Hematopoietic stem-cell transplantation (HSCT) refers to infusion of hematopoietic stem cells to restore bone marrow after bone-marrow–toxic doses of cytotoxic drugs and can use autologous, allogeneic, syngeneic, or umbilical cord blood sources harvested from marrow, peripheral blood, or cord blood.
For brain tumors, autologous HSCT is used to permit escalation of chemotherapy doses above marrow tolerance (rescue transplant) and has been tried in patients with high-risk brain tumors to eradicate residual disease and improve cure rates; tandem autologous HSCT is a preplanned sequence of transplants and may be used for high-risk embryonal tumors. Allogeneic HSCT is uncommonly used for solid tumors; its theoretical rationale is a graft-versus-tumor effect and it may be considered only if an autologous graft cannot be cleared of tumor or cannot be harvested.
CNS embryonal tumors are a heterogeneous group (including medulloblastoma and related entities such as ETMR, AT/RT, pineoblastoma, and others) that tend to disseminate via CSF pathways and are increasingly subclassified by molecular genetics for risk stratification and treatment planning. Medulloblastoma treatment centers on maximal surgical resection followed by craniospinal radiotherapy and risk-adapted chemotherapy; average-risk and high-risk groups have distinct prognoses and treatment regimens, and in children under three years alternative strategies (including high-dose chemotherapy with autologous HSCT) have been explored to delay or avoid radiotherapy.
Recurrent CNS embryonal tumors may be treated with high-dose chemotherapy and autologous HSCT as salvage therapy; objective response rates of 50%–75% have been reported but long-term disease control is seen in fewer than 30% of patients, primarily those in first relapse with localized disease.
Ependymoma arises from ependymal cells, is usually managed initially with maximal surgical resection followed by radiotherapy, and generally shows poor response to conventional-dose chemotherapy. Because relapse is common and further surgery or radiation may not be feasible, high-dose chemotherapy with autologous HSCT has been investigated as a possible salvage option, but HSCT for ependymoma is specifically addressed in coverage exclusions.