Showing posts with label maintenance. Show all posts
Showing posts with label maintenance. Show all posts

Friday, May 6, 2011

Still Stable


Pomalidomide Study:

After 41 cycles on the pomalidomide (CC-4047) study, my M-Spike is still 1.0 g/dL, and IgG is up only slightly. Lambda light chains are up significantly, but they were down a lot last month.

News from the International Myeloma Workship in Paris:

New data from the CALGB study showed that patients who were given Revlimid maintenance after a transplant achieved an overall survival rate of 90% after two years or more, compared with 83% for patients receiving a placebo. Some doctors believe that maintenance therapy of some kind will become the new standard of care. Here is the IMF article. The IMF is the International Myeloma Foundation.

That information and other myeloma facts were presented at a Journalists Workshop, a video press conference by the IMF, which is available for viewing on the web. It lasts about an hour, and is a summary of the high points of the Myeloma Workshop. At about 45 minutes there is a one-minute clip showing me running in a marathon in Providence, Rhode island last Sunday. The clip was included in the press conference as a demonstration of the effectiveness of the new study drug pomalidomide. You could fast forward through the running part, but the rest of the video is actually interesting and I recommend it.

Some Current Test Results:

Test    Feb 07    Mar 09    Apr 07    May 05     Remarks
M-spike g/dL 1.0 1.0 1.0 1.0 Best tumor measure?
IgG mg/dL 1200 1050 1080 1130 Best tumor measure?
L FLC mg/dL 2.47 2.50 2.08 3.07 L Free light chains
Calcium mg/dL 10.1 9.6 9.9 9.4 Dandy
Creatinine mg/dL 1.0 1.0 1.2 1.1 Kidney, OK
HGB g/dL 16.0 15.2 15.5 14.7 Hemoglobin, good
RBC M/uL 4.44 4.40 4.27 4.11 Red cells, marginal
WBC K/uL 4.1 5.3 4.9 4.6 White cells, OK
ANC K/uL 1.40 1.61 1.90 1.90 Neutrophils, sufficient

Related Links:

My Myeloma     A discussion of my myeloma, not very technical.
My Treatment History Not technical.
My Test Charts Graphic displays of several key test results over time.
My Test Result Table Somewhat technical. Best with a wide browser window.
My Supplement Regimen With links to where I buy them.


Today's lunch: Leftover roast organic chicken (I love cold chicken), hot organic broccoli with a little hot sauce, organic heritage plum tomatoes, and organic USA strawberries. Everything there is normal size except the strawberries, which are enormous. It's strawberry season!

Friday, February 11, 2011

Fighting Secondary Cancers

I'm cheerful today, after visiting Mayo Clinic for the end of the 38th 28-day cycle of pomalidomide. IgG is up a paltry 3%, from 1170 to 1200 mg/dL, but M-spike is down a whopping 17%, from 1.2 to 1.0 g/dL. I don't actually believe that my monoclonal proteins dropped that much, because last month's figure was a medical impossibility (higher than IgG), but it feels good anyway. See, it doesn't take a lot to make me happy. We celebrated with a couple of bowls of kettle-popped organic popcorn.

STABLE is the proper description:

The myeloma is stable. IgG has varied between 923 and 1350 mg/dL since July of 2008, two and a half years. I just want to stay on this regimen forever, running marathons and otherwise enjoying life. It doesn't work that way, but so far pomalidomide has given me nearly three years of normalcy.

When pomalidomide fails, what's next for me?

Every treatment fails eventually - that's a dependable feature of myeloma. Apparently, though, I will have plenty of options. I've had thalidomide, pomalidomide, dexamethasone, and low-dose naltrexone so far, no other doctor-prescribed treatments. There are Velcade studies at Mayo right now, and Carfilzomib, plus several new agents which work in magically new ways. Dr KDS mentioned Phase I, II, and III trials - lots going on, and I might be eligible for several of them. I'm feeling good about the future.

We even discussed bone marrow transplant, but I'm not sold on that, for me. I have a slow-moving variety of myeloma, and I'm hopeful that it can be managed by using the existing treatments in a serial fashion and, perhaps, by taking advantage of new ones as they come along. The cure for myeloma is to live long enough to die of something else, and that's my plan. Meantime, life is to be lived!

What About Secondary Cancers?

There is new evidence that long-term treatment with Revlimid, such as Revlimid maintenance after a transplant, may result in an increased risk of second primary cancers including lymphoma, leukemia, and solid tumors. The risk is still low, perhaps less than 5%, but studies seem to show that it is somewhat increased compared with people not on Revlimid maintenance. Doctors are trying to quantify this risk now, to determine whether it says anything for or against long-term maintenance. The Myeloma Beacon has a very current article on this issue.

So what about pomalidomide? Thalidomide, Revlimid (lenalidomide), and pomalidomide are all immunomodulatory drugs (IMiDs). They all "modulate" the immune system, suppressing it to some extent, in their multi-pronged campaign against monoclonal plasma cells.

THE FOLLOWING ARE THE SUPPOSINGS OF A NON-DOCTOR. READ AT YOUR OWN RISK: We know that an important role of the immune system is to kill cancers before they can get started. The DNA of a cell goes wacko (technical term) for whatever reason, say a coincidental zap from a gamma ray that left the star Alpha Centauri 4.2 years ago, or a treatment by an alkylating agent like melphalan, or a radiation treatment for something, or even a PET scan. The immune system detects the wacko cell and swats it down. Game over.

If the immune system is suppressed, however, maybe it wouldn't detect the wacko cell, or maybe not until that naughty cell has multiplied and the group has become too strong and adaptable for any immune system to swat it down. Thus the drug doesn't actually cause the cancer, it simply opens the door for it. Again, this is all supposition; I am not a doctor.

If something like that is happening, though, we might see secondary cancers in people taking other IMiDs like thalidomide, if we look, and eventually perhaps in those of us taking pomalidomide. Dr KDS says that there really is no information on that last point yet. Pomalidomide is too new. I don't know if anyone has yet looked at the information that does exist. But I do know that I've been on pomalidomide for nearly three years now, and that easily qualifies as long-term treatment. There was no transplant, but this is maintenance nonetheless.

How Do We Fight Secondary Cancers?

Job One, of course, is to discuss this with our doctors, and keep ourselves up to date.

Job Two, in my opinion, is to live a healthful lifestyle that fights cancer. That is a huge subject covering nutrition, exercise, sleep, addictions, and much more. It is, however, more or less in our own control. We can influence our own futures and make it more likely that we'll be here for our grandchildren. I've been thinking about writing a book about this (of course there are books out there already), and may blog about it, but here are some simple principles:
  • Nutrition: We simply avoid eating anything that does not contribute to health. Does soda contribute to health, or a jelly doughnut, or french fries? Of course not! So we choose a healthful alternative, like charged water, a slice of organic whole-grain bread with a little organic raspberry jam, or a banana. Further, we go for the very best foods, especially fruits and vegetables, organic where suggested by the "dirty dozen" lists. Good nutrition contributes in two ways: (1) we avoid ingesting foods that cause cancer, foods full of pesticides, bad fats, and empty sugars; and (2) we do eat high-quality foods containing nutrients that our bodies need to build a competent immune system, including antioxidants and other micronutrients. We are what we eat.
  • Exercise: Some is good, more is better. A good goal is a half hour, five days a week. We three try for an hour and usually make it. A balanced program, aimed at improving overall health, will include some resistance training (muscle building) and some aerobic exercise, with the prior advice of a doctor of course.
  • Sleep: How can our health be at its best if we shortchange ourselves on sleep? Studies show that most people need eight hours, some more and some a little less. One test: if I need to use an alarm clock to wake up, then perhaps I'm not getting enough.
  • Addictions:
    • Smoking: Oh, for God's sake, if you still smoke, do whatever it takes to stop. No excuses - it's killing you and everyone around you. Rehab if necessary. If you live with a smoker, move out.
    • Overweight: Overwhelming evidence points to overweight as a serious cancer risk. If you are obese (BMI 30+), or even overweight, please find a way back into your bathing suit, whatever it takes. This will require a serious lifestyle change - you will fail if you think it might not. Talk to people who have done it.
We three have followed these principles for years now. Does that mean we won't get additional cancers? No, it means that our risk is lower than it would be otherwise. That's all that any of us can do.

Some Current Test Results:

Test    Nov 18    Dec 16    Jan 13    Feb 07     Remarks
M-spike g/dL 1.2 1.0 1.2 1.0 Best tumor measure?
IgG mg/dL 1300 1080 1170 1200 Best tumor measure?
L FLC mg/dL 2.92 2.41 2.49 2.47 L Free light chains
Calcium mg/dL 10.3 9.8 10.3 10.1 OK
Creatinine mg/dL 0.9 1.0 1.4 1.0 Kidney, OK
HGB g/dL 15.0 14.6 15.3 16.0 Hemoglobin, good
RBC M/uL 4.26 4.23 4.48 4.44 Red cells, marginal
WBC K/uL 5.9 5.1 3.3 4.1 White cells, OK
ANC K/uL 2.30 2.50 1.19 1.40 Neutrophils, sufficient

Related Links:

My Myeloma     A discussion of my myeloma, not very technical.
My Treatment History Not technical.
My Test Charts Graphic displays of several key test results over time.
My Test Result Table Somewhat technical. Best with a wide browser window.
My Supplement Regimen With links to where I buy them.


High-quality food is often quite colorful. Canned wild-catch salmon baked under yogurt and a little shredded cheese, organic lettuce, pineapple, pickled organic beets, onions, organic peas:

Friday, June 4, 2010

ASCO Headline: Maintenance Works

And so does consolidation. This may be the most important new information for myeloma patients this weekend.

ASCO is the American Society of Clinical Oncology, currently holding its annual meeting at McCormick Place in Chicago, 30,000 strong. I am here as a guest of the International Myeloma Foundation (IMF), to observe the information presented by the many speakers, and to blog about it from the perspective of an ordinary patient. Yay for the IMF! And thank you. I love this stuff. But be advised: I am not a doctor, just an engineer. You should get your medical advice and even your facts from your doctor.

The ASH (American Society of Hematology) conference a half-year ago suggested that maintenance works, and ASCO confirms it. What is it?
  • Consolidation is a drug therapy given AFTER a stem cell transplant (SCT), to further reduce the tumor burden.
  • Maintenance is administration of a drug (Revlimid, Velcade, ...) for a long period AFTER a good response has been achieved from an SCT or other therapy, to keep the ugly buggers down.
I attended a session titled "Expert Perspectives in Individualized Treatment of Hematologic Malignancies" (yikes - what was I doing there?). Dr David Vesole of Hackensack University spoke on "Updates on Innovative Treatment for Newly Diagnosed and Relapsed/Refractive Myeloma. More about that in another post.

Consolidation:

Dr Vesole cited two different studies, one using Revlimid and another using Velcade, both showing a significant advantage for consolidation. In the revlimid study, two months of Revlimid increased the percentage of patients showing a very good partial response (VGPR) or better from 58% to 70%. In the other study, Velcade was started at three months after the SCT, and continued for six months. After those nine months, 49% of the patients taking Velcade were still in near-CR or better, contrasted with 33% of the control group.

Maintenance:

The brand-newest papers on post-SCT maintenance have not been presented yet, but the abstracts are available. As Dr Durie of the IMF has pointed out in a press release dated yesterday, the new studies may influence doctors toward continuing therapy (maintenance) as a means of preventing or delaying relapse. The study results are quite clear: maintenance works. One study was "unblinded," in fact, because those on the Revlimid maintenance arm were doing so much better than those on placebo. I will attend these sessions, and will report on them if I learn anything beyond what is in the abstracts.

What does this mean for us?

Unfortunately, it's both sweet and sour. In many cases, we should probably NOT enjoy a drug holiday after achieving stable disease from an SCT or other means. Instead, going on maintenance, we will incur: (1) side effects of Revlimid or Velcade; (2) the cost of those drugs, and (3) the nuisance of taking the pills or getting the infusions. But we may likely enjoy a longer period before relapse and quite possibly a longer life. Life is good - I'm in favor of it.

What about those who are already on a drug holiday? Should I start now? Is it too late to start? Ask your doctor - I don't think the studies answer that question.

No Kidding!