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NAACCR Data Dictionary
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Version 25
Data Item #3914: Progesterone Receptor Percent Positive or Range

* indicates required field

Length: 3
Source of Standard: NAACCR
Section Name: Stage/Prognostic Factors
Year Implemented: 2018
Version Implemented: 18
Record Types: A, M, C, I

XML NAACCR ID: progesteroneRecepPrcntPosOrRange

Parent XML Element: Tumor

Required Status:

NPCR Collect: . - No recommendations
CoC Collect: RS - Required, site specific
SEER Collect: RC - Collected by SEER from CoC-accredited hospitals
CCCR Collect: . - No recommendations

Description:

Progesterone Receptor, Percent Positive or Range is the percent of cells staining progesterone receptor positive measured by IHC.

Rationale:

Progesterone Receptor, Percent Positive or Range is a Registry Data Collection Variable in AJCC. It is a new data item for cases diagnosed 1/1/2018+.

Item Data Type:

text

Allowable Values

000, 001-100, R10, R20, R30, R40, R50, R60, R70, R80, R90, R99, XX7, XX8, XX9

Codes:

000

PR negative, or stated as less than 1%

001-100

1-100 percent

R10

Stated as 1-10%

R20

Stated as 11-20%

R30

Stated as 21-30%

R40

Stated as 31-40%

R50

Stated as 41-50%

R60

Stated as 51-60%

R70

Stated as 61-70%

R80

Stated as 71-80%

R90

Stated as 81-90%

R99

Stated as 91-100%

XX7

Test done, results not in chart

XX8

Not applicable: Information not collected for this case
(If this item is required by your standard setter, use of code XX8 will result in an edit error.)

XX9

Not documented in medical record
PR (Progesterone Receptor) Percent Positive or Range not assessed or unknown if assessed

Code Notes:

Note:

  • Physician statement of PR (Progesterone Receptor) Percent Positive or Range can be used to code this data item.
  • Code this data item using the same report used to record PR Summary.
  • If PR negative, or percentage less than 1%, code 000.
  • The actual PR (1-100%) percent takes priority over the range codes.
  • If PR positive but percentage unknown, code XX9.

Each Site-Specific Data Item (SSDI) applies only to selected primary sites, histologies, and years of diagnosis. Depending on applicability and standard-setter requirements, SSDIs may be left blank.