| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Division of Pediatric Oncology, The Children's Hospital of Philadelphia, and the Department of Pediatrics, The University of Pennsylvania School of Medicine [J. H. S., A. E. E.], and Department of Statistics, The University of Pennsylvania [M. F.], Philadelphia, Pennsylvania 19104
We report on the development of three multiple logistic regression models to predict death from childhood neuroblastoma in patients treated without bone marrow transplantation. The models have been developed using a data set of 125 patients for whom age, stage, serum ferritin, and/or histology were available from diagnosis. Seventy-seven patients had all four variables recorded at diagnosis, 34 had age, stage, and serum ferritin, and 14 had age, stage, and histology. Minimum time from diagnosis for all patients was 3 years. The four-variable (full) model showed a predictive value positive rate (or 1 the false positive rate) of 91.3% and a predictive value negative rate (or 1 the false negative rate) of 94.4%. Survival curves, based on derived "good" and "poor" prognosis, were constructed for the full model of 77 patients and for the same patients using subset models either without ferritin or without histology. Correcting for prognostic factors noted at diagnosis, no time trend could be identified over the study period. Point estimates for the probability of death in all three models are displayed in graphical form. The results suggest that serum ferritin and tumor histology at diagnosis have independent prognostic significance and that patient outcome in neuroblastoma can be very accurately predicted with a four-variable model. Such information will help sort patients into good and poor prognosis for bone marrow transplant and intensive chemotherapy protocol triage and will help evaluate the efficacy of future therapeutic innovations.
1 This research was supported by the American Cancer Society and NIH Grant KO4CA01480. Point estimates for the derived predictive models, along with 95% confidence intervals, are available upon request.
2 To whom requests for reprints should be addressed, at The Children's Hospital of Philadelphia, Division of Oncology, Room 9093, 34th & Civic Center Blvd., Philadelphia, PA 19104.
Received 7/25/90. Accepted 12/17/90.
This article has been cited by other articles:
![]() |
K. Kalantar-Zadeh, K. Kalantar-Zadeh, and G. H. Lee The Fascinating but Deceptive Ferritin: To Measure It or Not to Measure It in Chronic Kidney Disease? Clin. J. Am. Soc. Nephrol., September 1, 2006; 1(Supplement_1): S9 - S18. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. X. Tang, H. Zhao, B. Kung, D. Y. Kim, S. L. Hicks, S. L. Cohn, N.-K. Cheung, R. C. Seeger, A. E. Evans, and N. Ikegaki The MYCN Enigma: Significance of MYCN Expression in Neuroblastoma. Cancer Res., March 1, 2006; 66(5): 2826 - 2833. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Weinstein, H. M. Katzenstein, and S. L. Cohn Advances in the Diagnosis and Treatment of Neuroblastoma Oncologist, June 1, 2003; 8(3): 278 - 292. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. J. Nickerson, K. K. Matthay, R. C. Seeger, G. M. Brodeur, H. Shimada, C. Perez, J. B. Atkinson, M. Selch, R. B. Gerbing, D. O. Stram, et al. Favorable Biology and Outcome of Stage IV-S Neuroblastoma With Supportive Care or Minimal Therapy: A Children’s Cancer Group Study J. Clin. Oncol., February 1, 2000; 18(3): 477 - 477. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Raschella, V. Cesi, R. Amendola, A. Negroni, B. Tanno, P. Altavista, G. Paolo Tonini, B. De Bernardi, and B. Calabretta Expression of B-myb in Neuroblastoma Tumors Is a Poor Prognostic Factor Independent from MYCN Amplification Cancer Res., July 1, 1999; 59(14): 3365 - 3368. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. X. Tang, A. E. Evans, H. Zhao, A. Cnaan, W. London, S. L. Cohn, G. M. Brodeur, and N. Ikegaki High-Level Expression of EPHB6, EFNB2, and EFNB3 Is Associated with Low Tumor Stage and High TrkA Expression in Human Neuroblastomas Clin. Cancer Res., June 1, 1999; 5(6): 1491 - 1496. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Caron, P. van Sluis, J. de Kraker, J. Bokkerink, M. Egeler, G. Laureys, R. Slater, A. Westerveld, P.A. VoUte, and R. Versteeg Allelic Loss of Chromosome 1p as a Predictor of Unfavorable Outcome in Patients with Neuroblastoma N. Engl. J. Med., January 25, 1996; 334(4): 225 - 230. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. X. Tang, H. Zhao, M. E. Robinson, B. Cohen, A. Cnaan, W. London, S. L. Cohn, N.-K. V. Cheung, G. M. Brodeur, A. E. Evans, et al. Implications of EPHB6, EFNB2, and EFNB3 expressions in human neuroblastoma PNAS, September 26, 2000; 97(20): 10936 - 10941. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Cancer Research | Clinical Cancer Research |
| Cancer Epidemiology Biomarkers & Prevention | Molecular Cancer Therapeutics |
| Molecular Cancer Research | Cancer Prevention Research |
| Cancer Prevention Journals Portal | Cancer Reviews Online |
| Annual Meeting Education Book | Meeting Abstracts Online |