Time to repeal and replace response criteria for acute myeloid leukemia?

被引:54
作者
Bloomfield, Clara Derber [1 ]
Estey, Elihu [2 ]
Pleyer, Lisa [3 ,4 ,5 ]
Schuh, Andre C. [6 ]
Stein, Eytan M. [7 ,8 ]
Tallman, Martin S. [7 ,8 ]
Wei, Andrew [9 ,10 ]
机构
[1] Ohio State Univ, Columbus, OH 43210 USA
[2] Fred Hutchinson Canc Res Ctr, 1124 Columbia St, Seattle, WA 98104 USA
[3] Paracelsus Med Univ, Salzburg, Austria
[4] Salzburg Canc Res Inst, Ctr Clin Canc & Immunol Trials, Salzburg, Austria
[5] Canc Cluster Salzburg, Salzburg, Austria
[6] Princess Margaret Canc Ctr, Toronto, ON, Canada
[7] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[8] Weill Cornell Med Coll, New York, NY USA
[9] Alfred Hosp, Melbourne, Vic, Australia
[10] Monash Univ, Melbourne, Vic, Australia
关键词
Acute myeloid leukemia; AML; Response criteria; Minimal residual disease; MRD; Clinical trials; MINIMAL RESIDUAL DISEASE; INTERNATIONAL WORKING GROUP; ACUTE MYELOGENOUS LEUKEMIA; OLDER PATIENTS; COMPLETE REMISSION; GENE-MUTATIONS; ADULT PATIENTS; INDUCTION CHEMOTHERAPY; GEMTUZUMAB OZOGAMICIN; PROGNOSTIC RELEVANCE;
D O I
10.1016/j.blre.2018.03.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The International Working Group (IWG) response criteria for acute myeloid leukemia, published in 2003, have remained the standard by which the efficacy of new drugs is measured in clinical trials. Over the last decade, concepts related to treatment response have been challenged by several factors; for example, the dissociation between early clinical response and survival outcome in older patients, the recognition that epigenetic and newer differentiating-agent therapies may produce delayed responses and also hematologic improvement' transfusion independence without a morphologic response, and evidence that remissions without minimal (or measurable) residual disease (MRD) may result in outcomes superior to those of morphologic remissions with persistent MRD. The evolving role of MRD status as a potential surrogate for predicting long-term survival has enhanced the clinical need to standardize and incorporate emerging technologies that enable deeper responses beyond those recognized by the IWG, and to pre-emptively identify patients at risk of early relapse. The potential for therapeutic interventions to erase MRD and alter the natural history represents an important and open research question. Reviewed here are some of the implications and challenges associated with establishing and incorporating new treatment response criteria, initially into clinical research, and eventually into real-world practice.
引用
收藏
页码:416 / 425
页数:10
相关论文
共 87 条
[1]   Enasidenib induces acute myeloid leukemia cell differentiation to promote clinical response [J].
Amatangelo, Michael D. ;
Quek, Lynn ;
Shih, Alan ;
Stein, Eytan M. ;
Roshal, Mikhail ;
David, Muriel D. ;
Marteyn, Benoit ;
Farnoud, Noushin Rahnamay ;
de Botton, Stephane ;
Bernard, Olivier A. ;
Wu, Bin ;
Yen, Katharine E. ;
Tallman, Martin S. ;
Papaemmanuil, Elli ;
Penard-Lacronique, Virginie ;
Thakurta, Anjan ;
Vyas, Paresh ;
Levine, Ross L. .
BLOOD, 2017, 130 (06) :732-741
[2]  
[Anonymous], 2015, DACOGEN PRESCRIBING
[3]  
[Anonymous], 2016, BLOOD
[4]  
[Anonymous], 2016, VIDAZA AZACITIDINE P
[5]   The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia [J].
Arber, Daniel A. ;
Orazi, Attilio ;
Hasserjian, Robert ;
Thiele, Jurgen ;
Borowitz, Michael J. ;
Le Beau, Michelle M. ;
Bloomfield, Clara D. ;
Cazzola, Mario ;
Vardiman, James W. .
BLOOD, 2016, 127 (20) :2391-2405
[6]   Postinduction Minimal Residual Disease Predicts Outcome and Benefit From Allogeneic Stem Cell Transplantation in Acute Myeloid Leukemia With NPM1 Mutation: A Study by the Acute Leukemia French Association Group [J].
Balsat, Marie ;
Renneville, Aline ;
Thomas, Xavier ;
de Botton, Stephane ;
Caillot, Denis ;
Marceau, Alice ;
Lemasle, Emilie ;
Marolleau, Jean-Pierre ;
Nibourel, Olivier ;
Berthon, Celine ;
Raffoux, Emmanuel ;
Pigneux, Arnaud ;
Rodriguez, Celine ;
Vey, Norbert ;
Cayuela, Jean-Michel ;
Hayette, Sandrine ;
Braun, Thorsten ;
Coude, Marie Magdeleine ;
Terre, Christine ;
Celli-Lebras, Karine ;
Dombret, Herve ;
Preudhomme, Claude ;
Boissel, Nicolas .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (02) :185-+
[7]   Genomics of Acute Myeloid Leukemia Diagnosis and Pathways [J].
Bullinger, Lars ;
Doehner, Konstanze ;
Doehner, Hartmut .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (09) :934-946
[8]   The addition of gemtuzumab ozogamicin to low-dose Ara-C improves remission rate but does not significantly prolong survival in older patients with acute myeloid leukaemia: results from the LRF AML14 and NCRI AML16 pick-a-winner comparison [J].
Burnett, A. K. ;
Hills, R. K. ;
Hunter, A. E. ;
Milligan, D. ;
Kell, W. J. ;
Wheatley, K. ;
Yin, J. ;
McMullin, M. F. ;
Dignum, H. ;
Bowen, D. ;
Russell, N. H. .
LEUKEMIA, 2013, 27 (01) :75-81
[9]   Clofarabine doubles the response rate in older patients with acute myeloid leukemia but does not improve survival [J].
Burnett, Alan K. ;
Russell, Nigel H. ;
Hunter, Ann E. ;
Milligan, Donald ;
Knapper, Steven ;
Wheatley, Keith ;
Yin, John ;
McMullin, Mary F. ;
Ali, Sahra ;
Bowen, David ;
Hills, Robert K. .
BLOOD, 2013, 122 (08) :1384-1394
[10]   The impact of dose escalation and resistance modulation in older patients with acute myeloid leukaemia and high risk myelodysplastic syndrome: the results of the LRF AML14 trial [J].
Burnett, Alan K. ;
Milligan, Donald ;
Goldstone, Anthony ;
Prentice, Archibald ;
McMullin, Mary-Frances ;
Dennis, Michael ;
Sellwood, Elizabeth ;
Pallis, Monica ;
Russell, Nigel ;
Hills, Robert K. ;
Wheatley, Keith .
BRITISH JOURNAL OF HAEMATOLOGY, 2009, 145 (03) :318-332