Article and Video CATEGORIES

Cancer Journey

Search By

Dr. Jack West is a medical oncologist and thoracic oncology specialist who is the Founder and previously served as President & CEO, currently a member of the Board of Directors of the Global Resource for Advancing Cancer Education (GRACE)

 

Lessons on Who Benefit Most with Second Line and Later Therapies
Dr West
Author
Howard (Jack) West, MD

One very important trial that has changed how we treat previously treated patients with advanced NSCLC has been a trial coded JMEI by Lilly, which sponsored this phase III randomized trial that directly compared second line treatment with alimta (pemetrexed) against the only FDA-approved second line treatment at that time, taxotere (docetaxel). Essentially identical in activity, this trial led to alimta's approval for lung cancer because it was associated with less frequent and severe drops in blood counts and fewer hospitalzations than with taxotere (abstract here). But from this trial we've also been able to glean additional information on who benefits more or less from second-line treatment.

Dr. Glen Weiss published a follow-up paper (available here) that analyzed several variables in the JMEI trial. Some findings were definitely anticipated: patients with the best performance status of 0 had a far better survival than patients with a modestly or more significantly compromised performance status of 1 or 2 (median survival 12.7 vs. 8.3 vs 2.6 months for 0/1/2, respectively) -- we knew that healthier patients do better and live longer.

Weiss Ann Oncol PS and survival

(Click on image to enlarge)

We also saw that patients who had previously had an objective response (complete or partial) did especially well, with a median survival of 15.8 months, compared to patients who achieved stable disease (median 10.5 months) or progressive disease (median 4.6 months) on first line chemo. So "responders respond", and the patients who did best early continue to do better, and those with aggressive disease initially tended to continue to do the least well.

Weiss Prior Response and OS

And you might expect that the patients who went the longest time between completing first line therapy and starting second line treatment did the best, since they'd have the slowest progressing disease. There was a modest difference there as well, with those who needed to move promptly to second line treatment (< 3 months) having a median survival of 6.9 months vs. a longer survival if you had a longer interval before needing second line treatment (9.2 and 9.3 months for 3-6 month and >6 month interval, respectively).

As has been seen in some other trials, such as the BR.21 trial of tarceva vs. placebo for 2nd or 3rd line therapy (abstract here), patients with adenocarcinomas had the longest median overall survival (9.1 months), followed by "other/mixed" (7.8 months), with squamous a little further behind (6.5 months). And women had a significantly better median survival compared with men, a full two month difference (9.4 vs 7.2 months). Age of younger than 70 vs. 70 or older didn't make a difference in overall survival.

There is significant attention in the paper on a trend toward better survival in the patients who received a combination of a platinum (cisplatin or carboplatin) and gemcitabine compared with a platinum and a taxane (such as taxol) or another platinum-based doublet:

Weiss JMEI survival and prior chemo

But this difference really didn't emerge as statistically significant.

One other issue came up in the further analysis of the trial, and that was the difference in outcomes with alimta vs. taxotere in patients 70 and over. I'll cover that next.

Next Previous link

Previous PostNext Post

Related Content

Online Community

An antibody–drug conjugate (ADC) works a bit like a Trojan horse. It has three main components:

  1. The antibody, which serves as the “horse,” specifically targets a protein found on cancer...

Bispecifics, or bispecific antibodies, are advanced immunotherapy drugs engineered to have two binding sites, allowing them to latch onto two different targets simultaneously, like a cancer cell and a T-cell, effectively...

The prefix “oligo–” means few. Oligometastatic (at diagnosis) Oligoprogression (during treatment)

There will be a discussion, “Studies in Oligometastatic NSCLC: Current Data and Definitions,” which will focus on what we...

Radiation therapy is primarily a localized treatment, meaning it precisely targets a specific tumor or area of the body, unlike systemic treatments (like chemotherapy) that affect the whole body.

The...

Biomarkers are genetic mutations (like EGFR, ALK, KRAS, BRAF) or protein levels (like PD-L1) in tumor cells that help guide personalized treatment, especially NSCLC, directing patients to targeted therapies or immunotherapies...

Hi Stan!  So good to hear from you.  I'm sorry for the late response.  I too have been out of town with family and missed your post, probably because I was...

It is so good to hear from you!  And I am so happy to hear that your holidays have been good and that you are doing well.  It sounds like your...

Recent Comments

JOIN THE CONVERSATION
Biomarkers
By JanineT GRACE … on
Radiation Therapy
By JanineT GRACE … on
Oligometastatic vs Oligoprogression
By JanineT GRACE … on
Hi Stan!! and happiest of holidays!
By dbrock on