Cervical screening in Canada, 2023-24
HPV testing
On this page:
- Status of HPV primary screening implementation
- Activities to support the transition to HPV primary screening
- Current capacity in which HPV testing is being used
- Use of HPV testing after an abnormal cervical screening test result
Human Papillomavirus (HPV) testing is increasingly being recognized as the leading approach in cervical screening. The link between the persistent presence of HPV and the risk of developing cervical cancer has been established, making HPV primary screening advantageous as it identifies cervical pre-cancer earlier, resulting in a significantly lower likelihood of cervical cancer compared with Pap test screening. Learn more about HPV testing in Canada and the current state of the Elimination of Cervical Cancer.
One jurisdiction is currently using HPV testing as the primary screening method for cervical cancer. Eight provinces and two territories have plans to implement HPV testing for primary screening. Jurisdictions are currently undergoing activities to support the implementation of HPV primary screening, including developing guidelines and business and operation plans.
Status of HPV primary screening implementation
P/T | No current HPV primary screening activities | Planning for implementation | Piloting | Partially implemented | Jurisdiction-wide implemented | Plans to implement self-sampling to facilitate HPV primary screening implementation |
---|---|---|---|---|---|---|
YT | ✓ | |||||
NT | ✓ | ✓ | ||||
NU | ✓ | |||||
BC | ✓* | ✓* | ||||
AB | ✓ (preparing business case) | ✓ | ||||
SK | ✓ | |||||
MB | ✓ | ✓ | ||||
ON | ✓ | ✓^ | ||||
QC | ✓ | |||||
NB | ✓* | ✓~ | ||||
NS | ✓ | ✓ | ||||
PE | ✓ Implemented change in May 2023 | ✓ | ||||
NL | ✓ |
*BC: Self-screening is available province wide for eligible people. During BC’s 3-year transition, LBC samples will be triaged to either primary cytology or HPV, depending on the patient’s age. Not all samples will have HPV testing, but HPV testing is available through self-screening for those who choose that collection method.
^ON: Ontario plans to implement self-sampling for HPV testing in a phased approach which will enable the program to determine how best to implement self-sampling in the Ontario context (e.g., designing the best clinical pathways to ensure follow-up of positive test results and optimizing kit distribution and return processes).
~NB: As of March 2023, approval to proceed with the implementation of the phased-in transition from cytology based testing (Pap) to HPV primary screening, with an option for self-sampling.
Definitions
Levels of implementation status (to show incremental implementation progress by jurisdiction):
- No current HPV primary screening activities: “Status Quo” cervical screening activities.
- Planning for implementation: Conducting environmental scanning, gathering requirements to determine approach for implementation (i.e., preparing/submitting business cases, forming advisory committees) and/or planning for pilots/programs for HPV primary screening and/or self-sampling.
- Piloting: Pilot has been implemented to offer HPV primary screening. Pilots include time-bound screening activities that do not have confirmed sustainable funding.
- Partially implemented: Organized HPV primary screening has rolled out in certain sites or for certain populations across the jurisdiction. Partial implementation includes organized screening being phased-in over a time by gradually increasing capacity of screening sites or if plans are in place to implement organized screening at additional site locations. Partial implementation has secured sustained funding to offer long-term organized screening.
- Jurisdiction-wide implemented: A fully implemented organized HPV primary screening program, which is available jurisdiction-wide, with or without options for self-sampling and embeds a culturally safe approach to care. Note: An organized program would include elements such as eligibility criteria, quality assurance mechanisms, participant recall, abnormal follow-up, etc.
Activities to support the transition to HPV primary screening
Ten jurisdictions are working towards the transition to HPV primary screening. Activities to support the transition include developing business cases, updating existing infrastructure, developing recommendations and pathways, and implementing pilot programs.
P/T | Description of activities to support the transition to HPV primary screening |
---|---|
YT | Updating infrastructure to support implementation of program |
NT | Planning is underway for pilot |
NU | – |
BC | Transition to HPV primary screening completed as of January 2024* |
AB |
|
SK |
|
MB | – |
ON |
|
QC |
|
NB |
|
NS |
|
PE |
|
NL |
|
*BC: BC is considering the following self-sampling and lab assays: Copan FLOQSwabs®, eluded into PreservCyt, COBAS instrument.
^PE: PE is considering the following self-sampling and lab assays: Self-vaginal FLOQSwabs® with breakpoint (COPAN HPC146R03 Date 2021.01 — product description), and BD Onclarity™ HPV Assay.
-NU, MB: No information was provided at the time data were collected.
Current uses of HPV testing
Six provinces and two territories are using HPV testing in triage, with most specifying it is used in participants ≥30 years old with ASC-US. Some jurisdictions use HPV testing in post treatment, while others are researching its use for triage within their jurisdiction.
Current capacity in which HPV testing is being used
P/T | Capacity in which HPV testing is being used |
YT | Post treatment |
NT | Triage in participants |
NU | Triage in participants ≥30 with ASC-US |
BC | Post treatment and ASC-H follow-up |
AB | Triage in participants ≥30 with ASC-US or participants ≥50 with LSIL; posttreatment exit test |
SK | Healthcare providers can order an HPV test (i.e., non-reflexively) via requisition. Planning to implement HPV reflex testing for triage for clients ≥30 years of age with ASC-US and clients ≥50 years of age with LSIL in 2023 |
MB | HPV triage implemented in February 2022. Initiative supports individuals ≥30 with an ASC-US cytology result, and individuals ≥50 with a LSIL cytology result |
ON | HPV testing is not currently funded by the Ontario Ministry of Health. However, it is available on a patient pay basis or in some hospital settings. Recognizing that it is available, the OSCP provides guidance to healthcare providers on when to consider its use (e.g., for people with a first time ASCUS result over age 30 or to discharge eligible patients from colposcopy). |
QC | Triage in participants ≥30 with ASC-US |
NB | Triage in participants ≥30 with ASC-US or participants ≥50 with LSIL |
NS | Colposcopy clinic |
PE | Triage in participants ≥30 with ASC-US and no previous abnormal Pap HPV testing provided upon request by PCP or gynecologist as a 12-month follow-up test in treatment phase to confirm persistent or cleared HPV infection HPV testing as primary screening tool HPV testing provided as a follow-up test to confirm persistent or cleared HPV infection |
NL | Triage in participants ≥30 with ASC-US |
Use of HPV testing after an abnormal cervical screening test result
P/T | Pap primary screening with HPV triage/ reflex testing | When Pap primary screening with HPV triage/reflex testing is used | HPV with Pap Triage | When HPV with Pap Triage is used | Does HPV testing include HPV genotyping? | When HPV with genetic triage is used |
YT | To be determined | |||||
NT | ✓ | One-year follow-up for LSIL or ASC-US for 21-29 years ASC-US ≥30 years LSIL or ASC-US post-menopausal |
||||
NU | ✓ | Pap with HPV reflect testing for participants ≥30 years with ASCUS | ||||
BC | – | – | – | – | – | – |
AB | ✓ | Pap with HPV reflex testing for participants with ASC-US ≥30 and LSIL ≥50 | To be determined | To be determined | ||
SK | ✓ (2023) | Planning to implement Pap with HPV reflex testing for participants with ASC-US ≥30 and LSIL ≥50 in 2023 | ||||
MB | ✓ | Pap with HPV reflex testing for participants with ASC-US ≥30 and LSIL ≥50 | Yes, HPV is reported in 16, 18, and ‘other’ | |||
ON | ✓* | HPV testing is not currently funded by the Ontario Ministry of Health. However, it is available on a patient pay basis or in some hospital settings. Recognizing that it is available, the OCSP provides guidance to healthcare providers on when to consider its use (e.g., for people with a first time ASCUS result over age 30 or to discharge eligible patients from colposcopy). | ✓^ | |||
QC | ✓ After an abnormal Pap test screening, oncogenic HPV testing is used for participants ≥30 before following up with colposcopy, if HPV test is positive |
|||||
NB | ✓ | Recommended as triage for participants aged ≥30 with an ASC-US or ≥50 with LSIL | N/A | N/A | ✓ Includes HPV genotyping |
Triage for participants aged ≥30 with an ASC-US or ≥50 with LSIL
Some colposcopists may order ad hoc HPV test for cure post-colposcopy/treatment |
NS | – | – | – | – | – | – |
PE | ✓ Implemented HPV testing as primary screen, May 2023 |
Triage in participants ≥30 with ASC-US and no previous abnormal Pap.
Further HPV testing on request by PCP for treatment/exit management (e.g., repeat testing at 12 months to confirm persistent or cleared HPV infection) Implemented HPV testing as primary screen in May 2023 |
Yes | HPV-positive for other high-risk subtypes, not 16, 18, 45 | ✓ | Triage in participants ≥30 with ASC-US and no previous abnormal Pap
Further HPV testing on request by PCP for treatment/exit management (e.g., repeat testing at 12 months to confirm persistent or cleared HPV infection) Implemented HPV testing as primary screen in May 2023 |
NL | ✓ | Triage in participants ≥30 with ASC-US |
ON: * While in use in some cases, cytology screening alone is the current screening test recommended by the program. HPV testing with cytology triage is currently under development as part of planning for the implementation of HPV testing in Ontario.
Abbreviations:
- ASC-US: atypical squamous cells of undetermined significance
- LSIL: low-grade squamous intraepithelial lesion
- HSIL: high-grade squamous intraepithelial lesion