Tipifarnib for the Treatment of Advanced Solid Tumors, Lymphoma, or Histiocytic Disorders With HRAS Gene Alterations, a Pediatric MATCH Treatment Trial

Complete Title: APEC1621M: NCI-COG PEDIATRIC MATCH (MOLECULAR ANALYSIS FOR THERAPY CHOICE) - PHASE 2 SUBPROTOCOL OF TIPIFARNIB IN PATIENTS WITH TUMORS HARBORING HRAS GENOMIC ALTERATIONS
Trial Phase: II
Investigator: Katherine Tarlock

This phase II pediatric MATCH trial studies how well tipifarnib works in treating patients with solid tumors that have recurred or spread to other places in the body (advanced), lymphoma, or histiocytic disorders, that have a genetic alteration in the gene HRAS. Tipifarnib may block the growth of cancer cells that have specific genetic changes in a gene called HRAS and may reduce tumor size.

Keywords:
  • Glioma
  • Kidney Cancer
  • Medulloblastoma
  • Melanoma
  • Neuroblastoma
  • Lymphoma, Non-Hodgkin (NHL)
  • Sarcoma
  • Solid Tumors
  • Thyroid Cancer
  • Neoplasms, Germ Cell and Embryonal
  • Ependymoma
  • Rhabdomyosarcoma
  • Sarcoma, Ewing
  • Pheochromocytoma
  • Osteosarcoma
  • Sarcoma, Soft Tissue
  • Rhabdoid Tumor
  • Histiocytosis, Langerhans-Cell
  • Hepatoblastoma
  • Neuroectodermal Tumors, Primitive, Peripheral
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Adult
Pediatric
II
Katherine Tarlock
RG1123186
NCT04284774
APEC1621M: NCI-COG PEDIATRIC MATCH (MOLECULAR ANALYSIS FOR THERAPY CHOICE) - PHASE 2 SUBPROTOCOL OF TIPIFARNIB IN PATIENTS WITH TUMORS HARBORING HRAS GENOMIC ALTERATIONS
Glioma
Kidney Cancer
Medulloblastoma
Melanoma
Neuroblastoma
Lymphoma, Non-Hodgkin (NHL)
Sarcoma
Solid Tumors
Thyroid Cancer
Neoplasms, Germ Cell and Embryonal
Ependymoma
Rhabdomyosarcoma
Sarcoma, Ewing
Pheochromocytoma
Osteosarcoma
Sarcoma, Soft Tissue
Rhabdoid Tumor
Histiocytosis, Langerhans-Cell
Hepatoblastoma
Neuroectodermal Tumors, Primitive, Peripheral