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. 2021 Apr 17;100(6):1553–1567. doi: 10.1007/s00277-021-04514-y

Table 1.

Patient, disease, and transplant characteristics

Characteristics Overall Upfront-allo Auto-allo Relapse P Missing
N (%) 205 (100) 75 (37) 74 (36) 56 (27)
Age, years, median (range) 51.7 (26.3–66.1) 47.4 (26.3–59.7) 53.2 (30.7–65.1) 56.1 (41.9–66.1) < 0.001
< 50 83 (40) 47 (63) 24 (32) 12 (21)
50–60 98 (48) 28 (37) 42 (57) 28 (50)
> 60 24 (12) 0 (0) 8 (11) 16 (29)
Gender male/female 105/100 (51/49) 42/33 (56/44) 34/40 (46/54) 29/27 (52/48) 0.468
Myeloma subtype 0.092
IgG 121 (59) 45 (60) 47 (64) 29 (52)
IgA 33 (16) 8 (11) 9 (12) 16 (28)
IgD 5 (2) 4 (5) 1 (1) 0 (0)
Light chain 43 (21) 17 (23) 15 (20) 11 (20)
Nonsecretory 3 (2) 1 (1) 2 (3) 0 (0)
ISS stage 0.385 30 (14)
I 71 (35) 31 (41) 21 (28) 19 (34)
II 69 (34) 22 (29) 31 (42) 16 (29)
III 35 (17) 13 (17) 15 (20) 7 (13)
Cytogenetic risk 0.054 118 (58)
Standard 56 (27) 30 (40) 13 (18) 13 (23)
Higha 31 (15) 9 (12) 14 (19) 8 (14)
Extramedullary diseaseb 63 (31) 35 (47) 13 (18) 15 (27) 0.001 7 (3)
Number of pre-allo-SCT treatment lines < 0.001 1
1 74 (36) 31 (41) 43 (58) 0 (0)
2 67 (33) 25 (33) 23 (31) 19 (34)
3 44 (22) 14 (19) 7 (10) 23 (42)
≥ 4 19 (9) 5 (7) 1 (1) 13 (23)
Induction treatment < 0.001 1
AD/VAD 79 (39) 17 (23) 40 (54) 22 (39)
VCD 46 (23) 19 (25) 21 (28) 6 (11)
BorDex 27 (13) 11 (15) 5 (7) 11 (20)
Thalidomide-based combination 27 (13) 16 (21) 2 (3) 9 (16)
RVD 13 (6) 6 (8) 3 (4) 4 (7)
MP 2 (1) 0 (0) 0 (0) 2 (4)
Otherc 10 (5) 6 (8) 3 (4) 1 (2)
Novel drugs prior to allo-SCT < 0.001
IMID 110 (54) 44 (59) 22 (30) 44 (79)
PI 128 (62) 55 (73) 37 (50) 36 (64)
IMID and PI 82 (40) 35 (47) 18 (24) 29 (52)
None 49 (24) 11 (15) 33 (45) 5 (9)
Disease status prior to allo-SCT 0.093 1
sCR/CR 42 (20) 10 (14) 22 (30) 10 (18)
VGPR/PR 149 (73) 60 (80) 49 (66) 40 (71)
MR/SD 3 (1) 1 (1) 0 (0) 2 (4)
PD 10 (5) 4 (5) 2 (3) 4 (7)
Time between diagnosis and 1st auto-SCT, days, median (range) 206 (113–2643) 195 (119–2643) 219 (113–2300) 0.092
Time between last auto-SCT and allo-SCT, days, median (range)d 205 (63–4459) 161 (63–391) 750 (113–4459) < 0.001
Time between diagnosis and allo-SCT, days, median (range) 377 (137–5104) 261 (137–1721) 372 (218–2776) 1145 (246–5104) < 0.001
Karnofsky performance status ≥ 80 199 (97) 70 (93) 73 (99) 56 (100) 0.192 1
Donor source 0.030
Sibling 100 (49) 33 (44) 45 (61) 22 (39)
HLA matched 99 (48) 33 (44) 45 (61) 21 (38)
9/10 HLA matched 1 (1) 0 (0) 0 (0) 1 (1)
MUD 105 (51) 42 (56) 29 (39) 34 (61)
10/10 HLA matched 89 (43) 34 (45) 23 (31) 32 (57)
≤ 9/10 HLA matched 16 (8) 8 (11) 6 (8) 2 (4)
Donor/recipient gender 0.520
M/M 73 (36) 32 (43) 24 (32) 17 (30)
M/F 52 (25) 15 (20) 23 (31) 14 (25)
F/M 32 (16) 10 (13) 10 (14) 12 (22)
F/F 48 (23) 18 (24) 17 (23) 13 (23)
Graft type < 0.001
BM 39 (19) 28 (37) 4 (5) 7 (12)
PB 166 (81) 47 (63) 70 (95) 49 (88)
Conditioning regimen < 0.001
MACe 88 (43) 73 (97) 4 (5) 11 (20)
CyTBI 55 (27) 53 (70) 0 (0) 2 (4)
Treo14 33 (16) 20 (27) 4 (5) 9 (16)
RICf 117 (57) 2 (3) 70 (95) 45 (80)
FluTBI 52 (25) 1 (1) 42 (57) 9 (16)
Treo-RIC 65 (32) 1 (1) 28 (38) 36 (64)
Received ATG 119 (58) 35 (47) 27 (36) 23 (41) 0.409 1
GVHD prophylaxis < 0.001
CSA + short course of MTX 128 (63) 50 (67) 32 (43) 46 (82)
CSA + short course of MTX + MP 25 (12) 24 (32) 0 (0) 1 (2)
CSA + MMF 52 (25) 1 (1) 42 (57) 9 (16)

aDefined by the presence of del17p (any percentage), t(4;14), or t(14;16)

bThe presence of plasma cells or plasmacytomas outside the bone marrow

c4 patients received dexamethasone monotherapy; 3 bortezomib, doxorubicin, and dexamethasone; 2 cyclophosphamide-dexamethasone; 1 cyclophosphamide, doxorubicin, and dexamethasone

d11 patients received two auto-SCTs

eMAC regimens included CyTBI (cyclophosphamide 60 mg/kg for 2 days and total body irradiation 12 Gy) and Treo14 (treosulfan 14 g/m2 for 3 days and fludarabine 30 mg/m2 for 5 days)

fRIC regimens included FluTBI (fludarabine 30 mg/m2/3 days and total body irradiation 2 Gy) and Treo-RIC (treosulfan 10–12 g/m2 for 3 days and flurarabine 30 mg/m2 for 5 days)

Upfront-allo allo-SCT performed first line without a previous auto-SCT, auto-allo allo-SCT performed after auto-SCT in first line, relapse allo-SCT performed after relapse, ISS International Staging System, allo-SCT allogeneic hematopoietic stem cell transplantation, AD doxorubicin and dexamethasone, VAD vincristine, doxorubicin, and dexamethasone, VCD bortezomib, cyclophosphamide, and dexamethasone, BorDex bortezomib and dexamethasone, RVD bortezomib, lenalidomide, and dexamethasone, MP melphalan and prednisone, IMID immunomodulatory drug, PI proteasome inhibitor, sCR stringent complete response, CR complete response, VGPR very good partial response, PR partial response, MR minimal response, SD stable disease, PD progressive disease, auto-SCT autologous stem cell transplantation, HLA human leucocyte antigen, MUD matched unrelated donor, BM bone marrow, PB peripheral blood, MAC myeloablative conditioning, RIC reduced-intensity conditioning, ATG antithymocyte globulin, GVHD graft-versus-host disease, CSA cyclosporine, MTX methotrexate, MP methylprednisolone, MMF mycophenolate mofetil