CEA test

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JDinNC
Posts: 771
Joined: Fri Jul 05, 2013 9:49 pm
Location: Murphy, N.C.

CEA test

Postby JDinNC » Sat Sep 26, 2015 8:19 am

I never really thought about this...but how often should you have your CEA tested. My next one is in Dec. just before my next CT scan. My last one was before my last PET scan in July. I haven't personally seen my oncologist since maybe around June because he's retiring at the end of this year and he's always on vacation. Wouldn't you normally have one done between your scans to be sure your CEA hasn't risen any. And if so, they can take quicker actions?
61 y/o female @ DX...........
T3N0M1
6/13 DX- stage 4
Sigmoid colon cancer.
One met to lung
7/13 colon resection
8/13 lung resection
7/17 four years....NED
8/18 five years....NED
MELANOMA
63 y/o @ DX
6/15 stage 2a
7/15 surgery on arm
7/15 NED
4/16 recurrance
5/16 remove metastasis from back
5/16. Started immunotherapy
8/16 discontinue treatment
7/18...PET scan...NED

Nik Colon

Re: CEA test

Postby Nik Colon » Sat Sep 26, 2015 8:22 am

Idk what's standard, but that seems like a long time between. I would have to check mine. I know I just had another one done recently.

1/15/15 - 4.9
3/11/15 - 3.2
3/26/15 - 2.9

I know I have had at least 3 after that

1.2 after surgery 6/15
4.6 after starting folfiri 7/15
3.6 on last one 9/15

DarknessEmbraced
Posts: 3817
Joined: Sat Nov 01, 2014 4:54 pm
Facebook Username: Riann Fletcher
Location: New Brunswick, Canada

Re: CEA test

Postby DarknessEmbraced » Sat Sep 26, 2015 9:44 am

I have my CEA and CA 125 checked every 3 months.
Diagnosed 10/28/14, age 36
Colon Resection 11/20/14, LAR (no illeo)
Stage 2a colon cancer, T3NOMO
Lymph-vascular invasion undetermined
0/22 lymph nodes
No chemo, no radiation
Clear Colonoscopy 04/29/15
NED 10/20/15
Ischemic Colitis 01/21/16
NED 11/10/16
CT Scan moved up due to high CEA 08/21/17
NED 09/25/17
NED 12/21/18
Clear colonoscopy 09/23/19
Clear 5 year scans 11/21/19- Considered cured! :)

Joannerogers
Posts: 260
Joined: Tue Jun 16, 2015 4:50 pm

Re: CEA test

Postby Joannerogers » Sat Sep 26, 2015 10:52 am

Since I'm still undergoing treatment I have mine done monthly.
53yo married 27 years, 2 children, 24 and 25
Diagnosed april 23,2015 rectosigmoid
Starting CEA 1845
Port placement and liver bx April 27
Folfox started april 29
Avastin added on May 6
Stage IV crc with mets to 50% of liver

10/13/15 dc'd transfusion #12...toxic
Pet/ct scan on 11/3/15
20% liver resected all margins clear 11/30/15
8/18/15 cea 21.
9/15/15 cea 13.9
10/13/15 cea 14.4
1/22/2016 cea 2.5
LAR 02/15/16 all clear

rp1954
Posts: 1857
Joined: Mon Jun 13, 2011 1:13 am

Ideally...

Postby rp1954 » Sat Sep 26, 2015 11:55 am

Sounds like your dr has already checked out, I'd be shopping and interviewing. "... can [they] take quicker actions?" Yes - the real question is can you - we always have to advocate for ourselves.

Blood tests may not catch everything but the current "standards" (NCCN, ASCO, etc) are not well designed to protect attentive stage 4s in the zone between first NED and five years out. A CEA test is not very thorough coverage nor is even quarterly likely to be timely for a fast developing problem. Scheduled scan images are usually quarters behind what is possible with frequent biomarkers, trended. A large percent will recur sometime, and need timely treatment to either resolve it, while curative surgery is possible, or to yield the maximum chances and time. Biological and chemical tweaking also becomes possible.

Suppose you knew for absolute sure that you would recur at some random time in those 3-4 years, as most still do. What could you do? What would you do if you were a multimillionaire with a finger prick cancer test?

Multiple kinds of markers, blood taken and results accumulated weekly, reviewed bi/monthly by an expert analyst would be pretty protective. Few of the "oh-my-god" surprises we see and there would be better options. The limitations are the tests themselves, the physical limitations of sampling, personal psychology, economics and the expertise.
In the near future, it may be possible to drop by Walgreenmart, and get your finger/elbow stuck for a few drops and get 10-20 panels. I'd be willing to do that weekly, maybe 10 days, and have it automatically swept into my spreadsheet. Even now, with the current sanguineous blood draws and a budget, we've found 2-6 weeks doable. Second, is that most people have a lot of scatter in their data due to inflammation, (cancer) metabolism or lab test methods. This scatter can reduced and minimized in the NED period and with some treatments, but is a medically unaddressed/underserved area.
Psychologically, it would be best if the patient didn't have to see every high frequency test asap, but rather had a brief consult monthly, bimonthly or even quarterly that scored or reviewed a matrix of several accumulated tests that yielded more graded information and certainty, and some minor chemical recommendations.
Finally, the big sticker is expertise. Some medical papers are slowly admiting that various biomarker trends are very sensitive and predictive, useful in practice. Multiple markers in skillful combination is even further behind. However our doctors mostly seem to be ignorant or asleep on these subjects, and the national payers, HMOs, insurance companies or their stooge doctors would probably attack them if they weren't. We probably need a results oriented (inter)national colorectal subscriber service to do this.

Even today, given the costs of belated treatment, the economics should not be a barrier for monthly draws. Our system is just not arranged efficently and effectively for us.

FYI, we watch for problems, including liver, with CEA, (AFP or CA19-9, one frequent, one qtrly), ALP, GGT, LDH, adjusted and quality controlled with hsCRP and ESR, "monthly" (4-6 wks) in good times. If we had LEF prices available, we'd do quantitative D-dimer more often, at 4-9 week intervals.
watchful, active researcher and caregiver for stage IVb/c CC. surgeries 4/10 sigmoid etc & 5/11 para-aortic LN cluster; 8 yrs immuno-Chemo for mCRC; now no chemo
most of 2010 Life Extension recommendations and possibilities + more, some (much) higher, peaking ~2011-12, taper chemo to almost nothing mid 2018, IV C-->2021. Now supplements

jhocno197
Posts: 817
Joined: Mon May 11, 2015 9:33 pm

Re: CEA test

Postby jhocno197 » Sat Sep 26, 2015 2:17 pm

My husband's was being checked every two weeks. I don't know what they'll do now, though, since they've stopped his chemo.
DH - dx Dec 2014, stage IV with bladder & peritoneal involvement - non-resectable
Colostomy
FOLFOX failed
FOLFIRI failed
Tumor actually distending pelvic skin
Not a candidate for last-ditch pelvic exenteration
Stivarga finally begun 2/19/16
Tumor growing/fungating
Lonsurf started 11/18/16
Died 3/10/17

Lee
Posts: 6207
Joined: Sun Apr 16, 2006 4:09 pm

Re: CEA test

Postby Lee » Sat Sep 26, 2015 2:52 pm

I was a stage IIIC. For the first 3 yrs, I saw my Onc every 3 months, and had CEA done just prior to seeing Onc. I would get scans every 6 months. After 3 yrs, saw my Onc 2X yearly with no scans but 2X a year CEA test. When I had to switch Onc, I was getting yearly CEA and sometimes scan till the 10 yr mark. On this past visit, 11 yrs out, Onc announced I was cured and would not be testing me for CRC anymore. I will continue to see her because I'm an ex smoker and she will monitor my lungs, my choice.

Lee
rectal cancer - April 2004
46 yrs old at diagnoses
stage III C - 6/13 lymph positive
radiation - 6 weeks
surgery - August 2004/hernia repair 2014
permanent colostomy
chemo - FOLFOX
NED - 16 years and counting!

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dianetavegia
Posts: 2731
Joined: Sat May 16, 2009 8:47 pm
Facebook Username: Diane Weldy Tavegia
Location: Villa Rica, Georgia

Re: CEA test

Postby dianetavegia » Sat Sep 26, 2015 3:05 pm

Mine is always done after my MRI/ CT scan when I go for results, so every 6 months. Sometimes I have to beg for months to know the results, other times it's 3 or four weeks.
Stage III cc surgery 1/7/09. 12 tx FOLFOX
Stage IV PET = 1.5cm liver met. HR 4/11/12

14 years since dx and 11 years post liver resection.
Pronounced CURED and discharged by onc

“O Lord my God, I cried out to You, And You healed me.” Psalms 30:2

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ANDRETEXAS
Posts: 662
Joined: Fri Feb 14, 2014 11:01 am
Location: Austin, Texas (University of Tennessee alumnus)

Re: CEA test

Postby ANDRETEXAS » Sat Sep 26, 2015 4:22 pm

At my request, I have all my blood work and CEA tested every six weeks. My blood work is posted online two days afterward, and I go by and pick up a copy of my CT results the next day or two days after it is done.
2/10/14 - Colon resect
2/13 - DX- Stage IIIb
6 of 18 lymph nodes cancerous
3/7 - Port placed
3/11 - FOLFOX (12 rds w/full oxi)
8/14 - Chemo finish
8/25 - CT- Inc
9/5 - clean PET
12/10- clean CT

3/2/15 - Clean colonoscopy & port removed
3/4 - clean CT
9/21- clean CT

3/23/16 - clean CT

2/22/17- clean CT

3/21/18 - clean CT
4/1 - clean colonoscopy

3/11/19 - clean CT
9/23 - Five-year release - Annual visits now !

4/13/23 - clean colonoscopy

ONE DAY AT A TIME !


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