Thursday, August 13, 2009

What is Multiple Myeloma


Multiple Myeloma

by Rick Alan

Definition

Multiple myeloma is a relatively rare cancer of the bone marrow. It results from the abnormal growth of plasma cells in the bone marrow. Plasma cells normally produce antibodies. As these abnormal or malignant plasma cells multiply, they produce enormous quantities of abnormal antibodies. These abnormal antibodies accumulate in the blood and urine. As the plasma cell tumor grows, it also destroys the surrounding bone. These events lead to bone pain, kidney damage, and a compromised immune system.


Cancer occurs when cells in the body (in this case plasma cells) divide without control or order. Normally, cells divide in a regulated manner. If cells keep dividing uncontrollably when new cells are not needed. A mass of tissue forms, called a growth or tumor. The term cancer refers to malignant tumors, which can invade nearby tissue and can spread to other parts of the body. A benign tumor does not invade or spread.


© 2009 Nucleus Medical Art, Inc.


Causes

The cause of multiple myeloma is unknown.


Risk Factors

A risk factor is something that increases your chance of getting a disease or condition.

Risk factors for multiple myeloma include:

Age: 50 or older

Race: black


Symptoms

Symptoms of early stage multiple myeloma include:

Persistent bone pain, often severe. It is most commonly in the back but also in the limbs or ribs.

Fatigue

When the disease progresses, symptoms may include:

Fatigue

Weakness

Broken bones

Repeated infections

Nausea and vomiting

Constipation

Difficulty urinating

Abnormal bleeding

Headache

Visual problems

Confusion


Treatment

Once cancer is found, staging tests are performed to find out if the cancer has spread and, if so, to what extent. While treatment is sometimes capable of slowing the progression of the multiple myeloma, complete remission is rare. Treatment is also important for the control of symptoms. Treatment depends on your symptoms and the stage of your cancer.

Treatments include:

Chemotherapy

Chemotherapy is the use of drugs to kill cancer cells. Chemotherapy may be given in many forms including: pill, injection, and via a catheter. The drugs enter the bloodstream and travel through the body killing mostly cancer cells, but also some healthy cells.

The most common initial chemotherapeutic agents are melphalan , prednisone , or a three drug combination called VAD. When young patients develop myeloma, some oncologists feel they should first receive the VAD chemotherapy followed by a bone marrow transplant, if they have had a good response to the initial VAD.

Bone Marrow Transplant

The two types of bone marrow transplant used include an autologous and allogeneictransplant.

Autologous transplant—is one where the patient’s bone marrow is stunned with very high doses of chemotherapy, and it recovers with infused stem cells.

Allogeneic transplant—is a more involved process requiring the donation of bone marrow cells from a donor (usually a first-degree relative). The bone marrow of the patient is stunned with very high doses of chemotherapy (and sometimes with low doses of radiation therapy) followed by the infusion of the donor’s cells into the blood of the patient. The stem cells then seek out the bone marrow and re-populate it.

Both techniques are potentially deadly and have significant side effects associated with them. However, these procedures (particularly the allogeneic transplant) are the only ones that have shown to result in a prolonged survival, or even a cure.

Immunomodulatory Treatments

Immunomodulatory treatments help alter the way the myeloma cells live, and ultimately makes it difficult for them to survive, reproduce, and produce the proteins that cause secondary symptoms. Drugs used for this treatment include thalidomide , lenalidomide ,arsenic trioxide , neovastat, and velcade .

Other Medications

  • Strong oral analgesics to relieve bone pain
  • If anemia is present, erythropoietin to increase the amount of red blood cells
  • Prednisone and biphosphonate drugs to treat high calcium levels
  • Antibiotics to treat infections
  • Biphosphonates to protect bones from fractures and myeloma spreading

Radiation Therapy (Radiotherapy)

Radiation therapy is the use of radiation to kill cancer cells and shrink tumors. Radiation is most often given to relieve bone pain, and by itself is not considered curative.

Surgery

Surgery is done to remove a multiple myeloma tumor that causes pain or other debilitating symptoms, when radiation therapy is not considered feasible. Surgery is not curative.

Red Blood Cell Transfusion

Red blood cell transfusion is for patients with severe anemia.

Peripheral Stem Cell Transplant

Peripheral stem cell transplant involves giving patients immature, healthy blood cells to replace bone marrow cells that are destroyed during total body radiation and high-dose chemotherapy.

Lifestyle Measures

Lifestyle measures help reduce symptoms and maintain overall health:
  • Stay as active as possible.
  • Drink plenty of fluids to help avoid dehydration and kidney damage.
  • Eat a balanced diet.
  • Do not take high doses of vitamins.

Prevention

There are no guidelines for preventing multiple myeloma because the cause is unknown.

RESOURCES:

CANADIAN RESOURCES:

REFERENCES:

  • Mayo Clinic and Foundation for Medical Education and Research website. Available at:http://www.mayo.edu/ .
  • The Merck Manual of Medical Information . Merck & Co., Inc. Simon and Schuster, Inc.; 2000.
  • National Cancer Institute, National Institutes of Health (NIH) website. Available at:http://www.cancer.gov/ .
  • Rajkumar, SV, Hayman, SR, Lacy, MQ, et al. Combination therapy with lenalidomide plus dexamethasone (Rev/Dex) for newly diagnosed myeloma. Blood . 2005;106:4050 .

Infusions, Steroids & CT Angio

December 16, 2008


Hello all,


Here is an update as I promised on the latest of my treatments. Last Friday I began my infusions at UCLA. All went well and my body did beautifully with the medications. Along with the second set of steroids for this month. And great news is the medication we had been waiting for was delivered to me this morning!!! Thank you Lord!


There was a huge hang up with our insurance not wanting to approve this medication for some reason, but we think we finally figured out what the problem was. For the past 4 weeks they claimed they didn't have enough clinical information and kept saying they needed more in order to approve it. Well, Saturday night we received a call from the Specialist at UCLA saying that some of my blood work came back abnormal for and thought I might have had blood clotting, so he told Greg to take me to ER immediately for a CT Angio test to rule out a possible Pulmonary Embolism. Which you can imagine was was scary he was thinking there might be blood clotting which could be fatal if it traveled to the heart or brain. But thank God the Scan didn't show any clotting. But the scan did show pitting of the bones after all in my upper back where all the pain is. That would explain everything now. And this is the reason for the insurance approving this 3rd medicine on the spot. This has been the missing link that the insurance company needed to release the Chemo drug.


We believe this call Saturday night was a God send because if my Doctor had not called for us to go in for the Angiogram they probably wouldn't have detected the bone pitting for quite sometime since I've already done most of my scans recently. Another good thing is that while I was at UCLA for my treatment on Friday The Dr decided to start a bone treatment even though he didn't see anything wrong with my bones at the time he thought it would be a good idea to ease up the pain and at the same time it would strengthen and restore any damage to the bone if necessary. We think he must have had a gut feeling or inclination that the pitting was soon to come.


Overall, I have been feeling significantly better since Friday so far so we are very excited to see what the next 11 treatments has in store for me. Please keep the prayers going as you can see God is moving and answering your prayers quickly and most of all giving me the peace and the strength to get through this and to be strong for my family as well.


Just thought to give you a heads up on the latest, so I start my third Chemo drug tonight, hopefully my body will take well to this one as well.


Thank you again for your faithfulness,

Debbie

Wednesday, August 12, 2009

The Diagnosis...



















December 11, 2008


Dear friends,


As some of you know this has been a tough time for our family but God has truly been so good to us and has sustained us and has kept us under his wing. We have been blessed blessed blessed! We have been overwhelmed with the outpour of blessings which have surrounded us through family and friends and from people we don't know. We keep hearing of different prayer chains going on all over the place in different countries, from the East Coast to the West Coast and in between. Different churches, prayer groups, etc... it is amazing, we feel God smothering us with His Love and Comfort all over the place. We would like to thank those of you who have been praying for us.



The support up here in the high desert has been amazing, just when we were throwing in the towel and actively looking down the hill to move, God stopped us dead in our tracks with all of this and said you are not alone in this I have put people in your path who will help you guys get through this. Sure enough so many friends and family lovingly and consistently have been reaching out to us daily for prayer, meals on wheels, enouragement, babysitting, school carpool anything we need on a daily basis. It is so hard because our hearts are at home down the hill, but now God is showing us the love there is for us up here. We feel torn, but right now we believe God is faithfully providing for our family LOVE and SUPPORT from the family we never realized existed up here. We dont know what are future holds and where we are to go, but we are taking it day by day and letting God lead the way. We are standing on His Promises knowing there is a time and season for everything and right now this is Gods time for us to sit at His feet and patiently wait on HIM .... : ) TO BE STILL AND TO KNOW HE IS GOD!


We are not sure how much those of you who do know, or if you don't know at all but I (Debbie) was recently diagnosed with "Multiple Myeloma", a cancer of the plasma cells (which has excessive numbers of abnormal plasma cells in the bone marrow, it is incurable but a treatable disease. The average age for someone with this disease us usually found in the age of 60 and above. I am considered a VERY rare case because of my age which I fall into a category of 4% of those diagnosed under the age of 45. Crazy, I know...and God Chose me to run this race! The specialist at UCLA sounds very optimistic that I should respond to the Chemotherapy with no problem, seeing that I am very young, my general health is in very good health, and the good medicines they have to treat this and not to mention that my all over bone scan, CAT scan and MRI have all come out clean and show no cancer in the bones as of yet. Mostly I have the Lord at my side who will see me through. We are hoping this will be the treatment that takes it into remission, if not they I believe the next step will be a bone marrow transplant (yikes!!).


To catch you up on the latest, the past few days have been really hard on us. Our WHOLE family caught the stomach flu. We have been down but now we are up. It has been especially hard on me juggling my cancer ailments, the kids and this flu. Today is a much better day and looking forward to moving right along with this new venture.

As for the chemo, we still havn't started. For the past week weve been battling back and forth with our insurance company, medical group, the UCLA specialist, the pharmacy who is handling one of the chemo drugs and the oncologist up here. There are so many people involved who play significant roles in each part in order to get all the necessary approvals to get it all going, which has been anything but efficient up to this point. For lack of better words we are dealing with very "incompitent people" who cannot seem to pull it together which is making this very frustrating on us. The only ones who seem to have the ball rolling and keeping us going is the oncologist up here is who has been kind enough to order every test we have been asked for without the help of the specialist at Ucla. The Dr up here and his staff have been great, quick and on top of it, but sad to say he is the one who doesn't feel confident in handling this rare case. Unfortunately trying to get anything answered from our treating physician at Ucla has been nothing but headaches for 3 weeks now. We have been through many hurdles and hoops trying to get approvals. Yesterday we were challenged by our insurance company who called us yesterday morning to say that they were denying the request for the Revlamid, then they called in the afternoon to tell us that they were not going to allow us to treat at UCLA after all and that we had to treat up here (which you can imagine had us in a panic), but with God on our side and Gregs strong persistance he was able to get what we needed and it was all taken care of and our insurance agreed to let us treat at UCLA after all.


To somewhat sum up the treatment details. I will be treating with a 3 part chemo series for the next 3 months.


-The first part is "Dexamethazone" a high dose steriod which I had started taking on Thanksgiving Day which was 40 steroids in 4 days. With a 2 week break then will resume again in less than one week from now. The first course I have already taken my body reacted very bad to it, so we are praying the second time around will be different and not so harsh on my system since the quantity will be significantly less.


-The second is "Revlamid" a Chemo pill which is a HIGHLY regulated drug has been harder than the dickens to get approved. Apparently, this drug is only carried in 5 of the U.S states and very expensive ($8,000.00 per month). Our insurance company has to go through many channels before they can approve it. Each step has to be under a 24 hour evaluation by an insurance director. Once it has been approved it will be shipped to me within several hours out of L.A. and will have to be resubmitted for approval each month and thereafter for re-approval again and again. As of today, it is under final evaluation (so they say) and we hope to have it sent to us with in the next couple of days.


-The third form is "Valcaid" the infusion drug which will be introvenoiusly administered through IV at UCLA once a week. As of today we got the approval and the drug is on its away to L.A as we speak and we are still waiting for confirmation from the UCLA office that the approval has been faxed and that the medicine has arrived in order for me to set up the first appt, so this too is supposedly in its last stage of finalizing. We are praying to start this by Friday or early next week.

Ultimately we are being tried and stretched no doubt, but we know that God will faithfully carry us through, though the physical ailments may be hindering, our faith will not. God is at work and we are encouraged daily through His Grace and Mercy. This trial couldn't come at a better time of the year, this is a living testimony of how much we have to be thankful for and we are honored to be given the opportunity to excercise our faith in the Lord through the Holidays. We do thank you all for your prayers, help and encouragement. Please keep praying for Greg for strength and the boys that God guards thier little hearts, and that all goes well for the 3 month treatment and that my body will respond well to the chemo and bring healing. God is on the throne and is being given all the glory!

Thats all for now we will keep you updated and let you know when we start!


Love you all,

Greg & Debbie