Effect of time to complete remission on subsequent survival and disease-free survival time in AML, RAEB-t, and RAEB
Open Access
- 1 January 2000
- journal article
- Published by American Society of Hematology in Blood
- Vol. 95 (1) , 72-77
- https://doi.org/10.1182/blood.v95.1.72
Abstract
The authors examined the relationship between the time required to enter complete remission (CR) after a first course of chemotherapy for newly diagnosed acute myeloid leukemia (AML), refractory anemia with excess blasts in transformation (RAEB-t), or refractory anemia with excess blasts (RAEB). They also examined subsequent survival time and disease-free survival time after accounting for cytogenetic status, age, and treatment. The data set consisted of 1101 patients with these diagnoses treated at the M. D. Anderson Cancer Center between 1980 and 1996 for whom outcomes were established after first-course therapy. Of the 1101 patients, 740 (67%) were in CR after this time; 508 of these 740 (69%) have died (80% had disease recurrence before death). The authors used the parametric model of Shen and Thall to estimate, in particular, TC (time to CR), TC,D (time from CR to death = residual survival after CR), and TC,R (residual disease-free survival [DFS] after CR) as functions of the covariates noted above and to estimate the dependence of TC,D and TC,R on TC. There was a strong inverse association between TC and both TC,D and TC,R (P < .001 for both) that was independent of cytogenetic status, age, or treatment. The residual survival time of patients who required >50 days to enter CR was closer to the residual survival time of resistant patients than to that of patients known to be in CR within approximately 30 days of the start of treatment. Time to CR is an independent predictor of residual survival and disease-free survival in patients with newly diagnosed AML who achieve CR after 1 course of chemotherapy. (Blood. 2000;95:72-77)Keywords
This publication has 14 references indexed in Scilit:
- Randomized Phase II Study of Fludarabine + Cytosine Arabinoside + Idarubicin ± All-Trans Retinoic Acid ± Granulocyte Colony-Stimulating Factor in Poor Prognosis Newly Diagnosed Acute Myeloid Leukemia and Myelodysplastic SyndromeBlood, 1999
- Parametric likelihoods for multiple non-fatal competing risks and deathStatistics in Medicine, 1998
- Effect of Diagnosis (Refractory Anemia With Excess Blasts, Refractory Anemia With Excess Blasts in Transformation, or Acute Myeloid Leukemia [AML]) on Outcome of AML-Type ChemotherapyBlood, 1997
- Randomized Comparison of DAT Versus ADE as Induction Chemotherapy in Children and Younger Adults With Acute Myeloid Leukemia. Results of the Medical Research Council's 10th AML Trial (MRC AML10)Blood, 1997
- A randomized investigation of high-dose versus standard-dose cytosine arabinoside with daunorubicin in patients with previously untreated acute myeloid leukemia: a Southwest Oncology Group studyBlood, 1996
- Use of granulocyte colony-stimulating factor before, during, and after fludarabine plus cytarabine induction therapy of newly diagnosed acute myelogenous leukemia or myelodysplastic syndromes: comparison with fludarabine plus cytarabine without granulocyte colony-stimulating factor.Journal of Clinical Oncology, 1994
- Report of the National Cancer Institute-sponsored workshop on definitions of diagnosis and response in acute myeloid leukemia.Journal of Clinical Oncology, 1990
- A strategy for evaluation of new treatments in untreated patients: application to a clinical trial of AMSA for acute leukemia.Journal of Clinical Oncology, 1987
- Factors related to length of complete remission in adult acute leukemiaCancer, 1980
- The effect of chemotherapy on acute leukemia in the humanJournal of Chronic Diseases, 1961