BACKGROUND: The purpose of the current study was to evaluate the activity and toxicity of dexamethasone, high-dose cytarabine, and carboplatin (DAC) combination therapy in children with newly diagnosed large-cell non-Hodgkin lymphoma (NHL) and to estimate the event-free and overall survival rates achieved when DAC is incorporated into a conventional regimen. METHODS: From 1991 to 1997, 20 boys and 5 girls aged 4.2 to 17.7 years who had stage III (according to the St. Jude staging system) (n = 21) or stage IV (n = 4) large-cell NHL were treated in this study. DAC therapy was administered at the beginning of the induction phase in 2 sequential cycles and incorporated throughout a continuation phase (modified from the ACOP+ regimen, which features doxorubicin, cyclophosphamide, vincristine, and prednisone) with doxorubicin, cyclophosphamide, vincristine, and dexamethasone. The total duration of treatment was approximately 10 months. RESULTS: DAC therapy yielded a response in 22 of 25 patients (88%; 95% confidence interval [95% CI], 68%-97%): complete remission in 13 cases (52%), and partial response in 9 (36%). After additional treatment with doxorubicin, cyclophosphamide, vincristine, and dexamethasone, complete remission was attained in 18 patients (72%) and partial remission in 3 (12%). The event-free survival rate (+/- the standard error [SE]) was 64% +/- 9% and the overall survival rate was 80% +/- 8% at 5 years. CONCLUSIONS: The results of the current study indicate that the DAC regimen is well tolerated and effective for pediatric patients with large-cell NHL. 2008 American Cancer Society
BACKGROUND: The purpose of the current study was to evaluate the activity and toxicity of dexamethasone, high-dose cytarabine, and carboplatin (DAC) combination therapy in children with newly diagnosed large-cell non-Hodgkin lymphoma (NHL) and to estimate the event-free and overall survival rates achieved when DAC is incorporated into a conventional regimen. METHODS: From 1991 to 1997, 20 boys and 5 girls aged 4.2 to 17.7 years who had stage III (according to the St. Jude staging system) (n = 21) or stage IV (n = 4) large-cell NHL were treated in this study. DAC therapy was administered at the beginning of the induction phase in 2 sequential cycles and incorporated throughout a continuation phase (modified from the ACOP+ regimen, which features doxorubicin, cyclophosphamide, vincristine, and prednisone) with doxorubicin, cyclophosphamide, vincristine, and dexamethasone. The total duration of treatment was approximately 10 months. RESULTS:DAC therapy yielded a response in 22 of 25 patients (88%; 95% confidence interval [95% CI], 68%-97%): complete remission in 13 cases (52%), and partial response in 9 (36%). After additional treatment with doxorubicin, cyclophosphamide, vincristine, and dexamethasone, complete remission was attained in 18 patients (72%) and partial remission in 3 (12%). The event-free survival rate (+/- the standard error [SE]) was 64% +/- 9% and the overall survival rate was 80% +/- 8% at 5 years. CONCLUSIONS: The results of the current study indicate that the DAC regimen is well tolerated and effective for pediatric patients with large-cell NHL. 2008 American Cancer Society
Authors: R I Fisher; E R Gaynor; S Dahlberg; M M Oken; T M Grogan; E M Mize; J H Glick; C A Coltman; T P Miller Journal: N Engl J Med Date: 1993-04-08 Impact factor: 91.245
Authors: A Reiter; M Schrappe; M Tiemann; R Parwaresch; M Zimmermann; E Yakisan; R Dopfer; P Bucsky; G Mann; H Gadner Journal: J Clin Oncol Date: 1994-05 Impact factor: 44.544
Authors: J T Sandlund; C H Pui; V M Santana; H Mahmoud; W M Roberts; S Morris; S Raimondi; R Ribeiro; W M Crist; J S Lin Journal: J Clin Oncol Date: 1994-05 Impact factor: 44.544
Authors: A Reiter; M Schrappe; W D Ludwig; F Lampert; J Harbott; G Henze; C M Niemeyer; H Gadner; S Müller-Weihrich; J Ritter Journal: Blood Date: 1992-11-15 Impact factor: 22.113
Authors: J T Sandlund; V Santana; M Abromowitch; R Ribeiro; H Mahmoud; G D Ayers; J S Lin; R E Hutchison; C W Berard; C A Greenwald Journal: Leukemia Date: 1994-01 Impact factor: 11.528
Authors: J R Anderson; R D Jenkin; J F Wilson; C R Kjeldsberg; R Sposto; R R Chilcote; P F Coccia; P R Exelby; S Siegel; A T Meadows Journal: J Clin Oncol Date: 1993-06 Impact factor: 44.544