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Maintenance Alimta in Advanced NSCLC Shows Significant Improvement in Progression-Free Survival


May 17, 2008 - 3:05 pm printer friendly view / write comments
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Dr. West

   Last year, a provocative trial was presented at ASCO that compared early vs. later taxotere as second line therapy.  I described that study here, and it showed a very significant improvement in progression-free survival (PFS) and a near significant improvement in overall survival (OS) for the recipients of taxotere immediately after four cycles of first line chemo for advanced NSCLC.  These results were impressive enough that it would make us consider switching to a “maintenance” approach of giving second line treatment, in this case with taxotere, immediately after 4 cycles of first line chemo in non-progressing patients. 

    There were a few limitations to that work.  First, some prior, generally smaller studies didn’t clearly support the conclusion that maintenance or early second line chemo is definitely superior.  Because of that, most experts felt that it would be helpful to get another study that supported maintenance chemo before we declared it a standard of care.  Second, the prior trial waited a full three months before doing a repeat scan that would trigger a start of chemo in the delayed chemo arm — and about 1/3 of the patients on that arm were too sick to get chemo by the time they were found to have progression.  That’s too long, in my opinion, to wait before checking for progression, which is often found radiographically before a patient gets too sick for chemo.   With so many people in the delayed chemo arm not getting it, the trial was in some ways a study of everyone getting immediate chemo vs. 2/3 getting delayed chemo — not fair.

    But yesterday there was a press conference sponsored by ASCO to highlight the results of a trial sponsored by Eli Lilly and being presented at the oral presentation on advanced lung cancer at ASCO in two weeks (abstract here), and this result added to the prior study will likely change the standard of care, in my opinion.   The new trial, called JMEN by Lilly (every common has their own cryptic coding for trial names, and I don’t know if ANYONE really knows what JMEN refers to — it’s not an acronym), asked a very similar quesiton to the one from last year — does maintenance chemo (or early second line chemo, depending on your point of view) improve progression-free survival, the time before someone shows cancer progression and needs to change treatment plans?  The schema is as shown here:

JMEN Schema

(Click on image to enlarge)

As shown in the figure, 663 patients who had received four cycles of initial platinum-based chemo (without avastin) and didn’t show progression were randomized 2:1 to active chemo vs. an IV placebo every 3 weeks, and both groups received vitamin supplementation with B12 and folate, as is standard for alimta (who knows? maybe that leads to better results with a placebo as well). 

    The trial was clearly positive for demonstrating a benefit in progression-free survival as well as higher response rates achieved in patients overall who received an alimta “chaser” after initial platinum-based doublet:

JMEN efficacy

As shown in the table, there was a nearly two month improvement in PFS overall, and a nearly 20% increase in response rate for the general population.  These results were concentrated in the patients with non-squamous NSCLC, including adenocarcinoma, large cell carcinoma, and “other” (primilary histologies that couldn’t be assigned because the tumor is poorly differentiated or there is too little tissue to clarify a particular NSCLC histology), and they look especially impressive in the adenocarcinoma patients. 

   In a prior study called JMDB that compared cisplatin/alimta to cisplatin/gemcitabine in previously untreated patients with advanced NSCLC (described in a post here), the cisplatin/alimta arm looked better for non-squamous NSCLC, while cisplatin/gemcitabine looked borderline significantly superior for patients with squamous NSCLC.  Similar to that experience, in this maintenance trial there wasn’t an improvement in the median PFS with alimta for squamous cell NSCLC patients.  However,  according to the table in the abstract the “hazard ratio” (abbreviated HR in most of the tables and abstracts) that reflects the overall improvement in PFS over the course of the entire time line was 30% better and statistically significant despite that.  You can get a significantly better HR without improving the median if most of the improvement is before or after the median (which reflects just one spot in time, not the whole time course).   The other explanation is that there was no improvement and that the number in their table from the abstract was an error.  In any event, at the press conference, the lead investigator, Dr. Ciuleanu from Romania, said, ”In the squamous population there was little change in progression-free survival with pemetrexed therapy, consistent with previous phase III trials”.   I’ll let you know if the information in the table isn’t correct, but it’s fair to say that the results with maintenance alimta are at least less impressive in squamous NSCLC patients.

   The trial hasn’t collected enough long-term data to address any differences in overall survival, but the abstract and the press conference allude to a 20% improvement in OS with maintenance alimta, 13.0 vs. 10.2 months, that was just on the border of statistical significance (p = 0.06).  Although I might have hoped for new and updated information at the meeting, the comments from the press conference sound like we won’t learn more for another 6-12 months.

   This does bring up the question of how important PFS really is compared with OS.  I think this trial will be viewed as very influential because even if we consider OS to be far more important than PFS, the improvement by 2.8 months in the maintenance alimta arm is likely to be interpreted as very clinically valuable even if it isn’t necessarily statistically significant.  Combining these results with the Fidias trial of earlier vs. later taxotere, I believe that the new standard will be to use some kind of maintenance therapy after 4-6 cycles of first line chemo.  We are already doing that as a standard of care with avastin for avastin-eligible patients, but we will likely see more people adding chemo or tarceva to avastin based on these results.  While we don’t have trial results yet on whether tarceva will provide a similar benefit to chemo as a maintenance therapy, the trials that will answer that question should be available and presented in the next year or so.   And for the avastin-ineligible patients, I believe that while it will always be acceptable to give a treatment break to people who need it, our recommendation for patients without progression will be to transition immediately from first line chemo to a maintenance/early second line treatment. 

Posted in: Chemotherapy, Core Concepts, First-line treatment, Lung Cancer, Metastatic/Recurrent NSCLC, Second Line and Later, Non-Small Cell Lung Cancer (NSCLC), Second-line treatment, Stage IV/Advanced/Metastatic NSCLC, Treatment Digg    StumbleUpon    Furl    reddit    Delicious    printer friendly



  1. May 17, 2008 - 5:54 pm

    Hi Dr. West,

    This is a very interesting article and I hope that it helps future lung cancer patients. It did not help my husband. He had been taking Alimta for a couple of months prior to his passing. He also received the B12 and he took Folic Acid. I guess it was just too late in the game for him. Although he had been responding well to his treatments, he didn’t stand a chance. He was so weak from malnourishment that he couldn’t fight anymore. I hope that someday that lung cancer can be eradicated.

    cdejac

    cdejac
  2. May 18, 2008 - 7:45 pm

    hi dr.west this sounds really intresting ,but in our country like india our so called indian medical oncologists are not able to go for maintainance therapy immediately after firstline therapy.
    The reason for that is they are not well educated in terms of updating their knowledge and they are not ready to take the calculative risk as they dont want to loose their patients.please do the needful for our fool indian oncologists.

    amrish_gupta
  3. May 19, 2008 - 7:33 pm

    We’d all love to see more substantial gains in lung cancer. But our improvements have been pretty much evolutionary, not revolutionary. Alimta’s been a nice addition to our collection of useful drugs for lung cancer, and the concept of maintenance chemo immediately after first line therapy, whether with alimta or taxotere or something else, seems to provide a meaningful but not stunning improvement. A few months of benefit here, a few months there, and it adds up. But as you bring up, it’s not everyone who’s getting the same benefit. Some get many months, some get a few months, some stay about the same, and a few may even do worse. It’s only when we aggregate the results for everyone that we see an overall benefit. But our treatments are based on probabilities, and individuals fall all along a spectrum.

    -Dr. West

    Dr. West
  4. May 21, 2008 - 12:25 am

    Hi Dr West,
    I’m in my 12th week of alimta now, after 2 full radiation treatments (beyond maximim amount of rad recommended) and 3 chemo combinations during last 2 years. I see alimta doesn’t do well with my squamous type. Shortness of breath to black outs, total loss of appetite, worse fatigue (all red blood markers below range), scary constipation soonafter treatment, etc; i.e. quality of life much decreased with alimta. Probably soon i will need much more energy to find an interventional pulmonologist for possible laser and/or stent. Would you advise me getting off the alimta and getting some strength back? Thank you,

    Tom

    TomP
  5. May 21, 2008 - 7:38 pm

    Tom,

    I’m afraid I can’t give advice about how to manage a person who isn’t my patient. I would caution that this issue that alimta may be particularly favorable in patients with adenocarcinomas, while the gemcitabine-containing regimen was most favorable in patients with squamous cancers, can really be over-interpreted. The study that led to the idea of particularly effective chemo agents for different cancer subtypes is just one study, and it didn’t show that these drugs were useless in other lung cancer subtypes. It just indicated that some patients did better with one approach, while others did better with another.

    The bigger issue as I see it is your very significant side effects, which sound like they’re really at the outer limits of being bearable. It’s absolutely worth having a good discussion with your doctor(s) about whether having ongoing therapy is causing more harm than good.

    -Dr. West

    Dr. West
  6. October 3, 2008 - 5:38 am

    I have recently read and heard about new developments with an anti-cancer virus. The major breakthrough as compared to earlier anti-cancer virus developments is that the virus now developed will not be rejected by the body’s immune system. I gather this is a major development in destroying cancer cells of many types. A lead scientist in this development is Dr John Bell, of the Ottawa Health Research Institute, a foremost research facilty associated with the Ottawa Cancer Institute in Canada. Apparently they are on the edge of clinical trials. Have you any information on this development?
    Thanks
    Frank Leigh

    frankleigh
  7. October 3, 2008 - 7:21 pm

    Sorry, Frank. I can’t say that I’m familiar with this work.

    -Dr. West

    Dr. West
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