New Australian MonaLisa TouchTM clinical trial

MonaLisa TouchTM (MLT) is a new, non-hormonal
treatment for women with vaginal atrophy (VA).

Vaginal atrophy most commonly occurs after menopause, when
oestrogen levels fall and the walls of the vagina become thinner, drier and may
become inflamed. VA also affectS women who have had breast cancer, where
medications affect oestrogen levels and bring on menopausal symptoms. This
often distressing condition can cause painful burning, itching, dryness,
painful intercourse and pain during urination.

MLT is a type of fractional CO2 laser technology treatment
which involves pin-point laser applications to the vaginal lining. At present,
there is not enough evidence about the effectiveness of MonaLisa TouchTM for
it to be recommended as a medical treatment. It is currently expensive to
access and there is no Medicare rebate available. This
article
provides an interesting overview of fractional CO2 therapy for
vaginal atrophy.

University of NSW Associate Professor Jason Abbott (a gynaecologist
and obstetrician) is currently running a clinical trial in Australia which will
evaluate how effective MonaLisa TouchTM is in treating
postmenopausal VA symptoms in women with a history of breast cancer.

The study is being conducted in Sydney.

You can read more about the trial on our Clinical trials for women who have completed
active treatment
webpage. 

Tagged:
«1

Comments

  • Zoffiel
    Zoffiel Member Posts: 3,372
    Thanks Marianne. I'd register for that but, of course, being out in the sticks in another state I can't. 

    It takes a certain degree of confidence, or desperation, to agree to have ones vagina lasered, but it would be excellent if they had a big enough sample to establish if this treatment works. VA is one of the less recognised side effects of cancer treatment. I'd go to considerable trouble and expense to restore some semblance of my previous sex life if I thought the treatment would work.
  • mum2jj
    mum2jj Member Posts: 4,327
    Shame I live so far away, otherwise would be very interested.
  • MKitty68
    MKitty68 Member Posts: 261
    edited February 2018
    I would also be very interested in being a part of this, however I am in Brisbane, a shame someone here couldn't do the same. 
    In Brisbane these treatments are in the vicinity of $2,000 for the three treatments
  • Deanne
    Deanne Member Posts: 2,163
    edited February 2018
    Yes, I agree @MKitty68. I had to drive to Kedron for treatment from the Sunshine Coast as otherwise there was a waiting list for nearly 6 months locally. It cost $1800 for 3 treatments and gynaecologist reduced her fee to $450 for a further 2 treatments. I am on Femara which caused atrophy within the first 6 months. 
  • Afraser
    Afraser Member Posts: 4,352
    Interesting. Like @zoffiel I am wary about lasering my vagina, but would also like to see some more research done. I too have little doubt that Femara has been instrumental in the problem, which like @Deanne manifested itself within 6 months of starting hormonal treatment. 
  • mum2jj
    mum2jj Member Posts: 4,327
    @Deanne, how well did it work for you? @Afraser I don’t know if Fe area is solely to blame. I am triple neg and can’t take any of those drugs but did do chemo twice in 18mths and have vaginal atrophy. I think the chemopause has a lot to do with it too. 
    Hugs ladies. 
    Paula x
  • Deanne
    Deanne Member Posts: 2,163
    edited February 2018
    It improved things Paula, @mum2jj, but not back to completely normal. I was fine after chemo and for 2 years on Tamoxifen but having ovaries out at 49 and then 6 months on Femara seemed to be the problem for me. It was very sudden.
    Deanne xxx
  • Jane221
    Jane221 Member Posts: 1,193
    Thanks for this Marianne, I'm definitely going to see if I can be involved as this is an issue that plagues me. Jane xx
  • Afraser
    Afraser Member Posts: 4,352
    I was way past the menopause before cancer and before starting Femara - yes, it could be age related, but it's too much of a coincidence that I had no issue whatsoever, including during chemo, before starting Femara and non functional 6 months later!  I accept it as part of the treatment, and have simply worked around it, but It's still one of the side effects that isn't spoken too much about by oncologists and clearly can cause a lot of angst at an already difficult time for many women.
  • mum2jj
    mum2jj Member Posts: 4,327
    edited February 2018
    @Afraser maybe mine was just too much chemo in a short span of time. Who knows, mine was certainly a slower onset than you femera ladies. The only plus side is that being triple neg I can use (reluctantly) vagifem pessaries which have helped with the UTI’s I was plagues with and the dryness. @Deanne are you going to have more treatments ?  I agree it is something never mentioned by my oncologist as a side effect. @Jane221it will be great if you can get involved. Keep us posted as to what’s involved. Maybe I should plan a few more trips to Sydney. 
    Hugs all. 
    Paula x
  • Deanne
    Deanne Member Posts: 2,163
    I hope to keep up with the maintenance treatments @mum2jj. I think it has helped to avoid issues like UTI’s etc. I think that without being on Femara the results would be much better and last longer between treatments. While many women do suffer from these issues who are not on hormonal treatment for bc, the incidence is much higher if you are. I think I read something like 40% compared to 60%. 

     I did discuss my issues with my oncologist but she said pessaries are not something she would want me to try unless the situation was much worse. Then she has had women who use them for short periods of time. I definitely don’t want to compromise my recurrence chances! It seems that the laser treatment is my best option. I think it has helped.
    Deanne xxx
  • Afraser
    Afraser Member Posts: 4,352
    I too was interested (temporarily) in the vagifem pessaries and my oncologist was guardedly OK about trying them, but then I read the list of potential side effects on the product website! As with chemo, I am accustomed to a scary list and recognising this is just a list of possibilities and may never happen, but given existing conditions I went off the idea of using the product fairly quickly. 
  • mum2jj
    mum2jj Member Posts: 4,327
    I hear you both. If my cancer was not triple neg I would not go near them, ha unfortunately said that I don’t know what I would have done as I was getting a UTI every two to three weeks it was an awful time. I wish Mona Lisa was more affordable. Paula x
  • SoldierCrab
    SoldierCrab Member Posts: 3,445
    @Jane221 can you please post this into the Lets talk about Vaginas group ....