According to the National Cancer Institute, cancer is a “term for diseases in which abnormal cells divide without
control and can invade nearby tissues. Cancer cells can also spread to other parts of the body through the blood and
lymph systems”. While prostate cancer generally fits these criterion, there may be an exception to this rule in
the case of Gleason Score 6, also known as Grade Group 1, prostate cancer.
Unlike Gleason Score 7-10 prostate
cancer that can invade, spread and can result in death, Gleason 6 prostate cancer is a well-differentiated cancer that
is not known to locally invade or metastasize.1 Many men develop prostate cancer as they age
with many diagnosed with age-related Gleason 6 cancer that will have no impact on their life. The term “autopsy
cancer” has been used to describe the presence of any prostate cancer in older men who die from other causes and were
never diagnosed with prostate cancer. One of the arguments against prostate cancer screening is the over-diagnosis of
these non-life threatening cancers that may result in unnecessary treatment once detected.
The discussion
concerning proposed nomenclature change to remove the word cancer in Gleason Score 6 prostate cancer has been with us
for over 10 years.1,2 Several changes in the United States have rekindled this debate. A large
number of men today, with some estimates of up to 70% of those newly diagnosed, are found to have Gleason 6
cancers.3 Based on the non-aggressive nature of this cancer, active surveillance is now
commonly practiced as opposed to active treatment. However, current protocols for active surveillance still require
follow up testing, imaging and biopsy all of which may be unnecessary. In terms of Gleason 6 disease, this follow up
is often driven by the fear that a more aggressive cancer could be missed. The man with non-life threatening Gleason 6
disease is now labeled as having been diagnosed with cancer, a life changing event.
As medical knowledge advances
across many cancer types, the concept of reclassifying malignancies has taken place in other diseases. Some types of
melanoma, cervical cancer, breast cancer, thyroid cancer and others have been relabeled without the ominous “cancer”
moniker. Many of these reclassified tumor subtypes relate to the fact there is a high prevalence of indolent disease
in many healthy individuals. Such is the case for Gleason 6 prostate cancer as well.
We have seen changes in both
directions in the field of urologic oncology, towards and away from calling certain tumors “cancer”. Before the advent
of CT imaging, renal tumors less than 2 cm were often called renal adenomas because they did not spread beyond the
kidney. During surgical procedures on the kidney, these small tumors were often noted as incidental findings. Today
these are histologically and molecularly characterized as small renal cell carcinomas.
Another example of
reclassification of malignancy in urology is in bladder cancer. In the early 2000’s, the WHO/ International Society of
Urological Pathology (ISUP) consensus changed the nomenclature of a specific malignant bladder tumor. The group noted
that certain bladder cancers had a negligible risk of progression and defined a new entity now known as papillary
urothelial neoplasm of low malignant potential or PUNLMP.
Some alternate names for Gleason 6 prostate cancer have
been proposed to avoid the “c” word. These include
IDLE for indolent lesion of epithelial origin, or INERRT for
indolent neoplasm rarely requiring treatment.1,2
As this debate of renaming Gleason 6 prostate cancer
continues, a word of caution is needed. First, the renaming discussion only relates to the identification of pure
Gleason 6 cancer without any other associated higher-grade disease. Next, does a Gleason 6 prostate cancer in a
50-year-old male have the same implications as the same diagnosis in an 80-year-old? Does germ line testing for
prostate cancer associated mutated genes have an impact? Is there a difference between one biopsy core of Gleason 6
cancer and multiple Gleason 6 cores from the same biopsy session? Lastly, are there additional criteria that should be
met to make a renamed non-life threatening cancer subtype valid without calling it a cancer such as a defined PSA
level, MRI findings or a molecular marker?
Current advocates of renaming Gleason 6 prostate cancer have pointed
out, such as Eggener and associates, the diagnosis of even a non-life threatening cancer in a patient can have
devastating consequences on the patient and their family.4 In the case of the diagnosis of
prostate cancer, these include an increased risk of depression and suicide, insurance coverage implications,
additional interventions, and higher health care costs. All of these negative consequences can also come from the
diagnosis of a Gleason 6 prostate cancer that is unlikely to harm a man in his lifetime. As stated by Dr. Eggener ”…if
Gleason 6 cancer is biologically inert, the labeling is not…”.
Leonard G. Gomella, MD
Editor-in-Chief
Philadelphia, PA, USA
1. Carter HB, Partin AW, Walsh PC et al. Gleason Score 6 adenocarcinoma: Should it be labeled as cancer? J Clin Oncol 2012;30(35):4294-4296.
2. Esserman L, Shieh Y, Thompson I. Rethinking screening for breast cancer and prostate cancer. JAMA 2009;302(15):1685-1692.
3. Islami F, Ward EM, Sung H et al. Annual report to the nation on the status of cancer, Part 1: National Cancer Statistics. J Natl Cancer Inst
2021;113(12):1648-1669.
4. Eggener SE, Berlin A, Vickers AJ et al. Low-grade prostate cancer: time to stop calling it cancer. J Clin Oncol 2022;Apr 18:JCO2200123.
Online ahead of print.
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© The Canadian Journal of Urology™; 29(3); June 2022