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Time trends and prognostic factors for survival from childhood cancer: a report from the Childhood Cancer Registry of Piedmont (Italy)

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Abstract

Survival after childhood cancer has been improving since the late 1970s in most developed countries. The Childhood Cancer Registry of Piedmont has been recording malignant tumors in children (0–14 years) throughout Piedmont since 1967. The present paper is based on the records of the 2,970 children diagnosed during the period 1970–2001; survival rates are estimated up to June 30, 2004. Based on records from the Registrar Offices of the relevant towns of residence, 1,698 children were reported to be alive, 1,252 deceased, and 20 were of unknown vital status. Over the period 1970–2001, 5-year survival rates for all tumor types combined showed a statistically significant increasing trend (p<0.0001). For acute lymphocytic leukemia, the survival rate increased steadily from 24.7% (95% CI 15.0–34.3) in 1970–1974 to 87.8% (82.1–93.6) in 1995–1999. Five-year survival rates for central nervous system tumors increased from 32.8% (21.0–44.6) in 1970–1974 to 80.3% (72.6–88.0) in 1990–1994 and decreased thereafter. Age of less than 1 year at time of diagnosis was a favorable prognostic factor for neuroblastoma and ganglioneuroblastoma. The extent of disease at diagnosis was related to prognosis for neuroblastoma and ganglioneuroblastoma and other selected solid tumors. A white blood cell count greater than 50,000×106 cells/l was associated with decreased survival in children with acute lymphocytic leukemia and acute non-lymphocytic leukemia. We have found positive trends in survival for all tumor types in Piedmont, similar to those reported by other population-based cancer registries. Age, extent of disease, and white blood cell count at diagnosis are prognostic factors for selected cancer sites.

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Abbreviations

ALL:

Acute lymphocytic leukemia

ANLL:

Acute non-lymphocytic leukemia

CCRP:

Childhood Cancer Registry of Piedmont

CI:

Confidence interval

CNS:

Central nervous system

FAB:

French-American-British

HR:

Hazard ratio

ICCC:

International classification of childhood cancer

ICD-O:

International classification of diesease for oncology

LFU:

Lost to follow-up

MV:

Microscopic verification

SNS:

Sympathetic nervous system

STS:

Soft tissue sarcomas

WBC:

White blood cell

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Acknowledgements

The CCRP is supported by the Piedmont Region. This project was partly supported by the “Oncology Special Project”, Compagnia di San Paolo FIRMS, by the Italian Association for Research on Cancer (AIRC), by the special program “Ricerca Sanitaria Finalizzata” of the Piedmont Region and by “University of Eastern Piedmont, local research funds 2003”. We thank Prof. Benedetto Terracini and Prof. Neil Pearce for their insight and for reading the manuscript. We thank Prof. Giuseppe Masera, Prof. Modesto Carli, Prof. Enrico Madon, Prof. Andrea Pession, Dr. Bruno De Bernardi and Dr. Franca Fossati Bellani, chairmen of AIEOP protocols, and Dr Roberto Rondelli for supplying clinical data. A grateful thanks to Mrs. Marinella Nonnato for the careful management of the CCRP data and for the follow-up.

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Correspondence to Corrado Magnani.

Appendix

Appendix

Some categories were grouped together: non-Hodgkin lymphoma (ICCC category 02B) with Burkitt lymphoma (02C) and unspecified lymphomas (02E); other gliomas (03D) with other specified intracranial and intraspinal neoplasms (03E) and unspecified intracranial and intraspinal neoplasms (03F); neuroblastoma and ganglioneuroblastoma (04A) with other sympathetic nervous system tumors (04B); fibrosarcoma, neurofibrosarcoma and other fibromatous neoplasms (09B) with other specified soft tissue sarcomas (09D) and unspecified soft tissue sarcomas (09E).

The other categories not mentioned in the paper were all included in the 'other tumor types' group.

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Dama, E., Pastore, G., Mosso, M.L. et al. Time trends and prognostic factors for survival from childhood cancer: a report from the Childhood Cancer Registry of Piedmont (Italy). Eur J Pediatr 165, 240–249 (2006). https://doi.org/10.1007/s00431-005-0034-7

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  • DOI: https://doi.org/10.1007/s00431-005-0034-7

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