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Problems In The Prognosis Of Neuroblastoma

Dargeon, H. W. 1960Neuroblastoma

American Journal of Roentgenology 83(3): March 1960; 551-555

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Abstract

The author has collected a series of 58 children with neuroblastoma in whom no active treatment was undertaken, but it should be stressed that all these cases have been histologically confirmed, either by means of biopsy or at autopsy. The average survival period of the untreated fatal cases was four months from symptomatic onset. Among the 58 untreated children included, no less than 20 showed a symptomatic onset of the illness in the first year of life, and 19 of these succumbed to the disease, as did all the ones aged more than 1 year. The one solitary survivor in the untreated series is the only instance of spontaneous regression in our series. In November 1950, a new treatment was introduced, Vitamin B12 injections. A completely unselected series of 82 patients with neuroblastoma was given this treatment. Of these, 33 children have been complete clinical failures; 8 children have shown temporary improvement; 8 more were excluded because the length of treament was considered to be inadequate. Thirty-two children have been classified as clinical remissions; 30 of them are alive, 28 for periods of from more than 2 years to 12 years. Two children have died after Vitamin B12 therapy from other causes, with no evidence of tumor at autopsy.

Case Details

Personal Characteristics

Female child aged four months

Clinical Characteristics

Multiple subcutaneous nodules, one of which was biopsied and showed neuroblastoma, and a very enlarged liver

Remission Characteristics

Six months later the nodules began to disappear and in december 1958, at the age of two and one half years, she shows no signs of disease

Treatment & Mechanisms

Proposed Remission Mechanisms

Not discussed

Non-Clinical Treatment

No treatment

Additional Notes

The family refused any therapy and took her home against advice. At present this would be called a spontaneous clinical remission but we do not know whether reactivation of the recognized sites or growth of possible unrecognized sites may subsequently occur.