Articles tagged with: Robotic Surgery

24
April
2018

Gleason 3+4 - active surveillance or surgery

Gleason 3+4 - active surveillance or surgery

Can men with intermediate risk prostate cancer go on active surveillance?


Comparison of Pathological and Oncologic Outcomes of Favorable Risk Gleason Score 3 + 4 and Low Risk Gleason Score 6 Prostate Cancer: Considerations for Active Surveillance Journal of Urology, The, 2018-05-01, Volume 199, Issue 5, Pages 1188-1195

Some guidelines (eg. NCCN - National Comprehensive Cancer Network) suggest that men with small amounts of Gleason 4 (these are men with ISUP GG 2) on their biopsy can go onto active surveillance if other factors are suitable. But not much is known about long-term outcomes compared to that in men in the low risk Gleason score 3+3/Grade Group 1 group.

This study looked at the outcomes of both groups, but for men treated with surgery, to see if the cancer outcomes were equivalent. This is a roundabout way of seeing if active surveillance is safe in men in ISUP GG 2.

The findings showed that 94% of low GG1 and 83% of GG2 had prostate cancer that had not spread beyond the prostate. Invasion into the seminal vesicles was present in 2% of GG1 and in 5% of GG2. Cancer in lymph nodes was seen in 0.3% of GG1 abnd 2% of GG2.

The need for further (radiotherapy) treatment in the future was 6% in GG1 versus 12% in GG2. Finally, PSA remained undetectable in 89% of GG1 and 81% of GG2.


Categories: Updates

15
April
2018

The ISUP Groups for prostate cancer

The ISUP Groups for prostate cancer

Grade Group (ISUP Group) as the replacement for Gleason Score


The Gleason score has been ‘replaced’ by the ISUP Group for the scoring of the agressiveness of prostate cancer on biopsy or after radical prostatectomy. See below for a descritpion of the new scoring system:

  • GG 1(GS 3+3 = 6): cancers comprising only individual discrete and well-formed glands.

  • GG 2 (GS 3 + 4 = 7): cancers comprising predominantly discrete and well-formed glands with a lesser component of poorly formed/fused/glomeruloid/cribriform glands.

  • GG 3 (GS 4 + 3 = 7): cancers with predominantly poorly formed/fused/glomeruloid/cribriform glands with a lesser component of discrete and well-formed glands.

  • GG4 (GS4+4=8;3+5=8;5+3=8):cancers comprising only poorly formed/fused/glomeruloid/cribriform glands or tumours with discrete and well-formed glands and lesser component lacking glands, or tumour predominantly lacking glands with a lesser component of discrete and well-formed glands.
  • GG 5 (GS 4+5, 5+4 and 5+5): cancers without gland/luminal formation or with necrosis, with or without poorly formed/fused/glomeruloid/cribriform glands.

Categories: Updates

14
April
2018

The use of PSMA PET/CT for men who have a measurable PSA after radical prostatectomy

The use of PSMA PET/CT for men who have a measurable PSA after radical prostatectomy

The use of PSMA PET/CT for men who have a measurable PSA after radical prostatectomy


PSMA after radical prostatectomy

“Efficacy, Predictive Factors, and Prediction Nomograms for 68Ga-labeled Prostate-specific Membrane Antigen–ligand Positron-emission Tomography/Computed Tomography in Early Biochemical Recurrent Prostate Cancer After Radical Prostatectomy”. European Urology Volume 73, Issue 5, Pages 656–661

In this study, PSMA PET/CT was used to examine men who had measurable PSA readings after radical prostatectomy. Recurrent disease was seen on imaging in 55% of men (74 out of 134) with very low (0.2–0.5 ng/ml) PSA and in 74% (102/138) of men with low (>0.5–1.0 ng/ml) PSA.

Based on these findings it seems reasonable to perform PSMA PET/CT in men with early biochemical recurrence (measurable; PSA) , as it can help direct further treatment decisions. Predictors of a positive scan were PSA, current use of hormone treatment (ADT) and to a lesser extent ISUP grade group (Gleason score).


Categories: Updates

15
April
2018

Active surveillance and prostate biopsies

Active surveillance and prostate biopsies

Active surveillance for prostate cancer – how often do we see no cancer on a second biopsy?


Role of Surveillance Biopsy with No Cancer as a Prognostic Marker for Reclassification: Results from the Canary Prostate Active Surveillance Study. European Urology Volume 73, Issue 5, Pages 706–712

In this study, men on AS for prostate cancer were re-biopsied (surveillance biopsies) as per protocol. On first surveillance biopsy, 32% of men had no cancer, 43% had cancer that was the same ISUP group (Gleason score) as the first biopsy, and 25% had a change in the score on their biopsy.

For those men who had no change or no cancer on the first surveillance biopsy, when they came to their second surveillance biopsy, 38% had no cancer, 44% had the same cancer as originally, and 17% were reclassified. A finding of no cancer on the second surveillance biopsy meant men were less likely to have an upgrading in their cancer in the future. This means that it may be possible to slightly relax the frequency of surveillance in men who have a surveillance biopsy without cancer. It also means that for active surveillance protocols, one size does not fit all, and the frequency of follow up for prostate cancer needs to be tailored for the individual.

If you would like to discuss active surveillance for prostate cancer, please ask you GP to contact Nick Brook and this can be arranged.


Categories: Updates

10
February
2018

Focal prostate cancer treatment may be coming soon

Focal prostate cancer treatment may be coming soon

Focal therapy - prostate cancer treatment for the near future?


What is focal therapy of the prostate?

In some ways, prostate cancer treatment has fallen behind other cancers. Although robotic surgery is a less invasive way of removing the prostate than an open cut, we are still not at the stage of being able to target cancer cells or groups of cells, and leave behind other non-cancerous cells in the prostate. This focused, or focal, treatment could have advantages in that important nearby structures are less at risk of damage compared to an operation to remove the prostate.

One of the issues is that, for some men, prostate cancer can be a multi-focal disease, meaning that it can occur in multiple areas of the prostate. Others may just have one 'index' lesion that needs treating, and these people could be good candidates for focal treatment.

High quality imaging is key

The key is high quality imaging of the prostate. There have been steps in the right direction with the use of multiparametric MRI of the prostate- see here and here.

A well performed mpMRI read by an expert radiologist is a powerful tool in identifying areas of the prostate that need biopsy - see here and here.

Accurate biopsy is very important

If we can have accurate biopsy - see here - and be confident that this is a true representation of the degree of prostate cancer present, then it is just a small step to say that we could apply treatment to a focused area of the prostate to reduce the side effects of treatment for some men. Ask your urologist if he or she offers software fusion biopsy of the prostate.

Potential avenues for focal prostate cancer treatment

Currently, there are various options for development of focal therapy:

  • 1 - focal brachytherapy - see here for more information about brachytherapy - which is essentially just brachytherapy applied to one side of the prostate

  • 2 - High intensity focused ultrasound (HIFU) treatment. This has been used in the past to treat the whole prostate, and results were mixed. Although focal-HIFU is in theory a slightly different approach, a lot of work needs to be done before this could be an accepted treatment

  • 3 - Focal laser ablation using photodynamic treatment. Here a compound is injected, which is taken up by abnormal cells in the prostate. A laser is fired that is specific for the compound, and the laser causes a reaction in the compound that kills the targeted cells. The idea is that normal cells are not affected

  • 4 - Direct laser energy targeting of the abnormal area in the prostate. This is the simplest, most direct and elegant idea - the area that is known to be abnormal and cancerous (from the MRI and subsequent biopsy) is targeted directly by a laser fibre. This approach has been investigated and used by urologists at UCLA in the States, and may hold out promise for the future

Conclusion

As surgical treatments become more refined, we hope that an increasing number of patients will be offered focal treatments. It is important that your urologist is able to discuss and offer a range of treatment. Most important is that the treatment is the right one for you.


Categories: Updates

04
February
2018

Low dose rate (seed) brachytherapy for prostate cancer in men under 60 years

Low dose rate (seed) brachytherapy for prostate cancer in men under 60 years

Low dose rate (seed) brachytherapy for prostate cancer in men under 60 years


What did the study show?

Langley et al. reported (Jan 2018) on the outcomes of men treated with seed implant (LDR) brachytherapy. The study suggests that low-dose-rate brachytherapy is a very effective treatment, with excellent long-term control of prostate cancer in men aged ≤ 60 years at time of treatment.

597 patients with a median age of 57 (range 44-60) years were followed up for a median of 8.9 years (1.5- 17.2 years range of follow up). The 10-year relapse-free survival rates (this means the percentage of men who, at 10 years, have no evidence of recurrent cancer) using the Phoenix definition for biochemical failure were as follows:

  • 95% for low risk prostate cancer
  • 90% for intermediate risk prostate cancer
  • 87% for high-risk prostate cancer

Of the 597 men, only six (1%) died from prostate cancer during follow-up.

Erectile function was preserved in 75% of men who were potent before treatment.

Important points to highlight from the study?

1. These results are excellent. It is interesting to note that in Australia, LDR brachytherapy probably would not be used for high risk prostate cancer.

2. The follow up period is reasonably long, but prostate cancer has a long natural history, which means that it can take many years for it to declare itself if it is going to come back, and therefore it takes a long time to know if treatment has been effective.

3. The median follow-up was 8.9 years, but the calculation of biochemical recurrence (a sign of prostate cancer coming back by a continued rise in PSA) was worked-out from a median follow-up of 5.9 years. As we know with many other studies in cancer, the longer the follow up period, the more men may develop recurrent prostate cancer. This is true of any form of treatment, whether it be radical prostatectomy, radiation or brachytherapy.

4.The rate of prostate cancer mortality is very encouraging, but again, follow-up was relatively short, and recurrences and deaths can occur in the period 10-15 years after treatment.

5. Experience is important in prostate brachytherapy. This study reported excellent dosing of the prostate (how much radiation was delivered to the prostate). This can be measured by something called the D90, which indicates the quality of the seed implant. In this study, these values were excellent. In Adelaide, these figures are very carefully assessed by an expert team of radiation physicists after any seed implant.

6. Because this was not a randomised study, one cannot make any direct comparisons between surgery and brachytherapy, and this is an important discussion for any prostate cancer patient. It is ideal if you can discuss your treatment options with someone who is able to offer you both treatments, or at least work in a practice where both treatments are available. This is likely to reduce any bias in advice given to you.

Summary

These are excellent outcomes for both cancer control and preservation of erectile function. LDR brachytherapy is a very good treatment option for younger (or older) men with prostate cancer. The decision about your treatment needs to be discussed in detail with a urologist who can offer both options for treatment.

Langley SM, Soares R, Uribe J, et al. Long-term oncological outcomes and toxicity in 597 men ≤60 years of age at time of low dose rate brachytherapy for localised prostate cancer. BJU Int 2017

Categories: Updates

Affiliations

Urology Affiliations

Latest Tweets

Contact Us

  • Nick Brook Urology
    Calvary North Adelaide Hospital
    89 Strangways Tce,
    North Adelaide,
    Adelaide SA 5006
  • 08 8267 1424
  • 08 8267 1370