The Plasma Cell Disorder Post-HCT Data Form is one of the Comprehensive Report Forms. This form captures plasma cell disorder (PCD) post-HCT data such as: disease assessment at the time of best response, hematologic and organ parameters at the time of best response, post-HCT therapy, disease status at the time of evaluation for this reporting period, and current status of amyloidosis for this reporting period.

This form must be completed for all recipients whose primary disease reported on the Pre-TED Disease Classification Form (Form 2402) is “Multiple myeloma/plasma cell disorder (PCD).” The Post-HCT Plasma Cell Disorder form must be completed in conjunction with each Post-HCT follow-up form (Form 2100). This form is designed to capture specific data occurring within the timeframe of each reporting period (i.e., between day 0 and day 100; between day 100 and the six-month date of contact for six-month follow-up; and between the date of contact for the six-month follow-up and the date of contact for the one-year follow-up, etc.).

Links to Sections of the Form
Q1 – 2: Disease Specificity
Q3 – 53: Disease Assessment at the Time of Best Response to HCT or Cellular Therapy
Q54 – 109: Organ Parameters of Amyloidosis at the Time of Best Response
Q110 – 141: POEMS Syndrome Assessment at the Time of Best Response
Q142 – 210: Post-Infusion Therapy
Q211 – 252: Disease Status at the Time of Evaluation for this Reporting Period
Q253 – 311: Current Status of Amyloidosis for this Reporting Period
Q312 – 343: Current Status of POEMS Syndrome for this Reporting Period

Manual Updates:
Sections of the Forms Instruction Manual are frequently updated. The most recent updates to the manual can be found below. For additional information, select the manual section and review the updated text.

If you need to reference the historical Manual Change History for this form, please click here or reference the retired manual section on the Retired Forms Manuals webpage.

Date Manual Section Add/Remove/Modify Description
5/20/2022 2116: PCD Post-Infusion Add Clarification added that Q160 will not come due when NA is reported: Indicate if the date the radiation therapy stopped is Known, Unknown, or Not applicable. If Known, enter the date the line of radiation therapy ended. Report Not applicable if the recipient is still receiving therapy. When Not applicable is selected, the radiation dose will not be reported in the next question. However, once radiation stops (i.e., the radiation stop date is Known), the dose will be reported.
5/20/2022 2116: PCD Post-Infusion Add Instructions added on how to report the total dose when radiation continued from the prior reporting period: If radiation started in a previous reporting period (i.e., Not applicable was reported as the therapy end date for the prior reporting period) and continued into the current reporting period, report the total dose administered since radiation started (including the doses given in the previous reporting period).
Example B: A recipient started radiation at end of the Day 100 reporting period. 200 cGy for 3 doses were given (total dose in the Day 100 reporting period is 600 cGy). Radiation continued into the 6-month reporting period and an additional 200 cGy for 4 doses were given (total dose given in the 6-month reporting period is 800 cGy). The total dose of radiation should be reported as 1400 cGy (600 cGy + 800 cGy).
4/30/2021 2116: PCD Post-Infusion Modify Version 4 of the 2116: Plasma Cell Disorders (PCD) Post-Infusion Data section of the Forms Instruction Manual released. Version 4 corresponds to revision 5 of the Form 2116.
Last modified: May 20, 2022

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