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01.12.2016 | Research | Ausgabe 1/2016 Open Access

Journal of Hematology & Oncology 1/2016

Impact of conditioning intensity in T-replete haplo-identical stem cell transplantation for acute leukemia: a report from the acute leukemia working party of the EBMT

Zeitschrift:
Journal of Hematology & Oncology > Ausgabe 1/2016
Autoren:
Marie T. Rubio, Bipin N. Savani, Myriam Labopin, Simona Piemontese, Emmanuelle Polge, Fabio Ciceri, Andrea Bacigalupo, William Arcese, Yener Koc, Dietrich Beelen, Zafer Gülbas, Depei Wu, Stella Santarone, Johanna Tischer, Boris Afanasyev, Christoph Schmid, Sebastian Giebel, Mohamad Mohty, Arnon Nagler
Wichtige Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​s13045-016-0248-3) contains supplementary material, which is available to authorized users.
Marie T Rubio and Bipin N Savani are joint first co-authors
Mohamad Mohty and Arnon Nagler share senior authorship

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

MTR, BNS, ML, MM, and AN designed the research and/or analyzed data; FB, AB, WA, YK, DB, ZG, DW, PDB, JT, BA, CS, and SG provided clinical data; MTR, BNS, ML, MM, and AN wrote the manuscript; and all authors approved the final version of the manuscript.

Background

Haplo-identical hematopoietic stem cell transplantation (haplo-SCT) is an attractive transplant procedure since it provides a possibility of transplantation to almost all patients needing an allogeneic SCT. Historical approaches of haplo-SCT performed with unmanipulated bone marrow stem cell grafts, standard myeloablative conditioning, and graft-versus-host disease (GVHD) prophylaxis were associated with high risks of graft rejection and severe GVHD due to uncontrolled bi-directional recipient and donor allo-reactivity [ 14]. Although the development of T cell depleted haplo-SCT has allowed to control the risk of severe GVHD, the poor T cell immune reconstitution observed in these patients is associated with a high incidence of life-threatening infections [ 510]. In the last decade, several strategies of T cell replete bone marrow (BM) or peripheral blood (PB) haplo-SCT have been developed with both reduced intensity (RIC) and fully intensive myeloablative conditioning (MAC) regimens and variable GVHD prophylaxis strategies [ 1126]. While some groups have used a combination of anti-thymocyte globulin (ATG) with immunosuppressive agents with or without monoclonal antibodies such as rituximab and basiluximab [ 1116], others have adopted the Baltimore’s strategy [ 1726] of in vivo T cell depletion by the administration of high doses of cyclophosphamide (Cy) on days 3 and 4 post-SCT (PT-Cy). These approaches have improved immune reconstitution and reduced non-relapse mortality (NRM) of haplo-SCT [ 20, 2729]. In single center experiences, these new haplo-SCT platforms allow similar transplant outcomes than allo-SCT performed with HLA-matched donors [ 3037]. However, the optimal conditioning regimen for haplo-SCT in acute leukemia remains a question of debate.
In HLA-matched related or unrelated allogeneic SCT for acute leukemia, several studies have reported a dose-dependent effect of the intensity of the conditioning regimen on disease control [ 3840]. In this context, the reduced risk of relapse after MAC is counterbalanced by higher NRM leading to similar overall survival in MAC and RIC [ 4148]. In T-replete haplo-SCT, low risks of acute and chronic GVHD, resulting in <20 % NRM at 1 to 5 years after RIC and MAC, have been reported [ 1726]. Relapse incidence, however, varies from 35 to 60 % at 1-year post-transplant and remained the major event after haplo-SCT performed with RIC and PT-Cy [ 1719, 23, 26]. Although these differences could be related to disease risk at transplant [ 24, 25, 49], these observations raise the question of the role of the conditioning regimen intensity on leukemic control and transplant outcomes after T-replete haplo-SCT.
To address this question, we performed a large retrospective registry study to compare the transplant outcomes of 696 patients receiving a haplo-SCT after RIC ( n = 271) to those transplanted after MAC ( n = 425) for acute leukemia.

Results

Patient, disease, and transplant characteristics

Details of patients, disease, and transplant characteristics are summarized in Table  1. Six hundred and ninety-six patients with AL were included in the study. Two hundred and seventy-one patients received RIC and 425 MAC regimen before haplo-SCT between 2001 and 2012. Patients of the RIC group were older with median age of 53 years (range, 18–76) in comparison to 38 years (range, 18–4) for the MAC group ( p < 0.0001). Only 45 % of the patients were ≤50 years of age in the RIC group vs. 70 % in the MAC group ( p < 0.0001). The median follow-up of surviving patients in the RIC group was 15 (range, 1–73) months, while that of the MAC group was 22 (range, 1–142) months ( p = 0.007). Significantly higher numbers of patients were transplanted for acute myeloid (AML) in the RIC than in the MAC group (80 vs. 67 %), while more lymphoid leukemia (ALL) recipients were documented in the MAC cohort (33 vs. 20 %; p < 0.0001). There were more patients in CR1 in the MAC group (41 vs. 29 %) and with active disease in RIC compared to MAC groups (47 vs. 31 %; p < 0.0001). The other pre-transplant characteristics were similar between RIC and MAC groups, and the majority of patients were transplanted from 2008 to 2012 in both groups (91.5 % in RIC and 82.6 % in MAC) (Table  1).
Table 1
Patient and disease characteristics
Patient characteristics
RIC
MAC
p value
Number of patients
271
425
 
Recipient age at SCT (years, range)
53 (18–76)
38 (18–74)
<10 −4
Recipient age (by classes), n (%)
   
<0.0001
 < 30
46 (17.0 %)
148 (34.8 %)
 
 30–40
32 (11.8 %)
82 (19.3 %)
 
 40–50
45 (16.6 %)
98 (23.1 %)
 
 ≥ 50
148 (54.6 %)
97 (22.8 %)
 
Recipient gender, n (%)
   
0.42
 Male
153 (56.5 %)
252 (59.6 %)
 
 Female
118 (43.5 %)
171 (40.4 %)
 
Year of SCT (median), year (%)
2010
2011
0.65
 2001–2007
23 (8.5 %)
74 (17.4 %)
<0.0001
 2008–2012
248 (91.5 %)
351 (82.6 %)
Interval from diagnosis to SCT (days, range)
299 (52–3892)
272 (41–3689)
0.24
Donor age
37 years (19–71)
42 years (12–70)
0.83
Donor age (by classes), year (%)
   
0.55
 < 30
39 (29.3 %)
54 (29.2 %)
 
 30–40
32 (24.1 %)
33 (17.8 %)
 
 40–50
29 (21.8 %)
46 (24.9 %)
 
 ≥ 50
33 (24.8 %)
52 (28.1 %)
 
Donor gender, n (%)
   
0.69
 Male
138 (50.9 %)
223 (52.5 %)
 
 Female
133 (49.1 %)
202 (47.5 %)
 
Female donor to male recipient, n (%)
76 (28 %)
119 (28.1 %)
0.98
Diagnosis, n (%)
   
<0.0001
 AML
217 (80.1 %)
286 (67.3 %)
 
  Good cytogenetics
8 (6 %)
19 (14 %)
  Intermediate cytogenetics
47 (37 %)
53 (39 %)
 
  Poor cytogenetics
19 (15 %)
18 (13 %)
 
  Secondary AML
54 (42 %)
45 (33 %)
 
  Missing cytogenetics
89 (41 %)
151 (53 %)
 
 ALL
54 (19.9 %)
139 (32.7 %)
  Phi+ ALL
15 (54 %)
27 (36 %)
  Missing cytogenetics
26 (48 %)
64 (46 %)
 
Disease status at SCT, n (%)
   
<0.0001
 CR1
78 (28.8 %)
175 (41.2 %)
 
 ≥ CR2
67 (24.7 %)
118 (27.8 %)
 
 Active disease
126 (46.5 %)
132 (31.1 %)
 
Karnosky at SCT, n (%)
   
0.05
 ≤ 80 %
101 (39.9 %)
109 (32 %)
 
 > 80 %
152 (60.1 %)
232 (68 %)
 
 Missing
18 (6.7 %)
84 (19.8 %)
 
Patient positive CMV serology, n (%)
213 (79.8 %)
311 (78.3 %)
0.66
CMV risk, n (%)
   
0.06
 Low
35 (13.3 %)
59 (15.2 %)
 
 Intermediate
169 (64.2 %)
272 (69.3 %)
 
 High
59 (22.4 %)
56 (14.5 %)
 
AML acute myeloid leukemia, ALL acute lymphoid leukemia, CMV cytomegalovirus, CMV risk low = negative recipient and donor serology, high positive recipient and negative donor serology, intermediate all other combinations, CR complete remission, SCT stem cell transplantation
The indication for haplo-SCT was high risk disease in the majority of patients in both groups, with 71 and 59 % of patients in RIC and MAC groups, respectively, transplanted in advanced phase or active disease.
Details of transplant characteristics, conditioning, and GVHD prophylaxis regimens are summarized in Table  2. The majority of patients in the RIC group received PB stem cells (65 %) compared to a similar distribution of PB and BM as stem cell source in the MAC cohort (52.5 and 47.5 %, respectively; p = 0.001). The percentage of patients receiving in vivo T cell depletion, mainly performed with Thymoglobulin, was not significantly different between the two groups ( p = 0.26). Apart from in vivo T cell depletion, GVHD prophylaxis consisted of the combination of one calcineurin inhibitor with mycophenolate mofetyl (MMF) alone, or in association with methotrexate (MTX) +/− Basiluximab (anti-CD25) or post-transplant cyclophosphamide (PT-Cy). A calcineurin inhibitor + MMF and/or MTX +/− Basimuximab was used in 31 and 54 % of the patients in the RIC and MAC groups, respectively, while the association of a calcineurin inhibitor + MMF with PT-Cy (PT-Cy + CsA/Tacro + MMF) was applied in 25 and 32 % of patients of the RIC and MAC groups, respectively. Another frequent combination was sirolimus and MMF, used in 33 % of patients of the RIC group (Table  2). The choice of conditioning and GVHD prophylaxis was dependent on centers’ protocols and strategies of transplantation.
Table 2
Transplant characteristics
Transplant characteristics
RIC
MAC
p value
Number of patients
271
425
 
Source of stem cells
0.001
 BM
95 (35.1 %)
202 (47.5 %)
 
 PB
176 (64.9 %)
223 (52.5 %)
 
Conditioning regimen
 
 Chemotherapy-based
200 (73.8 %)
306 (72 %)
 
 TBI-based
71 (26.2 %)
119 (28 %)
 
In vivo T depletion
0.26
 Yes
140 (51.7 %)
201 (47.3 %)
 
 Thymoglobulin
127 (91 %)
185 (92 %)
 Lymphoglobulin
2 (1 %)
1 (0.5 %)
 
 Alemtuzumab
11 (8 %)
15 (7.5 %)
 
 No
131 (48.3 %)
224 (52.7 %)
Post-transplant GVHD prophylaxis
<0.0001
 CsA/FK506 + MMF or MTX
61 (23.2 %)
120 (30.3 %)
 
 CsA + MMF + MTX
2 (0.8 %)
55 (13.9 %)
 
 CsA + MMF + MTX + Basiliximab
19 (7.2 %)
40 (10.1 %)
 
 PT-Cy + CsA/FK506 + MMF
66 (25.1 %)
125 (31.6 %)
 
 Sirolimus + MMF
87 (33.1 %)
10 (2.5 %)
 
 Other
28 (10.6 %)
46 (11.6 %)
 
DLI
   
NS
 No DLI
247 (91.1 %)
389 (92.5 %)
 
 Pre-emptive DLI
11 (4.1 %)
14 (3.3 %)
 
 DLI after relapse
13 (4.8 %)
22 (5.2 %)
 
BM bone marrow, Bu busulfan, CSA cyclosporine, Cy cyclophosphamide, DLI donor lymphocyte injection, Flu fludarabine, MMF mycophenolate mofetyl, MTX methotrexate, PB peripheral blood, PT-CY post-transplant cyclophosphamide, TBI total body irradiation
Donor lymphocyte infusion (DLI) was reported in 24 (8.9 %) in RIC and 36 (8.5 %) in MAC groups. Among those, DLI was pre-emptive for 11 patients (4 % of patients) in RIC and 14 (3 %) in MAC groups.

Engraftment and GVHD

Conditioning regimen specific engraftment and GVHD are summarized in Table  3. Ninety percent of patients in the RIC group engrafted vs. 92 % in the MAC group ( p = 0.58). The median day for ANC > 500/μL was 17 (range, 3–75) and 18 (range, 6–63) days in MAC and RIC groups, respectively ( p = 0.007). The incidences of day 100 grade II–IV (29 vs. 24 %; p = 0.23) and III–IV (10.7 vs. 10.9 %; p = 0.96) acute GVHD were not significantly different between MAC and RIC groups, respectively. As shown in Table  5, in multivariate analysis, the only factor associated with increased grade II–IV acute GVHD was the use of PB in comparison to BM stem cells (hazard ratio (HR) 1.96; 95 % CI, 1.32–2.92; p = 0.0008). Two-year incidence of chronic GVHD was similar between the different conditioning groups: 25 % (95 % CI, 19–31) in RIC vs. 32 % (95 % CI, 28–37) in MAC groups; ( p = 0.14). There was no difference of incidence of cGVHD in AML and ALL groups (Table  4). In multivariate analysis, chronic GVHD was not significantly different between RIC and MAC groups (HR 0.80; 95 % CI, 0.56–1.14; p = 0.21). The only factor associated with chronic GVHD was the use of PB in comparison to BM stem cells (HR 1.64; 95 % CI, 1.16–2.30; p = 0.005) (Table  5).
Table 3
Engraftment and GVHD
 
RIC
MAC
p value
Total number of patients
271
425
 
Engraftment
235 (90.4 %)
383 (91.7 %)
0.58
 Non-engraftment
25 (9.8 %)
35 (8.4 %)
 
 Missing
11
7
 
Acute GVHD
     
 Grade 0–I, n (%)
202 (75.6 %)
293 (71.5 %)
0.23
 Grade II–IV, n (%)
65 (24.4 %)
117 (28.5 %)
 
 Grade III–IV, n (%)
29 (10.9 %)
45 (10.7 %)
0.96
 Missing, n
4
15
 
Chronic GVHD a
24.7 % (19–30.9)
32.1 % (27.3–37.1)
0.14
 Limited, n
29
76
 
 Extensive, n
22
36
 
 Missing, n
2
5
 
GVHD graft-versus-host disease
a2-year cumulative incidence
Table 4
Comparison of 2-year outcomes between MAC and RIC haplo-SCT according to disease status
Disease
Patients group and p value
RI
NRM
LFS
OS
cGVHD
Diagnosis
AML
36.1 % (31.6–40.6)
31.6 % (27.4–35.9)
32.2 % (27.7–36.7)
37.7 % (33.1–42.4)
29.2 % (24.8–33.7)
 
ALL
40 % (32.5–47.3)
32.9 % (28.6–37.2)
27.2 % (20.2–34.1)
33.3 % (25.9–40.7)
29.8 % (22.8–37.2)
 
p
0.43
0.87
0.45
0.40
0.67
All patients
           
 CR1
RIC
30.1 % (19.1–41.9)
31.1 % (24.1–38.3)
38.9 % (26.4–51.3)
46.9 % (34.1–59.8)
26 % (15–38.3)
 
MAC
21.5 % (15.4–28.3)
29.1 % (22.2–36.3)
49.1 % (41.2–57.1)
55.4 % (47.5–63.4)
41 % (32.8–48.9)
 
p
0.21
0.80
0.42
0.64
0.10
  ≥ CR2
RIC
38.5 % (25.8–51.1)
36.8 % (28.2–45.5)
24.6 % (13.1–36.1)
29.8 % (17.7–41.9)
29.6 % (17.5–42.8)
 
MAC
30 % (21.5–39)
27.8 % (19.7–36.4)
42.2 % (32.6–51.7)
47.7 % (38–57.5)
37 % (27.4–46.6)
 
p
0.38
0.25
0.06
0.07
0.53
 Active dis.
RIC
55.8 % (45.9–64.6)
32.9 % (24.5–41.5)
11.3 % (5–17.5)
14.3 % (7.3–21.3)
21.4 % (13.8–30.1)
 
MAC
51.9 % (42.3–60.6)
37.1 % (28.6–45.7)
11 % (4.7–17.2)
18.5 % (11.2–25.7)
15.2 % (9.2–22.7)
 
P
0.52
0.38
0.64
0.60
0.29
Active dis active disease, cGVHD chronic graft-versus-host disease, CR complete remission, LFS leukemia-free survival, NRM non-relapse mortality, MAC myeloablative conditioning, OS overall survival, RI relapse incidence, RIC reduced intensity conditioning
Table 5
Multivariate analysis
 
Relapse
NRM
Acute GVHD
Chronic GVHD
LFS
OS
 
p value
HR (95 % CI)
p value
HR (95 % CI)
p value
OR (95 % CI)
p value
HR (95 % CI)
p value
HR (95 % CI)
p value
HR (95 % CI)
RIC vs. MAC
 All
0.07
1.31 (0.98–1.75)
0.76
0.95 (0.69–1.31)
0.32
0.82 (0.55–1.21)
0.21
0.80 (0.56–1.14)
0.27
1.13 (0.91–1.40)
0.44
1.09 (0.87–1.36)
 AML
0.09
1.34 (0.95–1.87)
0.17
0.78 (0.54–1.12)
       
0.74
1.04 (0.81–1.34)
0.79
0.97 (0.75–1.25)
 ALL
0.5
1.23 (0.67–2.26)
0.18
1.5 (0.83–2.72)
       
0.17
1.34 (0.88–2.05)
0.10
1.44 (0.94–2.22)
Age at SCT
 1. <30 (ref)
 
1.00
 
1.00
 
1.00
 
1.00
 
1.00
 
1.00
 2. (30–40) vs. 1
0.91
1.02 (0.68–1.54)
0.27
0.79 (0.51–1.20)
0.98
1.01 (0.60–1.70)
0.25
0.75 (0.46–1.22)
0.47
0.90 (0.67–1.20)
0.52
0.91 (0.67–1.23)
 3. (40–50) vs. 2
0.43
0.84 (0.55–1.28)
0.74
1.08 (0.69–1.69)
0.98
1.01 (0.58–1.77)
0.70
0.91 (0.56–1.48)
0.74
0.95 (0.70–1.29)
0.79
0.96 (0.69–1.32)
 4. ≥ 50 vs. 3
0.11
1.33 (0.93–1.90)
0.48
0.87 (0.59–1.28)
0.06
1.62 (0.98–2.70)
0.44
1.18 (0.77–1.79)
0.52
1.09 (0.84–1.42)
0.79
1.04 (0.79–1.36)
ALL vs. AML
0.04
1.39 (1.021.91)
0.37
1.16 (0.84–1.61)
0.65
1.10 (0.73–1.66)
0.50
1.13 (0.79–1.63)
0.03
1.28 (1.021.61)
0.03
1.30 (1.031.64)
Status at SCT
 CR1 (ref)
 
1.00
 
1.00
 
1.00
 
1.00
 
1.00
 
1.00
  ≥ CR2 vs. CR1
0.05
1.46 (1.012.13)
0.45
1.15 (0.80–1.63)
0.35
1.24 (0.80–1.92)
0.23
1.25 (0.87–1.78)
0.05
1.30 (1.001.67)
0.01
1.40 (1.071.83)
 Active dis. vs. CR1
<104
4.43 (3.206.12)
0.0002
1.86 (1.342.59)
0.85
1.04 (0.68–1.60)
0.45
1.17 (0.78–1.75)
<104
2.94 (2.343.70)
<104
2.92 (2.303.72)
PB vs. BM
0.85
1.03 (0.77–1.37)
0.59
1.09 (0.80–1.48)
0.0008
1.96 (1.32–2.92)
0.005
1.64 (1.162.30)
0.63
1.05 (0.85–1.30)
0.58
1.06 (0.85–1.32)
PT-Cy-based vs. other
0.94
0.99 (0.72–1.36)
0.02
0.63 (0.440.92)
0.11
0.69 (0.44–1.09)
0.46
1.15 (0.79–1.69)
0.10
0.82 (0.64–1.04)
0.16
0.83 (0.65–1.07)
Year of SCT
 2001–2005 (ref)
 
1.00
 
1.00
 
1.00
 
1.00
 
1.00
 
1.00
 2005–2007
0.86
1.08 (0.48–2.43)
0.74
0.89 (0.45–1.77)
0.62
1.24 (0.44–3.51)
0.17
2.03 (0.74–5.56)
0.89
0.96 (0.57–1.63)
0.84
1.06 (0.61–1.83)
 2008–2012
0.98
0.99 (0.47–2.09)
0.22
0.68 (0.36–1.27)
0.27
1.68 (0.67–4.22)
0.14
2.04 (0.80–5.19)
0.40
0.81 (0.50–1.31)
0.60
0.87 (0.53–1.44)
Active dis active disease, BM bone marrow, PT-Cy-based post-transplant cyclophosphamide associated to one calcineurin inhibitor and mycophenolate mofetyl, CR complete remission, GVHD graft-versus-host-disease, LFS leukemia-free survival, NRM non-relapse mortality, MAC myeloablative conditioning, OS overall survival, PB peripheral blood, Ref reference, RIC reduced intensity conditioning, SCT allogeneic stem cell transplantation

Toxicity and NRM

There was no difference in NRM at 2 years between RIC and MAC groups in univariate (33 %; 95 % CI, 29–38; after RIC vs. 31 %; 95 % CI, 27–36 after MAC; p = 0.88) and multivariate analyses (HR 0.95; 95 % CI, 0.69–1.31; p = 0.76) (Table  5) in the total population of patients. When analyzed separately, there was no difference neither between AML and ALL in univariate analysis (31.6 %; 95 % CI, 27–36; in AML vs. 33 %; 95 % CI, 28–37 in ALL; p = 0.87) (Table  4). In addition, in multivariate analysis, the intensity of the conditioning had no significant impact on NRM in AML and ALL groups (Table  5).
Among all patients, in univariate analysis, there was no difference in NRM at 2 years between the two groups for patients transplanted in CR1 (Table  4 and Fig.  1), in ≥CR2 or with active disease (Table  4). In multivariate analysis, however, active disease at transplant was associated with a higher risk of NRM (HR 1.86; 95 % CI, 1.34–2.59; p = 0.0002), while the use of PT-Cy + CsA/Tacro + MMF was associated with decreased NRM as compared to other GVHD prophylaxis (HR 0.63; 95 % CI, 0.44–0.92; p = 0.02) (Table  5 and Fig.  3). There was no impact of recipient age at transplant, type of disease (ALL vs. AML), source of stem cells (PB vs. BM), and year of transplant (Table  5).
The main causes of NRM were infectious complications in 53 (32 %) vs. 75 (33 %) patients and GVHD in 23 (14 %) vs. 36 (16 %) of patients in RIC vs. MAC groups, respectively. Death from organ toxicity was very low in both groups. In particular, sinusoidal obstructive syndrome (SOS) was reported in 2 (1.2 %) and 5 (2.2 %) of patients in RIC and MAC groups, respectively.

Relapse

Overall RI at 2 years was comparable between AML and ALL (36.1 % in AML and 40 % in ALL, p = 0.43) (Table  4). However, since disease status at transplant was significantly different between the two conditioning groups (Table  1), relapse incidence and survivals were analyzed separately for all patients transplanted in CR1, ≥ CR2, and with active disease (Table  4). Overall RI at 2 years for patients transplanted in CR1, ≥ CR2, and with active disease were 23.9, 33.1, and 53.6 %, respectively. In univariate analysis, RI at 2 years was similar between RIC and MAC groups for patients in CR1 (30 %; 95 % CI, 19–42 vs. 22 %; 95 % CI, 14–28 %; respectively; p = 0.21) (Table  4 and Fig.  1), in ≥CR2 (39 %; 95 % CI, 26–51 vs. 30 %; 95 % CI, 22–39 %; respectively; p = 0.38) or with active disease (56 %; 95 % CI, 47–65 vs. 52 %; 95 % CI, 42–61 %; respectively; p = 0.52) (Table  4). In multivariate analysis, there was a trend to a slight increase of RI in the RIC vs. MAC group (HR 1.31; 95 % CI, 0.98–1.75; p = 0.07) (Table  5). This trend was particularly observed in AML patients (HR 1.34; 95 % CI, 0.95–1.87; p = 0.09) (Table  5). In addition, the risk of relapse was significantly higher for patients transplanted in ≥CR2 (HR 1.46; 95 % CI, 1.01–2.13; p = 0.05) or with active disease (HR 4.43; 95 % CI, 3.20–6.12; p < 0.0001) compared to CR1, and in ALL compared to AML (HR 1.39; 95 % CI, 1.02–1.91; p = 0.04) (Table  5). Despite reduced NRM, the RI was similar in patients having received PT-Cy + CsA/Tacro + MMF in comparison to other GVHD prophylaxis (HR 0.99; 95 % CI, 0.72–1.36; p = 0.94) (Table  5 and Fig.  2).

Leukemia-free survival

LFS at 2 years was comparable between AML and ALL (32.2 % in AML and 27.2 % in ALL, p = 0.67) (Table  4). Overall LFS at 2 years for all patients transplanted in CR1, ≥CR2, and with active disease were 46.3, 35.7, and 11.4 %, respectively. LFS at 2 years was similar between RIC and MAC groups for patients transplanted in CR1 (39 %; 95 % CI, 26–51 vs. 49 %; 95 % CI, 41–57 %, respectively, p = 0.42) (Table  4 and Fig.  1) or with active disease (11 %; 95 % CI, 5–18 vs. 11 %; 95 % CI, 5–17 %, respectively, p = 0.64) (Table  4). There was a trend towards worse LFS in RIC vs. MAC groups for patients transplanted in ≥CR2 (25 %; 95 % CI, 13–36 vs. 42 %; 95 % CI, 33–52 %; respectively; p = 0.06) (Table  4). However, in multivariate analysis, LFS was no different between RIC and MAC groups for all patients (HR 1.13; 95 % CI, 0.91–1.40, p = 0.27), as well as for AML (HR 1.04; 95 % CI, 0.81–1.34, p = 0.74) and ALL (HR 1.34; 95 % CI, 0.88–2.05, p = 0.17) patients (Table  5). Multivariate analysis showed lower LFS in patients transplanted in ≥CR2 (HR 1.30; 95 % CI, 1.00–1.67; p = 0.05) or with active disease (HR 2.94; 95 % CI, 2.34–3.70; p < 0.0001) compared to CR1, and in ALL compared to AML (HR 1.28; 95 % CI, 1.02–1.61; p = 0.03) (Table  5).

Overall survival

Overall survival (OS) at 2 years was comparable between AML and ALL (37.7 % in AML and 33.3 % in ALL, p = 0.40) (Table  4). Overall OS at 2 years for patients transplanted in CR1, ≥CR2, and with active disease were 53.2, 41, and 16.3 %, respectively. OS at 2 years was similar in RIC and MAC groups for patients transplanted in CR1 (47 %; 95 % CI, 34–60 vs. 55 %; 95 % CI, 48–63 %, respectively, p = 0.64) (Table  4 and Fig.  1) or with active disease (14 %; 95 % CI, 7–21 vs. 19 %; 95 % CI, 11–26 %, respectively, p = 0.60) (Table  4 and Fig.  2). There was a trend towards worse OS in RIC as compared to MAC groups for patients transplanted in ≥CR2 (30 %; 95 % CI, 18–42 vs. 48 %; 95 % CI, 38–58 %; respectively; p = 0.07) (Table  4 and Fig.  2). In multivariate analysis, OS was no different between RIC and MAC groups in the total cohort of patients (HR 1.09; 95 % CI, 0.87–1.36, p = 0.44) (Table  5) and in AML patients (HR 0.97; 95 % CI, 0.75–1.25, p = 0.79). Although not significant, there was a trend for a worse OS with RIC in ALL patients (HR 1.44; 95 % CI, 0.94–2.22, p = 0.10) (Table  5). Of note, 39 % of ALL patients receiving a RIC had active disease at transplantation in comparison to 24 % of those transplanted with MAC ( p = 0.03). Multivariate analysis also showed lower OS in patients transplanted in ≥CR2 (HR 1.40; 95 % CI, 1.07–1.83; p = 0.01) or with active disease (HR 2.92; 95 % CI, 2.30–3.72; p < 0.0001) compared to CR1, and in ALL compared to AML (HR 1.30; 95 % CI, 1.03–1.64; p = 0.03) (Table  5).

Discussion

The development of T-replete haplo-SCT for the treatment of hematological malignancies has been considerable over the last 5 to 10 years. Several RIC and MAC regimens have been designed by different groups at the same time with GVHD prophylaxis regimens based either on the Baltimore’s approach using PT-Cy [ 1726] or the combination of several immunosuppressive drugs with in vivo T cell depletion with monoclonal antibodies [ 1116]. They all demonstrated the feasibility of such transplants with limited NRM (≤20 % at 1 year) and promising survival rates, in particular in patients transplanted in CR [ 24, 25, 49]. However, comparative studies between the different transplant strategies had not been performed. Our study represents the first large retrospective analysis comparing transplant outcomes between RIC and MAC T-replete haplo-SCT for AML and ALL. In AML, our results show similar LFS and OS in patients receiving RIC and MAC regimens after adjustment for disease risk at transplant. In ALL, there was a trend for worse OS with RIC not related to increase relapse but rather a trend for increase NRM. This might be explained by higher proportions of patients with advanced disease in the RIC group.
In multivariate analysis, two factors impacted LFS and OS: disease status at transplant in all patients and in the AML and ALL subgroups (data not shown), and type of leukemia. Patients transplanted for ALL or in ≥CR2 had higher risk of relapse, while those transplanted with active disease had increased RI and NRM. Reduced anti-leukemic effect of allo-SCT with higher relapse rates in ALL in comparison to AML is well known in both non-haplo and haplo-SCT settings [ 50, 51]. As reported by other groups, outcome of RIC and MAC haplo-SCT in patients transplanted with active disease are poor, with relapse rates above 50 %, increased NRM, and OS below 20 % [ 13, 1719, 22], confirming the need for developing innovative transplant strategies for those patients. In this series, patients transplanted in advanced disease phase (CR2 and beyond) had a higher risk of relapse and lower survival rates in comparison to those transplanted in CR1. We also observed a trend in univariate analysis towards reduced LFS and OS after RIC vs. MAC in this subset of patients. These results are in contradiction with those reported in smaller series of patients allo-grafted with RIC or MAC haplo-SCT [ 13, 22]. However, in their last reports, the Bacigalupo’s group also showed poorer outcome of patients transplanted in ≥CR2 [ 24, 32]. Our results confirm better transplant outcomes in patients transplanted in CR1 with an OS of about 50 % at 2 years, independently of the intensity of the conditioning and of recipient age (data not shown). Altogether, these results suggest that haplo-SCT should be considered in the first line of treatment in high risk AML and ALL and can be performed with MAC or RIC according to patient’s age and co-morbidities.
Cumulative incidences of acute and chronic GVHD were similar between RIC and MAC. Grade II–IV acute GVHD occurred in 25 % of patients transplanted with RIC and 29 % of those receiving a MAC, while chronic GVHD was observed in 25 and 32 % of them, respectively. These results are in line with the reported incidences of GVHD after T-replete haplo-SCT associated with different strategies of in vivo T cell depletion [ 1315, 1726] and confirm the reduction of GVHD rates with such strategies in a multicenter experience. The use of PB vs. BM stem cells was associated with increased risk of acute and chronic GVHD but had no impact on the incidence of NRM and survivals. While the use of PB is also associated with increased chronic GVHD in other HLA-matched transplant settings [ 52, 53], its impact on the incidence of acute GVHD is more debatable. In haplo-SCT with RIC and PT-Cy, Castagna et al. could not find significant increase of acute GVHD with PB in comparison to BM [ 54]. In this study, the use of PB was associated with higher risk of grade II–IV acute GVHD independently of the intensity of the conditioning regimen and of the use of PT-Cy. Because of the heterogeneity of the conditioning and GVHD prophylaxis regimens, we believe that the potential impact of the stem cell source on the incidence of acute GVHD in haplo-SCT needs further investigation.
NRM was similar between RIC and MAC groups. However, NRM was above 30 % in both groups, including in patients transplanted in CR1, which is higher than the levels below 20 % reported with T-replete haplo-SCT independently of the type of GVHD prophylaxis in single centers’ experiences [ 12, 13, 1726]. Apart from disease status, the only factor impacting NRM in multivariate analysis was the use of PT-Cy in association to one calcineurin inhibitor and MMF in the prophylaxis of GVHD. NRM with PT-Cy + CsA/Tacro + MMF was closed to 20 % at 2 years (Fig.  3b), as described by the Baltimore’s group [ 1719]. Reduction of NRM with PT-Cy was due to decreased mortality from GVHD (data not shown) without significant reduction in the incidence of acute and chronic GVHD, suggesting that PT-Cy ameliorates the severity of GVHD. While there was a trend for an increased incidence of relapse in RIC vs. MAC in multivariate analysis adjusted for disease risk, as observed in non-haplo-identical SCT [ 3840], interestingly, patients receiving PT-Cy + CsA/Tacro + MMF did not have increased risk of relapse. Altogether, these data suggest that the association of PT-Cy with one calcineurin inhibitor and MMF represents a safer platform for GVHD prophylaxis in haplo-SCT with reduced NRM without impact on relapse incidence.
In comparison to the data reported by the Baltimore’s group of haplo-SCT performed with a Fludarabine-Cyclophosphamide-low dose TBI RIC and PT-Cy, the data of RIC with PT-Cy in this multicenter experience confirm that this approach is associated with low risks of GVHD and provides lower NRM. Although, PT-Cy is not associated to an increased risk of relapse, its incidence remains however the major post-transplant event with 30 % incidence at 2 years in patients transplanted in CR1 in our series. Thus, although this platform seems safer, strategies for improvement are needed. In this objective, adaptation of conditioning intensity, the use of PBSC together with post-transplant immunomodulation, and preventive anti-leukemia targeted strategies might improve the outcome.

Conclusions

We recognize that this study has several limitations. First, it is retrospective and registry-based with imperfectly reported cytogenetics data, and the reasons for the choice of the intensity of conditioning regimen and GVHD prophylaxis were unknown but mainly dependent on centers’ protocols and experience. Second, the conditioning regimens and GVHD prophylaxis used were very heterogeneous, and patient characteristics varied among the groups for multiple factors including age, type of leukemia, and disease status at transplantation. Despite these limitations, the results described in this large retrospective study confirm single center experiences of the validity of performing T-replete haplo-CST with MAC or RIC, in particular using PT-Cy as GVHD prophylaxis, in first line treatment of high risk AML and ALL. Prospective comparative studies are required to determine the optimal conditioning and GVHD prophylaxis as well as the place for post-transplant immunomodulation or targeted therapeutic strategies.

Methods

Study design and data collection

This was a retrospective multicenter analysis. Data were provided and approved for this study by the acute leukemia working party (ALWP) of the EBMT group registry. The latter is a voluntary working group of more than 500 transplant centers that are required to report all consecutive stem cell transplantations and follow-ups once a year. Audits are routinely performed to determine the accuracy of the data. The study protocol was approved by the institutional review board at each site and complied with country-specific regulatory requirements. The study was conducted in accordance with the Declaration of Helsinki and Good Clinical Practice guidelines. All patients provided written informed consent authorizing the use of their personal information for research purposes. Eligibility criteria for this analysis included adult patients (age >18 years) with AL, transplanted between 2001 and 2012, from an HLA-haplo-identical donor with bone marrow (BM) or G-CSF mobilized peripheral blood (PB) stem cells. All donors were HLA-mismatched at least at two loci (≤8/10) (-A, -B, -C, DRB1, -DQB1). Exclusion criteria were previous allogeneic or cord blood transplantation and ex vivo T cell depleted stem cell graft. Variables collected included recipient and donor characteristics (age, gender, CMV serostatus), disease status at transplant, transplant related-factors including conditioning regimen, pre-transplant immunosuppression (in vivo T cell depletion with anti-thymocyte globuline or alemtuzumab vs. none), stem cells source (BM or PB), GVHD prophylaxis (PT-Cy + CsA/Tacro + MMF vs. others), and outcome variables (acute and chronic GVHD, relapse, NRM, leukemia-free survival (LFS), OS, and causes of death). Regimens were classified as MAC or RIC based on published criteria [ 55]. Grading of acute and chronic GVHD was performed using established criteria [ 56]. Chronic GVHD was classified as limited or extensive according to usual criteria [ 57]. The list of institutions reporting data included in this study is provided in the supplemental data (Additional file 1: Table S1).

Statistical analysis

The primary end point of the study was overall (OS) and leukemia-free survival (LFS). Secondary endpoints included disease relapse incidence (RI), non-relapse mortality (NRM), engraftment, incidences, and severity of acute and chronic GVHD. LFS was defined as survival without relapse or progression and NRM as death without relapse/progression. The two groups according to the conditioning regimen were compared by the chi-square method for qualitative variables, whereas the Mann-Whitney test was applied for continuous parameters. Univariate comparisons were done using the log-rank test for OS, LFS, and Gray’s test for RI, NRM, and GVHD cumulative incidences. Multivariate analyses were performed using logistic regression for complete remission (CR) rate and Cox proportional hazards model for all other endpoints. Factors differing in terms of distribution between the two groups and factors associated with a p value less than 0.15 by univariate analysis were included in the final model. All tests were two-sided. The type I error rate was fixed at 0.05 for the determination of factors associated with time to event outcomes. Statistical analyses were performed with SPSS 22.0 (IBM Corp., Armonk, NY, USA) and R 3.1.1 software packages (R Development Core Team, Vienna, Austria).

Acknowledgements

MM thanks Prof. J.V. Melo (Adelaide, Australia) for critical reading of the manuscript. MM also acknowledges the educational grants received from the “Association for Training, Education and Research in Hematology, Immunology and Transplantation” (ATERHIT). The Saint-Antoine hospital group is supported by several grants from the Hospital Clinical Research Program from the French National Cancer Institute to MM.
A complete list of contributors, as well as members of the European Blood and Marrow Transplantation Group appears on the online data supplement.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

MTR, BNS, ML, MM, and AN designed the research and/or analyzed data; FB, AB, WA, YK, DB, ZG, DW, PDB, JT, BA, CS, and SG provided clinical data; MTR, BNS, ML, MM, and AN wrote the manuscript; and all authors approved the final version of the manuscript.

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