Locally advanced, or stage III, NSCLC, can potentially include patients for whom surgery is an option, but for many patients with stage IIIA and a majority of those with stage IIIB NSCLC, a non-surgical approach is the best treatment recommendation. It’s important to keep in mind that the goal of treatment for patients with locally advanced NSCLC but who don’t have a malignant pleural effusion (fluid inside the chest but outside of the lung, with cancer cells in it) can potentially be cured. The risk of doing poorly are from both local growth and distant micrometastatic spread (living cancer cells traveling elsewhere in the body through the bloodstream).
The old standard in the 1980s was radiation alone. An important clinical trial the “Dillman Trial” then compared the old standard of just radiation alone to chemo with a two drug combination of “cisplatin-based” chemo for two cycles followed by the same radiation plan. The cure rate was significantly better, although unfortunately we were still curing these patients far too rarely. However, it changed the standard of care from radiation alone to a combination of chemo and radiation together.
Over the last decade, the more timely question has been how best to combine chemo and radiation. Multiple trials from different countries have tested chemo and radiation given one at a time (”sequential chemoradiation”, as was done in the Dillman trial) to chemo and radiation given together (”concurrent chemoradation”). The vast majority of these studies have shown that concurrent chemo and radiation is associated with better chances for cure, at a cost of greater short-term toxicity during and shortly after treatment. The leading side effect problems with this approach are severe esophagitis, or burning/irritation of the esophagus that can make it very painful to swallow, and pneumonitis, which is inflammation of the lung tissue.
Patients with significant medical problems, particularly very compromised lung function, as well as patients with large tumors that would require very large radiation fields, are potentially not well served by this approach and may do better to receive sequential therapy, or possibly chemo alone to shrink the cancer somewhat so that the radiation field may be smaller. In general, stage III NSCLC is an area where the toxicity of treatment, and even the potential for dying from the challenging treatment, can limit the feasibility and potential benefit of a very aggressive approach.
Some physicians and centers routinely chemo and radiation together, followed by additional and often different chemo alone (generally docetaxel, or Taxotere). This is based on very encouraging early work by the Southwest Oncology Group (SWOG) that showed remarkably good results from a cisplatin-based doublet chemo (cisplatin/etoposide) with radiation followed by three cycles of taxotere. This is still controversial, since it can be very challenging to get patients through this approach safely, and the patients enrolled on this trial were unusually fit, not representative of a more general population of patients with marginal lung function and significant other medical problems. We still await further trials to clarify whether this approach is ideal. Other doctors commonly give carboplatin-based chemo on a weekly basis with radiation, but I don’t favor this approach as much, since our results tend to be a bit better with cisplatin than with carboplatin, and we don’t have as much evidence as we would like that carboplatin gives as good results. And the stakes are high, so we don’t want to cut the chances of cure even slightly if we don’t have to. We just need to balance that against the very real safety risks.
Current trials are focusing on newer chemo in this mix, adding targeted therapies to potentially improve cure, and adding prophylactic brain radiation after everything else. The last is an important ongoing question because we see a distressingly high rate of relapses in the brain first or brain only after all of the other treatment, presumably because the central nervous system acts as a “sanctuary site” where chemo cannot easily penetrate and fight micrometastatic disease. However, we still don’t know that brain radiation is appropriate here, so I don’t recommend it in this setting outside of a clinical trial. Together, the improvements in our treatment plans have led to significant gains in our cure rate for stage III NSCLC over the past 20 years, but we still need to build on this momentum.
posted by Dr. West @ 10:59 pm link to this post





November 19th, 2006 at 4:58 pm
I have had two brain surgeries for ONE met two yrs apart2004 snd 2006. Had SRS for residual 2004. 2nd surgey neuos did, didn’t work. Just had Cyberknife for one met. My onc. has basically sent me to pasture. No followup. Last chemo Oct 2003. Dx 3/2003 taxol/Carbo and 38 radiation tx to chest(completed 5/2003)… Tumor in right lung stable. If I were your patient, what would you suggest I do next. CK info I have is from people on lchelp website, their treatments.. Thank you, Karen
PS I like your site, Is this a site to ask questions? No need to reply if it is not…
November 19th, 2006 at 6:54 pm
I can’t be too specific because I don’t know the details of your case and really can’t and shouldn’t give you specific medical advice. However, I can address how I have approached similar cases. In my patients who have nothing growing right now in the brain or in your chest/anyplace else, I would often watch things but not necessarily recommend any treatment. Our treatments like chemo are generally not considered especially effective for getting into the brain and controlling metastases there. Although there are reported responses of brain metastases to EGFR inhibitors like Tarceva, they’re not that common either. Regardless, it sounds to me like the surgery and CK have treated everything they could see. Whole brain radiation at this point is debatable. There is no proven survival benefit for it, but it can substantially decrease the risk of subsequent brain metastases; on the other hand, long-term neurologic toxicity can sometimes be seen. That would be a leading consideration, worth talking to a radiation oncology specialist about pros and cons.
Brain relapses after definitive chemotherapy and radiation for locally advanced NSCLC are unfortunately far more common than we’d like to see (25-40% in some series), but prophylactic whole brain radiation is quite controversial and unproven after chemo and chest radiation. It’s the subject of a national ongoing trial (randomization to prophylactic whole brain radiation or observation). Many patients are skittish about that kind of randomization, but we just don’t know if brain radiation after treatment for stage III NSCLC is a good thing or not.
So in the absence of any evidence of anything growing right now, there’s just no obvious best answer here. Taxotere, Alimta, and Tarceva all have been approved by the FDA for recurrence/progression after prior treatment, but it’s tough to be too enthusiastic about a treatment with some side effects in a situation where there is no obvious evidence of anything currently to treat if the spot in your chest hasn’t been growing.
Good luck.