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Publication, Part of

Cancer Registration Statistics, England, 2021 - Full release

National statistics, Accredited official statistics

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Reported measures

Counts

Counts of cancer incidence are presented for diagnoses registered in 2021.

Counts of mortality are presented for deaths from cancer registered in 2021.

Crude rates (age-specific and non-standardised)

The crude rate is the number of events in a specific population during a time period per 100,000 people. An event can either be a tumour diagnosis where the measure would be an incidence rate, or a death from cancer where the measure would be a mortality rate. A crude rate is calculated using the following equation:

(total number of events)/(total population) X 100,000

In this publication and the accompanying data tables, the non-standardised rate refers to the crude rate for all ages combined, where as the age-specific rate refers to the crude rate for individual age bands.

Age-standardised rate

Age-standardised cancer incidence and mortality rates are presented. An age-standardised rate is a weighted average of the age-specific rates, where the weights uses age-specific proportions of a standardised population European Standard Population 2013 (ESP). Standardising rates with the ESP accounts for the differing age structure of different populations. This means that geographical and time comparisons of the rates can be made.

Main and detailed cancer groupings

Most official statistics reporting on cancer use cancer sites that are based only on where the cancer started growing in the body. This can be a helpful way to summarise cancers but may sometimes hide the different types of cancer that grow in the same place. These different types of cancer can need different treatments even though they are found in the same part of the body. 

To better reflect the variety of cancers that patients are diagnosed and treated with, this publication introduces a wide range of subtypes of cancer that may require different treatments and may have different outcomes.  The next update of the cancer survival publication will examine these outcomes using the groupings in this publication. 

The different cancer groupings introduced have been consulted upon with patient representatives, charities and clinicians. These cancer groupings will gradually evolve to reflect changes in medical knowledge and clinical practice; some parts of the body have yet to mapped in detail and these will be added to over time. 

There are two levels of cancer grouping, a main level of up to 36 cancer groups which cover every registerable diagnosis and a detailed level that allow the reporting by appropriate sub-types of cancer. Table 2 presents these main and detailed cancer groups.

The coding systems used to define each main or detailed cancer group are ICD-10 for the location in the body (sometimes with the definitions of the cancer cell type from ICD-O-2) or ICD-O-3 for both the location in the body and the cancer cell type (where needed).

Table 2: A list of the main and detailed cancer groups used in this publication.

Main group Detailed group
Anus Not applicable
Bladder All Bladder
Bladder Bladder - malignant or in situ
Bladder Bladder - uncertain or unknown
Blood All Blood 
Blood Acute lymphoblastic leukaemia (ALL)
Blood Acute myeloid leukaemia (AML)
Blood Chronic lymphocytic leukaemia (CLL) or small lymphocytic lymphoma (SLL)
Blood Chronic myeloid leukaemia (CML)
Blood Chronic myelomonocytic leukaemia (CMML)
Blood Diffuse large B-cell lymphoma (DLBCL) and other high grade mature B-cell neoplasms
Blood Essential thrombocythaemia (ET)
Blood Follicular lymphoma
Blood Hodgkin lymphoma
Blood Lymphoplasmacytic lymphoma (LPL) or Waldenstrom
Blood Mantle cell lymphoma (MCL)
Blood Marginal zone lymphoma (nodal, extranodal, MALT)
Blood Mature T-cell and NK-cell neoplasms
Blood Myelodysplastic syndromes (MDS)
Blood Myeloma
Blood Other blood cancer
Blood Polycythaemia vera (PCV)
Bone Sarcoma  All Bone
Bone Sarcoma  Bone tumours of intermediate behaviour
Bone Sarcoma  Chondrosarcoma
Bone Sarcoma  Chordoma
Bone Sarcoma  Ewing sarcoma
Bone Sarcoma  Osteosarcoma
Bone Sarcoma  Other malignant bone tumours
Bowel Bowel
Bowel Colon
Bowel Rectosigmoid junction
Bowel Rectum
Brain All Brain
Brain Benign endocrine
Brain Malignant brain
Brain Non-benign endocrine
Brain Non-malignant brain
Breast Not applicable
Cancer of unknown primary All Cancer of unknown primary
Cancer of unknown primary CUP - Malignant neoplasm, without specification of site
Cancer of unknown primary CUP - Secondary and unspecified malignant neoplasm of lymph nodes
Cancer of unknown primary CUP - Secondary malignant neoplasm of other and unspecified sites
Cancer of unknown primary CUP - Secondary malignant neoplasm of respiratory and digestive organs
Cervix Not applicable
Endocrine glands excluding brain All Endocrine glands excluding brain
Endocrine glands excluding brain Non-thyroid endocrine glands
Endocrine glands excluding brain Thyroid
Eye Not applicable
Head and neck All Head and neck
Head and neck Hypopharynx
Head and neck Larynx
Head and neck Major salivary glands
Head and neck Middle ear, and other, and ill-defined head and neck sites
Head and neck Nasal cavity and sinus
Head and neck Nasopharynx
Head and neck Oral cavity
Head and neck Oropharynx
Heart, mediastinum, pleura and ill-defined Not applicable
Kidney All Kidney
Kidney Chromophobe RCC
Kidney Clear cell RCC
Kidney Kidney - other
Kidney Papillary RCC
Kidney Renal cell carcinoma NOS
Kidney Wilms (Nephroblastoma)
Liver and biliary tract All Liver and biliary tract
Liver and biliary tract Ampulla of Vater
Liver and biliary tract Cholangiocarcinoma
Liver and biliary tract Gallbladder
Liver and biliary tract Liver excluding intrahepatic cholangiocarcinoma
Lung All Lung
Lung Non-small cell lung cancer
Lung Small cell lung cancer
Mesothelioma Not applicable
Oesophagus All Oesophagus
Oesophagus Oesophagogastric junction
Oesophagus Oesophagus - overlapping lesion and unspecified
Oesophagus Oesophagus lower third
Oesophagus Oesophagus upper and middle third
Ovary All Ovary
Ovary Ovary - borderline
Ovary Ovary - malignant epithelial
Ovary Ovary - miscellaneous and unspecified
Ovary Ovary - non-specific site
Ovary Ovary - sex cord-stromal and germ cell
Pancreas All Pancreas
Pancreas Pancreas - Carcinoma and Other
Pancreas Pancreas - Neuroendocrine
Prostate Not applicable
Renal pelvis and ureter All Renal pelvis and ureter
Renal pelvis and ureter Renal pelvis and ureter - malignant or in situ
Renal pelvis and ureter Renal pelvis and ureter - uncertain or unknown
Skin tumour All Skin diagnoses
Skin tumour Melanoma  
Skin tumour Non melanoma skin cancer  
Skin tumour Other skin tumours
Small intestine Not applicable
Soft Tissue Sarcoma All Soft Tissue Sarcoma
Soft Tissue Sarcoma Dermatofibrosarcoma protuberans
Soft Tissue Sarcoma Endometrial stromal sarcoma
Soft Tissue Sarcoma Gastrointestinal stromal sarcoma (GIST)
Soft Tissue Sarcoma Kaposi sarcoma
Soft Tissue Sarcoma Leiomyosarcoma
Soft Tissue Sarcoma Liposarcoma
Soft Tissue Sarcoma Malignant peripheral nerve sheath tumour (MPNST)
Soft Tissue Sarcoma Myofibrosarcomas and other fibroblastic sarcomas
Soft Tissue Sarcoma Myxoid fibroblastic sarcomas
Soft Tissue Sarcoma Other malignant soft tissue tumours
Soft Tissue Sarcoma Phyllodes
Soft Tissue Sarcoma Rhabdomyosarcoma
Soft Tissue Sarcoma Soft tissue tumours of intermediate behaviour
Soft Tissue Sarcoma Synovial
Soft Tissue Sarcoma Tumours of uncertain differentiation
Soft Tissue Sarcoma Undifferentiated Sarcoma
Soft Tissue Sarcoma Vascular Tumours
Stomach All Stomach
Stomach Cardia
Stomach GIST located in stomach
Stomach Non-Cardia
Stomach Stomach - overlapping lesion and unspecified
Testes All Testes
Testes Non-seminoma
Testes Seminoma
Testes Testes - other
Thymus Not applicable
Urethra Not applicable
Uterus All Uterus
Uterus Uterus - endometrial
Uterus Uterus - non-endometrial
Vagina Not applicable

Hormone receptor statuses for diagnoses of breast cancer

Breast cancer estimates for England are also given according to their hormone receptor status markers as set out in Table 3. The way in which a breast cancer is sensitive to different hormone receptor statuses influences the treatments offered to patients and their likely outcomes. The hormone statuses included in this publication are oestrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor 2 (HER2).

Table 3: combinations of hormone receptor statuses used with breast cancer in this publication.

Oestrogen (ER)  Progesterone (PR) 
Human epidermal growth
factor receptor 2 (HER2) 
Sometimes called 
Any 
Any 
Any 
 
Borderline 
Any 
Any 
 
Negative 
Any  Any   
Positive 
Any  Any   
Unknown 
Any  Any   
Any 
Borderline 
Any 
 
Any 
Negative 
Any   
Any 
Positive 
Any   
Any 
Unknown 
Any   
Any 
Any 
Borderline 
 
Any  Any 
Negative 
 
Any  Any 
Positive 
 
Any  Any 
Unknown 
 
Negative 
Negative 
Negative 
Triple negative 

More information can be found about hormone receptors ER and PR at https://breastcancernow.org/about-breast-cancer/diagnosis/hormone-receptors-and-breast-cancer/ and HER2 at https://breastcancernow.org/about-breast-cancer/diagnosis/her2/  

Gleason Grade Group for diagnoses of prostate cancer

Prostate cancer estimates are also given according to their Gleason Grade Group (sometimes called a Cambridge Prognostic Group). Like hormone receptor statuses in breast cancer patients, they can influence the treatments offered to patients and indicate the likely outcomes.

Table 4: Gleason Grade Groups used in this publication for diagnoses of prostate cancer.

Gleason Grade Group 
Gleason scores (the two most common scores added together) 
6 (3+3) 
7 (3+4) 
7 (4+3) 
4 & 5 
8, 9 or 10 (4+4, 4+5, 5+4 or 5+5) 
Unknown 
Not recorded 
All 
Scores 6 to 10 and not recorded 

 More detail on Gleason Grade Groups can be found at https://www.cancerresearchuk.org/about-cancer/prostate-cancer/stages/grades 



Last edited: 23 May 2024 10:39 am