CNS Involvement at Initial Diagnosis and Risk of Relapse After Allogeneic HCT for Acute Lymphoblastic Leukemia in First Complete Remission
Mohamed A. Kharfan-Dabaja,
Myriam Labopin,
Ali Bazarbachi,
Urpu Salmenniemi,
Stephan Mielke,
Patrice Chevallier,
Marie Thérèse Rubio,
Marie Balsat,
Pietro Pioltelli,
Anne-Lise Menard,
Gerard Socié,
Anne Huynh,
Nicolaas Schaap,
Arancha Bermúdez Rodríguez,
Jan J. Cornelissen,
Ibrahim Yakoub-Agha,
Mahmoud Aljurf,
Sebastian Giebel,
Eolia Brissot,
Zina Peric,
Arnon Nagler,
Mohamad Mohty
Affiliations
Mohamed A. Kharfan-Dabaja
1 Dvision of Hematology-Oncology and Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, FL, USA
Myriam Labopin
2 Sorbonne University, Department of Hematology, Hôpital Saint Antoine and INSERM UMRs 938, Paris, France
Ali Bazarbachi
3 Blood and Marrow Transplantation Program, Department of Internal Medicine, American University of Beirut, Lebanon
Urpu Salmenniemi
4 HUCH Comprehensive Cancer Center, Stem Cell Transplantation Unit, Helsinki, Finland
Stephan Mielke
5 Karolinska Institute and University Hospital, Department of Laboratory Medicine, CAST, Stockholm, Sweden
Patrice Chevallier
6 CHU Nantes, Department D’Hématologie, Nantes, France
Marie Thérèse Rubio
7 CHRU BRABOIS, Service Hématologie, Vandoeuvre Nancy, France
Marie Balsat
8 Centre Hospitalier Lyon Sud, Service Hematologie, Lyon, France
Pietro Pioltelli
9 Ospedale San Gerardo, Clinica Ematologica dell`Universita Milano-Biocca, Monza, Italy
Anne-Lise Menard
10 Centre Henri Becquerel, Hematology, Rouen, France
Gerard Socié
11 Hopital St. Louis, Department of Hematology – BMT, Paris, France
Anne Huynh
12 CHU, Institut Universitaire du Cancer Toulouse, Oncopole, Toulouse, France
Nicolaas Schaap
13 Radboud University Medical Centre, Department of Hematology, Nijmegen, The Netherlands
Arancha Bermúdez Rodríguez
14 Hospital U. Marqués de Valdecilla, Servicio de Hematología-Hemoterapia c/ Marqués de Valdecilla s/n, Santander, Spain
Jan J. Cornelissen
15 Department of Hematology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, The Netherlands
Ibrahim Yakoub-Agha
16 CHU de Lille LIRIC, Univ Lille, INSERM U1286, France
Mahmoud Aljurf
17 King Faisal Specialist Hospital & Research Centre, Oncology (Section of Adult Haematolgy/BMT), Riyadh, Saudi Arabia
Sebastian Giebel
18 Department of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland
Eolia Brissot
2 Sorbonne University, Department of Hematology, Hôpital Saint Antoine and INSERM UMRs 938, Paris, France
Zina Peric
19 University Hospital Centre Zagreb and School of Medicine, University of Zagreb, Croatia
Arnon Nagler
20 Division of Hematology and Bone Marrow Transplantation, The Chaim Sheba Medical Center, Tel-Hashomer, Ramat-Gan, Israel
Mohamad Mohty
2 Sorbonne University, Department of Hematology, Hôpital Saint Antoine and INSERM UMRs 938, Paris, France
Outcomes of allogeneic hematopoietic cell transplantation (allo-HCT) for adult acute lymphoblastic leukemia (ALL) have improved over time. Studies have shown that total body irradiation (TBI) is the preferable type of myeloablative conditioning (MAC). However, outcomes based on central nervous system (CNS) involvement, namely CNS-positive versus CNS-negative, have not been compared. Here, we evaluated outcomes of 547 patients (CNS-positive = 96, CNS-negative = 451) who were allografted in the first complete remission (CR1) between 2009 and 2019. Primary endpoint was leukemia-free survival (LFS). Median follow-up was not different between the CNS-positive and CNS-negative groups (79 versus 67.2 months, P = 0.58). The CNS-positive group were younger (median age 31.3 versus 39.7 years, P = 0.004) and were allografted more recently (median year 2012 versus 2010, P = 0.003). In both groups, MAC was the preferred approach (82.3% versus 85.6%, P = 0.41). On multivariate analysis, the CNS-positive group had higher incidence of relapse (RI) (hazard ratio [HR] = 1.58 [95% confidence interval (CI) = 1.06-2.35], P = 0.025), but no adverse effect on LFS (HR = 1.38 [95% CI = 0.99-1.92], P = 0.057) or overall survival (OS) (HR = 1.28 [95% CI = 0.89-1.85], P = 0.18). A subgroup multivariate analysis limited to CNS-positive patients showed that a TBI-based MAC regimen resulted in better LFS (HR = 0.43 [95% CI = 0.22-0.83], P = 0.01) and OS (HR = 0.44 [95% CI = 0.21-0.92], P = 0.03) and lower RI (HR = 0.35 [95% CI = 0.15-0.79], P = 0.01). Another subgroup analysis in CNS-negative patients showed that MAC-TBI preparative regimens also showed a lower RI without a benefit in LFS or OS. While a MAC-TBI allo-HCT regimen may not be suitable to all, particularly for older patients with comorbidities, this approach should be considered for patients who are deemed fit and able to tolerate.