TBI Using IMRT and Cyclophosphamide Prior to Stem Cell Transplant for the Treatment of Severe Systemic Sclerosis

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-65
SponsorCity of Hope Medical Center

About this trial

This early phase I trial studies the side effects and feasibility of total body irradiation using intensity modulation radiation therapy (IMRT) when given in combination with cyclophosphamide prior to stem cell transplant to treat severe systemic sclerosis. IMRT delivers total body radiation therapy more precisely and may reduce radiation exposure to sensitive normal organs. Giving chemotherapy, such as cyclophosphamide, and total body irradiation before a donor stem cell transplant helps kill cancer cells in the body and helps make room in the bone marrow for new blood-forming cells (stem cells) to grow. Giving IMRT and cyclophosphamide prior to stem cell transplant may work better in treating severe systemic sclerosis and reduce radiation doses to lung and kidneys compared to cyclophosphamide alone.

Eligibility criteria

Qualifiers

Karnofsky performance status (KPS) >= 70

Systemic sclerosis patients evaluated within 30 days of start of conditioning regimen who would be candidates for TBI-cyclophosphamide (Cy) per City of Hope (COH) guidelines and standard operating procedures (SOP) for autologous hematopoietic cell transplant

Patients must be suitable for TBI conditioning regimens as part of transplant per radiation the referring hematologist

Patients must have adequate organ function for HCT as determined by the hematologist

Disqualifiers

Patients should not have any uncontrolled illness including ongoing or active infection

Prior history of radiation therapy must be presented to study principal investigator (PI) for eligibility determination

Pregnant women are excluded from this study because total body irradiation is an agent with the potential for teratogenic or abortifacient effects

Subjects, who in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study

Trial design

Treatments tested in this trial

  • Allogeneic Hematopoietic Stem Cell Transplantation
  • Cyclophosphamide
  • Intensity-Modulated Radiation Therapy
  • Total-Body Irradiation

Treatment groups

15 Participants
are divided into 1 treatment group

Sponsors and collaborators

City of Hope Medical Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator