Table 1.

Demographic characteristics, leukemia genetics, and therapeutic interventions of patients with low Vitamin C

Patient no.SexAge, yAML genetics Recent or current chemotherapy treatmentTreatment linePlatelet countVc level (μmol/L)Malnutrition present (yes/no) Parental nutrition
SubtypePathologic variants presentKaryotype
57 AML-MRC BRAF, NF1, NPM1, DNMT3A  46,XX,-18,+r[5]/46.XX[15] Liposomal daunorubicin-cytarabine Induction 20 Yes No 
73 M5 DNMT3A, FLT3, NPM1, BRCA2, SMC1A  47,XY,+mar[2]/46,XY[18] 7 + 3 and midostaurin Induction <5 Yes Yes 
66 M5 DNMT3A, IDH2, PTPN11, EZH2  Normal Decitabine and venetoclax R/R 24 Yes Yes 
60 t-AML IKZF1, BRAF, ETV6, RUNX1  47,XX,+8[20] Liposomal daunorubicin-cytarabine R/R 10 <5 No No 
65 t-AML NF1, TP3, CD79a  Complex (monosomal) Busulfan & cyclophosphamide Conditioning for HSCT 53 Yes Yes 
62 t-AML DNMT3A, JAK2, PLCG1  45,X,-Y,t(7;21;8)(q11.2;q22;q21.3)[19]/46,XY[1] Azacitidine and venetoclax R/R 26 Yes No 
Patient no.SexAge, yAML genetics Recent or current chemotherapy treatmentTreatment linePlatelet countVc level (μmol/L)Malnutrition present (yes/no) Parental nutrition
SubtypePathologic variants presentKaryotype
57 AML-MRC BRAF, NF1, NPM1, DNMT3A  46,XX,-18,+r[5]/46.XX[15] Liposomal daunorubicin-cytarabine Induction 20 Yes No 
73 M5 DNMT3A, FLT3, NPM1, BRCA2, SMC1A  47,XY,+mar[2]/46,XY[18] 7 + 3 and midostaurin Induction <5 Yes Yes 
66 M5 DNMT3A, IDH2, PTPN11, EZH2  Normal Decitabine and venetoclax R/R 24 Yes Yes 
60 t-AML IKZF1, BRAF, ETV6, RUNX1  47,XX,+8[20] Liposomal daunorubicin-cytarabine R/R 10 <5 No No 
65 t-AML NF1, TP3, CD79a  Complex (monosomal) Busulfan & cyclophosphamide Conditioning for HSCT 53 Yes Yes 
62 t-AML DNMT3A, JAK2, PLCG1  45,X,-Y,t(7;21;8)(q11.2;q22;q21.3)[19]/46,XY[1] Azacitidine and venetoclax R/R 26 Yes No 

AML-MRC, AML with myelodysplasia-related changes; F, female; HSCT, hematopoietic stem cell transplantation (both allo/auto); IDG2, isocitrate dehydrogenase 2; M, male; R/R, relapsed/refractory; 7 + 3, cytarabine and daunorubicin; t-AML, treatment-related AML.

At the time of AML diagnosis.

Severe protein calorie malnutrition, as established by a registered dietician.

Variant of unknown significance; however, the allele frequency was >15%.

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