TABLE 2.
FIGO (Designate primary: Tov, Tft, Tp, or Tx) | UICC | ||
---|---|---|---|
T | N | M | |
Stage | |||
IA | T1a | N0 | M0 |
IB | T1b | N0 | M0 |
IC | T1c | N0 | M0 |
IIA | T2a | N0 | M0 |
IIB | T2b | N0 | M0 |
IIIA | T3a | N0 | M0 |
T3a | N1 | M0 | |
IIIB | T3b | N0 | M0 |
T3b | N1 | M0 | |
IIIC | T3c | N0−1 | M0 |
T3c | N1 | M0 | |
IV | Any T | Any N | M1 |
Regional nodes (N) | |||
Nx | Regional lymph nodes cannot be assessed | ||
N0 | No regional lymph node metastasis | ||
N1 | Regional lymph node metastasis | ||
Distant metastasis (M) | |||
Mx | Distant metastasis cannot be assessed | ||
M0 | No distant metastasis | ||
M1 | Distant metastasis (excluding peritoneal metastasis) |
1. The primary site—that is, ovary, fallopian tube, or peritoneum—should be designated where possible. In some cases, it may not be possible to clearly delineate the primary site, and these should be listed as “undesignated”.
2. The histologic type should be recorded.
3. The staging includes a revision of the Stage III patients and allotment to Stage IIIA1 is based on spread to the retroperitoneal lymph nodes without intraperitoneal dissemination, because an analysis of these patients indicates that their survival is significantly better than those who have intraperitoneal dissemination.
4. Involvement of retroperitoneal lymph nodes must be proven cytologically or histologically.
5. Extension of tumor from omentum to spleen or liver (Stage IIIC) should be differentiated from isolated parenchymal splenic or liver metastases (Stage IVB).
Source: Prat J. 17