Stage II neuroblastoma-does adjuvant irradiation contribute to cure?

Twenty‐one children with Stage II neuroblastoma diagnosed between 1973 and 1983 were analyzed retrospectively. Median age at diagnosis was eleven months (1 week to 153 months). Primary tumor was above the diaphragm in 67% and below the diaphragm in 33%. All patients underwent surgical resection and...

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Veröffentlicht in:Medical and pediatric oncology 1985, Vol.13 (3), p.117-121
Hauptverfasser: McGuire, Warren A., Simmons, Doyle, Grosfeld, Jay L., Baehner, Robert L.
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container_end_page 121
container_issue 3
container_start_page 117
container_title Medical and pediatric oncology
container_volume 13
creator McGuire, Warren A.
Simmons, Doyle
Grosfeld, Jay L.
Baehner, Robert L.
description Twenty‐one children with Stage II neuroblastoma diagnosed between 1973 and 1983 were analyzed retrospectively. Median age at diagnosis was eleven months (1 week to 153 months). Primary tumor was above the diaphragm in 67% and below the diaphragm in 33%. All patients underwent surgical resection and pathologic diagnosis was neuroblastoma in 76% and ganglioneuroblastoma in 24%. Regional lymph nodes were positive in three of eleven patients sampled. Sixty‐seven percent had gross residual disease, and thirty‐three percent had microscopic residual disease. Seventeen patients received postoperative irradiation and none has relapsed (median follow‐up 57 months). Four patients received surgery alone (median follow‐up 24 months); one local relapse occurred in this group and was subsequently treated with irradiation. All patients are alive and disease free, with a median length of follow‐up of 55 months. Radiation dosage was 1000‐1800 rad in patients less than 12 months of age, and 1800‐3000 rad in those greater than 12 months of age at diagnosis. The high disease‐free survival rate in both groups of patients, but especially in the group receiving adjuvant irradiation, emphasizes the need for a controlled, prospective study to determine which Stage II neuroblastoma patients, if any, would be benefitted by postoperative irradiation.
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Median age at diagnosis was eleven months (1 week to 153 months). Primary tumor was above the diaphragm in 67% and below the diaphragm in 33%. All patients underwent surgical resection and pathologic diagnosis was neuroblastoma in 76% and ganglioneuroblastoma in 24%. Regional lymph nodes were positive in three of eleven patients sampled. Sixty‐seven percent had gross residual disease, and thirty‐three percent had microscopic residual disease. Seventeen patients received postoperative irradiation and none has relapsed (median follow‐up 57 months). Four patients received surgery alone (median follow‐up 24 months); one local relapse occurred in this group and was subsequently treated with irradiation. All patients are alive and disease free, with a median length of follow‐up of 55 months. Radiation dosage was 1000‐1800 rad in patients less than 12 months of age, and 1800‐3000 rad in those greater than 12 months of age at diagnosis. 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Pediatr. Oncol</addtitle><description>Twenty‐one children with Stage II neuroblastoma diagnosed between 1973 and 1983 were analyzed retrospectively. Median age at diagnosis was eleven months (1 week to 153 months). Primary tumor was above the diaphragm in 67% and below the diaphragm in 33%. All patients underwent surgical resection and pathologic diagnosis was neuroblastoma in 76% and ganglioneuroblastoma in 24%. Regional lymph nodes were positive in three of eleven patients sampled. Sixty‐seven percent had gross residual disease, and thirty‐three percent had microscopic residual disease. Seventeen patients received postoperative irradiation and none has relapsed (median follow‐up 57 months). Four patients received surgery alone (median follow‐up 24 months); one local relapse occurred in this group and was subsequently treated with irradiation. All patients are alive and disease free, with a median length of follow‐up of 55 months. Radiation dosage was 1000‐1800 rad in patients less than 12 months of age, and 1800‐3000 rad in those greater than 12 months of age at diagnosis. The high disease‐free survival rate in both groups of patients, but especially in the group receiving adjuvant irradiation, emphasizes the need for a controlled, prospective study to determine which Stage II neuroblastoma patients, if any, would be benefitted by postoperative irradiation.</description><subject>Age Factors</subject><subject>Biological and medical sciences</subject><subject>Child, Preschool</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Ganglioneuroma - mortality</subject><subject>Ganglioneuroma - pathology</subject><subject>Ganglioneuroma - radiotherapy</subject><subject>Ganglioneuroma - surgery</subject><subject>Humans</subject><subject>Infant</subject><subject>irradiation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neoplasm Metastasis</subject><subject>Neoplasm Recurrence, Local</subject><subject>Neuroblastoma - mortality</subject><subject>Neuroblastoma - pathology</subject><subject>Neuroblastoma - radiotherapy</subject><subject>Neuroblastoma - surgery</subject><subject>Neurology</subject><subject>Radiotherapy Dosage</subject><subject>Retrospective Studies</subject><subject>Stage II neuroblastoma</subject><subject>Tumors of the nervous system. 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subjects Age Factors
Biological and medical sciences
Child, Preschool
Combined Modality Therapy
Female
Follow-Up Studies
Ganglioneuroma - mortality
Ganglioneuroma - pathology
Ganglioneuroma - radiotherapy
Ganglioneuroma - surgery
Humans
Infant
irradiation
Male
Medical sciences
Neoplasm Metastasis
Neoplasm Recurrence, Local
Neuroblastoma - mortality
Neuroblastoma - pathology
Neuroblastoma - radiotherapy
Neuroblastoma - surgery
Neurology
Radiotherapy Dosage
Retrospective Studies
Stage II neuroblastoma
Tumors of the nervous system. Phacomatoses
title Stage II neuroblastoma-does adjuvant irradiation contribute to cure?
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