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Thursday, March 28, 2013

Success with Adjuvant PVNS Radiation Treatment, Story


Why Did I Choose To Have Adjuvant PVNS Radiation Treatment

 I had my first "open knee synovectomy" for diffuse Pigmented Villonodular Synovitis on Dec 14, 2011. My oncologist orthopedic surgeon assured me that she had removed all visible signs of the pvns - which is a very aggressive nonmalignant tumor of joints with synovial tissue such as the knees, hips, elbows, ankles etc.  She emphasized that it only takes a single PVNS cell to reseed and begin the process of tumor growth. I was uncomfortable with the variable yet high recurrence rate of up to  60%, even when all visible tumor had been excised.

I read many research studies comparing the short and long term statistics of  chemotherapy, and radiation therapy as an adjuvant treatment for diffuse pvns.  I found that I wasn't a candidate for chemotherapy due to having polyneuropathy, so the only other treatment available in my case was external radiation treatment. 

Radiology Oncologist Assessment

I constructed a {list of questions} to ask my radiology oncologist, at my consultation appointment. The answers to these questions are case specific, but the following is in general.

In my case, pvns recurrence after an open synovectomy was estimated to be in the high 40 percentile. Open synovectomy with adjuvant external radiation would reduce my recurrence rate to the mid-teen percentile. 

I was concerned about rumors of external radiation treatment dangers such as the possibility of forming a secondary cancer. I was assured by my radiology oncologist and years worth of research, that this fear was totally unfounded. There has never been a reported case of secondary cancer from PVNS radiation treatment. 

The level of risk as explained by my radiology oncologist..."you are much more likely to suffer from a serious adverse reaction to anesthesia during surgery than to experience a secondary malignancy caused by radiation treatment for pvns." There are possible complications and risks associated with all treatments, including repeated surgeries... so the risks and benefits must be carefully evaluated.
I'm neither for or against radiation or chemo in the treatment of PVNS, because they both have a place in it's treatment with their own unique risks. Recent studies are showing that they have nearly the same effectiveness. However there are additional concerns that should seriously be looked at when using a systemic drug on a disease that is confined to one joint. Unfortunately, I've found that many of the physician promoting chemotherapy agents have some type of association or financial interest in promoting chemotherapy drugs and their trials. A consultation with an oncologist or radiology oncologist will be able to provide you with a personal risk for these adjuvant treatments.

Radiation Therapy Experience

On my seventh week post synovectomy, I decided to have 18 external radiation treatments of 200 greys each, Monday - Friday for 3 1/2 weeks.  This is the normal radiation dose used by most physicians for the treatment of diffuse pvns in the knee. 

Second week of radiation treatment: I've had four treatments, flexion range of motion (ROM) 84º, extension is normal, pain 3-4 with increased activity, increasing fatigue and swelling.

Third week: I've had nine treatments, flexion ROM 84º, I'm feeling the cumulative effects, pain 3-5, slight burning sensation, vice grip feeling, heat at site, darkening of skin, swelling, fatigue is overwhelming. I had to back off on physical therapy due to the swelling interfering with proper positioning of my knee during RT delivery. Compression, elevation, ice, and medication is helping to control the side effects.  

Fourth week: I've had 14 treatments, flexion ROM 74º. I'm finding that it's a challenge to keep my attitude in check as the fatigue drains my ability to keep pace with my normal daily activities. I'm told that the fatigue will pass as my body recovers from the treatment. 

Fifth week: I've had 18 treatments and I'm now finished with radiation. Flexion ROM 81º It is now 12 weeks post op and I have physical therapy 3-4 days a week to work on increasing my ROM.

16 wk post synovectomy, 4 wks post radiation therapy and my flexion ROM has been stuck at 81 degrees for 2 wks. Prior to RT my ROM was at 84 degrees. I lost 10 degrees during RT= 74 degrees, regained 7 degrees the 1st 2 wks post RT

18 week post op my flexion ROM is stuck at 81º and I am now having  a knee manipulation under anesthesia followed up by aggressive physical therapy. This procedure worked well in breaking up scar tissue and my flexion ROM is now at 113º.

PVNS and Pain Free 15 months post synovectomy, RT, manipulation, false pvns recurrence and arthroscopy, several months of physical therapy, partial knee replacement with flexion ROM now at 118º. Normal knee flexion is 130º

In summary, I feel that I've attacked this disease as aggressively as possible, and only time will tell if my choices were worth the risks. I know that the radiation treatment damaged my knee in the sense that it caused additional scar tissue. Although, surgery also caused scar tissue. Hopefully I will remain in remission, and I'll  have MRIs done every six months and eventually yearly for the rest of my life. The partial knee replacement will make the MRIs even more difficult to read, but it was necessary since the pvns and treatments left me with painful bone on bone arthritis.  

Making The Right Decision

I will be very cautious in approaching any surgery for a possible recurrence of pvns, since I've already had one false positive recurrence on the MRI reading (scar tissue). One year after my synovectomy, I had an arthroscope which ruled out a pvns recurrence, my meniscus was repaired, and that's when they discovered that I needed a knee replacement. 

Nearly a year after making my decision to have external radiation treatment after my first synovectomy....I'm seeing a trend toward more aggressive treatment on the onset of pvns and not waiting until there has been a recurrence. I honestly don't know if this is a good thing or not. Once again only time will tell. Obviously my thoughts were to throw every weapon  at it, to kill it off on the initial assault, and so far it has worked for me. I can't say this is the right route for others because there are just too many variables in each case, and I'm not a doctor. The information that I share, are links to empirical studies, otherwise it's just my personal opinion based on my experience, and it should not be taken as medical advice. 


When I was under the impression that there was a recurrence of the pvns...I questioned whether I made right decision to be treated with radiation. However, I feel strongly that it was worth decreasing my recurrence rates by having the radiation treatment, and I would do it again. Only time will tell if I will remain in remission. One year after my open synovectomy I had a partial knee replacement.  Nearly three years later, I remain pvns and pain free, but I will never know for sure if RT has played a role in my positive outcome or not. Statistics point to yes, but there are others that have had less than satisfactory outcomes. 


7 comments:

  1. Dear CJ,

    I am contacting you about an important PVNS and GCT-TS study that may advance research! PVNS and GCT-TS tumors are rare and input from participants with these tumors is very important.

    We are conducting this interview study so that we can learn from you and better understand the symptoms of PVNS or GCT-TS and the impact that these symptoms may have on your life.

    You may be eligible to participate in the study if;
    • You are 18 years of age and older
    • You are able to read and speak English
    • You have or had a PVNS or GCT-TS tumor and this can be clinically confirmed by your physician

    The study involves an interview lasting about 60-90 minutes, no treatments are given as part of this study. If you are eligible and participate in this study you will receive $100 for your time.

    If you would like more information about the study, please call 866-766-2344 and ask for Kelly McQuarrie or Adam Weinberger.

    Please feel free to share this invitation with others that you may know who have PVNS or GCT-TS who may be interested in participating in the study.

    Thank you for considering this important research study!

    Adam Weinberger
    Research Assistant
    Outcomes Research
    United BioSource Corporation
    7101 Wisconsin Avenue, Suite 600
    Bethesda, MD 20814
    Phone: +1 240 235 2502 ext. 62502
    Cell: +1 301 219 8683
    Fax: +1 301 654 9864
    Email: adam.weinberger@unitedbiosource.com
    www.unitedbiosource.com

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  2. Thank you for this blog. I am going through treatment for PVNS right now. So far I've had an arthroscopic synovectomy and removal of a portion of my gastrocnemius muscle because the tumor had spread. It has been difficult. I had my first MRI 2 weeks after a c-section and then surgery 10 weeks later. My Dr has talked about manipulation under anesthesia if my ROM is still limited. It is nice to hear someone who has a positive outcome.

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  3. Thanks for sharing the post. It was really helpful.

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  4. Thank you for sharing your experience. My daughter just had an arthroscopic synovectomy, which failed to bring any improvement. We'll be going on to an open synovectomy soon. We'll both be reading up on your experiences with this. Thanks again!

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    1. You're very welcome. I'm so sorry to hear of your daughter troubles with PVNS. Thankfully, I've been PVNS free for nearly 5 1/2 years. As you know I decided upon an open synovectomy , followed with external radiation. Between age, PVNS, surgery and radiation, my cartilage was destroyed in my knee, so I had a partial knee replacement. Since that point, I'm back to life as usual and I haven't had any more issues.

      I know that the PVNS could come back at any point, but for now I'm enjoying not having any knee pain or problems. I really hope that your daughter will a stellar outcome. It can be disheartening reading about the many failed cases, but remember that the successes usually don't keep writing about PVNS when they're cured or in remission.

      There is life after PVNS, and I wish your family the very best. It's always great to hear from people utilizing this site. Thank you for your kind comments.

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  5. I would like to participate in the study

    ReplyDelete