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Publication, Part of

Cancer Registration Statistics, England, 2022

National statistics, Accredited official statistics

Accredited official statistics logo.

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