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DiscussionAnyone else have Clonal Cytopenia of Undetermined Significance (CCUS)?
Blood Cancers & Disorders | Last Active: Oct 20 2:20pm | Replies (74)Comment receiving replies
Hi @loribmt and @pixiesusan. First, thank you, Lori, for being willing to share your story and for serving as support to those who have blood cancer or their precursors. Having someone who has gotten so sick (then received successful transplantation) as a resource and patient advocate is invaluable. 🙂
@pixiesusan I am so sorry for what you are going through. I agree with @loribmt. Please do not admonish yourself for not understanding what is happening with your body. ITP is an autoimmune cause of low platelets. I assume this is why you may have fallen through the cracks early on…. When were you formally diagnosed with CCUS? When was your bone marrow biopsy done that confirmed CCUS? Have you had any others since then? I have done a lot of reading over my ten plus year course with CCUS. I also happen to be a nurse. So it is easier for me to read and understand what is happening. However, this can be both a blessing and a curse. I also tend to worry… it’s hard not to… when we know CCUS is a precursor to MDS or AML .
Having a standard of care that is to simply follow blood work closely without early treatment is somehow counterintuitive. I have been to several specialists over the span of my illness. (This is due to change in insurance, MD retiring, another changing to academia.) I have also had a second opinion. I have received care from both BI/Lahey Health and Dana Farber, where I am now. I’ve had a second opinion at Sloan Kettering in NY. These are all top institutions. They all have the same thoughts about treating only for symptomatic patients or those whose numbers are declining. This is because the treatment can make patients sicker sooner than if they had just taken a wait and see approach.
I am concerned about your bone pain and declining platelet counts. As a note of reference, normal platelet counts should be in the range of 150k-450K. Mild “thrombocytopenia” or (low platelets) is 101K-140K; Moderate thrombocytopenia is between 51K and 100K and severe thrombocytopenia is below 51K. (Cleveland Clinic 2022). Your platelet counts have been severely low for a long time, thus the easy bruising. It is imperative you see your hematologist sooner than later, especially since you are now also having additional symptoms. (Bone pain and severe exhaustion.)
You mentioned not having any other blood work abnormalities. In CCUS, there are many variations in the course of the disease. It seems no two patients are exactly the same. You can have changes in platelets, white blood counts and/or red blood cell counts. The standard of care for treatment is based on the IPSS or International Prognostic Scoring System. This uses three prognostic indicators to predict the course of a patient’s disease.
You mentioned not knowing what VAF and NGS is. VAF is Variant Allelle Frequency. This refers to mutations and its definition is the “frequency with which a variant is detected in the specimen.” My understanding of this is that the higher the VAF, the higher the risk the particular mutation is of contributing to progression of the disease. NGS (next generation sequencing) is a blood test that is often used to “determine the mutation status of recurrently mutated genes that play an important role in the diagnosis, prognosis and clinical management of blood cancers. It is also used in CCUS for timely and accurate diagnosis.” Dana Farber developed a rapid heme panel. I am unsure of how or even if this is different from NGS. But the RHP is defined as “a high-tech genetic test that provides an unprecedented amount of critical information to aid in the choice of treatment in a matter of days.”
From what you have shared, I would encourage you to reach out to your hematologist at Dana Farber. I would ask her to repeat your bone marrow biopsy and also to order a rapid heme panel. This test may require a call to your insurance company to ensure coverage, as it can be expensive.
If you should have any further questions, please reach out to me at any time. I hope that I have helped in some small way. I will keep you in thought and prayer. It is my hope you will receive timely and effective treatment in the very near future.
Replies to "Hi @loribmt and @pixiesusan. First, thank you, Lori, for being willing to share your story and..."
Audrey, thank you so much for this incredibly helpful reply for @pixiesusan! Sharing your experience with CCUS and all of this information you’ve provided…well, it’s priceless! What a lifeline for someone like Susan who is just recently diagnosed and looking for answers. Your compassion as a nurse is showing through loud and clear. 🥰
This is what I just love about Connect! It’s such a caring and supportive forum where we help take care of each other. Your post today has left me feeling so uplifted and grateful for you, for your taking the time to write such a helpful and informational reply.
Audrey, are you still active in nursing or retired?