Prediction of survival with lower intensity therapy among older patients with acute myeloid leukemia

被引:6
作者
Sasaki, Koji [1 ,3 ]
Ravandi, Farhad [1 ]
Kadia, Tapan M. [1 ]
Borthakur, Gautam [1 ]
Short, Nicholas J. [1 ]
Jain, Nitin [1 ]
Daver, Naval G. [1 ]
Jabbour, Elias J. [1 ]
Garcia-Manero, Guillermo [1 ]
Loghavi, Sanam [2 ]
Patel, Keyur P. [2 ]
Montalban-Bravo, Guillermo [1 ]
Masarova, Lucia [1 ]
DiNardo, Courtney D. [1 ]
Kantarjian, Hagop M. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Hematopathol, Houston, TX USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, 1515 Holcombe Blvd Box 428, Houston, TX 77030 USA
关键词
acute myeloid leukemia; early mortality; lower-intensity chemotherapy; molecular abnormalities; mutations; predictive model; survival; RISK MYELODYSPLASTIC SYNDROME; LOW-DOSE CYTARABINE; CONVENTIONAL CARE REGIMENS; GEMTUZUMAB OZOGAMICIN; ELDERLY-PATIENTS; INDUCTION CHEMOTHERAPY; SINGLE-CENTER; OPEN-LABEL; PHASE-II; AZACITIDINE;
D O I
10.1002/cncr.34609
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThe aim of this study was to develop a prognostic model for survival in older/unfit patients with newly diagnosed acute myeloid leukemia (AML) who were treated with lower-intensity chemotherapy regimens. MethodsThe authors reviewed all older/unfit patients with newly diagnosed AML who received lower-intensity chemotherapy from 2000 until 2020 at their institution. A total of 1462 patients were included. They were divided (3:1 basis) into a training (n = 1088) and a validation group (n = 374). ResultsIn the training cohort of 1088 patients (median age, 72 years), the multivariate analysis identified 11 consistent independent adverse factors associated with survival: older age, therapy-related myeloid neoplasm, existence of previous myelodysplastic syndrome or myeloproliferative neoplasms, poor performance status, pulmonary comorbidity, anemia, thrombocytopenia, elevated lactate dehydrogenase, cytogenetic abnormalities, and the presence of infection at diagnosis, and therapy not containing venetoclax. The 3-year survival rates were 52%, 24%, 10%, and 1% in favorable, intermediate, poor, and very poor risk, respectively. This survival model was validated in an independent cohort. In a subset of patients in whom molecular mutation profiles were performed in more recent times, adding the mutation profiles after accounting for the effects of previous factors identified IDH2 (favorable), NPM1 (favorable), and TP53 (unfavorable) mutations as molecular prognostic factors. ConclusionThe proposed survival model with lower-intensity chemotherapy in older/unfit patients with newly diagnosed AML may help to advise patients on their expected outcome, to propose different strategies in first complete remission, and to compare the results of different existing or future investigational therapies. Plain Language Summary Lower intensity therapy can be considered for older patients to avoid severe toxicities and adverse events.However, survival prediction in AML was commonly developed in patients who received intensive chemotherapy.In this study, we have proposed a survival model to guide therapeutic approach in older patients who received lower-intensity therapy.
引用
收藏
页码:1017 / 1029
页数:13
相关论文
共 95 条
  • [1] Phase 1 dose escalation multicenter trial of pracinostat alone and in combination with azacitidine in patients with advanced hematologic malignancies
    Abaza, Yasmin M.
    Kadia, Tapan M.
    Jabbour, Elias J.
    Konopleva, Marina Y.
    Borthakur, Gautam
    Ferrajoli, Alessandra
    Estrov, Zeev
    Wierda, William G.
    Alfonso, Ana
    Chong, Toh Han
    Chuah, Charles
    Koh, Liang-Piu
    Goh, Boon-Cher
    Chang, Julie E.
    Durkes, Daniel E.
    Foudray, Maria Cielo
    Kantarjian, Hagop M.
    Dong, Xiao Qin
    Garcia-Manero, Guillermo
    [J]. CANCER, 2017, 123 (24) : 4851 - 4859
  • [2] International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data
    Arber, Daniel A.
    Orazi, Attilio
    Hasserjian, Robert P.
    Borowitz, Michael J.
    Calvo, Katherine R.
    Kvasnicka, Hans-Michael
    Wang, Sa A.
    Bagg, Adam
    Barbui, Tiziano
    Branford, Susan
    Bueso-Ramos, Carlos E.
    Cortes, Jorge E.
    Dal Cin, Paola
    DiNardo, Courtney D.
    Dombret, Herve
    Duncavage, Eric J.
    Ebert, Benjamin L.
    Estey, Elihu H.
    Facchetti, Fabio
    Foucar, Kathryn
    Gangat, Naseema
    Gianelli, Umberto
    Godley, Lucy A.
    Gokbuget, Nicola
    Gotlib, Jason
    Hellstrom-Lindberg, Eva
    Hobbs, Gabriela S.
    Hoffman, Ronald
    Jabbour, Elias J.
    Kiladjian, Jean-Jacques
    Larson, Richard A.
    Le Beau, Michelle M.
    Loh, Mignon L. -C.
    Lowenberg, Bob
    Macintyre, Elizabeth
    Malcovati, Luca
    Mullighan, Charles G.
    Niemeyer, Charlotte
    Odenike, Olatoyosi M.
    Ogawa, Seishi
    Orfao, Alberto
    Papaemmanuil, Elli
    Passamonti, Francesco
    Porkka, Kimmo
    Pui, Ching-Hon
    Radich, Jerald P.
    Reiter, Andreas
    Rozman, Maria
    Rudelius, Martina
    Savona, Michael R.
    [J]. BLOOD, 2022, 140 (11) : 1200 - 1228
  • [3] Mayo Clinic experience with 1123 adults with acute myeloid leukemia
    Begna, Kebede H.
    Ali, Walid
    Gangat, Naseema
    Elliott, Michelle A.
    Al-Kali, Aref
    Litzow, Mark R.
    Christopher Hook, C.
    Wolanskyj-Spinner, Alexandra P.
    Hogan, William J.
    Patnaik, Mrinal M.
    Pardanani, Animesh
    Zblewski, Darci L.
    Chen, Dong
    He, Rong
    Viswanatha, David
    Hanson, Curtis A.
    Ketterling, Rhett P.
    Tefferi, Ayalew
    [J]. BLOOD CANCER JOURNAL, 2021, 11 (03)
  • [4] Early mortality and overall survival of acute myeloid leukemia based on facility type
    Bhatt, Vijaya R.
    Shostrom, Valerie
    Giri, Smith
    Gundabolu, Krishna
    Islam, K. M. Monirul
    Appelbaum, Frederick R.
    Maness, Lori J.
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2017, 92 (08) : 764 - 771
  • [5] Estimating and comparing time-dependent areas under receiver operating characteristic curves for censored event times with competing risks
    Blanche, Paul
    Dartigues, Jean-Francois
    Jacqmin-Gadda, Helene
    [J]. STATISTICS IN MEDICINE, 2013, 32 (30) : 5381 - 5397
  • [6] Gemtuzumab ozogamicin with fludarabine, cytarabine, and granulocyte colony stimulating factor (FLAG-GO) as frontline regimen in patients with core binding factor acute myelogenous leukemia
    Borthakur, Gautam
    Cortes, Jorge E.
    Estey, Elihu E.
    Jabbour, Elias
    Faderl, Stefan
    O'Brien, Susan
    Garcia-Manero, Guillermo
    Kadia, Tapan Mahendra
    Wang, Xuemei
    Patel, Keyur
    Luthra, Rajyalakshmi
    Koller, Charles
    Brandt, Mark
    Ravandi, Farhad
    Kantarjian, Hagop
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2014, 89 (10) : 964 - 968
  • [7] ANALYSIS OF SURVIVAL DATA UNDER PROPORTIONAL HAZARDS MODEL
    BRESLOW, NE
    [J]. INTERNATIONAL STATISTICAL REVIEW, 1975, 43 (01) : 45 - 58
  • [8] A comparison of low-dose cytarabine and hydroxyurea with or without all-trans retinoic acid for acute myeloid leukemia and high-risk myelodysplastic syndrome in patients not considered fit for intensive treatment
    Burnett, Alan K.
    Milligan, Donald
    Prentice, Archie G.
    Goldstone, Anthony H.
    McMullin, Mary F.
    Hills, Robert K.
    Wheatley, Keith
    [J]. CANCER, 2007, 109 (06) : 1114 - 1124
  • [9] Flai (fludarabine, cytarabine, idarubicin) plus low-dose Gemtuzumab Ozogamicin as induction therapy in CD33-positive AML: Final results and long term outcome of a phase II multicenter clinical trial
    Candoni, Anna
    Papayannidis, Cristina
    Martinelli, Giovanni
    Simeone, Erica
    Gottardi, Michele
    Iacobucci, Ilaria
    Gherlinzoni, Filippo
    Visani, Giuseppe
    Baccarani, Michele
    Fanin, Renato
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2018, 93 (05) : 655 - 663
  • [10] Venetoclax and azacitidine compared with induction chemotherapy for newly diagnosed patients with acute myeloid leukemia
    Cherry, Evan M.
    Abbott, Diana
    Amaya, Maria
    McMahon, Christine
    Schwartz, Marc
    Rosser, Julie
    Sato, Audrey
    Schowinsky, Jeffrey
    Inguva, Anagha
    Minhajuddin, Mohd
    Pei, Shanshan
    Stevens, Brett
    Winters, Amanda
    Jordan, Craig T.
    Smith, Clayton
    Gutman, Jonathan A.
    Pollyea, Daniel A.
    [J]. BLOOD ADVANCES, 2021, 5 (24) : 5565 - 5573