2.
Include the information specified in subsection (A) and the following
information in the case report:
a. The
patient's unique accession number, separate from a medical record number, that
was assigned by the hospital's cancer registry to the patient for
identification purposes;
b. The
unique sequence number assigned by the cancer registry to the specific cancer
within the body of the patient being reported;
c. The date the patient was admitted to the
hospital for diagnostic evaluation, cancer-directed treatment, or evidence of
cancer, carcinoma in situ, or a benign tumor of the central nervous system, if
applicable;
d. The date the patient
was discharged from the hospital after the patient received diagnostic
evaluation or treatment at the hospital, if applicable;
e. The source of payment for diagnosis or
treatment of cancer, or both;
f.
The level of the facility's involvement in the diagnosis or treatment, or both,
of the patient for cancer, including the code that represents the earliest
source that identified the cancer;
g. The year in which the hospital first
provided diagnosis or treatment to the patient for the cancer being
reported;
h. The patient's county
of residence at diagnosis of cancer;
i. The patient's marital status and age at
diagnosis of cancer, place of birth, and, if applicable, name of the patient's
spouse;
j. If the patient is under
18 years of age and unmarried, the name of the patient's parent or legal
guardian;
k. A narrative
description of how the cancer was diagnosed, including a description of the
primary site and the microscopic structure of the tumor cells and surrounding
tissues;
l. The number of regional
lymph nodes examined and the number in which evidence of cancer was
detected;
m. The clinical,
pathological, or other staging classification, based on the analysis of tumor,
lymph node, and metastasis;
n. The
patient's clinical, pathological, or other stage group;
o. If the cancer was diagnosed before 2018,
the code for the person who determined the stage group of the
patient;
p. A narrative description
of the clinical evaluation of x-ray diagnostic films and scans of the patient,
and the dates of the films or scans;
q. A narrative description of laboratory
tests performed for the patient, including the date, type, and results of and
code related to any of the patient's laboratory tests;
r. A narrative description of the results of
the patient's clinical evaluation;
s. The procedures used by the reporting
facility to obtain a diagnosis and staging classification, including:
i. The dates on which the procedures were
performed; and
ii. The name of the
facilities where the procedures were performed, if different from the reporting
facility;
t. A narrative
description of any cancer-related surgery on the patient, including the:
i. Date of surgery;
ii. Name of the facility where the surgery
was performed, if different from the reporting facility; and
iii. Type of surgery;
u. The code associated with the type of
surgery performed on the patient and the date of surgery;
v. The codes associated with the:
i. Extent of lymph node surgery;
ii. Number of lymph nodes removed;
iii. Surgery of regional sites, distant
sites, or distant lymph nodes; and
iv. Reason for no surgery or that surgery was
performed;
w. Whether
reconstructive surgery on the patient was performed as a first course of
treatment, delayed, or not performed;
x. A narrative description of cancer-related
radiation treatment administered to the patient, including the:
i. Date of radiation treatment;
ii. Name of the facility where the radiation
treatment was performed, if different from the reporting facility;
and
iii. Type of
radiation;
y. As
applicable, the code specifying that radiation treatment was administered or
associated with the reason for no radiation treatment;
z. The code associated with the type of
radiation treatment administered to the patient and the date of radiation
treatment;
aa. A narrative
description of cancer-related chemotherapy administered to the patient,
including the:
i. Date of cancer-related
chemotherapy;
ii. Name of the
facility that administered the chemotherapy, if different from the reporting
facility; and
iii. Type of
chemotherapy;
bb. The
code associated with the type of chemotherapy administered to the patient and
the date of chemotherapy;
cc. The
code associated with any other types of cancer- or non-cancer-directed first
course of treatment, not otherwise coded on the case report for the patient,
including:
i. Hormone therapy, immunotherapy,
hematologic transplant, or endocrine procedures administered to the
patient;
ii. Additional surgery,
radiation, or chemotherapy administered to the patient; or
iii. Other treatment administered to the
patient;
dd. If
applicable, a narrative description of any other types of cancer or
non-cancer-directed first course of treatment, including:
i. The dates of the treatment;
ii. The names of the facilities where the
treatment was performed, if different from the reporting facility;
and
iii. The type of
treatment;
ee. If the
patient's treatment included both surgery and another type of treatment, the
sequence of the two treatments;
ff.
The code for the status of the patient's treatment, including whether the
patient received any treatment or the tumor was being actively observed and
monitored;
gg. The code for whether
the patient has had a reappearance of a cancer, carcinoma in situ, or benign
tumor of the central nervous system, and, if additional cancer of the type
diagnosed at the primary site is found after cancer-directed treatment:
i. The date of the reappearance;
and
ii. A narrative description of
the nature of the reappearance, including whether the additional cancer was
found at the primary site, a regional site, or a distant
site;
hh. If the patient
has died, the place and cause of death and whether an autopsy was
performed;
ii. The name of the
individual or the code that identifies the individual completing the case
report;
jj. The type of records
used by the reporting facility to complete the case report;
kk. If applicable, a code that indicates the
reason for a required date not to be included in the case report required in
subsection (B)(1); and
ll. If
applicable, a code that indicates that an apparently inconsistent code has been
reviewed and is correct; and