NEWLY DIAGNOSED?
Glossary of Terms for Men Considering Active Surveillance
A plain-language guide for men who are newly diagnosed with prostate cancer
Being newly diagnosed can feel like learning a whole new language. This glossary explains common words and phrases you may hear as you begin Active Surveillance — or decide whether it is the right approach for you.
Active Surveillance is a research-based, evidence-supported approach to managing prostate cancer. For men with low-risk localized prostate cancer, it is not just an option — it is the preferred management approach and standard of care in major guidelines. Research and guidelines also support Active Surveillance for some men with Grade Group 2 / Gleason 3+4 disease.
This glossary is designed to help you better understand the terms you may hear, read your results with more confidence, and feel more prepared for conversations with your healthcare team.
How to use this glossary
Use this glossary to quickly understand words you may see in biopsy reports, MRI reports, PSA results, or conversations with your doctor. You can search by term, abbreviation, or phrase, browse by category, or open only the sections you need.
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Most useful terms for Active Surveillance
Start with these terms if you are newly diagnosed, reviewing test results, or trying to understand whether Active Surveillance may fit your situation.
Terms worth asking your doctor about
Some terms do not mean you should panic, but they may be important to discuss because they can affect whether Active Surveillance is still a safe fit.
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Aggressive cancer
Cancer that is more likely to grow, spread, or require treatment sooner. One of the main goals of Active Surveillance is to watch for signs that a cancer may be acting more aggressively than it first appeared.
Active Surveillance is designed for cancers that appear slow-growing. Signs of more aggressive disease are one of the main reasons doctors may recommend closer testing or treatment.
Cancer grade
A way of describing how abnormal the cancer cells look under the microscope. Lower-grade cancers usually grow more slowly than higher-grade cancers.
Cancer stage
A way of describing where the cancer is located and whether it has spread. Men on Active Surveillance usually have localized prostate cancer.
Clinical stage
A way of describing how far the cancer appears to have grown based on exams, imaging, and biopsy information. You may hear terms such as T1c or T2a, which help describe whether the cancer seems confined to the prostate. These terms can be part of deciding whether Active Surveillance is a reasonable option.
Active Surveillance is usually considered when the cancer appears confined to the prostate. Clinical stage helps show whether that still seems true.
Confirmatory biopsy
A follow-up biopsy done after diagnosis to confirm the original findings and make sure a more aggressive cancer was not missed. This can be an important part of deciding whether Active Surveillance is a safe option.
A confirmatory biopsy can help make sure the cancer truly fits a lower-risk picture before you settle into long-term monitoring.
Favorable intermediate-risk prostate cancer
A group between low-risk and higher-risk prostate cancer. Some men in this category may still discuss Active Surveillance with their doctors, depending on the details of their biopsy, PSA, MRI, and overall health.
Some men in this group may still be candidates for Active Surveillance, but the decision is usually more individualized and often needs closer review.
Genitourinary pathologist
A pathologist who specializes in cancers of the urinary and male reproductive systems, including prostate cancer. Some men seek a second review from this type of specialist when treatment decisions feel close or uncertain.
Gleason score
A system used to describe how prostate cancer cells look under the microscope. It helps estimate how aggressive the cancer may be.
Grade Group
A newer grading system for prostate cancer, from 1 to 5. Grade Group 1 is the least aggressive-looking cancer and is the group most often associated with Active Surveillance.
Grade Group is one of the most important parts of deciding whether Active Surveillance is a safe fit. Grade Group 1 most often supports Active Surveillance, while higher groups raise more concern.
What is my Grade Group, and how does it affect whether Active Surveillance is a good fit?
Intermediate-risk prostate cancer
Prostate cancer that falls between low-risk and high-risk. Some men with favorable intermediate-risk disease may still be considered for Active Surveillance, depending on their situation.
Localized prostate cancer
Cancer that appears to be confined to the prostate and has not spread elsewhere. This is the setting in which Active Surveillance may be considered.
Low-risk prostate cancer
Prostate cancer that appears unlikely to grow or spread quickly based on PSA, biopsy findings, and other test results. Many men offered Active Surveillance fall into this group.
Pathologist
A doctor who examines biopsy tissue under the microscope and determines whether cancer is present and how aggressive it looks.
Risk category
A general way of describing how likely a cancer is to grow or spread. Common categories include low-risk, intermediate-risk, and high-risk.
Upgrade / upgrading
When repeat testing shows the cancer is more aggressive than first thought. This can be one reason to move from Active Surveillance to treatment.
One goal of Active Surveillance is to catch any meaningful change early. Upgrading is one of the main reasons a doctor may recommend changing the plan.
What changed in my results, and does it mean treatment is now recommended?
Active Surveillance (AS)
A way of managing low-risk or favorable prostate cancer with careful monitoring instead of immediate treatment. The aim is to avoid or delay treatment unless the cancer changes. Follow-up usually includes PSA tests, clinical exams, repeat biopsy, and often MRI.
Baseline PSA
Your first recorded PSA result, used as a starting point for comparing future PSA tests over time.
Doctors often learn more from how your PSA changes over time than from any single PSA number.
Biomarker test
A test that adds information about how likely a prostate cancer is to be more aggressive or need treatment. It is usually considered alongside MRI, biopsy results, PSA, and other clinical information.
Biopsy
A procedure in which small pieces of prostate tissue are taken and examined under a microscope.
Biparametric MRI (bpMRI)
A shorter type of prostate MRI that uses fewer imaging sequences than a multiparametric MRI and does not use contrast dye. In some centres it may be used to assess the prostate while reducing scan time, although mpMRI remains the more established approach in prostate imaging.
Confirmatory testing
Follow-up testing done after diagnosis to make sure the cancer is truly low risk before settling into Active Surveillance. This may include repeat PSA testing, repeat imaging, repeat biopsy, or selected biomarker or genomic tests.
Confirmatory testing helps reduce the chance that a higher-risk cancer was missed at the start.
Digital rectal exam (DRE)
A physical exam in which a doctor gently feels the prostate through the rectum to check for changes such as firmness or lumps.
Genetic testing
Testing for inherited gene changes that may affect prostate cancer risk or aggressiveness. It may be discussed more often when there is a strong family history or cancer at a younger age.
Genomic test
A test that looks at the biology of the cancer itself to help estimate risk and support decision-making. These tests can add information, but they do not replace biopsy, MRI, or follow-up monitoring.
Imaging
Scans or pictures of the body used to look more closely at the prostate and surrounding areas.
Magnetic Resonance Imaging (MRI)
A scan that produces detailed images of the prostate. It can help identify suspicious areas and guide biopsies.
micro-Ultrasound (microUS)
A newer, high-resolution ultrasound that can help doctors see suspicious areas in real time and guide a targeted biopsy during the same visit. In some centres, it is being used as another imaging option before biopsy or during follow-up.
Monitoring
The regular follow-up used during Active Surveillance. This often includes PSA tests, MRI scans, doctor visits, and repeat biopsies.
Active Surveillance is not “doing nothing.” Monitoring is the active part of the plan and helps catch changes early if they happen.
Monitoring schedule
The plan for PSA tests, MRI scans, doctor visits, and biopsies during Active Surveillance. Exact timing varies, but the schedule helps make sure changes are caught early if they happen.
A clear follow-up schedule helps you know what comes next and makes it easier to stay on track with monitoring.
Multiparametric MRI (mpMRI)
A more detailed kind of prostate MRI that combines different types of images to help assess suspicious areas. It is commonly used in Active Surveillance to help guide monitoring and biopsy decisions.
PI-RADS
A scoring system used by radiologists to describe how suspicious an area looks on a prostate MRI. It can help decide whether a biopsy or closer follow-up may be needed.
Higher PI-RADS scores can make doctors more concerned that a more significant cancer may be present or developing.
What is my PI-RADS score, and does it suggest biopsy or closer follow-up?
PRI-MUS
A scoring system used with micro-ultrasound to describe how suspicious an area looks. Like PI-RADS on MRI, it helps doctors judge whether an area may need closer attention or biopsy.
PRI-MUS can help show whether an area looks reassuring or whether it may need targeted biopsy or closer follow-up.
Prostate-Specific Antigen (PSA)
A protein made by the prostate that can be measured with a blood test. PSA levels can rise for many reasons, not just cancer.
Prostate volume
The size of the prostate, usually measured on imaging. This helps doctors calculate PSA density and put a PSA result into better context.
Prostate volume helps make PSA density possible, and PSA density is one of the more useful numbers in Active Surveillance.
PSA density
The PSA level in relation to the size of the prostate. This can be especially helpful in Active Surveillance because it may give a clearer sense of whether a PSA result is reassuring or more concerning. A lower PSA density can sometimes support a more reassuring picture when it is considered together with MRI and biopsy findings.
PSA density is one of the most useful ways to add context to a PSA result, especially when deciding whether the overall picture still looks low risk.
What is my PSA density, and how does it affect whether Active Surveillance still looks appropriate for me?
PSA kinetics
How PSA changes over time, such as how quickly it rises. During Active Surveillance, PSA changes are usually looked at alongside MRI findings, biopsy results, and other information rather than on their own.
A PSA trend may lead to closer review, but doctors usually interpret it together with imaging and biopsy results rather than by itself.
PSA retest / repeat PSA
A repeat PSA blood test done to make sure an elevated result is real and not caused by something temporary, such as infection, recent ejaculation, biking, or a recent procedure.
Repeating a PSA can help avoid making a big decision based on a number that may not reflect your usual PSA level.
PSMA PET scan
A scan that looks for prostate cancer using a tracer that attaches to a protein called PSMA. It is most often used when doctors are concerned that cancer may have spread or returned after treatment, so it is not usually part of standard Active Surveillance.
Repeat biopsy
A biopsy done during follow-up to see whether the cancer still appears low-risk or has changed. This can help show whether Active Surveillance continues to be a safe choice.
Repeat biopsy helps confirm that the cancer still fits the lower-risk picture that made Active Surveillance reasonable in the first place.
Systematic biopsy
A biopsy that samples several standard areas of the prostate rather than aiming at one specific suspicious spot. It is sometimes described as a standard biopsy.
This approach can still be helpful, especially when imaging does not show a clear target, but it may miss some cancers that a targeted biopsy can better sample.
Targeted biopsy
A biopsy aimed directly at a suspicious area seen on MRI or micro-ultrasound. This can help doctors sample the part of the prostate that looks most concerning.
Targeted biopsy can make the results more informative by focusing on the area most likely to contain higher-grade disease.
Transperineal biopsy (TP biopsy)
A biopsy taken through the skin between the scrotum and anus rather than through the rectum. In Active Surveillance, this approach is often discussed because it may lower infection risk and can sometimes sample the prostate more thoroughly, including areas toward the front of the gland.
For men who need repeat biopsies over time, the lower infection risk and more complete sampling can be important.
Transrectal biopsy
A biopsy taken through the rectum, often using ultrasound guidance. This has been widely used for many years, though some centres now prefer the transperineal approach because of infection concerns.
Transrectal ultrasound (TRUS)
An ultrasound done through the rectum, often used during prostate biopsy.
Ultrasound
An imaging method that uses sound waves to create pictures. It is commonly used during prostate biopsies.
These are some of the words that often show up in MRI reports, biopsy reports, and follow-up conversations. They can be especially helpful when you are trying to understand what your doctor means by “reassuring,” “needs closer follow-up,” or “may no longer fit Active Surveillance.”
Red-flag terms to know
Some words deserve a follow-up question because they may suggest a higher chance that the cancer is more aggressive than it first appeared.
- Concerning imaging change
- Cribriform pattern
- Higher-volume disease
- IDC-P
- Upgrade / upgrading
Seeing one of these terms does not mean you should panic. It usually means it is worth asking your doctor how that finding affects whether Active Surveillance is still a safe fit.
Biopsy core
One small sample of prostate tissue taken during a biopsy.
The number of cores taken and the number that contain cancer help doctors understand how much cancer was found.
Concerning imaging change
A change on MRI or micro-ultrasound that makes an area look more suspicious than before. This might include a new lesion, growth of an existing lesion, or a higher imaging score.
Changes on imaging are often reviewed alongside PSA density and biopsy findings when deciding whether more testing is needed.
What changed on imaging, and does it mean I need biopsy or closer follow-up?
Cribriform pattern
A growth pattern seen on biopsy that can suggest the cancer may behave more aggressively than the Grade Group alone might suggest.
When this pattern is present, especially in a larger amount, many doctors become more cautious about recommending or continuing Active Surveillance.
Does the amount or type of cribriform pattern change whether Active Surveillance is still recommended?
Higher-volume disease
A general way of saying that cancer was found in more of the biopsy samples, in a greater percentage of a sample, or in a broader area of the prostate than expected.
More cancer found on biopsy can shift the conversation from lower-risk to more concerning disease.
Intraductal carcinoma of the prostate (IDC-P)
A biopsy finding that is usually treated as a warning sign for more aggressive disease elsewhere in the prostate.
IDC-P often argues strongly against Active Surveillance and usually leads to closer review and discussion of treatment.
Was IDC-P found in my biopsy, and what does that mean for my options?
Lesion
An area on imaging that looks different from the surrounding prostate tissue and may need closer attention.
The size, location, and imaging score of a lesion can help guide whether a targeted biopsy or closer follow-up is needed.
Pattern 4
A more aggressive-looking prostate cancer pattern seen under the microscope. In biopsy reports, even a small amount of pattern 4 can matter.
Grade Group 2 disease often means Gleason 3+4, so doctors pay attention to how much pattern 4 is present, not just whether it is present.
How much pattern 4 was found, and does it include any concerning patterns such as cribriform?
Pattern 5
A high-grade prostate cancer pattern that looks more concerning under the microscope and is associated with more aggressive disease.
Pattern 5 is generally not compatible with Active Surveillance.
Was any pattern 5 found, and what treatment discussion does that lead to?
Positive core
A biopsy core that contains cancer.
The number of positive cores can help doctors judge how much cancer is present and whether the findings still look lower risk.
Progression
Evidence that the cancer may be changing over time, such as a higher grade on biopsy, more concerning imaging, or a worrisome overall pattern.
Progression is one of the main reasons doctors may recommend more testing or a move to treatment.
Candidate for Active Surveillance
A general way of saying that, based on the test results and the overall picture, Active Surveillance may be a reasonable and safe option to discuss. Being a candidate does not mean every doctor will make the same recommendation, but it means the option is worth reviewing carefully.
This phrase often means your results are reassuring enough that monitoring is worth serious consideration, not that treatment must happen right away.
Clinical trial
A research study that tests a medical approach, test, or monitoring strategy. Some men on Active Surveillance choose to participate in studies related to imaging, biomarkers, monitoring, or quality of life.
Family history
The pattern of cancer in your close relatives, such as a father, brother, or several family members with prostate, breast, ovarian, or pancreatic cancer. Family history can affect how doctors think about inherited risk and whether extra testing may help.
A stronger family history may lead to a more cautious discussion, additional testing, or closer monitoring.
Life expectancy
An estimate of how long a person is likely to live based on age and overall health. In prostate cancer care, it can help guide whether Active Surveillance, watchful waiting, or treatment makes the most sense.
This helps put the risks and benefits of monitoring versus treatment into context over the years ahead.
Overtreatment
Treatment that may not have been necessary, especially when a cancer was unlikely to cause harm. One of the main goals of Active Surveillance is to reduce overtreatment.
Pathology review
A second look at biopsy slides by another pathologist, often to confirm the grade and check for important features that may affect treatment decisions. Some men find this especially helpful when their case seems close to the line between Active Surveillance and treatment.
A second pathology review can sometimes strengthen confidence in Active Surveillance or identify features that deserve a more cautious plan.
Second opinion
When another doctor reviews your diagnosis or treatment options. This can be helpful when deciding whether Active Surveillance is right for you.
Treatment trigger
A change in results that suggests treatment may now be the safer choice. This may be based on biopsy findings, imaging, PSA-related changes, or a combination of factors.
Knowing your possible treatment triggers can make Active Surveillance feel more concrete and help you understand what changes your care team is watching for.
What specific changes would make you recommend treatment rather than continued monitoring?
Treatment-free interval
The period of time a man remains safely on Active Surveillance without needing treatment. For some men this may be many years, and for others treatment may eventually become the better option if the cancer changes.
This helps explain one of the main benefits of Active Surveillance: safely delaying or avoiding treatment and its side effects for as long as the cancer remains suitable for monitoring.
Watchful waiting
A less intensive approach than Active Surveillance, usually focused on symptom management rather than cure. It is more often considered for men who are older, have other significant health issues, or are unlikely to benefit from repeated testing or curative treatment. This distinction matters because Active Surveillance is meant for careful monitoring with the option of curative treatment later if needed.
Patients often hear these terms used as though they mean the same thing, but they are different. Active Surveillance is a structured monitoring plan with the option of curative treatment later if needed.
Are you recommending Active Surveillance or watchful waiting, and what would the follow-up plan include?
Monitoring and diagnosis
- ASActive Surveillance
- bpMRIBiparametric MRI
- DREDigital Rectal Exam
- GGGrade Group
- GUGenitourinary
- IDC-PIntraductal Carcinoma of the Prostate
- microUSmicro-Ultrasound
- MRIMagnetic Resonance Imaging
- mpMRIMultiparametric MRI
- PI-RADSProstate Imaging Reporting and Data System
- PRI-MUSProstate Risk Identification using Micro-Ultrasound
- PSAProstate-Specific Antigen
- PSMA PETProstate-Specific Membrane Antigen positron emission tomography scan
- TP biopsyTransperineal biopsy
- TRUSTransrectal Ultrasound
Symptoms and daily life
- BPHBenign Prostatic Hyperplasia
- LUTSLower Urinary Tract Symptoms
- QoLQuality of Life