13.1 The Abstracting Process: Workflow, Source Documents, Timeliness & Text Documentation

Key Takeaways

  • Abstracting follows a predictable order: confirm reportability, check the patient index for prior tumors, apply the multiple primary rules, gather source documents, code the items, write supporting text, then run edits.

  • Priority lists for conflicting documentation come from the standard setters: the Solid Tumor Rules for histology, the Grade Manual for grade, STORE for lymph node counts, and AJCC for staging time frames.

  • CoC's 2020 standards make abstracting timeliness part of each program's Standard 6.1 quality control plan, and STORE's Date Case Completed–CoC [2092] records when required items pass the "Hosp: CoC Required - All" edit set.

  • NAACCR text fields (for example Text--DX Proc--PE [2520], Text--DX Proc--Path [2570], Text--Staging [2600] and RX Text--Surgery [2610]) are required by NPCR and SEER; STORE notes that text is sent to state registries but not to the NCDB.

  • NAACCR says text must be entered manually from the medical record and must not be generated from coded values, because generated text cannot be used to check the codes.

Last updated: September 2026

The abstracting workflow

  1. Case identification. Casefinding (Chapter 9) flags a possible case. Confirm that the tumor is reportable under STORE, SEER or NPCR, and state rules, and that it was diagnosed on or after the reference date.
  2. Check the patient index. Search the registry for the patient. If the patient already has an accession number, this tumor gets the same accession number and the next sequence number (Section 11.1).
  3. Decide the number of primaries. Apply the Solid Tumor Rules or the Hematopoietic and Lymphoid Neoplasm Coding Manual before coding anything else. A new primary gets a new abstract, and a recurrence is recorded in the follow-up items.
  4. Assign Class of Case (Chapter 11). This controls which items CoC requires.
  5. Gather source documents from every relevant setting: history and physical, imaging, endoscopy, laboratory, operative and pathology reports, consultations, treatment summaries, and outside records.
  6. Code the items. These include demographics, diagnosis (site, histology, behavior, grade, laterality, Diagnostic Confirmation), staging (AJCC, Summary Stage 2018, SSDIs), first-course treatment, and follow-up.
  7. Write the text. Document the evidence for each coded item in the NAACCR text fields.
  8. Run edits. Correct the errors, apply override flags only when the unusual combination is verified, and let the software set the completion date.

Source documents and what they answer

SourceBest for
History and physical; consultation notesPresenting symptoms, history, family and tobacco history, physical exam findings (for example, palpable nodes), treatment plan and intent
Imaging reportsClinical tumor size and extension, lymph nodes and metastases before treatment
Endoscopy reportsLocation (for example, distance from the anal verge), appearance and biopsy
Operative reportsGross extension, what was removed, residual disease, surgical approach
Pathology and cytology reportsHistology and behavior, grade, size and extension, margins, lymph nodes, LVI, biomarkers
Laboratory reportsTumor markers and other values for SSDIs (PSA, CEA, LDH, AFP)
Radiation and systemic therapy recordsModality, dose, fractions, agents, dates
Discharge summaryA useful index to the stay; confirm details in the original reports

Official priority lists

When documents disagree, do not rely on a general "most authoritative document" idea. Use the priority list the standard setter publishes for the specific item:

  • Histology: each Solid Tumor Rules module gives a priority order for documentation. Tissue from the primary site comes first, and histology is coded from the diagnosis before neoadjuvant therapy. Code the more specific histology when the final diagnosis and the synoptic report differ.
  • Grade: the Grade Manual's priority is the synoptic report (CAP protocol), then the final diagnosis, then a physician statement.
  • Lymph node counts: STORE's priority is final diagnosis, then synoptic report, then microscopic description, then gross description.
  • Primary site: follow ICD-O-3 and the Solid Tumor Rules site instructions. Consult the physician advisor when the record does not identify a site.
  • Staging: AJCC rules define which information belongs to the clinical and the pathological time frames. For example, operative findings can support pathological T when the surgeon's resection meets AJCC criteria, and the pathology report does not automatically override every clinical fact.

Timeliness

  • CoC Standard 6.1 requires each program's quality control plan to evaluate abstracting timeliness every year, together with casefinding and the percentage of unknown values. The 2020 standards leave the specific timeliness target to the program's plan.
  • Date Case Completed–CoC [2092] is set automatically by the registry software once the items required for the case's Class of Case are abstracted and pass the "Hosp: CoC Required - All" edit set. It was created to measure abstracting timeliness and "may also be used as part of CoC Standard 6.1" timeliness monitoring. Follow-up information, delayed treatment and corrections may be added afterward.
  • RCRS (Standard 6.4) expects monthly submission of cases to the NCDB, so the registry must keep abstracting current throughout the year.
  • State central registries set their own reporting deadlines in law or rule. Many require facilities to report within about six months of diagnosis or first contact; check your state's rule.

Items required by Date Case Completed–CoC

Class of CaseItems that must be complete
00–22Identification, demographic and diagnostic items
10–22Staging and hospital-specific treatment
10, 12, 14, 20, 22Summary treatment (treatment at any facility)
00NPI of the facility or physician the patient was referred to
20–22NPI of the referring facility or physician who diagnosed or treated the patient

NAACCR text fields

ItemText fieldContents
2520Text--DX Proc--PEHistory and physical findings about this tumor
2530Text--DX Proc--X-ray/ScanImaging results
2540Text--DX Proc--ScopesEndoscopic findings
2550Text--DX Proc--Lab TestsLab and tumor marker results
2560Text--DX Proc--OpOperative findings
2570Text--DX Proc--PathCytology and histopathology findings
2580 / 2590Text--Primary Site Title / Text--Histology TitleWritten description of site and histology
2600Text--StagingStaging information not entered elsewhere
2610–2670RX Text--Surgery, Radiation (Beam), Radiation Other, Chemo, Hormone, BRM, OtherFirst-course treatment details
2680Text--RemarksOverflow and supplemental information
2690Text--Place of DiagnosisFacility, physician office, city or state where the diagnosis was made

Rules for good text

  • Manual entry: NAACCR's rationale says text "must contain a description that has been entered by the reporter independently from the code(s)." Text that software generates from codes cannot be used to check those codes.
  • Justify the codes: each text item lists the coded items it should support. For example, RX Text--Surgery supports the surgery, lymph node surgery, margins and sequence items.
  • Include dates and sources: for example, "04/02/26 CT C/A/P: 3.1 cm R lower lobe mass, no adenopathy, no mets."
  • Use NAACCR-approved abbreviations, and do not repeat the same information in several fields.
  • Who uses it: NPCR and SEER list the text fields as required. Central registries use text to consolidate reports from several facilities and for quality control and special studies. STORE notes that text is not transmitted to the NCDB.

Worked example

A right hemicolectomy pathology report shows "adenocarcinoma, 5.2 cm, invades through the muscularis propria into pericolic fat, 0/18 nodes." The operative note mentions "dense adhesions to the retroperitoneum" but no invasion.

  • Text--DX Proc--Path: "03/14/26 R hemicolectomy: adenoca, mod diff, 5.2 cm, invades thru MP into pericolic fat; margins neg; LVI absent; 0/18 LN."
  • Text--DX Proc--Op: "03/14/26 open R hemicolectomy; dense adhesions to retroperitoneum, taken en bloc; no residual gross disease."
  • Coding: because adhesions are not tumor invasion, the pathological T comes from the pathology finding, pT3. That gives Regional Nodes Examined 18 and Positive 00.
Loading diagram...
Abstracting workflow
Test Your Knowledge

A registry's software offers to fill Text--DX Proc--Path automatically with "8500/3, grade 2, C50.4." What does NAACCR guidance say about this?

A

It is acceptable because the text matches the codes exactly.

B

It is required for CoC-accredited programs.

C

It is not acceptable; text must be entered manually from the medical record, because text generated from codes cannot be used to verify those codes.

D

It is acceptable only for pathology-only (Class 43) cases.

Test Your Knowledge

According to STORE, how is Date Case Completed–CoC [2092] assigned?

A

The registrar enters the date the abstract was started.

B

It is the date the case was submitted to the state registry.

C

It is always six months after the Date of First Contact.

D

The registry software records it when the items required for the case's Class of Case have been abstracted and the case passes the "Hosp: CoC Required - All" edit set.

Test Your Knowledge

The final diagnosis and the CAP synoptic report on a colon resection give different histologies: "adenocarcinoma" versus "mucinous adenocarcinoma." Which source rule applies?

A

Follow the Solid Tumor Rules instruction to code the more specific histology when the final diagnosis and the synoptic report differ.

B

Always use the final diagnosis, because it is the pathologist's conclusion.

C

Use the operative report, because it describes the whole tumor.

D

Code adenocarcinoma NOS, because the documents conflict.

Sections you finish are checked off in the contents.