Literature DB >> 23983148

Outcomes of elderly de novo acute myeloid leukemia treated by a risk-adapted approach based on age, comorbidity, and performance status.

Jae-Ho Yoon1, Byung-Sik Cho, Hee-Je Kim, Jung-Ho Kim, Seung-Hwan Shin, Seung-Ah Yahng, Sung-Eun Lee, Ki-Seong Eom, Yoo-Jin Kim, Seok Lee, Chang-Ki Min, Seok-Goo Cho, Dong-Wook Kim, Jong-Wook Lee, Woo-Sung Min, Chong-Won Park.   

Abstract

Several criteria to define fitness for induction chemotherapy in elderly acute myeloid leukemia (AML) have been proposed; however, no studies have reported outcomes according to the application of a risk-adapted approach. We treated 256 consecutive patients with elderly AML (≥60 years) with a risk-adapted approach based on age, comorbidity score (CS), and performance status (ECOG). Eighty-five low-risk patients (age ≤ 65 years and ECOG 0-1 with CS < 2), 86 intermediate-risk patients (age > 65 years or ECOG = 2 with CS < 2), and 85 high-risk patients (ECOG > 2 or CS ≥ 2) were treated with induction chemotherapies, including standard intensive regimens, abbreviated-scheduled regimens, and modified low-dose cytarabine with oral etoposide (mLDAC), respectively. Overall response rates (ORR; complete response and complete response with incomplete recovery) for these three groups were 71.8%, 60.5%, and 41.2%, respectively, without a significant difference in early death rate (17.6%, 25.6%, 23.5%, P = 0.415). Among three abbreviated-scheduled regimens, a gemtuzumab ozogamicin (GO)-containing regimen (n = 43) showed a similar ORR rate (72.1%) to the intensive regimen. After achieving remission, 142 patients went on postremission treatments, including reduced-intensity allogeneic transplantation (RIC, n = 41), standard consolidation (n = 71), and repeated mLDAC (n = 30) according to donor availability, age, ECOG, and CS. Multivariate analyses revealed that not only RIC, but also repeated mLDAC, resulted in significantly superior survival outcomes to standard consolidation independent of age, ECOG, and CS. Clinical benefits of mLDAC for high-risk patients and abbreviated induction with GO for intermediate-risk patients should be confirmed with further studies. Our results also suggest that RIC should be actively considered in elderly AML as a postremission treatment.
Copyright © 2013 Wiley Periodicals, Inc.

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Year:  2013        PMID: 23983148     DOI: 10.1002/ajh.23576

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  6 in total

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2.  Prior hypomethylating agent use lacks impact on clinical outcome in patients with secondary acute myeloid leukemia arising from myelodysplastic syndromes treated with standard induction chemotherapy.

Authors:  Salih Subari; Firas Baidoun; Muhanad Hreh; Mrinal Patnaik; Shahrukh Hashmi; Michelle Elliott; William Hogan; Mark Litzow; Aref Al-Kali
Journal:  Int J Hematol       Date:  2016-01-18       Impact factor: 2.490

3.  Outcome and late effects among acute myeloid leukemia survivors: a nationwide population-based study.

Authors:  Kuang-Hsi Chang; Wen-Li Hwang; Chih-Hsin Muo; Chung Y Hsu; Chieh-Lin Jerry Teng
Journal:  Support Care Cancer       Date:  2016-08-09       Impact factor: 3.603

4.  How old is old: the beginning of a new era for therapeutic challenges for elderly patients with AML.

Authors:  Hee-Je Kim
Journal:  Blood Res       Date:  2014-06

5.  Comparison of the modified low-dose cytarabine and etoposide with decitabine therapy for elderly acute myeloid leukemia patients unfit for intensive chemotherapy.

Authors:  Seung-Hwan Shin; Byung-Sik Cho; Sung-Soo Park; Sung-Yeon Cho; Young-Woo Jeon; Jae-Ho Yoon; Seung-Ah Yahng; Sung-Eun Lee; Dong-Gun Lee; Ki-Seong Eom; Yoo-Jin Kim; Seok Lee; Chang-Ki Min; Seok-Goo Cho; Dong-Wook Kim; Jong-Wook Lee; Woo-Sung Min; Hee-Je Kim
Journal:  Oncotarget       Date:  2017-12-23

6.  Quantitative fragment analysis of FLT3-ITD efficiently identifying poor prognostic group with high mutant allele burden or long ITD length.

Authors:  Y Kim; G D Lee; J Park; J-H Yoon; H-J Kim; W-S Min; M Kim
Journal:  Blood Cancer J       Date:  2015-08-14       Impact factor: 11.037

  6 in total

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