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Impact of remission induction chemotherapy on survival in older adults with acute myeloid leukemia

✍ Scribed by Rachid Baz; Cristina Rodriguez; Alex Z. Fu; Rony Abou Jawde; Matt Kalaycio; Anjali Advani; Ronald Sobecks; Mikkael A. Sekeres


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
124 KB
Volume
110
Category
Article
ISSN
0008-543X

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✦ Synopsis


Abstract

BACKGROUND.

Significant controversy surrounds the use of remission induction chemotherapy (IC) in older adults with acute myeloid leukemia (AML). Earlier clinical trials have yielded conflicting results and possibly a minor survival benefit, often offset by a longer hospitalization time.

METHODS.

To evaluate the role of IC in patients with AML, a case control study of patients 60 years or older treated at the Cleveland Clinic Taussig Cancer Center between 1997 and 2005 was conducted. Forty‐four patients who did not receive IC were matched by a propensity analysis to 138 patients who received an anthracycline‐based regimen.

RESULTS.

The unadjusted median survival of patients who did not receive IC was 53 days, compared with 197 days (P < .001) for those who did. After further adjusting for age, gender, race, leukocyte count at presentation, AML cytogenetics, history of prior hematologic disorder, and assessing for comorbidities, not receiving IC was still associated with worse survival (hazards ratio of 1.88; 95% confidence interval, 1.15–3.05 [P = .01]). Additional predictors of poor outcomes in older adults with AML included higher leukocyte count at presentation, poor‐risk cytogenetics, and African‐American race (compared with Caucasians).

CONCLUSIONS.

The study suggests improved outcomes in older adults with AML who undergo remission induction therapy. Cancer 2007. Β© 2007 American Cancer Society.


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## Abstract Eighty‐one patients with acute myeloid leukemia who had persistent leukemia following standard induction therapy with cytarabine plus daunorubicin (7+3 regimen) underwent reinduction therapy with a combination of mitoxantrone, etoposide, and high‐dose cytarabine (HiDAC). Patients achiev