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. 2021 May 13;137(19):2585–2597. doi: 10.1182/blood.2020009471

Table 1.

Characteristics of patients treated in the adjuvant arm

Never relapsed after HCT
ID Donor DL Age/sex Adverse-risk features Prior treatments Time to T cells after HCT (in days) Donor chimerisms (blood or marrow), % Ongoing tacrolimus on day of infusion
1 MRD 1 57/F FLT3-ITD CIA→sorafenib→CIAx2→RIC-HCT 117 100 Yes
2 MRD 1 18/F FLT3-ITD AAML 1031 (arm C-sorafenib)→MAC-HCT 155 90 Yes
3 MRD 1 55/F MLL-r 7+3→HiDAC→MAC-HCT 76 100 Yes
5 MRD 2 53/F DNMT3A mut 7+3→HiDAC→MAC-HCT 63 100 Yes
8 MRD 2 65/M MLL-r 7+3×2→5-Azax11→RIC-HCT 156 100 Yes
9 MRD 3 45/M Ph+AML 7+3+Imatinib→MAC-HCT 106 100 yes
10 MRD 3 51/F AML CR2 7+3→HiDAC→relapse→FLA→HiDAC→MAC-HCT 106 100 Yes
4 MRD 1 54/F Complex-rIPSS: Int-2 5-Azax11→transf-dep→RIC-SCT 66 100 Yes
11 MRD 3 53/F CR2 (MRD+ at HCT) 7+3→HiDAC→relapse→FLA→ MRD+→MAC-HCT 112 100 None
14 MRD 3 18/F FLT3-ITD (MRD+ at HCT) AAML1031→relapse→CPX-351→FLA(G)→Ara-C/peg/midostaurin→refractory→venetoclax/decitabine→MRD+→MAC-HCT 132 100 Unknown
13 MRD 3 26/M TP53 mut MDS-EB2 5-aza+ venetoclax→MAC-HCT 132 100 Yes
15 MUD 5 67/M CMML→AMML (PIF) 7+3→residual disease→venetoclax+5-aza→RIC-HCT 230 91 None
Relapsed after HCT, but in CR after salvage therapy
ID Donor DL Age/sex Adverse-risk features Prior treatments Time to relapse after HCT (in days) Donor chimerisms (blood or marrow), % Ongoing tacrolimus on day of infusion
6 MRD 2 70/F AML CR3 7+3→HiDAC→CIA→RIC-HCT-relapse→7+3 800 100 None
12 MRD 3 55/M Ph+, t-AML 7+3→RIC-HCT→relapse→7+3 2130 100 None
7 MRD 2 58/M RAEB-1 rIPSS: Int-2→t-AML in CR2 Decitabine→RIC-HCT→relapse with RAEB→CIA→relapse as MDS→DLI (×4) 356 100 None
9 MRD 4 47/M Ph+AML in CR2 7+3+Imatinib→MAC-HCT→mLST→molecular relapse→decitabine-dasatinib 460 100 None
6 MRD 4 73/F AML CR5 7+3→HiDAC→IA→RIC-HCT-relapse→7+3→mLST→relapse→IT chemo and XRT→relapse→IT chemo and XRT 1330 100 None

All patients were in morphological CR and with no detectable disease on preinfusion flow cytometry or genetic analysis. Bold, italicized text highlights major events during the course of the patient's disease.

5-aza, 5 azacytidine; 7+3, 7 d of cytarabine infusion and 3 d of idarubicin; AAML 1031, up-front pediatric treatment protocol; Ara-C, cytarabine; CIA, clofarabine, idarubicin, and cytarabine; CMML→AMML, acute converted from chronic myelomonocytic leukemia; DNMT3A mut, DNA methyltransferase, 3A mutation; F, female; FLA(G), fludarabine and cytarabine with G-CSF; FLT3-ITD, fms-like tyrosine kinase 3 receptor1-internal tandem duplication; HiDAC, high dose (>1 g/m2 cytarabine), ID, patient ID number; Int-2, intermediate-2; IT chemo, intrathecal chemotherapy only; M, male; MAC, fully myeloablative pre-HCT conditioning chemotherapy; MDS-EB2, myelodysplastic syndrome-excess blasts-2; MLL-r, mixed lineage leukemia-1 gene rearrangement; MRD+, measurable residual disease present; Peg, pegasparaginase; Ph+, Philadelphia chromosome–positive (BCR-ABL rearranged); PIF, primary induction failure; RAEB, refractory anemia with excess of blasts; RIC, reduced-intensity pre-HCT conditioning chemotherapy; rIPSS, revised International Prognostic System for MDS; t-AML, therapy-related AML; TP53 mut, mutated TP53 gene, XRT, radiotherapy.