Dose and dose intensity are believed critical for attaining a maximal therapeutic effect in drug-responsive tumor systems. Childhood acute lymphoblastic leukemia may be an example of such a drug-responsive system as it is cured with current chemotherapy in a majority of cases. Between August 1981 an
Day 7 marrow response and outcome for children with acute lymphoblastic leukemia and unfavorable presenting features
✍ Scribed by Gaynon, Paul S. ;Bleyer, W. Archie ;Steinherz, Peter G. ;Finklestein, Jerry Z. ;Littman, Phillip ;Miller, Denis R. ;Reaman, Gregory ;Sather, Harland ;Hammond, G. Denman
- Book ID
- 102949870
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 604 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0098-1532
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The percent of marrow blasts on day 7 of therapy was determined for 128 children with previously untreated acute lymphoblastic leukemia and white blood count (WBC) ± 50,000/μl and/or lymphomatous features enrolled in the Childrens Cancer Study Group trial of the Berlin Frankfurt Munster 76/79 regimen (CCG‐193P). Patients received four‐drug induction therapy including vincristine, prednisone, l‐asparaginase, and daunomycin. Ninety‐seven patients had fewer than 25% marrow blasts on day 7. Of these, 94 survived and maintained remission through day 28 and were designated early responders. Thirty‐one patients had greater than 25% marrow blasts on day 7. Of these, 28 survived and achieved remission on day 28 and were designated late responders. The outcome of patients who underwent a day 7 marrow aspiration was similar to those who did not. Early responders had a 77.4% ± 4.5% (standard deviation) 3‐year estimated disease free survival, while late responders had 47.3% ± 9.8% (P<0.001). Early responders had a superior outcome both in the subset with an initial WBC<50,000/μl (P = 0.025) and in the subset with a WBC ± 50,000/μl (P = 0.01). The day 7 marrow response had prognostic value in this population of children with unfavorable presenting features who received four‐drug remission induction therapy.
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