* indicates required field
Length: 1
Source of Standard: NAACCR
Section Name: Stage/Prognostic Factors
Year Implemented: 2021
Version Implemented: 21
Record Types: A, M, C, I
XML NAACCR ID: alkRearrangement
Parent XML Element: Tumor
Required Status:
NPCR Collect: . - No recommendations
CoC Collect: RS - Required, site specific
SEER Collect: R - Required
CCCR Collect: . - No recommendations
Description:
Testing for ALK rearrangement is performed for patients with advanced non-small cell lung cancer (NSCLC) to identify tumors which are sensitive to small-molecule ALK kinase inhibitors.
Rationale:
ALK rearrangement is recommended by treatment guidelines for patients with advanced lung cancer as a prognostic marker and factor in determining appropriate therapy. It is a new data item for cases diagnosed 01/01/2021+.
Item Data Type:
text
Allowable Values
0-2, 4, 7-9, Blank
Codes:
0 |
Normal |
---|---|
1 |
Abnormal Rearrangement identified/detected: EML4-ALK, KIF5B-ALK, TFG-ALK, and/or KLC1-ALK |
2 |
Rearrangement identified/detected: Other ALK Rearrangement not listed in code 1 |
4 |
Rearrangement, NOS |
7 |
Test ordered, results not in chart |
8 |
Not applicable: Information not collected for this case |
9 |
Not documented in medical record |
Blank |
Diagnosis year is prior to 2021 |
Code Notes:
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.