𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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.


📜 SIMILAR VOLUMES


Association of delivered drug dose and o
✍ Gaynon, Paul S. ;Steinherz, Peter G. ;Bleyer, W. Archie ;Finklestein, Jerry Z. ; 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 640 KB

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

Features at presentation predict childre
✍ Tony H. Truong; Joseph Beyene; Johann Hitzler; Oussama Abla; Anne Marie Maloney; 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 99 KB

## Abstract ## BACKGROUND. Tumor lysis syndrome (TLS) is a well‐recognized complication of acute lymphoblastic leukemia (ALL). The ability to predict children at differing risk of TLS would be an early step toward risk‐based approaches. The objectives of the current study were 1) to describe the p

Outcome of acute lymphoblastic leukemia
✍ Ishii, Eiichi ;Eguchi, Haruhiko ;Matsuzaki, Akinobu ;Koga, Hiroyuki ;Yanai, Fumi 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 177 KB

## Abstract ## Background In our previous studies, the outcome of high‐risk ALL was still poor. In the present study, all children with ALL were classified into three groups and treated with a new regimen (AL90). ## Patients and Methods Between 1990 and 1996, 220 children with ALL, treated with

Comparison of the cellularity and presen
✍ Kidd, Pamela G.; Saminathan, Thamarai; Drachtman, Richard A.; Ettinger, Lawrence 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 23 KB 👁 3 views

Background. Many pediatric chemotherapy protocols for treatment of ALL require a bone marrow examination at day 7 or day 14 after initiation of therapy. The usefulness of a bone marrow biopsy, in addition to an aspirate, has been a frequently asked question. Procedure. This study addresses the eval

Levels of the soluble, 55-kilodalton iso
✍ Shuling Wu; Alexander Korte; Reinhard Gessner; Guenter Henze; Karlheinz Seeger 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 95 KB

## Abstract ## BACKGROUND It has been shown that the soluble, 55‐kilodalton isoform of tumor necrosis factor receptor (sTNFRp55) enhances tumor survival by exhibiting competitive ligand binding. The objective of the current study was to determine the levels of sTNFRp55 and their impact on outcome