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Vol. 47. Núm. S3.
HEMO 2025 / III Simpósio Brasileiro de Citometria de Fluxo
(Outubro 2025)
Vol. 47. Núm. S3.
HEMO 2025 / III Simpósio Brasileiro de Citometria de Fluxo
(Outubro 2025)
ID - 2329
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EXPERIENCE WITH AUTOLOGOUS PERIPHERAL BLOOD STEM CELL (PBSC) COLLECTION AND TRANSPLANTATION (HSCT) IN CHILDREN WEIGHTING 25 KG OR LESS
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OMWO Félix, ACL Alves, MRA Gomes, AS Ramos, EH Goto, DVB Cruz, KCA Sassaki, LL Quintino, LS Domingues, MGMA Dias, RV Gouvea, VC Ginani, CMV Alferi, ASS Ibanez, CMM Parrode, CM Lustosa, A Seber
Grupo de Apoio ao Adolescente e a Criança com Câncer, São Paulo, SP, Brazil
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Vol. 47. Núm S3

HEMO 2025 / III Simpósio Brasileiro de Citometria de Fluxo

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Introduction

The collection of autologous PBSC from small children may be challenging, especially to professionals proficient in adult Hematology and Hemotherapy. The reason for these autologous collections, now go beyond HSCT, also including therapy with CAR-T cells. Over 26 years of activity and over 1,000 transplants in children and adolescents, approximately 28% were performed in children weighting 25 kg or less.

Aim

The objective of this study is to report the experience of autologous HSCT in patients weighing 25 kg or less.

Material and methods

This is a review of the Laboratory forms and electronic medical records of all transplants performed between Dec,99 and July,25. The PBSC were collected by apheresis through a central venous catheter using the COBE Spectra® with ACD-A, 1:15 ratio, processing around 6 blood volumes. The procedures were repeated until 5 × 106 CD34+ cells/kg were collected. As of 2012, the target dose was tripled for patients undergoing tandem HSCT. The priming used irradiated and leukocyte poor red blood cells, filtered and resuspended in Normal Saline. During the apheresis, the patients received IV Na, K, Ca, Mg. As of 2016, the PBSC were collected by Spectra Optia®, ACD-A 1:12-1:15 depending on the duration of the procedure, platelet count, and outlet flow. The number of blood volumes was calculated based on the targeted CD34+ and the number on the peripheral blood on the day of the collection. The cells were cryopreserved with a final solution HAES 6%, albumin 4%, and DMSO 5%, and stored in an ultrafreezer. On the day of the infusion, a water bath 37°C was used for thawing the cells in the laboratory, where the quality control samples were drawn. DMSO was initially removed in children < 25 kg, with renal or heart failure, and infusions with > 1g/DMSO/kg using Rubinstein&apos;s protocol with a 1:1 dilution in a dextran-albumin solution 5% at 4ºC. Quality control samples were obtained and it was centrifuged at 400 g, 4°C for 20 min. The buffy coat was resuspended in the same solution and sent to the floor for infusion. In 2018, patient had DMSO removed if < 15 kg and as of October 2021 weight was no longer considered a criterion, only the presence of comorbidities.

Results

A total of 171 transplants were performed in 129 patients weighting < 25 kg: simple thawing in 65 transplants and 106 with DMSO removal. The conditioning regimens were used according to the underlying diseases: 24 Bu-Mel, 21 Carbo-Thiotepa (TT), 7 Carbo-VP-TT, 12 CEM, 62 CEM-TT, 2 CTX-Mel, 1 Temodal-TT-Carbo. No patient had graft failure and 72% are alive.

Discussion and conclusion

Leukoaphereses in our service were performed safely, even large volume procedures. The protocol we propose for children < 25 kg include priming with packed red blood cells, infusion of electrolytes during the procedure and continuous monitoring of the patients. Autologous transplantation is safe and feasible in these children.

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Hematology, Transfusion and Cell Therapy
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