids Dph and Microtubulesmentioning
confidence: 96%