18 staging systems and 8 prognostic scores across 31 cancers: the groupings quoted at every tumour board, each with its source and a link to the matching standard of care. Scores are interactive: tick the factors and read the published outcome for the group. Nothing you enter leaves the page.
UK reports stage against the UICC 8th edition, whose anatomic groups these are; the Royal College of Pathologists dataset in force (G148 version 3, November 2024) reprints it and advises against substituting AJCC TNM 8, because the AJCC edition also defines prognostic stage groups that move tumours up or down by grade, ER, PR and HER2 status and, for T1-2 N0 HR-positive HER2-negative disease, a low-risk genomic assay result. The UICC 9th edition, recommended from 1 January 2026, leaves the breast classification unchanged and clarifies only the post-treatment yp classification, basing ypT on the largest continuous focus of residual invasive cancer and recommending that residual cancer burden be reported beside it.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| 0 | Tis (DCIS). | Ductal carcinoma in situ |
| IA / IB | T1 (2 cm or smaller) N0 / T0-1 N1mi (micrometastases 0.2-2 mm). | Early disease, all types, Fertility and early menopause, decided before treatment starts |
| IIA / IIB | T0-1 N1 or T2 (2-5 cm) N0 / T2 N1 or T3 (over 5 cm) N0. | Early disease, all types, Fertility and early menopause, decided before treatment starts |
| IIIA / IIIB / IIIC | T0-2 N2 or T3 N1-2 / T4 (chest wall, skin, inflammatory) N0-2 / any T N3 (10 or more axillary nodes, infraclavicular, internal mammary plus axillary, supraclavicular). | - |
| IV | M1: distant metastases. | - |
UK reports stage against the UICC 8th edition, whose anatomic groups these are; the Royal College of Pathologists dataset in force (G148 version 3, November 2024) reprints it and advises against substituting AJCC TNM 8, because the AJCC edition also defines prognostic stage groups that move tumours up or down by grade, ER, PR and HER2 status and, for T1-2 N0 HR-positive HER2-negative disease, a low-risk genomic assay result. The UICC 9th edition, recommended from 1 January 2026, leaves the breast classification unchanged and clarifies only the post-treatment yp classification, basing ypT on the largest continuous focus of residual invasive cancer and recommending that residual cancer burden be reported beside it.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| 0 | Tis (DCIS). | - |
| IA / IB | T1 (2 cm or smaller) N0 / T0-1 N1mi (micrometastases 0.2-2 mm). | Stage I (≤2-3 cm, node-negative), Stage II-III, neoadjuvant |
| IIA / IIB | T0-1 N1 or T2 (2-5 cm) N0 / T2 N1 or T3 (over 5 cm) N0. | Stage II-III, neoadjuvant, Post-neoadjuvant, pathologic complete response, Post-neoadjuvant, residual invasive disease |
| IIIA / IIIB / IIIC | T0-2 N2 or T3 N1-2 / T4 (chest wall, skin, inflammatory) N0-2 / any T N3 (10 or more axillary nodes, infraclavicular, internal mammary plus axillary, supraclavicular). | Stage II-III, neoadjuvant, Post-neoadjuvant, pathologic complete response, Post-neoadjuvant, residual invasive disease |
| IV | M1: distant metastases. | Metastatic, first line, Metastatic, second line, Metastatic, later lines |
UK reports stage against the UICC 8th edition, whose anatomic groups these are; the Royal College of Pathologists dataset in force (G148 version 3, November 2024) reprints it and advises against substituting AJCC TNM 8, because the AJCC edition also defines prognostic stage groups that move tumours up or down by grade, ER, PR and HER2 status and, for T1-2 N0 HR-positive HER2-negative disease, a low-risk genomic assay result. The UICC 9th edition, recommended from 1 January 2026, leaves the breast classification unchanged and clarifies only the post-treatment yp classification, basing ypT on the largest continuous focus of residual invasive cancer and recommending that residual cancer burden be reported beside it.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| 0 | Tis (DCIS). | - |
| IA / IB | T1 (2 cm or smaller) N0 / T0-1 N1mi (micrometastases 0.2-2 mm). | Early stage, deciding on chemotherapy, Early stage, adjuvant endocrine therapy, Early stage, high risk: adjuvant CDK4/6 |
| IIA / IIB | T0-1 N1 or T2 (2-5 cm) N0 / T2 N1 or T3 (over 5 cm) N0. | Early stage, deciding on chemotherapy, Early stage, adjuvant endocrine therapy, Early stage, high risk: adjuvant CDK4/6 |
| IIIA / IIIB / IIIC | T0-2 N2 or T3 N1-2 / T4 (chest wall, skin, inflammatory) N0-2 / any T N3 (10 or more axillary nodes, infraclavicular, internal mammary plus axillary, supraclavicular). | - |
| IV | M1: distant metastases. | Metastatic, first line, Metastatic, molecular progression on first line, Metastatic, second line by genotype |
UK reports stage against the UICC 8th edition, whose anatomic groups these are; the Royal College of Pathologists dataset in force (G148 version 3, November 2024) reprints it and advises against substituting AJCC TNM 8, because the AJCC edition also defines prognostic stage groups that move tumours up or down by grade, ER, PR and HER2 status and, for T1-2 N0 HR-positive HER2-negative disease, a low-risk genomic assay result. The UICC 9th edition, recommended from 1 January 2026, leaves the breast classification unchanged and clarifies only the post-treatment yp classification, basing ypT on the largest continuous focus of residual invasive cancer and recommending that residual cancer burden be reported beside it.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| 0 | Tis (DCIS). | - |
| IA / IB | T1 (2 cm or smaller) N0 / T0-1 N1mi (micrometastases 0.2-2 mm). | Stage I (T1a-b N0), Stage II-III, Germline BRCA1 or BRCA2 carriers: early-stage choices |
| IIA / IIB | T0-1 N1 or T2 (2-5 cm) N0 / T2 N1 or T3 (over 5 cm) N0. | Stage II-III, Choice of neoadjuvant backbone: the platinum debate, Germline BRCA1 or BRCA2 carriers: early-stage choices |
| IIIA / IIIB / IIIC | T0-2 N2 or T3 N1-2 / T4 (chest wall, skin, inflammatory) N0-2 / any T N3 (10 or more axillary nodes, infraclavicular, internal mammary plus axillary, supraclavicular). | Choice of neoadjuvant backbone: the platinum debate |
| IV | M1: distant metastases. | Metastatic, first line, PD-L1 CPS ≥10, Metastatic, first line, PD-L1 negative or PD-1 ineligible, Metastatic, later lines |
Diagnosis is molecular first: IDH and 1p/19q status define the tumour type; grade is then assigned within the type. IDH-wild-type diffuse astrocytoma with TERT promoter mutation, EGFR amplification or +7/−10 is glioblastoma regardless of histology.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Astrocytoma, IDH-mutant, grade 2 | IDH1/2-mutant, 1p/19q intact, ATRX loss; low mitotic activity. | IDH-mutant grade 2, IDH-mutant grade 2 glioma, Paediatric low-grade glioma |
| Astrocytoma, IDH-mutant, grade 3 | As above with anaplasia and mitotic activity. | IDH-mutant grade 2, IDH-mutant grade 2 glioma, Oligodendroglioma grade 3 / astrocytoma grade 3 |
| Astrocytoma, IDH-mutant, grade 4 | As above with necrosis, microvascular proliferation or CDKN2A/B homozygous deletion. | IDH-mutant grade 2, IDH-mutant grade 2 glioma |
| Oligodendroglioma, IDH-mutant and 1p/19q-codeleted, grade 2-3 | Codeletion defines the type; grade 3 with anaplasia. | Oligodendroglioma grade 3 / astrocytoma grade 3, Paediatric low-grade glioma |
| Glioblastoma, IDH-wild-type, grade 4 | IDH-wild-type with necrosis or microvascular proliferation, or TERT promoter mutation, EGFR amplification or +7/−10. | Glioblastoma, Glioblastoma, newly diagnosed, Glioblastoma, recurrent |
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| 0 (very early) | Single tumour 2 cm or smaller, preserved liver function, ECOG 0. | Early, Very early / early (BCLC 0-A) |
| A (early) | Single tumour, or up to 3 nodules each 3 cm or smaller, preserved liver function, ECOG 0. | Early, Very early / early (BCLC 0-A) |
| B (intermediate) | Multinodular, preserved liver function, ECOG 0; subclassified by transplant candidacy and tumour burden. | Intermediate, Intermediate (BCLC B) |
| C (advanced) | Portal invasion or extrahepatic spread, preserved liver function, ECOG 1-2. | Advanced, Advanced (BCLC C), first line, Advanced, second line and beyond |
| D (terminal) | End-stage liver function or ECOG 3-4: best supportive care. | - |
ALBI grade (albumin and bilirubin only) is a more objective alternative used in trials.
Source: Pugh et al., Br J Surg 1973. Outcomes are those of the published cohort and do not account for treatments since.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Low risk | Primary, solitary, Ta, low grade, under 3 cm, no CIS. | NMIBC, Low / intermediate-risk NMIBC, High-risk NMIBC, BCG-naive |
| Intermediate risk | Ta low-grade tumours that are recurrent, multiple or 3 cm or larger, without high-risk features. | NMIBC, Low / intermediate-risk NMIBC, High-risk NMIBC, BCG-naive |
| High risk | T1, high grade, or CIS. | NMIBC, Low / intermediate-risk NMIBC, High-risk NMIBC, BCG-naive |
| Very high risk | Combinations such as T1 high grade with CIS, multiple large recurrent T1 high grade, variant histology or lymphovascular invasion; early cystectomy is discussed. | BCG-unresponsive NMIBC (CIS ± papillary), After cystectomy (no perioperative IO) |
The five-tier model NICE recommends for everyone with newly diagnosed localised or locally advanced prostate cancer, assigned by the urological cancer MDT. It replaced the three-tier D'Amico model in the 2021 amendment because that model could not separate Gleason 3+4 from 4+3. PSA is in micrograms per litre, which is the same number as nanograms per millilitre. NICE's treatment recommendations are written in these group numbers.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| CPG 1 | Gleason score 6 (grade group 1) and PSA under 10 and stage T1 to T2. Active surveillance is offered first (NG131 1.3.8). | - |
| CPG 2 | Gleason 3+4=7 (grade group 2) or PSA 10 to 20, with stage T1 to T2. Active surveillance, radical prostatectomy and radical radiotherapy are offered as a choice (NG131 1.3.9). | - |
| CPG 3 | Gleason 3+4=7 (grade group 2) and PSA 10 to 20 and stage T1 to T2, or Gleason 4+3=7 (grade group 3) at stage T1 to T2. Radical treatment is offered; active surveillance is considered only for people who decline it (NG131 1.3.10). | - |
| CPG 4 | Any one of: Gleason score 8 (grade group 4), PSA above 20, stage T3. Active surveillance is not offered (NG131 1.3.11). | High risk, Very high risk and node-positive |
| CPG 5 | Two or more of Gleason score 8 (grade group 4), PSA above 20 and stage T3; or Gleason 9 to 10 (grade group 5); or stage T4. | High risk, Very high risk and node-positive |
The five-tier model NICE recommends for everyone with newly diagnosed localised or locally advanced prostate cancer, assigned by the urological cancer MDT. It replaced the three-tier D'Amico model in the 2021 amendment because that model could not separate Gleason 3+4 from 4+3. PSA is in micrograms per litre, which is the same number as nanograms per millilitre. NICE's treatment recommendations are written in these group numbers.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| CPG 1 | Gleason score 6 (grade group 1) and PSA under 10 and stage T1 to T2. Active surveillance is offered first (NG131 1.3.8). | - |
| CPG 2 | Gleason 3+4=7 (grade group 2) or PSA 10 to 20, with stage T1 to T2. Active surveillance, radical prostatectomy and radical radiotherapy are offered as a choice (NG131 1.3.9). | Favourable intermediate risk, Unfavourable intermediate risk |
| CPG 3 | Gleason 3+4=7 (grade group 2) and PSA 10 to 20 and stage T1 to T2, or Gleason 4+3=7 (grade group 3) at stage T1 to T2. Radical treatment is offered; active surveillance is considered only for people who decline it (NG131 1.3.10). | Favourable intermediate risk, Unfavourable intermediate risk |
| CPG 4 | Any one of: Gleason score 8 (grade group 4), PSA above 20, stage T3. Active surveillance is not offered (NG131 1.3.11). | - |
| CPG 5 | Two or more of Gleason score 8 (grade group 4), PSA above 20 and stage T3; or Gleason 9 to 10 (grade group 5); or stage T4. | - |
The five-tier model NICE recommends for everyone with newly diagnosed localised or locally advanced prostate cancer, assigned by the urological cancer MDT. It replaced the three-tier D'Amico model in the 2021 amendment because that model could not separate Gleason 3+4 from 4+3. PSA is in micrograms per litre, which is the same number as nanograms per millilitre. NICE's treatment recommendations are written in these group numbers.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| CPG 1 | Gleason score 6 (grade group 1) and PSA under 10 and stage T1 to T2. Active surveillance is offered first (NG131 1.3.8). | Very low and low risk, preferred, Low risk, men who prefer treatment |
| CPG 2 | Gleason 3+4=7 (grade group 2) or PSA 10 to 20, with stage T1 to T2. Active surveillance, radical prostatectomy and radical radiotherapy are offered as a choice (NG131 1.3.9). | - |
| CPG 3 | Gleason 3+4=7 (grade group 2) and PSA 10 to 20 and stage T1 to T2, or Gleason 4+3=7 (grade group 3) at stage T1 to T2. Radical treatment is offered; active surveillance is considered only for people who decline it (NG131 1.3.10). | - |
| CPG 4 | Any one of: Gleason score 8 (grade group 4), PSA above 20, stage T3. Active surveillance is not offered (NG131 1.3.11). | - |
| CPG 5 | Two or more of Gleason score 8 (grade group 4), PSA above 20 and stage T3; or Gleason 9 to 10 (grade group 5); or stage T4. | - |
The five-tier model NICE recommends for everyone with newly diagnosed localised or locally advanced prostate cancer, assigned by the urological cancer MDT. It replaced the three-tier D'Amico model in the 2021 amendment because that model could not separate Gleason 3+4 from 4+3. PSA is in micrograms per litre, which is the same number as nanograms per millilitre. NICE's treatment recommendations are written in these group numbers.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Grade Group 1 | Gleason 3+3 = 6. Only individual, well-formed glands. | - |
| Grade Group 2 | Gleason 3+4 = 7. Predominantly well-formed glands with a lesser component of poorly formed, fused or cribriform glands. | - |
| Grade Group 3 | Gleason 4+3 = 7. Predominantly poorly formed, fused or cribriform glands. | - |
| Grade Group 4 | Gleason 8 (4+4, 3+5, 5+3). | - |
| Grade Group 5 | Gleason 9-10. Lack of gland formation, necrosis, or both. | - |
Derived in the VEGF-TKI era; survival on immunotherapy combinations is longer in every group, but the groups still select first-line regimens (nivolumab-ipilimumab is approved for intermediate and poor risk).
Source: Heng et al., Lancet Oncology 2013 (validation); JCO 2009 (derivation). Outcomes are those of the published cohort and do not account for treatments since.
The 2018 revision allows imaging and pathology to assign stage and adds IIIC for nodal disease (IIIC1 pelvic, IIIC2 para-aortic).
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| IA1 / IA2 | Microscopic invasion under 3 mm / 3-5 mm. | - |
| IB1 / IB2 / IB3 | Invasion 5 mm or more and largest dimension under 2 cm / 2-4 cm / 4 cm or more. | Stage IA1-IB1 (≤2 cm), Stage IB2-IIA (surgical candidates) |
| IIA1 / IIA2 / IIB | Upper two-thirds of vagina under 4 cm / 4 cm or more / parametrial involvement. | Locally advanced, Locally advanced (IB3, IIB-IVA), standard, Locally advanced, high risk (node-positive IB2-IIB, III-IVA) |
| IIIA / IIIB / IIIC1 / IIIC2 | Lower third of vagina / pelvic wall or hydronephrosis / pelvic nodes / para-aortic nodes. | Locally advanced, Locally advanced (IB3, IIB-IVA), standard, Locally advanced, high risk (node-positive IB2-IIB, III-IVA) |
| IVA / IVB | Bladder or rectum invasion / distant metastasis. | Recurrent/metastatic, Persistent, recurrent, or metastatic, first line |
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| I (IA-IC) | Confined to ovaries or tubes; IC for surgical spill, capsule rupture or positive washings. | Newly diagnosed stage I-II, Newly diagnosed stage III-IV: surgery and chemotherapy |
| II | Pelvic extension or primary peritoneal cancer confined to the pelvis. | Newly diagnosed stage III-IV: surgery and chemotherapy |
| III (IIIA1-IIIC) | Spread to the peritoneum outside the pelvis or retroperitoneal nodes: IIIA1 nodes only, IIIA2 microscopic, IIIB 2 cm or smaller, IIIC over 2 cm. | Newly diagnosed, Newly diagnosed stage I-II, Newly diagnosed stage III-IV: surgery and chemotherapy |
| IV (IVA-IVB) | Distant metastasis: IVA pleural effusion with positive cytology; IVB parenchymal or extra-abdominal metastases. | Newly diagnosed, Newly diagnosed stage I-II, Newly diagnosed stage III-IV: surgery and chemotherapy |
Staging decides when to treat (iwCLL active-disease criteria), not what to treat with; CLL-IPI (below) and TP53/IGHV status guide therapy choice.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Binet A | Fewer than 3 involved lymphoid areas, haemoglobin 100 g/L or above, platelets 100 × 10⁹/L or above (Rai 0-II). | Early stage, asymptomatic (Rai 0-II, Binet A-B) |
| Binet B | 3 or more involved areas, counts preserved (Rai I-II). | Early stage, asymptomatic (Rai 0-II, Binet A-B) |
| Binet C | Haemoglobin under 100 g/L or platelets under 100 × 10⁹/L (Rai III-IV). | Early stage, asymptomatic (Rai 0-II, Binet A-B) |
Outcomes predate BTK and BCL-2 inhibitors; with targeted therapy the survival gap between groups narrows but TP53 status still changes the regimen.
Source: International CLL-IPI working group, Lancet Oncology 2016. Outcomes are those of the published cohort and do not account for treatments since.
Limited stage is I-II; advanced stage is III-IV. B symptoms (fever, night sweats, weight loss over 10% in 6 months) are recorded for Hodgkin lymphoma only. Bulk is a single mass of 10 cm or over a third of the transthoracic diameter (Hodgkin) or per histology for NHL.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| I | One node or group of adjacent nodes; or a single extranodal lesion without nodal involvement (IE). | Limited stage (I-II, non-bulky), Limited stage (I to II), non-bulky, low risk: four cycles, and often no radiotherapy |
| II | Two or more nodal groups on the same side of the diaphragm; or stage I-II by nodal extent with limited contiguous extranodal involvement (IIE). | Limited stage (I-II, non-bulky), Limited stage (I to II), non-bulky, low risk: four cycles, and often no radiotherapy |
| II bulky | Stage II with bulky disease; treated as limited or advanced by histology and prognostic factors. | Limited stage (I-II, non-bulky), Advanced stage, IPI 0-1, Advanced stage, IPI 2-5 |
| III | Nodes on both sides of the diaphragm, or nodes above the diaphragm with spleen involvement. | Advanced stage, IPI 0-1, Advanced stage, IPI 2-5, Advanced stage, IPI 0 to 1: R-CHOP for six cycles |
| IV | Additional non-contiguous extralymphatic involvement (marrow, liver, lung, CNS). | Advanced stage, IPI 0-1, Advanced stage, IPI 2-5, Advanced stage, IPI 0 to 1: R-CHOP for six cycles |
Original IPI groups: low 0-1, low-intermediate 2, high-intermediate 3, high 4-5 with 5-year OS 73%, 51%, 43% and 26% before rituximab (Shipp 1993). NCCN-IPI (Zhou 2014) refines age and LDH bands.
Source: Sehn et al., Blood 2007 (R-IPI); Shipp et al., NEJM 1993 (IPI). Outcomes are those of the published cohort and do not account for treatments since.
Limited stage is I-II; advanced stage is III-IV. B symptoms (fever, night sweats, weight loss over 10% in 6 months) are recorded for Hodgkin lymphoma only. Bulk is a single mass of 10 cm or over a third of the transthoracic diameter (Hodgkin) or per histology for NHL.
FLIPI2 (Federico 2009) uses β2-microglobulin, node over 6 cm, marrow involvement, haemoglobin and age; PRIMA-PI uses β2-microglobulin and marrow alone.
Source: Solal-Céligny et al., Blood 2004. Outcomes are those of the published cohort and do not account for treatments since.
Limited stage is I-II; advanced stage is III-IV. B symptoms (fever, night sweats, weight loss over 10% in 6 months) are recorded for Hodgkin lymphoma only. Bulk is a single mass of 10 cm or over a third of the transthoracic diameter (Hodgkin) or per histology for NHL.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| I | One node or group of adjacent nodes; or a single extranodal lesion without nodal involvement (IE). | Early stage, favourable (I-II), Early stage, unfavourable (I-II bulky or risk factors) |
| II | Two or more nodal groups on the same side of the diaphragm; or stage I-II by nodal extent with limited contiguous extranodal involvement (IIE). | Early stage, favourable (I-II), Early stage, unfavourable (I-II bulky or risk factors) |
| II bulky | Stage II with bulky disease; treated as limited or advanced by histology and prognostic factors. | Advanced stage, Early stage, unfavourable (I-II bulky or risk factors), Advanced stage (III-IV), age ≤60 |
| III | Nodes on both sides of the diaphragm, or nodes above the diaphragm with spleen involvement. | Advanced stage, Advanced stage (III-IV), age ≤60, Advanced stage, age >60 |
| IV | Additional non-contiguous extralymphatic involvement (marrow, liver, lung, CNS). | Advanced stage, Advanced stage (III-IV), age ≤60, Advanced stage, age >60 |
Limited stage is I-II; advanced stage is III-IV. B symptoms (fever, night sweats, weight loss over 10% in 6 months) are recorded for Hodgkin lymphoma only. Bulk is a single mass of 10 cm or over a third of the transthoracic diameter (Hodgkin) or per histology for NHL.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| I | One node or group of adjacent nodes; or a single extranodal lesion without nodal involvement (IE). | - |
| II | Two or more nodal groups on the same side of the diaphragm; or stage I-II by nodal extent with limited contiguous extranodal involvement (IIE). | - |
| II bulky | Stage II with bulky disease; treated as limited or advanced by histology and prognostic factors. | - |
| III | Nodes on both sides of the diaphragm, or nodes above the diaphragm with spleen involvement. | - |
| IV | Additional non-contiguous extralymphatic involvement (marrow, liver, lung, CNS). | - |
Ki-67 of 30% or more adds independent risk (MIPI-c). Outcomes predate BTK inhibitors and cytarabine-based induction.
Source: Hoster et al., Blood 2008. Outcomes are those of the published cohort and do not account for treatments since.
ISS uses β2-microglobulin and albumin only. R-ISS adds interphase FISH (del(17p), t(4;14), t(14;16)) and LDH. R2-ISS (2022) further weights 1q gain. Use the interactive R-ISS scorer below.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| ISS I | β2-microglobulin under 3.5 mg/L and albumin 35 g/L or above. | - |
| ISS II | Neither I nor III. | - |
| ISS III | β2-microglobulin 5.5 mg/L or above. | - |
| R-ISS I | ISS I, standard-risk cytogenetics and normal LDH. | Newly diagnosed, Newly diagnosed, transplant-eligible, Newly diagnosed, transplant-ineligible |
| R-ISS II | Not R-ISS I or III. | Newly diagnosed, Newly diagnosed, transplant-eligible, Newly diagnosed, transplant-ineligible |
| R-ISS III | ISS III with either high-risk cytogenetics or raised LDH. | Newly diagnosed, High-risk smouldering myeloma, Newly diagnosed, transplant-eligible |
Points here are a device to reproduce the R-ISS rules: stage III needs ISS III plus at least one of high-risk FISH or raised LDH; stage I needs ISS I with neither. Median OS was not reached, 83 months and 43 months.
Source: Palumbo et al., JCO 2015. Outcomes are those of the published cohort and do not account for treatments since.
Limited stage is I-II; advanced stage is III-IV. B symptoms (fever, night sweats, weight loss over 10% in 6 months) are recorded for Hodgkin lymphoma only. Bulk is a single mass of 10 cm or over a third of the transthoracic diameter (Hodgkin) or per histology for NHL.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| I | One node or group of adjacent nodes; or a single extranodal lesion without nodal involvement (IE). | - |
| II | Two or more nodal groups on the same side of the diaphragm; or stage I-II by nodal extent with limited contiguous extranodal involvement (IIE). | - |
| II bulky | Stage II with bulky disease; treated as limited or advanced by histology and prognostic factors. | - |
| III | Nodes on both sides of the diaphragm, or nodes above the diaphragm with spleen involvement. | - |
| IV | Additional non-contiguous extralymphatic involvement (marrow, liver, lung, CNS). | - |
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| IA1-IA3 | T1a-c (3 cm or smaller) N0 M0; IA1 up to 1 cm, IA2 1-2 cm, IA3 2-3 cm. | Stage I-II resectable, Stage III unresectable |
| IB | T2a (3-4 cm, or main bronchus or visceral pleura) N0. | Stage I-II resectable, Stage III unresectable |
| IIA | T2b (4-5 cm) N0. | Stage I-II resectable, Stage III unresectable |
| IIB | T1-2 N1, or T3 (5-7 cm, chest wall, separate nodule same lobe) N0. | Stage I-II resectable, Stage III unresectable |
| IIIA | T1-2 N2, T3 N1, or T4 (over 7 cm, mediastinal invasion, nodule in another ipsilateral lobe) N0-1. | Stage III unresectable |
| IIIB | T1-2 N3, or T3-4 N2. | Stage III unresectable |
| IIIC | T3-4 N3. | Stage III unresectable |
| IVA | M1a (pleural or pericardial spread, contralateral lung nodule) or M1b (single extrathoracic metastasis). | Metastatic, EGFR exon 19 del / L858R, Metastatic, EGFR exon 20 insertion, Metastatic, ALK-rearranged |
| IVB | M1c: multiple extrathoracic metastases. | Metastatic, EGFR exon 19 del / L858R, Metastatic, EGFR exon 20 insertion, Metastatic, ALK-rearranged |
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Limited stage | Confined to one hemithorax and regional nodes, encompassable in a tolerable radiotherapy field (roughly TNM I-III without malignant effusion); about a third of patients. | Very limited stage (T1-2 N0, ~5%), Limited stage |
| Extensive stage | Beyond one hemithorax, malignant pleural or pericardial effusion, or distant metastases (TNM IV); about two-thirds. | Extensive stage, first line |
UK skin carcinoma reports stage against UICC, not the American AJCC: the Royal College of Pathologists assessed both and chose UICC because AJCC 8 covers only the head and neck while UICC covers the whole body surface, and because UICC TNM is the version favoured by NCRAS. The table combines the UICC head-and-neck and carcinoma-of-the-skin chapters and covers basal cell, squamous cell and adnexal carcinoma; it excludes Merkel cell carcinoma and carcinomas of the eyelid, vulva, penis, non-hair-bearing lip and non-hair-bearing perianal skin. Most people with a keratinocyte cancer are never given a stage at all, because it would not change what is done; the words that decide care in Britain are low risk and high risk.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Stage 0 | Tis N0 M0: carcinoma in situ, which in the skin usually means Bowen's disease. | - |
| Stage I | T1 N0 M0: tumour 20 mm or less in maximum dimension, usually the clinical measurement. | - |
| Stage II | T2 N0 M0: tumour over 20 mm and up to 40 mm. | - |
| Stage III | T3 N0 M0, or T1 to T3 with N1. T3 is over 40 mm, or minor bone erosion, or perineural invasion, or deep invasion (beyond the subcutaneous fat, or more than 6 mm from the granular layer of adjacent normal epidermis). N1 is a single ipsilateral node 30 mm or less. | Adjuvant after surgery and radiotherapy |
| Stage IV | T1 to T3 with N2 or N3, or any T4, or any M1. T4a is gross cortical or marrow invasion; T4b is axial skeleton invasion including the vertebral foramen and epidural space. Nodal categories differ between the head and neck, where extranodal extension subdivides them, and the trunk and limbs, where a contralateral node counts as distant metastasis. | Locally advanced or metastatic, first line |
Not a UK reporting standard and not used in UK pathology reports, which stage against UICC. It is included because it is the evidence behind the general agreement that the anatomical stage alone does not identify the dangerous tumours, and because American sources quote it. It counts four risk factors rather than measuring the tumour: poor differentiation, perineural invasion, diameter 2 cm or more, and invasion beyond the subcutaneous fat, with bone invasion automatically T3. The ten-year outcomes below come from 1,818 primary tumours at one American referral centre and are higher than an unselected population would show; the ranking rather than the percentage is what transfers. The Royal College of Pathologists has published its objection to the risk bands derived from this system.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| T1 | No risk factors. In the validation cohort, T1 and T2a together carried 10-year cumulative incidences of 1.4 percent local recurrence, 0.6 percent nodal metastasis and 0.2 percent death from the cancer. | - |
| T2a | One risk factor. | - |
| T2b | Two or three risk factors. In the derivation cohort T2b was 19 percent of cases but 72 percent of nodal metastases and 83 percent of deaths from the cancer. | Adjuvant after surgery and radiotherapy |
| T3 | Four risk factors, or bone invasion. T2b and T3 together were 5 percent of the validation cohort and carried 60 percent of poor outcomes, with 10-year incidences of 24 percent local recurrence, 24 percent nodal metastasis and 16 percent death from the cancer. | Locally advanced or metastatic, first line |
UK skin carcinoma reports stage against UICC, not the American AJCC: the Royal College of Pathologists assessed both and chose UICC because AJCC 8 covers only the head and neck while UICC covers the whole body surface, and because UICC TNM is the version favoured by NCRAS. The table combines the UICC head-and-neck and carcinoma-of-the-skin chapters and covers basal cell, squamous cell and adnexal carcinoma; it excludes Merkel cell carcinoma and carcinomas of the eyelid, vulva, penis, non-hair-bearing lip and non-hair-bearing perianal skin. Most people with a keratinocyte cancer are never given a stage at all, because it would not change what is done; the words that decide care in Britain are low risk and high risk.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Stage 0 | Tis N0 M0: carcinoma in situ, which in the skin usually means Bowen's disease. | - |
| Stage I | T1 N0 M0: tumour 20 mm or less in maximum dimension, usually the clinical measurement. | - |
| Stage II | T2 N0 M0: tumour over 20 mm and up to 40 mm. | - |
| Stage III | T3 N0 M0, or T1 to T3 with N1. T3 is over 40 mm, or minor bone erosion, or perineural invasion, or deep invasion (beyond the subcutaneous fat, or more than 6 mm from the granular layer of adjacent normal epidermis). N1 is a single ipsilateral node 30 mm or less. | - |
| Stage IV | T1 to T3 with N2 or N3, or any T4, or any M1. T4a is gross cortical or marrow invasion; T4b is axial skeleton invasion including the vertebral foramen and epidural space. Nodal categories differ between the head and neck, where extranodal extension subdivides them, and the trunk and limbs, where a contralateral node counts as distant metastasis. | Locally advanced or metastatic |
UK skin carcinoma reports stage against UICC, not the American AJCC: the Royal College of Pathologists assessed both and chose UICC because AJCC 8 covers only the head and neck while UICC covers the whole body surface, and because UICC TNM is the version favoured by NCRAS. The table combines the UICC head-and-neck and carcinoma-of-the-skin chapters and covers basal cell, squamous cell and adnexal carcinoma; it excludes Merkel cell carcinoma and carcinomas of the eyelid, vulva, penis, non-hair-bearing lip and non-hair-bearing perianal skin. Most people with a keratinocyte cancer are never given a stage at all, because it would not change what is done; the words that decide care in Britain are low risk and high risk.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Stage 0 | Tis N0 M0: carcinoma in situ, which in the skin usually means Bowen's disease. | - |
| Stage I | T1 N0 M0: tumour 20 mm or less in maximum dimension, usually the clinical measurement. | - |
| Stage II | T2 N0 M0: tumour over 20 mm and up to 40 mm. | - |
| Stage III | T3 N0 M0, or T1 to T3 with N1. T3 is over 40 mm, or minor bone erosion, or perineural invasion, or deep invasion (beyond the subcutaneous fat, or more than 6 mm from the granular layer of adjacent normal epidermis). N1 is a single ipsilateral node 30 mm or less. | - |
| Stage IV | T1 to T3 with N2 or N3, or any T4, or any M1. T4a is gross cortical or marrow invasion; T4b is axial skeleton invasion including the vertebral foramen and epidural space. Nodal categories differ between the head and neck, where extranodal extension subdivides them, and the trunk and limbs, where a contralateral node counts as distant metastasis. | - |
UK skin carcinoma reports stage against UICC, not the American AJCC: the Royal College of Pathologists assessed both and chose UICC because AJCC 8 covers only the head and neck while UICC covers the whole body surface, and because UICC TNM is the version favoured by NCRAS. The table combines the UICC head-and-neck and carcinoma-of-the-skin chapters and covers basal cell, squamous cell and adnexal carcinoma; it excludes Merkel cell carcinoma and carcinomas of the eyelid, vulva, penis, non-hair-bearing lip and non-hair-bearing perianal skin. Most people with a keratinocyte cancer are never given a stage at all, because it would not change what is done; the words that decide care in Britain are low risk and high risk.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Stage 0 | Tis N0 M0: carcinoma in situ, which in the skin usually means Bowen's disease. | - |
| Stage I | T1 N0 M0: tumour 20 mm or less in maximum dimension, usually the clinical measurement. | Localised low- and high-risk |
| Stage II | T2 N0 M0: tumour over 20 mm and up to 40 mm. | Localised low- and high-risk |
| Stage III | T3 N0 M0, or T1 to T3 with N1. T3 is over 40 mm, or minor bone erosion, or perineural invasion, or deep invasion (beyond the subcutaneous fat, or more than 6 mm from the granular layer of adjacent normal epidermis). N1 is a single ipsilateral node 30 mm or less. | High-risk after surgery and radiotherapy, Follow-up, the lymph nodes, and the chance of a second one, Radiotherapy after surgery, and what not to add to it |
| Stage IV | T1 to T3 with N2 or N3, or any T4, or any M1. T4a is gross cortical or marrow invasion; T4b is axial skeleton invasion including the vertebral foramen and epidural space. Nodal categories differ between the head and neck, where extranodal extension subdivides them, and the trunk and limbs, where a contralateral node counts as distant metastasis. | Locally advanced or metastatic |
Not a UK reporting standard and not used in UK pathology reports, which stage against UICC. It is included because it is the evidence behind the general agreement that the anatomical stage alone does not identify the dangerous tumours, and because American sources quote it. It counts four risk factors rather than measuring the tumour: poor differentiation, perineural invasion, diameter 2 cm or more, and invasion beyond the subcutaneous fat, with bone invasion automatically T3. The ten-year outcomes below come from 1,818 primary tumours at one American referral centre and are higher than an unselected population would show; the ranking rather than the percentage is what transfers. The Royal College of Pathologists has published its objection to the risk bands derived from this system.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| T1 | No risk factors. In the validation cohort, T1 and T2a together carried 10-year cumulative incidences of 1.4 percent local recurrence, 0.6 percent nodal metastasis and 0.2 percent death from the cancer. | Localised low- and high-risk |
| T2a | One risk factor. | Localised low- and high-risk |
| T2b | Two or three risk factors. In the derivation cohort T2b was 19 percent of cases but 72 percent of nodal metastases and 83 percent of deaths from the cancer. | Follow-up, the lymph nodes, and the chance of a second one |
| T3 | Four risk factors, or bone invasion. T2b and T3 together were 5 percent of the validation cohort and carried 60 percent of poor outcomes, with 10-year incidences of 24 percent local recurrence, 24 percent nodal metastasis and 16 percent death from the cancer. | Locally advanced or metastatic |
UK skin carcinoma reports stage against UICC, not the American AJCC: the Royal College of Pathologists assessed both and chose UICC because AJCC 8 covers only the head and neck while UICC covers the whole body surface, and because UICC TNM is the version favoured by NCRAS. The table combines the UICC head-and-neck and carcinoma-of-the-skin chapters and covers basal cell, squamous cell and adnexal carcinoma; it excludes Merkel cell carcinoma and carcinomas of the eyelid, vulva, penis, non-hair-bearing lip and non-hair-bearing perianal skin. Most people with a keratinocyte cancer are never given a stage at all, because it would not change what is done; the words that decide care in Britain are low risk and high risk.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Stage 0 | Tis N0 M0: carcinoma in situ, which in the skin usually means Bowen's disease. | - |
| Stage I | T1 N0 M0: tumour 20 mm or less in maximum dimension, usually the clinical measurement. | - |
| Stage II | T2 N0 M0: tumour over 20 mm and up to 40 mm. | - |
| Stage III | T3 N0 M0, or T1 to T3 with N1. T3 is over 40 mm, or minor bone erosion, or perineural invasion, or deep invasion (beyond the subcutaneous fat, or more than 6 mm from the granular layer of adjacent normal epidermis). N1 is a single ipsilateral node 30 mm or less. | Neoadjuvant, Radiotherapy and local options |
| Stage IV | T1 to T3 with N2 or N3, or any T4, or any M1. T4a is gross cortical or marrow invasion; T4b is axial skeleton invasion including the vertebral foramen and epidural space. Nodal categories differ between the head and neck, where extranodal extension subdivides them, and the trunk and limbs, where a contralateral node counts as distant metastasis. | Locally advanced, first line, Metastatic disease |
UK skin carcinoma reports stage against UICC, not the American AJCC: the Royal College of Pathologists assessed both and chose UICC because AJCC 8 covers only the head and neck while UICC covers the whole body surface, and because UICC TNM is the version favoured by NCRAS. The table combines the UICC head-and-neck and carcinoma-of-the-skin chapters and covers basal cell, squamous cell and adnexal carcinoma; it excludes Merkel cell carcinoma and carcinomas of the eyelid, vulva, penis, non-hair-bearing lip and non-hair-bearing perianal skin. Most people with a keratinocyte cancer are never given a stage at all, because it would not change what is done; the words that decide care in Britain are low risk and high risk.
| Stage | Definition | Standard of care on the cancer page |
|---|---|---|
| Stage 0 | Tis N0 M0: carcinoma in situ, which in the skin usually means Bowen's disease. | - |
| Stage I | T1 N0 M0: tumour 20 mm or less in maximum dimension, usually the clinical measurement. | - |
| Stage II | T2 N0 M0: tumour over 20 mm and up to 40 mm. | - |
| Stage III | T3 N0 M0, or T1 to T3 with N1. T3 is over 40 mm, or minor bone erosion, or perineural invasion, or deep invasion (beyond the subcutaneous fat, or more than 6 mm from the granular layer of adjacent normal epidermis). N1 is a single ipsilateral node 30 mm or less. | Radiotherapy, and who it suits |
| Stage IV | T1 to T3 with N2 or N3, or any T4, or any M1. T4a is gross cortical or marrow invasion; T4b is axial skeleton invasion including the vertebral foramen and epidural space. Nodal categories differ between the head and neck, where extranodal extension subdivides them, and the trunk and limbs, where a contralateral node counts as distant metastasis. | - |
ASCO and NCCN suggest offering apixaban or rivaroxaban thromboprophylaxis to ambulatory patients scoring 2 or more (AVERT, CASSINI), after weighing bleeding risk.
Source: Khorana et al., Blood 2008. Outcomes are those of the published cohort and do not account for treatments since.
Outcomes are quoted from the derivation or validation cohort named in each source and reflect the treatments of that era: R-IPI and CLL-IPI predate CAR-T and BTK inhibitors, IMDC predates immunotherapy doublets. They rank risk; they do not predict an individual. Stage tables are summarised to the level quoted in clinic; consult the AJCC/UICC manual for the full T, N and M definitions.
Lines of therapy lays out what is done at each stage; the calculators cover body surface area, renal function and RECIST; the glossary explains TNM staging, Lugano and R-ISS. Not medical advice.