Publication, Part of Cancer registrations statistics, England
Cancer Registration Statistics, England, 2022
National statistics, Accredited official statistics
New data added:
- Incidence counts and rates have been re-stated for cancers diagnosed between 2012 to 2022, reflecting the updated populations available using the 2021 census
- Counts and rates have been provided for Persons in addition to Males and Females
- We now use https://fingertips.phe.org.uk/documents/2021-lsoa-imd-lookup.xlsx to align deprivation scores with 2021 LSOAs
- The data downloads for Cancer Registrations (Incidence) now contain counts and age-standardised rates for England only. The interactive dashboard contains counts, age-specific, non-standardised and age-standardised rates for England and sub-national geographies
Coming Summer 2025:
- Incidence counts and rates for small geographic areas including, Upper Tier Local Authority (UTLA) 2024 boundaries, Local authority district / unitary authority (LAUA) 2024 boundaries and Middle layer super output area (MSOA) using census 2021
5 June 2025 11:00 AM
Correction notice:
A coding error has resulted in incorrect populations being used as a denominator for age-specific rates for sub-national estimates. This has affected Tables 1 to 4. The coding error has been fixed and the age-specific rates for Government office regions, Cancer alliances, and Integrated care boards have been updated to the correct values.
12 November 2024 12:25 PM
Things you need to know about this release
What’s included in this bulletin
The counts and rates of cancer registration are designated as Accredited Official Statistics. Accredited Official Statistics are a subset of Official Statistics, which have been certified by the UK Statistics Authority as compliant with its code of practice for statistics.
This bulletin reports on registered diagnoses of cancers which were diagnosed in the 2022 calendar year. Counts are presented for England, the 9 former Government office regions (provided to support regional communications activity by the charity sector), the 21 Cancer alliances and 42 Integrated care boards, as well as by gender, age groups from under 1 to 90 years and older, Index of Multiple Deprivation quintile and stage at diagnosis (where a staging system exists). In addition, the data tables contain in-situ tumours and benign tumours for completeness (in Table 3 of the accompanying data release).
Using the ICD-10 coding system, registerable diagnoses include cancers (C00.0 to C97), in situ tumours (D00.0 to D09.9), selected benign tumours (D32.0 to D33.9, D35.2 to D35.4), and tumours of uncertain or unknown behaviour (D37.0 to D48.9). Using ICD-O-3, some blood cancers are also now registerable, which correspond to the ICD-10 codes for amyloidosis (E85*) and amyloidosis of skin (L99*).
For sub-national estimates, data is provided where a non-standardised (all age) rate can be reliably estimated in at least half the geographies for that combination of main and detailed cancer groups, gender, deprivation or stage. To avoid re-identification through slivers, an additional detailed cancer group will be suppressed as required.
Diagnoses are presented both by ICD-10 codes and by main and detailed cancer groups (see the reported measures section for details) which use information on the type of cancer cells as well as their location in the body.
Care should be taken when making comparisons between the historic and latest available data.
Cancer registrations in England can take up to 5 years after the end of a given calendar year to reach 100% completeness, due to the continuing accrual of late registrations. Further changes may still occur after 5 years following later diagnostic testing. However, these late changes are uncommon.
Diagnoses of cancer are registered for each separate cancer; a person may be diagnosed with more than one type of cancer and would then appear more than once in the incidence statistics; the progression or recurrence of previous cancer diagnoses are not counted as new diagnoses.
Reported measures
Counts
Counts of cancer incidence are presented for diagnoses registered in 2022.
Counts of mortality are presented for deaths from cancer registered in 2022.
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, whereas 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. ONS recommends that Accredited Official Statistics outputs use the 2013 ESP aggregated to 90 and over, due to the availability of population estimates of assured quality for this age band.
Main and detailed cancer groupings
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 |
All Anus |
Bladder |
All Bladder |
Bladder |
Bladder - malignant or in situ |
Bladder |
Bladder - uncertain or unknown |
Blood cancer |
All Blood cancer |
Blood cancer |
Acute lymphoblastic leukaemia (ALL) |
Blood cancer |
Acute myeloid leukaemia (AML) |
Blood cancer |
Chronic lymphocytic leukaemia (CLL) or small lymphocytic lymphoma (SLL) |
Blood cancer |
Chronic myeloid leukaemia (CML) |
Blood cancer |
Chronic myelomonocytic leukaemia (CMML) |
Blood cancer |
Diffuse large B-cell lymphoma (DLBCL) and other high grade mature B-cell neoplasms |
Blood cancer |
Essential thrombocythaemia (ET) |
Blood cancer |
Follicular lymphoma |
Blood cancer |
Hodgkin lymphoma |
Blood cancer |
Lymphoplasmacytic lymphoma (LPL) or Waldenstrom |
Blood cancer |
Mantle cell lymphoma (MCL) |
Blood cancer |
Marginal zone lymphoma (nodal, extranodal, MALT) |
Blood cancer |
Mature T-cell and NK-cell neoplasms |
Blood cancer |
Myelodysplastic syndromes (MDS) |
Blood cancer |
Myeloma |
Blood cancer |
Other blood cancer |
Blood cancer |
Polycythaemia vera (PCV) |
Bone sarcoma |
All Bone sarcoma |
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 |
All 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 |
All Breast |
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 |
All Cervix |
Endocrine glands excluding brain |
All Endocrine glands excluding brain |
Endocrine glands excluding brain |
Non-thyroid endocrine glands |
Endocrine glands excluding brain |
Thyroid |
Eye |
All Eye |
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 |
Head and neck |
Nasopharynx |
Head and neck |
Oral cavity |
Head and neck |
Oropharynx |
Heart, mediastinum, pleura, other and ill-defined |
All Heart, mediastinum, pleura, other and ill-defined |
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 |
All Mesothelioma |
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 |
All Prostate |
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 cancer |
All Skin cancer |
Skin cancer |
BCC |
Skin cancer |
cSCC |
Skin cancer |
Melanoma |
Skin cancer |
Rare |
Small intestine |
All Small intestine |
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 |
All Thymus |
Urethra |
All Urethra |
Uterus |
All Uterus |
Uterus |
Uterus - endometrial |
Uterus |
Uterus - non-endometrial |
Vagina |
All Vagina |
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). Triple negative breast cancer occurs when the status for each of the three hormone receptors are negative – these are included as a separate category in the downloadable data tables.
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) |
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* |
*Known as triple (all) negative breast cancer
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/
Last edited: 10 June 2025 11:46 am