Questions 1 – 2: Specify the indication for CIBMTR data reporting

Indicate whether the individual will be receiving an Infusion (e.g., hematopoietic cellular transplant (HCT), gene therapy, cellular therapy), Marrow toxic injury, or Non-cellular therapy (e.g., study enrollment, chemotherapy, immunotherapy, etc.).

For more information on infusion types, review Appendix D.

Marrow toxic injury should only be reported by Radiation Injury Treatment Network (RITN) centers in the event of mass casualty incident resulting in marrow toxic injury. Do not report marrow toxic injury for individuals receiving pre-infusion radiation therapy or for accidental, isolated exposures to radiation. If the indication is Marrow toxic injury, specify the date of the marrow toxic injury (i.e., radiation event).

If completing this form for a patient at a RITN center and it is uncertain if the patient’s data should be reported using the marrow toxic injury indication, contact CIBMTR Center Support or email RITN@nmdp.org.

Non-cellular therapy may include vaccine or immunomodulatory trials; report non-cellular therapy when the patient is enrolled on a trial or protocol requiring data submission to CIBMTR.

Section Updates:

Question Number Date of Change Add/Remove/Modify Description Reasoning (If applicable)
1 1/28/2025 Modify Added new floating text to the non-cellular therapy option: Indicate whether the individual will be receiving an Infusion (e.g., hematopoietic cellular transplant (HCT), gene therapy, cellular therapy), Marrow toxic injury, or Non-cellular therapy (e.g., study enrollment, chemotherapy, immunotherapy, etc.). Floating text was updated in January 2025 release
1 1/28/2025 Remove Removed the red warning box: Non-cellular Therapy: There are currently no active studies for this option. If this seems to be incorrect, submit a CIBMTR Center Support ticket Validation was updated in January 2025 release
1 1/28/2025 Add New blue note box added: CMS Innovation Center’s Cell and Gene Therapy (CGT) Access Model for Sickle Cell Disease (SCD)
Select “non-cellular therapy” when completing this form for the first time for a CRID to be enrolled in the CMS Innovation Center’s Cell and Gene Therapy (CGT) Access Model for Sickle Cell Disease (SCD). Contact CIBMTR Center Support with any questions.
Validation was updated in January 2025 release
Last modified: Jan 28, 2025

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