Background. Mass population screening of infants for neuroblastoma was introduced in Japan in 1985. Other investigations of screening have been carried out in North America and Europe. Procedure. This paper summarizes the epidemiological results from the reports published from the infant screening p
Infants younger than 1 year of age with rhabdomyosarcoma
โ Scribed by Dr. Abdelsalam H. Ragab; Ruth Heyn; Melvin Tefft; Daniel N. Hays; William A. Newton Jr.; Mohan Beltangady
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 388 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
โฆ Synopsis
Of a total of 1561 patients registered in the Intergroup Rhabdomyosarcoma Study (IRS) as of May 1983, 78 patients (5%) were younger than 1 year of age. These infants did not differ from the older children (1-20 years of age) in male/female ratio, clinical grouping, or survival rates. Infants younger than 1 year of age had a significantly greater frequency of undifferentiated sarcoma, 18% versus 7% in older children (P < 0.005). Infants 'also had a significantly greater proportion of cancers with botryoid pathology, 10% versus 4% in older children (P < 0.005). When reviewed by the newly proposed IRS cytopathologic classification, there was no difference in pathologic types between the two age groups. Infants younger than 1 year of age had a higher rate of bladder-prostate-vagina primary tumor sites than older children, 24% versus 10% (P < 0.05). In addition, infants tended to receive less of the prescribed doses of chemotherapy and radiation therapy than older children, and to develop more toxicity to treatment than older chi!dren. Despite these differences, the overall survival curve for the two age groups appears to be similar. In contrast to Wilms' tumor and neuroblastoma, in which age ( 4 year) is a favorable prognostic factor, age does not appear to be an important prognostic factor in rhabdomyosarcoma.
Cancer 58:
๐ SIMILAR VOLUMES