Abstract

Total body irradiation (TBI) in combination with chemotherapy is widely used as a conditioning regimen in pediatric and adult hematopoietic stem cell transplantation (HSCT). The combination of TBI with chemotherapy has demonstrated superior survival outcomes in patients with acute lymphoblastic and myeloid leukemia when compared with conditioning regimens based only on chemotherapy. The clinical application of intensity-modulated radiation therapy (IMRT)-based methods (volumetric modulated arc therapy (VMAT) and TomoTherapy) seems to be promising and has been actively used worldwide. The optimized conformal total body irradiation (OC-TBI) method described in this study provides selected dose reduction for organs at risk with respect to the most significant toxicity (lungs, kidneys, lenses). This study included 220 pediatric patients who received OC-TBI with subsequent chemotherapy and allogenic HSCT with TCRαβ/CD19 depletion. A group of 151 patients received OC-TBI using TomoTherapy, and 40 patients received OC-TBI using the Elekta Synergy™ linac with an Agility-MLC (Elekta, Crawley, UK) using volumetric modulated arc therapy (VMAT). Twenty-nine patients received OC-TBI with supplemental simultaneous boost to bone marrow—(SIB to BM) up to 15 Gy: 28 patients (pts)—TomoTherapy; one patient—VMAT. The follow-up duration ranged from 0.3 to 6.4 years (median follow-up, 2.8 years). Overall survival (OS) for all the patients was 63% (95% CI: 56–70), and event-free survival (EFS) was 58% (95% CI: 51–65). The cumulative incidence of transplant-related mortality (TRM) was 10.7% (95% CI: 2.2–16) for all patients. The incidence of early TRM (<100 days) was 5.0% (95% CI: 1.5–8.9), and that of late TRM (>100 days) was 5.7 (95% CI: 1.7–10.2). The main causes of death for all the patients were relapse and infection. The concept of OC-TBI using IMRT VMAT and helical treatment delivery on a TomoTherapy treatment unit provides maximum control of the dose distribution in extended targets with simultaneous dose reduction for organs at risk. This method demonstrated a low incidence of severe side effects after radiation therapy and predictable treatment effectiveness. Our initial experience demonstrates that OC-TBI appears to be a promising technique for the treatment of pediatric patients.

Highlights

  • Total body irradiation (TBI) in combination with chemotherapy is widely used worldwide as a conditioning regimen prior to transplanting hematopoietic stem cells in patients with malignant hematological diseases.The main benefits of TBI include tumor cell elimination and general immunosuppressive effects

  • There is no capability to measure the dose in a small voxel volume and to create dose/volume histograms (DVHs) for the planning target volume (PTV) and organs at risk (OARs) to correlate toxicities with received radiation doses

  • The optimized conformal total body irradiation (OC-TBI) method described in this study provides reproducible dose reduction for OARs that are prone to significant radiotoxicity

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Summary

Introduction

Total body irradiation (TBI) in combination with chemotherapy is widely used worldwide as a conditioning regimen prior to transplanting hematopoietic stem cells in patients with malignant hematological diseases.The main benefits of TBI include tumor cell elimination and general immunosuppressive effects. Total body irradiation (TBI) in combination with chemotherapy is widely used worldwide as a conditioning regimen prior to transplanting hematopoietic stem cells in patients with malignant hematological diseases. The combination of TBI with chemotherapy has demonstrated superior survival results in patients with acute lymphoblastic and myeloid leukemia when compared with conditioning regimens, including chemotherapy alone [1,2,3,4,5,6,7]. The incidence of pneumonitis after TBI-conditioning regimens varies, covering a range of 10.3%–45%, and it depends on many factors, such as patient characteristics and treatment technique [10,11,12]. The disadvantage of the conventional TBI treatment technique is the lack of sparing organs at risk (OARs), with the exception of the lungs. There is no capability to measure the dose in a small voxel volume and to create dose/volume histograms (DVHs) for the planning target volume (PTV) and OARs to correlate toxicities with received radiation doses

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