Skip to main content

tumor treating fields for meso - what are they actually doing and does it help

Family · · 86 views
So Joe's oncologist at Moffitt brought this up last week and honestly I had no idea what she was talking about. TTFields or tumor treating fields or whatever the acronym is. She said it's something they're using more now for meso patients, especially pleural, and I'm trying to figure out if this is something we should be considering or if it's just another thing they throw at you when you're desperate.

From what I can gather it's like... electrical patches you wear? And they're supposed to mess with cancer cells somehow. The science part lost me but basically electrical currents that make it harder for the cells to divide. It's FDA approved for brain cancer and they're doing trials with meso now.

What I'm trying to figure out is whether anybody here has actual experience with this. Like are people doing it alongside their immunotherapy or chemo? Does it actually improve survival numbers or is it more of a "we might as well try everything" kind of thing? And I'm guessing it's gotta be expensive even if insurance covers some of it.

Joe starts his next round of treatment in early January and I want to go into that appointment with real questions instead of just nodding along while I'm panicking about what comes next. Has anyone on here dealt with TTFields or had their doctor recommend it?

11 Replies

Veteran
Haven't done TTFields myself but my oncologist mentioned it during my treatment planning and honestly I was skeptical too. Best thing I did was ask for the actual trial data they're using for meso instead of just the brain cancer stuff, made it easier to decide what made sense for my situation.
Family
That's smart, asking for the actual meso data instead of just taking the brain cancer stuff at face value. I'm gonna do that at Joe's next appointment - you're right, there's a big difference between what works for glioblastoma and what might work for pleural. Did your oncologist have any data on how it combines with immunotherapy or did they present it more as a standalone option?
Family
I haven't dealt with TTFields myself but honestly this post is hitting me hard because my mom's oncologist at Mayo brought it up too and I did exactly what you're doing - just nodded and panicked later. What I ended up doing was asking if it was part of the trial they had going or if she was just recommending it as an add-on, because those are totally different conversations right? Like one thing nobody mentioned yet is whether your insurance even covers it outside of a trial. We found out in October that if it's not trial-based they basically don't touch it, which felt like a gut punch when we were already drowning in copays.

The electrical patches thing freaked me out at first because I'm imagining my mom wearing some sci-fi vest under her shirt all day but apparently once you get used to it it's just... there. One of the nurses told us some patients forget they have it on which made me laugh because my mom forgets where she put her phone so that tracks.

I think the real question for Joe's appointment is whether it's something that would replace part of his current plan or add to it, because that changes everything about managing side effects and honestly your own sanity as a caregiver. I'm juggling teaching and helping my mom and I legit cannot imagine adding more appointments or logistics right now. Your question about whether it actually improves numbers is the right one though. Don't let them brush past that one.
Family
Oh man yeah, that's such a good point about the trial vs add-on thing. I didn't even think to ask that specifically and now I'm kicking myself because that changes everything doesn't it. Did you end up getting a straight answer on whether your mom's was trial-based or if Mayo was just recommending it as something extra? And honestly the insurance question is huge too because Joe's been through enough without us getting hit with some crazy bill we weren't expecting. I'm definitely making that my first question when we go in next month.
Patient
I haven't gone the TTFields route myself, but I've been digging into this pretty heavily since my oncologist mentioned it as a possible addition to my treatment plan. The mechanism is actually interesting once you parse through the jargon. They're using alternating electric fields at specific frequencies to disrupt mitotic spindle formation in dividing cells, which theoretically slows or stops the cancer cells from multiplying. It's approved for glioblastoma and they started the STRIVE-Meso trial back in 2021 looking at it combined with pemetrexed and cisplatin for pleural cases.

The thing that made me dig deeper was finding the actual trial data. The STRIVE-Meso preliminary results showed some promise with progression-free survival improvements, but I want to be real with you, the numbers weren't dramatic enough that I felt comfortable committing to wearing those vests for hours every day. It's not just the electrical patches, it's the time commitment and the skin irritation issues people report. I have peritoneal, not pleural like Joe, so the positioning might be different for him anyway.

What I'd actually recommend is asking specifically if Joe qualifies for an active trial versus just using it off-label. The trial data is more robust and sometimes insurance navigates differently with trial enrollment. We got our second opinion at Cleveland Clinic back in December and their oncologist was more cautious about TTFields than Moffitt was, which tells me there's genuine debate in the medical community about how much it really adds to outcomes right now.

Pull the actual STRIVE-Meso results before that January appointment. Don't just ask if it helps, ask what the baseline survival numbers are for his specific stage without it and what the trial showed with it included.
Patient
Yeah my onco mentioned that too when we were talking options after my EPP, said it's still pretty new for meso but the early numbers look decent. Haven't done it myself yet but definitely worth asking about since Joe's starting fresh with treatment in January.
Veteran
Haven't done TTFields myself but my oncologist mentioned it too, said it's mainly being used in combination with chemo right now. Worth asking if Moffitt has any trial data on their pleural cases since that's what matters for Joe's situation.
Family
Yeah that's a good point about the trial data. I'm gonna ask specifically about their outcomes with pleural cases since that's what we're dealing with. Frank makes sense that they'd use it alongside chemo rather than solo. Did your oncologist say whether it was something they'd recommend for your stage or more of a "here's an option" kind of thing?
Patient
I haven't done TTFields myself but I've been following the clinical data on this pretty closely since my diagnosis. From what I can find in the literature, the results for pleural meso have been mixed so far and most of the stronger evidence is still in brain cancer, so honestly I'd push his oncologist for specifics on which trials she's referencing and what the actual progression-free survival numbers look like for meso patients before committing to wearing those patches full time.
Family
That's exactly what I needed to hear, honestly. I was getting all caught up in the "it's FDA approved so it must be good" thing but you're right that I should ask her for the actual numbers instead of just the sales pitch version. I'm gonna write down some specific questions about the meso trials before we go in January. Did she mention anything about how much time people have to wear them daily, or is that something that varies?
Family
honestly i'm so glad you asked this because my mom's team at Banner mentioned it too back in september and i was completely lost. like you i'm sitting there nodding and then going home googling "electrical cancer patches" at midnight which is never a good sign lol.

from what i gathered talking to her oncologist here in phoenix, the whole idea is those vest things with the electrodes create these alternating electrical fields that basically mess with how cancer cells divide. it's wild because it sounds so sci-fi but apparently there's actual data backing it up, especially for meso specifically. the FDA approval for brain tumors came first but yeah they're definitely expanding trials to pleural cases.

my mom hasn't done it yet because her stage 3 diagnosis came with some other complications that made her team say let's hold off for now, but we had a whole conversation about it in october and honestly the thing that made me feel better was just understanding it's not some desperate hail mary. it's being offered because there's legitimate research. that helped me stop spiraling about it being a sign things were worse than we thought, you know?

the practical stuff though - she'd have to wear it like 18 hours a day which sounds brutal when you're already dealing with chemo side effects and fatigue. and yeah insurance stuff is its own nightmare but her oncologist's office actually has someone who handles that specifically so that part wasn't as scary as i expected. the cost question is real though and definitely worth asking about at your appointment.

good luck with joe's january round. asking real questions is exactly the right move and honestly his team will probably respect that way more than just going along with it.

Share Your Experience

Sign in or create a free account to share your experience.

Discussions in this community are for informational and emotional support purposes only. They do not constitute legal advice, medical advice, or an attorney-client relationship. Always consult a qualified professional for advice specific to your situation. Community Guidelines

Call Now: (800) 400-1805 Free Case Review • Available 24/7