Cervical cancer screening in Canada, 2026
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 cancer 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.
Six jurisdictions have partially or fully implemented jurisdiction-wide HPV testing. Additional jurisdictions 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 | ✓ | Implemented province-wide | ||||
| AB | ✓ Planning for provincial transitions to other age groups and HPV self-sampling implementation | ✓ Implemented HPV primary screening for age cohort 50-69 years in November 2025 | ✓ | |||
| SK | ✓ | ✓ | ||||
| MB | ✓ | ✓ | ||||
| ON | ✓ | ✓* | ||||
| QC | ✓ 13/18 regions have implemented HPV primary screening on an opportunistic basis. However, no organized screening program with established funding has been formally implemented. | |||||
| NB | ✓* | ✓* | ||||
| NS | ✓ | ✓ | ||||
| PE* | ✓ Implemented change in May 2023 | ✓ | ||||
| NL | ✓ | ✓ Spring 2026 |
Data current as of February 2026.
*Footnotes:
YT: HPV primary will be made available, but in the absence of an organized program, YT can only offer this through a primary care provider at this time. YT is working towards offering home self-sampling.
NT: A pilot program to mail out self-sampling screening kits is in progress.
ON: In March 2025, Ontario launched self-collected HPV testing with a small number of primary care clinics across the province and will expand access through a phased approach to implementation.
NB: Implementation of the phased-in transition from cytology based testing (Pap) to HPV primary screening, with an option for self-sampling planned to begin in 2026.
PE: Self screening is available at Provincial Cervical Screening Clinics, and in many Medical Homes and health services across PEI.
NL: NL is planning a phased in transition to HPV primary screening in Spring 2026.
Definitions
Levels of implementation status (to show incremental implementation progress by jurisdiction):
- No current HPV primary screening activities: “Status Quo” cervical cancer 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
Jurisdictions continue to work 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 | Transitioned to HPV primary self-sample screening completed April 2025. Currently piloting an HPV self-sample mail out kit project. |
| NU | Development of the new guidelines and planning for pilot |
| BC | Transition to HPV primary screening started January 2024* |
| AB |
|
| SK |
|
| MB | Ongoing activities planning for transition to HPV primary testing
|
| ON |
|
| QC |
|
| NB | Planning activities include:
|
| NS |
|
| PE |
|
| NL |
|
Data are current as of February 2026.
*Footnotes:
YT: YT is actively exploring strategic partnerships to develop or offer at-home HPV self-screening options.
BC: BC is considering the following self-sampling and lab assays: Copan FLOQSwabs®, eluded into PreservCyt, COBAS instrument.
PE: PE self-sampling and lab assays in use: Self-vaginal FLOQSwabs® with breakpoint (COPAN HPC146R03 Date 2021.01 — product description), and BD Onclarity™ HPV Assay.
Current uses of HPV testing
HPV testing is used for primary screening, triage and/or post treatment.
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 |
Data are current as of October 2023, except for Ontario which is current as of March 2024. Data for Nunavut and Yukon presented here is from data collected for the 2021-2022 E-Scan. For the most up-to-date information, please reference each jurisdiction’s program website.
Use of HPV testing after an abnormal cervical cancer 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* | ✓
Implemented HPV testing as primary screen, April 2025 |
N/A – HPV primary screening
Pap screening only if indicated by gynecologist High risk HPV positive other (non genotype 16/18/31/45) Pap required to test forASC-US/LSIL, ASC-H/HSIL, AGC, or AIS |
HPV completed as primary screen
Pap completed when indicated |
✓
From HPV primary testing prior to Pap |
Negative HPV test: Repeat HPV screening in 3 years
Positive HPV test:
Unsatisfactory HPV test: Repeat HPV screening in 3 months |
|
| NU | ✓ | Pap with HPV reflex testing for participants aged ≥30 years with ASCUS | ||||
| BC | ✓ | For any abnormal cytology | ✓ | For any LBC sample when HPV is detected | ✓
For 16 and 18 |
All samples are assessed for HPV 16 and 18 |
| AB | ✓ | Pap with HPV reflex testing for participants with ASC-US aged ≥30 and LSIL aged ≥50 | HPV positive results for 16 and 18 and “Other” | ✓ | ||
| SK | ✓ | Pap with HPV reflex testing for participants with ASC-US aged ≥30 and LSIL aged ≥50 in 2023* | ||||
| MB | ✓ | Pap with HPV reflex testing for participants with ASC-US aged ≥30 and LSIL aged ≥50 | ✓
HPV is reported in 16, 18, and ‘other’ |
|||
| ON | ✓ | HPV primary screening with reflex cytology implemented March 2025 | ✓
HPV is reported as type 16, 18/45 or other-high risk types. |
Partial genotyping is performed on all HPV-positive results
HPV types 16 and 18/45 are referred directly to colposcopy |
||
| QC | ✓ For regions where HPV primary screening with liquid-based cytology has been rolled out, follow-up on test results occurs in accordance with the INESSS algorithm for individuals aged 25–65 with a cervix: Investigation, treatment and follow-up algorithms | See the INESSS algorithm: Investigation, treatment and follow-up algorithms | ✓ 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 aged ≥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 | Yes | HPV OHR (other high-risk types – not 16, 18, 45) | ✓
DNA genotyping |
If HPV OHR (not 16/18/45) and LBC (Pap) test is NEGATIVE, ASCUS or LSIL -> repeat HPV test in 12 months
If HPV OHR (not 16/18/45) and LBC (Pap) test is ASC-H, HSIL or worse -> refer to colposcopy |
||
| NL | ✓ | All abnormal cytology beginning Spring 2026 | HPV (+) 16/18 and other
Implemented Spring 2026 |
Planning for potential options |
Data are current as of February 2026.
*Footnotes:
YT: YT follows BC algorithm
NT: HPV primary, Pap indicated for high risk HPV positive individuals with other genotypes (not 16/18/31/45)
SK: Implemented HPV reflex (triage) testing of cytology results in 2023
Abbreviations:
- ASC-US: atypical squamous cells of undetermined significance
- LSIL: low-grade squamous intraepithelial lesion
- HSIL: high-grade squamous intraepithelial lesion