TY - JOUR
T1 - A heavy metal baseline score predicts outcome in acute myeloid leukemia
AU - Ohanian, Maro
AU - Telouk, Philippe
AU - Kornblau, Steven
AU - Albarede, Francis
AU - Ruvolo, Peter
AU - Tidwell, Rebecca S.S.
AU - Plesa, Adriana
AU - Kanagal-Shamanna, Rashmi
AU - Matera, Eva Laure
AU - Cortes, Jorge
AU - Carson, Arch
AU - Dumontet, Charles
N1 - Funding Information:
Partial funding for this project was provided by the following: Southwest Center for Occupational and Environmental Health, a National Institute for Occupational Safety and Health (NIOSH) Education and Research Center, and awardee of Grant No. 5T42OH008421 from NIOSH and the Centers for Disease Control and Prevention; the National Institutes of Health/National Cancer Institute Cancer Center Support Grant P30CA016672 to MD Anderson Cancer Center (Biostatistics Resource Group); the University of Texas MD Anderson Cancer Center Duncan Family Institute for Cancer Prevention and Risk Assessment; the Leukemia Texas Foundation; Ladies Leukemia League; the Khalifa Foundation Gift; the Global Academic Programs Sister Institute Network Fund; a Gillson‐Longenbaugh Foundation Grant; the Max Cure Foundation; and the Cancer Recovery Foundation; INSU (Institut National des Sciences de l'Univers); CLARA (Cancéropôle Lyon Auvergne Rhône Alpes); MD Anderson Cancer Center Leukemia SPORE CA100632. Funding information
Publisher Copyright:
© 2020 Wiley Periodicals, Inc.
PY - 2020/4
Y1 - 2020/4
N2 - Despite abundant epidemiological data linking metals to leukemia and other cancers, baseline values of toxic and essential metals in patients with leukemia and the clinical impact of these metals remain unknown. Thus, we sought to quantify metal values in untreated patients with acute myeloid leukemia (AML) and controls and determine the impact of metal values on AML patients' survival. Serum samples from patients with untreated AML and controls at Hospices Civils de Lyon were analyzed and compared for trace metals and copper isotopic abundance ratios with inductively coupled plasma mass spectrometry. Survival analysis was performed as a function of metal values, and a multi-metal score was developed for patients with AML. Serum samples were collected from 67 patients with untreated AML and 94 controls. Most patients had intermediate-risk cytogenetics (63.1%) without FLT3 internal tandem duplication mutations (75.6%) or NPM1 mutations (68.1%). Most metal values differed significantly between AML and control groups. Patients with lower magnesium and higher cadmium values had the worst survival rates, with only 36% surviving at 6 months (P =.001). The adverse prognostic effect of this combination was maintained on multivariate analysis. Based on this, we developed a novel metal score, which accounts for multiple relative abnormalities in the values of five toxic and five essential metals. Patients with a higher metal score had significantly worse survival, which was maintained on multivariate analysis (P =.03). This baseline metal scoring system was also prognostic when we applied it to a separate population of front-line AML patients.
AB - Despite abundant epidemiological data linking metals to leukemia and other cancers, baseline values of toxic and essential metals in patients with leukemia and the clinical impact of these metals remain unknown. Thus, we sought to quantify metal values in untreated patients with acute myeloid leukemia (AML) and controls and determine the impact of metal values on AML patients' survival. Serum samples from patients with untreated AML and controls at Hospices Civils de Lyon were analyzed and compared for trace metals and copper isotopic abundance ratios with inductively coupled plasma mass spectrometry. Survival analysis was performed as a function of metal values, and a multi-metal score was developed for patients with AML. Serum samples were collected from 67 patients with untreated AML and 94 controls. Most patients had intermediate-risk cytogenetics (63.1%) without FLT3 internal tandem duplication mutations (75.6%) or NPM1 mutations (68.1%). Most metal values differed significantly between AML and control groups. Patients with lower magnesium and higher cadmium values had the worst survival rates, with only 36% surviving at 6 months (P =.001). The adverse prognostic effect of this combination was maintained on multivariate analysis. Based on this, we developed a novel metal score, which accounts for multiple relative abnormalities in the values of five toxic and five essential metals. Patients with a higher metal score had significantly worse survival, which was maintained on multivariate analysis (P =.03). This baseline metal scoring system was also prognostic when we applied it to a separate population of front-line AML patients.
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U2 - 10.1002/ajh.25731
DO - 10.1002/ajh.25731
M3 - Article
C2 - 31944361
AN - SCOPUS:85082312825
SN - 0361-8609
VL - 95
SP - 422
EP - 434
JO - American Journal of Hematology
JF - American Journal of Hematology
IS - 4
ER -