Umbilical cord blood transplants facilitated by the French cord blood banks network. On behalf of the Agency of Biomedicine, Eurocord and the French society of bone marrow transplant and cell therapy (SFGM-TC).

The public French Cord Blood Banks Network was established in 1999 with the objective of standardizing the practices governing umbilical cord blood (UCB) banking in France. The Network adopted a strategy to optimize its inventory and improve the quality of its banked units based on a quality improvement process using outcome data regularly provided by Eurocord. This study aimed to describe the results, over 10 years, of UCBT facilitated by a national network that used the same criteria of UCB collection and banking and to assess how modifications of banking criteria and unit selection might influence transplant outcomes. Nine hundred and ninety-nine units (593 single-unit and 203 double-unit grafts) were released by the Network to transplant 796 patients with malignant (83%) and non-malignant (17%) diseases. Median cell dose exceeded 3.5 × 107 TNC/kg in 86%. There was a trend to select units more recently collected and with higher cell dose. Neutrophil engraftment was 88.2% (85.7-90.7) and 79.3% (72.6-86.5) respectively for malignant and non-malignant diseases with a trend to faster recovery with higher cell doses. The respective 3-year transplant-related mortality were 31.1% (27.5-35.1) and 34.3% (27.0-43.5). OS was 49% ± 4 in malignant and 62% ± 4 in non-malignant disorders. In multivariate analysis, cell dose was the only unit-related factor associated with outcomes. Our results reflect the benefit on clinical outcomes of the strategy adopted by the Network to bank units with higher cell counts.

Introduction

Since the first cord blood transplant [1], improvement in umbilical cord blood (UCB) unit selection resulted in better outcomes after both single- and double-unit cord blood transplants [2-5]. Major limitations remain delayed hematopoietic recovery and high incidence of graft failure, resulting in an increased risk of non-relapse mortality compared to other stem cell sources [6-11]. To date, HLA matching and cell dose are the most important criteria when selecting UCB units for transplantation [12-17]. Historically, HLA was typed based on HLA-A, -B antigen level, and -DRB1 allele level. Subsequently, it was demonstrated that HLA-C match and high-resolution were important factors for outcomes. Increasing the total nucleated cell (TNC) above the recommended minimum pre-freezing dose of 2.5–3 × 107/kg has also been suggested to improve engraftment and survival [17, 18]. The French Cord Blood Banks Network (in French, Réseau Français de Sang Placentaire, called the Network throughout the article) was established in 1999 under the auspices of the National Agency for Organs and Bone Marrow Transplantation later replaced by the Agency of Biomedicine (ABM), with the aim of standardizing practices governing collection, storage, and release of UCB units across the national cord blood banks (CBB) [19]. In France, cord blood banking can only be performed in public banks authorized by competent National Health Authorities to process and store UCB units. For this propose, standard criteria for cord blood banking that resulted in collection and storage of UCB units of similar quality have been established and implemented through regular meetings and discussions organized by ABM between the CBBs, maternity wards, and transplant physicians. Methods for collection, cryopreservation and thawing, measurement of cell dose, and viability were standardized to fulfill the Foundation for the Accreditation of Cellular Therapy (FACT) - NetCord standards adopted by the Network [20]. The Network recommendations have been modified overtime based on transplant outcome data regularly provided by Eurocord and used as quality improvement indicators that assess the performance of the Network.

This study aims to describe the characteristics and distribution in quality categories of the French UCB units collected and released over a period of 10 years and to analyse the outcomes of transplants performed with these units during the same period, considering the modifications of the banking criteria carried out in the context of the quality improvement process, in terms of standardized collection and processing policies, pre-freezing unit eligibility criteria (collected volume, minimal TNC, and CD34 counts) and HLA typing.

Materials and methods

In this registry-based retrospective study, we included all consecutive patients who received unrelated single or double UCBT (sCBT or dCBT) in an EBMT center, with units released by the Network between 1 January 2008 and 31 December 2017. Patients having prior allogeneic transplantation, those transplanted in non-EBMT centers, and those receiving double units that were not both released by the Network were excluded. Data related to patients, UCB unit characteristics, and transplant outcomes were collected from the Eurocord and SYRENAD registries in accordance with the ethical standards of the institutional committees and the Helsinki declaration. The European Society for Blood and Marrow Transplantation (EBMT) and the Société Française de Greffe de Moelle et Thérapie Cellulaire (SFGM-TC) approved this study.

Definitions

The primary endpoint was overall survival (OS) defined as the interval from UCBT to death from any cause. Event-free survival (EFS) was defined as the interval from UCBT to either relapse or death. Transplant-related mortality (TRM) was defined as death in remission. Neutrophil engraftment was defined as the achievement of an absolute neutrophil count >0.5 × 109/L for three consecutive days. Early graft failure was defined as failure to achieve neutrophil engraftment, loss of donor engraftment or autologous recovery within day 100 after HSCT.

Diagnosis and grading of acute and chronic graft versus host diseases (aGVHD and cGVHD) were performed according to standard criteria [21, 22]. Cell doses were calculated as TNC or CD34+ cell counts by recipient weight in sCBT or as the cumulative number of TNC or CD34+ cells present in both units by recipient weight in dCBT. HLA compatibility was determined considering antigen-level for HLA-A and -B loci and allele-level for the HLA-DRB1 locus. HLA compatibility for dCBTs was classified according to the unit with the highest HLA disparity with the recipient. The conditioning regimen was defined as myeloablative (MAC) or reduced intensity (RIC) based on EBMT criteria [23].

Statistical analysis

Separate analyses were performed for malignant and non-malignant diseases. The transplant period was analyzed as a binary variable with the cut-off defined by the cohort’s median year of UCBT.

Probabilities of OS and EFS were estimated using the Kaplan–Meier method; two-sided log-rank test was used for univariate comparisons. The cumulative incidences were estimated for neutrophil recovery, aGVHD, cGVHD, TRM, and relapse with adjustment for competing risks. Multivariate analyses (MVA) were performed using Cox proportional hazards regression models [24], to adjust for all factors with a p value < 0.10 in univariate analysis. A threshold level of 0.05 was applied for statistical significance [25]. Statistical analyses were performed using SPSS 21 and R 3.2.0 software packages.

Organization of the Network

The Network currently includes five active public CBBs and 22 maternity wards authorized to perform UCB collection by the Regional Agency of Health. An additional site dedicated to UCB storage only and five other CBBs that have stopped all collection activities following the Network restructuring, continue to manage and release their previously stored UCB units. The reduction in the total number of active banks and associated maternity wards over the years was part of the global improvement strategy adopted by the network aiming to facilitate the implementation of uniform collection and processing high-quality standards. The processing and storage of UCB units in France can only be performed in public CBBs that are authorized for banking by the National competing authorities.

Results

Characteristics of UCB units stored in the Network during the study period

By the end of 2008, the Network inventory included 7051 UCB units. Due to increasing demand for UCB, the Network increased its activities with the goal of storing 30,000 units by 2015. In 2012, the Network included 16,154 units in its inventory and, in 2015, 34,115 units were available for transplantation. Once the quantitative objective achieved, the Network adopted a qualitative approach based on the “2015 banking criteria” that restricted cryopreservation to units with post-processing TNC counts ≥16 × 108. This resulted in the storage of only 10% of the collected units (2 076 new UCB units) between 2015 and 2017 (Fig. 1a).

Fig. 1

The Network inventory (2008–2017).

a Cumulative number of UCBs stored; b Numbers of UCBs released per year.

A total of 36,191 UCB units were available in the Network inventory on 31 December 2017; 62% of the stored units had pre-freezing cell counts >12 × 108 TNC. Only 249 units had TNC counts lower than 6 × 108. All units were typed for HLA -A, -B, and -DRB1 at different resolution levels and 67% were typed for HLA-C (Table 1).

Table 1

Characteristics of UCBs available in the Network inventory on 31 December 2008 and 2017.

HLA typing	HLA-A		HLA-B		HLA-C		HLA- DRB1
	2008	2017	2008	2017	2008	2017	2008	2017
Antigen-level	5485 (78%)	8117 (22%)	5408 (76%)	7691 (21%)	638 (9%)	1053 (3%)	3770 (53%)	2227 (6%)
Intermediate resolution (NMDP code)a,b	1566 (22%)	23,262 (65%)	1643 (24%)	23,510 (65%)	757 (11%)	16,830 (46%)	3281 (47%)	15,995 (44%)
Allele-level	–	4812 (13%)	–	4990 (14%)	–	6372 (18%)	–	17969 (50%)
Total UCB typed	7051 (100%)	36,191 (100%)	7051 (100%)	36,191 (100%)	1395 (20%)	24,255 (67%)	7051 (100%)	36,191 (100%)

UCB umbilical cord blood unit, TNC total nucleated cells.

ahttps://bioinformatics.bethematchclinical.org/hla-resources/allele-codes/.

bRef. [[60]].

Characteristics of the UCB units used for transplantation

Of the 2002 UCB units released by the Network over 10 years, 999 units fulfilled the criteria for inclusion in our study and were used to transplant 796 patients (593 sCBT and 203 dCBT) in 25 countries and 132 transplant centers (54% for transplants performed in France). Despite the transient early decrease between 2008 and 2010, the release activity improved dramatically after 2012 reaching a peak in 2014 followed by a slow decrease, which was likely due to the increasing use of related haploidentical donors (Fig. 1b). All released units had intermediate to high-resolution typing for HLA -A, -B, -C, and -DRB1 and 54% (n = 532) had allele-level typing. We observed a sustained increase in the total cell content of the units over the years, most prominent after 2012 (Table 2). A total of 106 units (11%) had pre-freezing TNC counts of 6 × 108–12 × 108, 193 (19%) had TNC counts of 12 × 108–16 × 108, and 709 (72%) had TNC counts ≥16 × 108. Only 4 UCB units with TNC count lower than 6 × 108 were released in the 10-year period considered in the analysis. Volume reduction was performed in 70% of the units (n = 700). UCB used for transplantation were collected between 1995 and 2016 and seventy percent (n = 693) were collected after 2005 (median year of collection). The median pre-freezing cell doses were 3.50 × 107 TNC/kg (2.61–5.70) and 1.28 × 105 CD34 + cells/kg (0.76–2.40) for the units collected before 2005 and 4.02 × 107 TNC/kg (2.92–6.93) and 1.75 × 105 CD34+ cells/kg (1.14–3.21) for those collected after 2005. The median cell loss at transplantation was 23% (7-49%) for TNCs and 30% (3-51%) for CD34+ cells. This percentage was roughly stable and was not affected by the cryopreservation duration (Table 2). The increased cell counts and available higher resolution HLA typing that characterized the units collected after 2005 might explain the trend towards the enhanced utilization of these units for transplantation in recent years (Fig. 2).

Table 2

Median TNC and CD34+ cell counts of the units released during the study period according to storage year.

UCB storage year	UCB units releaseda (n)	Median TNC count at freezing (×108)	Median TNC count at UCBT (×108)	TNC loss (%)	Median CD34+ count at freezing (×106)	Median CD34+ count at UCBT (×106)	CD34+ cell loss (%)
1995	6	19.9	12.5	37	7	5.2	26
1996	4	18.4	9.4	49	3.9	2.9	26
1997	6	18.1	13.4	26	4.9	3.3	33
1998	7	16.9	13.1	22	9.9	4.9	51
1999	48	19.1	14.7	23	6.7	4	40
2000	85	18.8	14.8	21	6.1	5.1	16
2001	64	19.4	15.1	22	6	3.6	40
2002	45	18.6	13.4	28	7.4	3.6	51
2003	32	19.1	15.4	19	6.1	3.8	38
2004	9	17.6	10.5	40	5.9	5.7	3
2005	14	17.4	11.9	32	5.4	4.5	17
2006	29	18.1	13.1	28	6.7	4.8	28
2007	36	17.3	13.6	21	6.5	4.8	26
2008	39	19.4	15.3	21	7.5	5.3	29
2009	53	17.0	14.5	15	6.8	4.6	32
2010	90	19.5	13.7	30	8.6	5.9	31
2011	127	19.8	15.4	22	7.8	5.3	32
2012	142	19.8	15.3	23	7.5	5.3	29
2013	111	22.4	17.3	23	8.3	5.7	31
2014	39	24.9	19.6	21	11.7	7	40
2015	10	22.9	21.4	7	7.8	6.6	15
2016	3	25.1	21.6	14	11.6	9.7	16

aEligible units released during the study period.

Fig. 2

Percentage of UCB units released yearly.

a UCB released according to median year of collection (=<2005 vs >2005); b UCB released by collection period.

Patient and transplant characteristics

A total of 796 patients underwent unrelated sCBT (n = 593, 75%) or dCBT (n = 203, 25%) with grafts released by the Network (Table 3). Indications for UCBTs were malignant (n = 661, 83%) or non-malignant (n = 135, 17%) disorders, with acute leukemia (AL) being the most common diagnosis. Median pre-freezing TNC dose was 5 × 107/kg (3.9–6.8) for recipients with hematological malignancies and 12.5 × 107/kg (6.9–21.1) for non-malignant disorders. This difference reflects the younger age (and lower bodyweight) of the recipients in the non-malignant group.

Table 3

Patients and transplant characteristics.

	Malignant diseases		Non-malignant disorders
UCBT period	2008–2012	2013–2017	2008–2012	2013–2017
No. of patients, N (%)	313 (47%)	348 (53%)	52 (39%)	83 (61%)
Median age, years (IQR)	35 (11–53)	34 (9–54)	1.65 (0.9–7.7)	1.5 (0.7–7)
Children (<18 y)	100 (32%)	133 (38%)	48 (92%)	77 (93%)
Adults (≥18 y)	213 (68%)	215 (62%)	4 (8%)	6 (7%)
Median weight, kg (IQR)	60 (40–72)	60 (31–74)	11 (8–25)	11 (7–24)
Gender, Male, N (%)	167 (53%)	189 (55%)	31 (60%)	48 (58%)
Recipient CMV serology, N (%)
Negative	137 (46%)	151 (47%)	19 (38%)	35 (47%)
Positive	161 (54%)	170 (53%)	31 (62%)	39 (53%)
Not reported	15	27	2	9
Diagnosis, N (%)
Acute leukemias	209 (67%)	237 (68%)
Myelodysplastic/Myeloproliferative disorders	42 (13%)	71 (21%)
Lymphoproliferative disorders	49 (16%)	35 (10%)
Plasma cell disorders	13 (4%)	5 (1%)
Primary immune deficiency			15 (29%)	33 (40%)
Bone marrow failure syndromes			16 (31%)	19 (23%)
Inborn errors of metabolism			14 (27%)	21 (25%)
Other non-malignant disorders			7 (13%)	10 (12%)
Time from diagnosis to UCBT, median months (IQR)	11.5 (6–33)	7.86 (5–22)	9.16 (3.4–20.6)	5 (2.6–15)
Graft type
sCBT	215 (69%)	248 (71%)	49 (94%)	81 (98%)
dCBT	98 (31%)	100 (29%)	3 (6%)	2 (2%)
HLA parity (low-intermediate resolution)
6/6	17 (5%)	23 (8%)	6 (12%)	18 (22%)
5/6	93 (31%)	126 (43%)	37 (71%)	41 (49%)
4/6	183 (59%)	131 (45%)	8 (15%)	15 (18%)
3/6	13 (4%)	12 (4%)	1 (2%)	0
2/6	2 (1%)	0	0	0
Missing	5	56	0	9 (11%)
HLA parity (high resolution)
8/8	2 (1%)	6 (3%)	1 (4%)	10 (19%)
7/8	7 (4%)	26 (13%)	5 (19%)	11 (21%)
6/8	26 (16%)	55 (27%)	6 (23%)	17 (32%)
5/8	64 (40%)	56 (27%)	8 (31%)	9 (17%)
4/8	42 (26%)	52 (25%)	5 (19%)	3 (6%)
3/8	18 (11%)	10 (5%)	1 (4%)	3 (6%)
2/8	3 (2%)	1 (<1%)
ABO compatibility, N (%)
ABO compatible	117 (38%)	120 (36%)	24 (46%)	31 (38%)
Minor ABO Incompatibility	80 (26%)	76 (23%)	12 (23%)	18 (22%)
Major ABO Incompatibility	112 (36%)	135 (41%)	16 (31%)	32 (40%)
Missing	4	17	0	2
Gender compatibility, N (%)
M/M or F/F	126 (40%)	160 (47%)	26 (50%)	44 (54%)
M/F or F/M	187 (60%)	182 (53%)	26 (50%)	38 (46%)
Missing		6	0	1
Conditioning regimen
MAC	164 (53%)	223 (66%)	32 (63%)	60 (75%)
RIC	146 (47%)	115 (34%)	19 (37%)	20 (25%)
Not reported	3	10	1	3
TBI containing regimen	186 (59%)	141 (41%)	8 (16%)	12 (20%)
ATG administration	149 (49%)	145 (62%)	39 (77%)	66 (93%)
GVHD Prophylaxis
CSA ± MMF based	300 (96%)	305 (88%)	45 (87%)	74 (89%)
Others	13 (4%)	43 (12%)	7 (13%)	9 (11%)
UCB characteristics
• UCB median volume, ml (IQR)	136 (117–163)	162 (140–183)	124 (108–143)	145 (126–168)
• UCB volume reduction, n (%)	191 (46%)	410 (92%)	23 (43%)	76 (89%)
Cell dose, Median (IQR)
• TNC collected (×107/kg)	4.8 (3.8–6.5)	5.1 (3.9–7.2)	11 (7.0–20.1)	12.9 (6.9–21.1)
• CD34 collected (×105/kg)	1.9 (1.3–2.8)	2.3 (1.5–3.4)	4.3 (2.3–9.3)	4.5 (2.5–7.9)
• TNC infused (×107/kg)	3.7 (2.9–5.3)	4.1 (3.0–6.1)	8.3 (5.1–15.41)	9.2 (4.8–15.1)
• CD34 infused (×105/kg)	1.4 (1.0–2.3)	1.7 (1.1–2.5)	2.5 (1.3–5.4)	3.1 (1.5–5.5)
Follow-up, median months (range)	65.8 (1.9–128)	23.6 (2.5–67)	74 (3.4–124)	25 (2.9–60)

UCBT cord blood transplant, IQR interquartile range (Q1–Q3), sCBT single unit UCBT, dCBT double unit UCBT, MAC myeloablative conditioning, RIC reduced intensity conditioning, TBI total body irradiation, ATG anti-thymocyte globulins, GVHD graft versus host disease, CSA ciclosporine A, MMF mycophenolate mefotil, UCB umbilical cord blood unit, TNC total nucleated cells.

Hematological malignancies

Of the 661 patients with hematological malignancies, 67% were transplanted for AL (acute lymphoblastic leukemia (ALL = 168); acute myeloblastic leukemia (AML = 278), 17% for other myeloid malignancies, and 16% for lymphoproliferative disorders. The median age at UCBT was 35 years (0.3–74) with 35% of patients aged <18 years. Single-unit UCB represented the graft source in 70% of cases; 87% of the donor-recipient pairs had ≤2/6 HLA disparities (antigen level HLA-A, -B, and allele level DRB1) with the recipients. Allele-level typing for HLA-A, -B, -C, -DRB1 was available for 52% (n = 162) of the patients transplanted before 2012 and 59% (n = 206) of those transplanted after 2012. There was a trend towards selecting UCB units with less HLA mismatches (≤3/8 HLA disparities in 70%) and higher cell counts (5.1 × 107 TNC/kg) for transplants performed after 2012. (Table 3)

Outcomes (Table 4)—The median follow-up for survivors was 36 months (1.9–128). The 60 days cumulative incidence of neutrophil recovery was 88.2% (95% CI 85.7–90.7) within a median time of 21 days (5–76), with better engraftment (90.7% versus 85.5%; p = 0.001) after 2012 in comparison to an earlier period. Acute GVHD grade II–IV was observed in 243 patients (54% of Grade II; 29% of Grade III and 17% of Grade IV), within a median of 25 days (7–94) and a cumulative incidence of 36.4% (95% CI 32.9–40.3) at 100 days with a trend for higher incidence after 2012 (33.1% vs 40.1% p = 0.044) that might reflect the use of higher cell doses and MAC regimen in recent years; 134 patients developed cGVHD within a median of 164 days (70–1015), and an incidence of 25.5% (95% CI 22.0–29.6%) at 3 years. Overall, 321 patients died, 170 of TRM, and 139 of relapse. The cause of death for the remaining 12 patients was unknown. The 3-year incidence of TRM was 31.1% (95% CI 27.5–35.1); the most common causes being infection (n = 63) and GVHD (n = 42). The 3-year cumulative incidence of relapse was 23% (95% CI 19.7–26.7) with a trend for less relapse in transplants performed after 2012 (25.9% vs 19.7% p = 0.088). The EFS was 46% ± 2 at 3 years. The OS was 49% ± 3 at 3 years (46% ± 3 before 2012; 53% ± 3 after 2012; p = 0.24) (Fig. 3A).

Table 4

Outcomes for malignant and non-malignant diseases by transplant period.

	Total	2008–2012	2013–2017	P value
3 y Overall survival
Malignant diseases	49% ± 3	46% ± 3	53% ± 3	0.241
Non-malignant disorders	62% ± 4	59% ± 6	65% ± 5	0.500
3 y Event-free survival
Malignant diseases	46% ± 2	42% ± 3	50% ± 3	0.108
Non-malignant disorders	NA	NA	NA
d60 CI Engraftment
Malignant diseases	88.2% (85.7–90.7)	85.5% (81.7–89.6)	90.7% (87.7–93.8)	0.001
Non-malignant disorders	79.3% (72.6–86.5)	71.2% (59.6–85.0)	84.3% (76.7–92.7)	0.02
d100 CI aGVHD
Malignant diseases	36.4 % (32.9–40.3)	33.1% (28.2–38.8)	40.1% (35.2–45.7)	0.044
Non-malignant disorders	33.1% (25.9–42.2)	35.3% (24.2–51.4)	31.7% (23.0–43.7)	0.736
3 y CI cGVHD
Malignant diseases	25.5% (22.0–29.6)	26.0% (21.1–32.2)	24.8% (20.1–30.5)	0.968
Non-malignant disorders	20.9% (14.2–30.7)	20.9% (11.2–39.1)	15.2% (8.5–27.0)	0.585
3 y CI relapse
Malignant diseases	23.0% (19.7–26.7)	25.9% (21.3–31.6)	19.7% (15.7–24.9)	0.088
Non-malignant disorders	NA	NA	NA
3 y CI TRM
Malignant disorders	31.1% (27.5–35.1)	31.8% (26.8–37.7)	30.1% (25.3–35.7)	0.861
Non-malignant disorders	34.3% (27.0–43.5)	37.9% (26.4–54.3)	31.7% (23.0–43.7)	0.495

Statistically significant p-values are in bold italic and Statistically non-significant p-values are in italic.

Fig. 3

Probabilities of 3-year overall survival by transplant period.

a OS for malignant diseases and b OS for non-malignant disorders.

In MVA, higher pre-freezing TNC dose (>3.5 × 107/kg) was the only unit characteristic associated with improved OS [HR = 0.67; 95% CI (0.50–0.91); p = 0.009] and lower TRM [HR = 0.67; 95% CI (0.46–0.97); p = 0.03]; while pre-freezing CD34+ cell dose (≥2.5 × 106/kg) was predictive of better engraftment [HR = 1.38; 95% CI (1.14–1.65); p = 0.002]; and higer incidence of aGVHD [HR = 1.39; 95% CI (1.02–1.92); p = 0.04]. The transplant period was not predictive of aGVHD. None of the UCB unit characteristics were predictive of relapse or cGVHD. Importantly, the administration of ATG was the only factor predictive of increased relapse incidence [HR = 1.47; 95% CI (1.01–2.15); p = 0.04] (Table 5).

Table 5

Multivariate analysis for overall survival, engraftment, aGVHD, cGVHD, TRM and relapse by disease type.

Malignant diseases
Covariatesa	HR	95% CI		p value
		Lower	Higher
Overall survival
Recipent CMV (positive vs negative)	1.32	1.04	1.66	0.020
Age (≥18y vs <18y)	1.59	1.18	2.15	0.002
Pre-cryopreservation TNC (≥3.5 vs <3.5)	0.67	0.50	0.91	0.009
PMN engraftment
UCBT period (>2012 vs ≤2012)	1.20	1.01	1.43	0.040
Pre-cryopreservation CD34 (≥2.5 vs <2.5)	1.38	1.14	1.65	0.0016
aGVHD
RIC vs MAC	0.63	0.45	0.89	0.008
ATG vs No ATG	0.31	0.19	0.50	<0.001
Pre-cryopreservation CD34 (≥2.5 vs <2.5)	1.39	1.02	1.92	0.040
cGVHD
dCBU vs sCBU	1.34	0.95	1.91	0.098
TRM
Recipient CMV (positive vs negative)	1.49	1.10	2.03	0.010
Age (≥18y vs <18y)	2.24	1.47	3.39	<0.001
Pre-cryopreservation TNC (≥3.5 vs <3.5)	0.67	0.46	0.97	0.030
RI
ATG vs No ATG	1.47	1.01	2.15	0.040
Event-free survival
Recipent CMV (positive vs negative)	1.35	1.06	1.73	0.020
Age (≥18y vs <18y)	1.40	1.02	1.93	0.030
No CR vs CR	1.51	1.14	1.99	0.004
TBI vs no TBI	0.67	0.52	0.87	0.003

Statistically significant p-values are in bold italic and Statistically non-significant p-values are in italic.

aGVHD acute graft vs host disease, ATG anti-tymocyte globulins, cGVHD chronic graft vs host disease, CMV cytomegalovirus, CR complete remission, dCBT double cord blood transplant, MAC myeloablative conditioning, PMN polymorphonuclear cells, RI relapse incidence, RIC reduced intensity conditioning, sCBT single-unit cord blood transplant, TBI total body irradiation, TNC total nucleated cells, TRM transplant-related mortality, UCBT umbilical cord blood transplant.

aCovariates included in the multivariate model: transplant period, age, recipient CMV, myolablative nature of the conditioning regimen, TBI, ATG, remission status, cell dose and graft type.

Clinical results in non-malignant disorders

UCBT was performed in 135 patients with non-malignant disorders. Indications for transplant were primary immunodeficiency (PID, n = 48), bone marrow failure syndromes (BMF, n = 35), an inborn error of metabolism (IE n = 35), histiocytic disorders (HIS, n = 11), hemoglobinopathy (HGP, n = 5) and autoimmune disease (AID, n = 1). The median age at transplant was 1.6 (0.1–43) years; only ten patients were older than 18 years. Single UCBT was administered to most patients and MAC regimen was administered to 92 patients. The median infused cell doses were 8.3 × 107 TNC/kg (5.1–15.41) and 2.5 × 105 CD34+ cells/kg (1.3–5.4). All grafts exceeded the minimal cell dose requirements due to the population age and low patients weight. Ninety-three percent of the grafts had ≤2/6 HLA disparities with their recipients. Allelic level typing for HLA -A, -B,-C and -DRB1 was available for 59% (n = 79) of the patients-UCB pairs with majority (n = 67) having ≤3/8 disparities (Table 3).

Outcomes (Table 4)—The median follow-up for survivors was 31 (2.9–124) months. The cumulative incidence of neutrophil recovery at day 60 was 79.3% (95%CI 72.6–86.5%) with a median engraftment time of 19 days (6–77) and better engraftment for UCBTs performed after 2012 (84.3% vs 71.2%; p = 0.02). Grade II–IV aGVHD was reported in 44 patients (22 Grade II, 13 Grade III, and 9 Grade IV) within a median time of 37 days (7–85) and with a cumulative incidence of 33.1% (95% CI 25.9–42.2) at 100 days; cGVHD was reported in 21 patients (extensive in five patients) within a median period of 164 days (101–727) and a 3-year incidence of 20.9% (95% CI 14.2–30.7). Overall, 47 patients died; the 3-year cumulative incidence of TRM was 34.3% (95% CI 27.0–43.5). The most common causes of TRM were infection (n = 17) and GVHD (n = 8). Twenty-seven patients developed primary graft failure, 19 died in a median time of 3.9 months, seven patients were alive at last follow-up after a second allogeneic transplant, and one patient after autologous reconstitution. Three-year OS was 59% ± 6 for patients transplanted before 2012 and 65% ± 5 for those after 2012 (Fig. 3B) with large heterogeneity among diagnosis (49% for BMF, 53% for HIS, and 75% for both IE and HbP). In MVA (Table 5), positive recipient CMV serology was the only factor associated with adverse OS [HR = 2.66; 95% CI(1.36–5.19); p = 0.004] and TRM [HR = 2.76; 95% CI (1.37–5.55); p = 0.004]. Other factors did not show any significant impact on transplant outcomes.

Discussion

The first successful UCBT was performed in 1988 at Saint-Louis hospital in Paris [1] in a patient with Fanconi anemia who received an UCB unit from his HLA-identical sibling. Subsequently, encouraging outcomes of HLA-matched sibling UCBTs provided the proof-of-concept that UCB was a good alternative source of hematopoietic stem cells. The first promising unrelated UCBT results were reported shortly after in children [26-29] and adults, promoted by improved patient and UCB unit selection and better supportive care [3, 4].

The first French CBB was set in Paris in 1990 and started collecting UCB units and developing its registry. With the growing evidence that UCB units could be stored without compromising their biological properties [30] and the acceptance of UCB as an alternative stem cell source, several public institutions, started to create CBBs in the US [31, 32] and Europe [33-37].

Subsequently, an international cooperative CBB network, the NetCord group, was created in 1998 to ensure the high and uniform quality of all UCB units [38]. The group promoted the creation of registries, such as Eurocord, to document and evaluate transplant outcomes in recipients of units released by CBBs.

According to the World Marrow Donors Association (WMDA) reports [39], more than 790,000 UCB units are available worldwide in the public CBBs and more than 40,000 UCBTs have been performed to date [40]. Such numbers highlight the significant clinical achievements over the last 30 years which established UCB as an alternative stem cell source for transplantation in children and adults. However, the use of new transplant protocols involving related haploidentical donors in recent years, has led to a dramatic decrease in utilization of UCB worldwide, thus challenging the sustainability of the public CBB economic model. Many publications addressing this issue advised the CBBs to re-calculate the size of their inventory defining banking decisions based on higher thresholds for cell counts and stronger quality criteria [41-43].

Despite setting up its first bank in 1990, the French Network had stored only 7051 allogeneic UCB units in three operational CBBs by the end of 2008. Adapted from the French bone marrow registry model [44], the optimal size for the French Network was estimated to include 46,737 CBU, which would provide national patients an 83% chance of finding a compatible CBU. To respond to the increase in demand for UCB grafts by transplant centers and to reduce the costly dependence on imported UCB units, the Network, supported by the French health authorities, set a target to store 30,000 UCB units by 2015, then adopted in 2015 a qualitative approach for banking UCB based on higher thresholds for cell counts (prefreezing TNC > 16 × 108). More importantly, the Network imposed very stringent quality standards for collection procedures. These standards used to be regularly modified and updated in the context of a quality improvement process using recipients’ outcomes results provided yearly by Eurocord. Consequently, on 31 December 2017, more than 36% of the units in the Network inventory had a cell content exceeding 15 × 108 TNCs, compared to only 20% of the units listed worldwide in WMDA 2018 reports [39], underscoring a successful quality improvement process adopted by the Network.

In our study, we report 999 UCB units collected and released by the Network for transplantation in EBMT centers. The units collected in recent years were characterized by higher cell counts and allele-level HLA typing which translated into an enhanced utilization rate and a shorter storage period, mainly for those collected after 2015. When compared to current unit selection guidelines [5, 15, 18, 45, 46], 98% of the donor-recipient pairs had 0-2/6 HLA disparities at antigen level HLA- A, -B and allele-level HLA_DRB1) and 52% had 0-4/8 allele level HLA mismatches. In addition, 86% of the patients received a pre-freezing cell dose exceeding the minimum requirement for TNC (>3.5 × 107/kg), and 75% received a CD34+ cell dose ≥ 1.5 × 105/kg, with higher cell doses in the non-malignant setting reflecting younger population age and lower body weight. The median TNC loss after thawing was 23% and was not affected by the length of storage or the processing CBB, demonstrating well-standardized methods of cryopreservation across the Network through time. UCBTs performed after 2012 were significantly associated with faster neutrophil recovery both for malignant (90.7% vs 85.5%, p = 0.001) and non-malignant disorders (84.3% vs 71.2%, p = 0.02) reflecting improved selection criteria for patients and UCB units in recent years.

As previously reported by other groups, we were not able to detect a clear association of HLA disparity with acute [2, 29] or chronic GVHD [10, 47, 48] occurrence, although 46% of the transplants had ≥2/6 HLA mismatches.

The reduced incidence of relapse (25% relapse at 3 years) in our cohort was broadly similar to that reported in hematological malignancies [15, 49, 50] with significantly higher rates in ATG-recipients (p = 0.04). The incidence of TRM was 33.1% for malignant and 34.3% for non-malignant disorders and did not improve overtime despite better unit selection. The OS rate was 49% ± 4 in hematological malignancies and 62 ± 4% in non-malignant disorders and compares favorably with previously published results for UCBT. When looking at MVA of outcomes in malignant diseases, cell dose was the only unit-related factor for OS, EFS, engraftment, acute GVHD, and TRM indicating that improvement could be obtained by further increase of the cell dose, especially in adults. None of the unit-related factors was predictive of outcomes in the non-malignant disorders probably due to younger age and higher cell counts.

Despite lower release rates in recent years with the emergence of haploidentical transplants, 6% of the network inventory were released over the 10-year study period and 2.7% were exported (2% after 2012), reflecting the high-quality standards of the French banked units and their probable HLA diversity. This high release activity represented a significant source of income for the Network close to €8500 per unit transplanted nationally and €17,000 per exported unit.

Based on the data from the WMDA reports [39], France maintained the greatest utilization rates (0.3–0.4% of the Network inventory) in Europe over the last 10 years and the highest ratio of exporting units (0.1%), promoted by high-quality of the units facilitated by the Network, and an exportation fee 15–20% lower than the average fee charged by other countries (€20,000–€25,000).

Our study has limitations inherent to its retrospective registry-based nature and the heterogenous group of diseases included. Another limitation is the consequence of the unavailability of donor’s ethnical background data due to restrictions imposed by the French legislation. Consequently, the analysis of the diversity of HLA haplotypes available in the network inventory (including rare and ethnic minorities) could not be performed. Finally, with the very strict and ambitious criteria for selecting the units eligible to be stored, the Network had to regularly address the economic challenges to remain viable and increase the utilization rates of the units available in its inventory.

Like the French Network, many National banks around the world [5, 51–58] started to question how to reach the optimal size of their inventory in the best cost-effective way and to reorganize their CBB networks to become economically sustainable without compromising the probability of finding optimal grafts for their patients. Consequently, the 2018 WMDA report [39] summarizing trends in stem cell registries in Europe, showed dramatic decrease in the numbers of new banked unrelated UCB units, from 90,000 new CB units listed worldwide in 2010 to less than half (40,000) in 2015, and 10,000 in December 2017.

In conclusion, despite the obvious decrease in the use of CBT in the latest years, with the development of haploidentical transplants, UCB remains an important source of stem cells mainly in children and for patients belonging to ethnic minorities [56, 59]. The Network still has to face two major challenges: expanding the diversity of HLA profiles represented in its inventory and achieving financial sustainability while maintaining the same or improved quality standards. Because all cryopreserved units are tested and ready for immediate use, UCB is also an invaluable resource in urgent situations as in the recent COVID-19 epidemics which resulted in a 15% increase in the number of units released by the Network to transplant national recipients over 2020 (82 units from January through October 2020 compared to 71 in the same period in 2019). Novel approaches aiming to speed-up hematopoietic recovery using ex-vivo expansion systems for hematopoietic stem cells and innovative cell and gene therapies using cord blood-derived immune cells (CAR, NK, MSC) are still being explored for the treatment of hematological diseases as well as autoimmune, neurological, and inflammatory disorders, thus determining the beginning of a new era in UCB therapy.