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Bone Metastases in Lung Cancer: An Introduction


February 17, 2007 - 4:50 pm printer friendly view / write comments
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Dr. West

   I’ve discussed the general management of metastatic lung cancer, both SCLC and NSCLC, but there are also several common complications that sometimes require particular management.  Bone metastases, for instance, may be treated by the same “whole body” approach with chemotherapy that treats other areas of tumor involvement, but may also benefit from additional approaches.  Bone metastases are common in oncology, and approximately 30-40% of lung cancer patients develop bone metastases at some point, about half presenting with evidence of bone involvement at the time of diagnosis (bone metastases general review abstract here).  These metastases often have a significant impact on a patient’s quality of life, leading not only to pain but also a risk for pathologic fractures (bone breaks because the bone is weakened by cancer involvement leading to reduced structural integrity), potential compression of the spinal cord and other nerves, and high blood calcium levels as bone is broken down (which can lead to confusion, constipation, numbness/tingling, and other problems).   With bone metastases comes a risk of impaired mobility, problems with sleeping and eating normally, and a somewhat worse prognosis overall, although there’s a lot of variability in the population. 

  Treating the underlying cancer with chemotherapy and/or targeted therapy (systemic, or “whole body”) can also lead to improvement in disease in the bones, but sometimes local therapy is indicated.  The goals of treating bone disease are primarily  to relieve pain and to reduce the risk of fracture, which tends to occur in “weight-bearing” bones like the legs, hips, and spine. 

  Of the patients with lung cancer who ultimately develop bone metastases (somewhere in the range of 50% of patients with advanced disease), the metastases are without symptoms in 30-60% initially, which leads to this being an underdiagnosed and undertreated problem.  The majority of these are in the spine (thoracic or lumbar vertebrae, mainly), ribs, and pelvis; and less likely but sometimes seen the cervical spine (in the neck), femurs (thighs), humerus (upper arm), scapula (shoulder blade), skull, sternum.  It’s fair to say that they can be anywhere in the spine, but more likely in the torso, and in the extremities more likely to be higher up. 

  The most common way to detect bone metastases used to be bone scans, but they used less and less now as PET scans have become more widely available.  Bone scans are falsely positive (light up as abnormal but not really cancer) in the setting of prior trauma or degenerative joint disease, and many people have one or more of those, so it can be very difficult or impossible to tell if the spine abnormality on the bone scan is metastatic disease or just garden variety disk disease, the kind that makes back pain one of the top reasons for people to see a health care professional.  PET scans are more sensitive (able to pick up disease better) and more specific (what they pick up is more likely to really be cancer) (one abstract on PET for bone mets here), and they’ve become much more widely available.  However, many if not most PET scans stop at the mid-femur level, so it’s possible to miss disease lower down in the legs –  an uncommon but certainly possible place to develop bony metastases.

   Often, those scans still can’t definitely proclaim an abnormal area as cancer.  MRI scans are often very, very good at determining details of bony disease and clarifying whether an abnormality is cancer or degenerative changes.  Some people can’t undergo an MRI scan because they’re loud and pretty tight, leading about 10% of people just unable to tolerate the close confines.  CT scans with “bone windows”, just a way of setting the contrast on the scans, can be useful to assess the bones in people who can’t get an MRI.  And then there’s also plain old x-rays, which are also potentially useful in assessing the hips or ribs or other places.  They aren’t as clear as an MRI, but they can sometimes provide the added information you need and are certainly widely available and a lot less expensive. 

  Even with additional studies, sometimes it’s not possible to say definitively whether abnormal areas on these scans are cancer or benign musculoskeletal disease.  Occasionally, we need to recommend that patients undergo a biopsy to confirm or exclude bone metastasis.  That wouldn’t be widely recommended in most situations in which a patient already has advanced lung cancer, since it’s not as likely to dramatically change treatment plans or prognosis, but in patients who are being staged and may be candidates for surgery and/or aggressive chemo/radiation plans for earlier stage disease, it often makes sense to pursue such a challenging approach only if it wouldn’t be proved futile by progression of metastatic disease in the forseeable future.

   I’ll talk about various treatment approaches for bone metastases in some upcoming posts.

Posted in: Evaluation and Work-Up, General Lung Cancer Issues, Lung Cancer, Management of Bone Metastases Digg    StumbleUpon    Furl    reddit    Delicious    printer friendly



  1. February 17, 2007 - 6:09 pm

    Dr West,
    Thank you so much for posting this article on bone metastases. My husband has had his 2nd opinion from Moffitt Center in Tampa and they recommend the same as his Onc in Orlando and that is a second-line chemo for his bone mets. We will see his Onc on Tuesday the 20th but are assuming that Topotecan will be the drug of choice. We don’t know any more than that right now, but from what I’ve read, it should be approximately 30 minute drip for 5 days and then resumed again on the 22nd day. What we’re trying to determine is if this drug will actually kill the cancer or just halt it for a while. I have a very hard time finding information on bone mets treatment. I am on message boards constantly but cannot actually find anyone who can tell me their experiences.

    Thank you again for your dedication to this site and education all of us on lung cancer. I look forward to any and all information on SCLC with bone mets.

    Laurie

    lban
  2. February 17, 2007 - 7:06 pm

    Dr. West, Thanks so much for your article on bone mets. I have mets to the left femur (95% undetected after chemo) tiny spot on illum (also almost gone) and 6 small lymph nodes in peri-hilar region completely resolved. and the primary tumor in the left lung is shrunk 50% around 2mm now. All the information that you supply us with is so valuable and God Bless you so much for your time, talents and caring. I will continue to keep up with your valuable information. Terry Durham

    ttdurham
  3. February 19, 2007 - 8:41 am

    Again a timely post for me. I was diagnosed Feb. 2006 with stage IV. Had low back pain and MRI suggested bone mets. Found tumor in one lung. PET scans found mets on ribs, lumbar vertebrae, and pelvis. Took 6 rounds of taxol, carboplatin and avastin, plus monthly dose of Zometa for bones. In August, PET scan showed lung tumor reduced 50% and dormant. Bone mets were “dramatically improved”, down to a few spots. PET scan in Nov. though showed bone mets increasing in activity (lung still dormant). So started Tarceva. PET scan 2 weeks ago showed bone mets stable. However, a year ago I had severe lower back pain, had trouble walking upstairs at home. Since November, my pain is minimal. I was able to get off pain meds, even otc ones since November. Thanks so much for your sharing of your knowledge.

    johnsegars
  4. August 28, 2007 - 8:12 am

    My mum has lung cancer and bone mets. And she has just started Chemo. She has pain in the lower back (where the mets is) and pain in her arm from the tumor. Alot of stuff i read says that If you have bone mets 6months usually about how long you may have left. Please someone give me there opinion.

    Johnsegars, your post is good, hope you keep well, my mum seems to be in a similar situation to what you were in.

    thanks

    michellem
  5. August 28, 2007 - 1:09 pm

    Michelle,

    I don’t think that there’s much evidence to say that patients with bone metastases have a significantly shorter survival than other patients with metastatic disease. Advanced disease doesn’t have a typical survival that any of us would be happy with, but it’s typically more than 6 months with treatment.

    -Dr. West

    Dr. West
  6. September 11, 2007 - 1:44 am

    Thank you for your reply Dr. West. We spoke to the doctors and they are saying that it doesnt look good. We are Desperate and need to do something for our mum. She is on so many pain killers. I asked about stuff for the bone like Zometa but they said that it haas side affects and the important thing at the moment is the chemo. I am terrified, because the chemo might not even be doing anything to help. the pain is worse every day

    michellem
  7. September 11, 2007 - 6:49 am

    Michelle,
    I can’t second guess your doctors, but I took Zometa while I was taking chemo. Since I last posted, my cancer has started spreading again and I just started chemo again. But I am still taking Zometa once a month. The pain is under control.

    johnsegars
  8. September 11, 2007 - 9:23 pm

    I would consider the zometa to be a relatively minor factor, likely less than the chemo. I do try to add it, but in patients in whom I’m worried about their kidneys, or who have dental problems that would be associated with higher risk of osteonecrosis of the jaw, I don’t recommend it, and I really don’t think they’re missing out on anything amazing. It doesn’t keep cancer from progressing into the bones, but it just slows that progression, on average.

    I know you’re saying that she’s on too many pain medicines, but also that the pain is worse every day. If the cancer is causing her pain to worsen, I’m afraid it’s possible that nothing will have a significant impact on the cancer. I definitely agree with trying to treat her cancer effectively with chemo, but I really hope she can get adequate pain control along the way and wouldn’t want to be stingy with her medicines just because they seem like a lot — some people need it, and it may be the most important thing to help her.

    -Dr. West

    Dr. West
  9. December 19, 2007 - 11:44 am

    Hi Dr. West. I just read all the posts about bone metastesis but didn’t see much about radiation. I have recently had a very painful shoulder problem which appeared from the MRI to be related to my NSCLC as well as involving a tear in the rotator cuff. I took a two week break from Tarceva to have radiation treatments which were supposed to help the pain by targetting the tumor. Actually my shoulder is even worse now. My onc says that the pain and loss of movement I experience sound like they are more of an orthopedic problem because radiation usually makes it feel better. He also says that they oftem find these bone metasteses in places with previous injury or surgery (In my case, I had acromioplasty in that shoulder two years ago.)Is that your experience? I am back on Tarceva now. I have not yet had any chemo because my small tumor has only grown a very tiny bit in the seven months of treatment and I still have no lung or breathing symptoms. In a month if my tumor has grown more I may start Alimta.
    My main questions: Do you find radiation effective for this type of thing? Do you see bone metastases in previously compromised places? Do you think it is safe to wait another month to start chemo?
    Thanks for all your help.
    Carlee

    Carlee
  10. December 20, 2007 - 4:27 pm

    Carlee,

    I definitely see that the clear majority of patients experience at least partial improvement in pain for bone metastases — not all, but certainly most. Absence of improvement would also lead me to think of alternative causes as an explanation.

    I’m not as aware of the finding of bone metastases in previously injured or otherwise compromised areas. I don’t mean to say that this is incorrect, because I haven’t heard about this being a myth — I am just not aware of any correlation.

    In someone who has shown very slow progression over a prolonged period of follow-up, and I’d say that 7 months qualifies, it seems quite appropriate to continue to follow without changes. Yes, cancer can always change its behavior and progress more quickly, but that’s unlikely.

    -Dr. West

    Dr. West
  11. March 23, 2008 - 3:32 am

    Dr. West: Hello again. Mari just had a Pet Scan which reveals bone metastasis. The doctor gives her 8-12 months and says she will have quality of life and no pain. How is this possible? Is there different types of bone cancer with no pain? Should she continue treatment or stop? Also, I met with a pharmacist who is into alternative medicine (Chinese herbs, roots, etc.) who says her brother had 6 months and has live 5 years with bone cancer. Is this possible? We are really desperate.
    Thanks again in advance.

    Maruchi

    maruchi2323
  12. March 23, 2008 - 1:15 pm

    Maruchi,

    Some patients have little or no pain from bone metastases, and others have more pain, but there are no rules about what happens.  The most important factor, though, is that oncologists and other doctors have a wide range of pain medicines available to treat and manage pain effectively. Most patients can be kept pretty comfortably and without significant pain control issues if the doctor and patient aren’t shy about treating the pain adequately, which often requires a steady escalation of narcotics, and bowel medications with that, to be adjusted to keep pain controlled.

    I an not an expert in alternative medicines, and I have significant biases against it. My perception is that a distressing proportion of alternative medicine practitioners make very optimistic claims based on a case or two, when we all have cases that defy the odds. The case this pharmacist described may have had an astounding result and beaten the odds, but if this long survivor actually has bone metastases from prostate cancer, a five year survival is not unusual at all, and perhaps the thing that made him seem miraculous is that the other doctor was way off base predicting six months. When I look at alternative medicine marketing pieces, the vast majority hype a case of someone who defied the odds. Every week I see a few people who defy the odds, but I don’t claim that it was because I laid hands on them. My personal opinion is that a lot of the alternative medicine industry capitalizes on the desperate need for hope to trump rational assessment of a situation. When you want to believe something enough, you won’t allow yourself to be skeptical, and all it takes is a lottery winner to make you expect that you will also win the lottery. But they don’t highlight that their odds of winning are also 1 in 100 or 1000 or worse.

    I wish the role of educating about what to expect from cancer, and lung cancer in particular, didn’t include such a sober view of what to expect (although there is still room for hope, and when I am positive, I really mean it). It’s easier and probably more profitable to withhold information and be unrealistically optimistic. But I feel that people deserve the truth and not a sugar-coated version.

    -Dr. West

    Dr. West
  13. March 30, 2008 - 10:31 am

    Hi Dr. West and everyone else.

    Just a comment about the claim that bone mets often occur at the site of a previous injury or surgery — my ONE bone met is precisely at the site (on the iliac crest) where they harvested bone for a bone graft for a spinal fusion 8 years ago. The oncs also never heard of such a site ‘attracting’ a metastasis and I found it such an extreme coincidence that I demanded a biopsy — and it was in fact a met. So maybe there is something to that claim…

    Ellen in PA
  14. March 30, 2008 - 10:41 am

    Ellen,

    I don’t think we know nearly enough about why mets settle in one place and not another. Perhaps there is something about the microenvironment around the site of prior injury that leads to a stronger blood supply or more “adhesion molecules” that make the area stickier to passing cancer cells. It does seem to be the case that we often find areas of micrometastatic deposits in places that don’t grow to become visible, clinically important metastases, so there are likely several variables that contribute to why one micrometastatic outpost thrives and 4 others just stay microscropic or die — sort of the way some startup companies or early town settlements become big while others fade away. There are likely many factors, and we’re still a ways away from understanding.

    -Dr. West

    Dr. West
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