Cyclophosphamide/doxorubicin vs. Cisplatin/teniposide in the treatment of children older than 12 months of age with disseminated neuroblastoma: A pediatric oncology group randomized phase II study
Autor: | Teresa J. Vietti, Nancy B. McWilliams, E. Ide Smith, Geoffrey Altshuler, F. Ann Hayes, Ruprecht Nitschke, Jonathan J. Shuster, Alexander A. Green, Robert P. Castleberry |
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Rok vydání: | 1995 |
Předmět: |
Cancer Research
medicine.medical_specialty Cyclophosphamide medicine.medical_treatment Phases of clinical research Gastroenterology Disease-Free Survival Neuroblastoma Internal medicine Antineoplastic Combined Chemotherapy Protocols medicine Humans Prospective Studies Neoplasm Metastasis Child Prospective cohort study Survival rate Teniposide Cisplatin Chemotherapy business.industry Remission Induction Infant Prognosis United States Surgery Survival Rate Oncology Doxorubicin Child Preschool Pediatrics Perinatology and Child Health Toxicity business medicine.drug |
Zdroj: | Medical and Pediatric Oncology. 24:176-180 |
ISSN: | 1096-911X 0098-1532 |
DOI: | 10.1002/mpo.2950240307 |
Popis: | This prospective study was designed to estimate the response rates and to compare two drug pairs, cyclophosphamide/doxorubicin (Cy/A) and cisplatin/teniposide (P1/VM) in previously untreated patients with disseminated neuroblastoma > 12 months of age at diagnosis. Estimated complete clinical response rates after five courses of therapy were 13% (70 patients) and 22% (64 patients) for Cy/A and P1/VM, respectively (P = 0.17). After surgical removal of residual tumors in patients with partial response, the complete response rates were 27% and 34% (P = 0.50), respectively. The overall CR/PR rates after induction and surgery were 59% and 73% (P = 0.077). There was no significant difference in event free survival (P = 0.48) or survival (P = 0.40). Five year survival on the two arms were 14% (SE = 5%) and 12% (SE = 4%), respectively. Toxicity was significant but manageable. The Cy/A arm had significantly higher hematopoietic toxicity but significantly lower GI toxicity. Significant allergic reactions were seen with the P1/VM arm, none in the Cy/A arm. Given the activity of these two regimens, further therapy with a combination of these regimens is suggested. |
Databáze: | OpenAIRE |
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