After oxi is done

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Volfan
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After oxi is done

Postby Volfan » Sat Aug 26, 2017 2:32 pm

I only have two more treatments with oxi.
For the people that went through oxi did you have any side effects go away after you were done with it?
Also doc talks like he will give me a choice between the pump and the pills.
Not having the pump would be great but I've gotten to a point I can manage the side effects for the most part. I'm worried that with the pills I might have a different set of side effects from them.
Stage IV Rectal cancer with liver mets
Oxaliplatin, avastin, 5fu
48 yr dude

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mypinkheaven
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Re: After oxi is done

Postby mypinkheaven » Sat Aug 26, 2017 3:26 pm

Most people seem to do fine with the pill Xeloda. I wasn't one of them. I felt really terrible. I have the pump now and it is better.
MSS, KRAS Wild NRAS Mutated
9/2012 CRC IIB Lft Colectomy 0 lymph nodes 0 Chemo
10/2013 CT clear
11/15 CEA 2.7 to 4.6
11/15 Spread to uterus. Hysterectomy
2/16 Pelvic radiation 25, brachytherapy 3
4/16 - 6/16 Xeloda
6/16 CT Several lung nodules 5 mm
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11/16 Transfer to UCSD Moores
12/16 Folfox + Avastin failed
2/17 Folfiri + Erbitux
8/17 5FU+Erbitux No 5FU bolus
7/18 Spread to vagina
6/18 Folfiri + Avastin + Trametinib
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Achilles Torn
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Re: After oxi is done

Postby Achilles Torn » Sat Aug 26, 2017 3:42 pm

I had Oxy discontinued since June and am on maintenance of 5FU pump with Avastin Infusion since. The cold sensitivity went away which is nice but I had my neuropathy steadily get worse for about a month and half (Numb fingers and feet, and a feeling of tingling in feet when moving my neck up and down) All in all manageable stuff.

It seems to have leveled off now or getting slightly better the last week or so.

I too am considering a switch to the pills as the pump is a drag especially with my kids.

AT
Diagnosed as 40 yo Male. BC Canada. Sigmoid Colectomy Dec. 2016
Pathology T3N2bM1 19 of 24 Nodes Positive + tumour deposits
PET scan - Para-Aortic and Iliac Lymph node spread. Stage VI.
Moderately differentiated. MSS. KRAS/BRAF Wild.
Mutations: TP53, ERBB4, MLL3, PDCD1LG2, PRKDC, SMAD3
FOLFOX + Bevacizumab Commenced Jan 9/2017 PET Scan July 2017 - on maintenance 5FU/Bev every 2 weeks.
Progression after Covid19 induced break June 2020. Resume Maintenance chemo of Capecitabine and Bev

Deb m
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Re: After oxi is done

Postby Deb m » Mon Aug 28, 2017 1:50 pm

My husband made it thru 10 rounds of Oxi. He had numbness on his fingers and the bottom of his feet. His fingers completely recovered after about 3-4 months. His feet recovered after about 6-8 months, but not completely, maybe 80%, but what little bit that's left in his feet does not bother him much at all.

deb m

NHMike
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Re: After oxi is done

Postby NHMike » Mon Aug 28, 2017 2:15 pm

A short discussion of this on another board.

https://csn.cancer.org/node/311615
6/17: ER rectal bleeding; Colonoscopy
7/17: 3B rectal. T3N1bM0. 5.2 4.5 4.3 cm. Lymphs: 6 x 4 mm, 8 x 6, 5 x 5
7/17-9/17: Xeloda radiation
7/5: CEA 2.7; 8/16: 1.9; 11/30: 0.6; 12/20 1.4; 1/10 1.8; 1/31 2.2; 2/28 2.6; 4/10 2.8; 5/1 2.8; 5/29 3.2; 7/13 4.5; 8/9 2.8, 2/12 1.2
MSS, KRAS G12D
10/17: 2.7 2.2 1.6 cm (-90%). Lymphs: 3 x 3 mm (-62.5%), 4 x 3 (-75%), 5 x 3 (-40%). 5.1 CM from AV
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susie0915
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Re: After oxi is done

Postby susie0915 » Mon Aug 28, 2017 3:02 pm

My neuropathy really didn't kick in until a few weeks after I finished my six rounds of xelox. The Dr. did reduce the dosage along the way due to diarrhea mostly. I'm 16 months out from xelox and still have some tingling and numbness in my feet. My hands are much better. As long as I wear something on my feet it's okay hasn't really prohibited me from doing anything just annoying. Not good barefoot though. Especially on hard surfaces. I did have raynauds in my hands before the cancer so when it's cold hands do get numb still. I don't think it's worse than before the cancer though. My oncologist prescribed me Neurontin but I really don't want to take it, can make you feel kind of loopy so I'm trying to just muddle through and hope it subsides some more. I find as long as I keep moving it helps.
58 yrs old Dx @ 55
5/15 DX T3N0MO
6/15 5 wks chemo/rad
7/15 sigmoidoscopy/only scar tissue left
8/15 PET scan NED
9/15 LAR
0/24 nodes
10/15 blockage. surgery,early ileo rev, c-diff inf :(
12/15 6 rds of xelox
5/16 CT lung scarring/inflammation
9/16 clear colonoscopy
4/17 C 4mm lung nod
10/17 pel/abd CT NED
11/17 CEA<.5
1/18 CT/Lung no change in 4mm nodule
5/18 CEA<.5, CT pel/abd/lung NED
11/18 CEA .6
5/19 CT NED, CEA <.5
10/19 Clear colonscopy
11/19 CEA <.5

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juliej
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Re: After oxi is done

Postby juliej » Mon Aug 28, 2017 5:55 pm

Oxi is tricky. Some of the side effects actually worsen in the weeks after your last dose! :shock: Neuropathy, especially, tends to keep building for a few more weeks, then levels out and starts going down. The other side-effects -- nausea, diarrhea, mouth sores, low blood counts, fatigue, loss of taste buds/appetite, muscle cramps -- they start going away almost immediately unless you are on other chemo.

For me, personally, there was a huge difference in my muscle cramping, fatigue, and loss of taste buds when I stopped oxi. I continued to take Avastin and Xeloda (pill form of 5FU) so I still had side effects from them, but oxi was responsible for my worst symptoms and I felt so much better when it was gone!

If you're fine with the pump, stick with it. Xeloda has its own set of side-effects but to me they were manageable and I didn't want to haul the pump around. If you're managing the pump's side-effects pretty well, then I'd stay with it if I were you.
Stage IVb, liver/lung mets 8/4/2010
Xelox+Avastin 8/18/10 to 10/21/2011
LAR, liver resec, HAI pump 11/2011
Adjuvant Irinotecan + FUDR
Double lung surgery + ileo reversal 2/2012
Adjuvant FUDR + Xeloda
VATS rt. lung 12/2012 - benign granuloma!
VATS left lung 11/2013
NED 11/22/13 to 12/18/2019, CEA<1

fumaros
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Re: After oxi is done

Postby fumaros » Tue Aug 29, 2017 12:30 pm

I had neuropathy in my hands and feet. It has been 9 months. Neuropathy is gone from hands, feet have improved drastically I still have tingly toes though. Congrats on being close to finishing.
Diagnosed 4/8/16, age 29
Colectomy 4/20/16
Stage III, T4bN1 Tumor 7x6.5x2. Muscinous Adenocarcinoma with SRC features
2/16 lymph nodes
Stage IV, Peri mets 5/2019
CEA 4/14/16 - 16.8
CEA 6/2/16 - 1.9
CEA 6/17/16 - 0.87, 7/16 - 1.33, 12/16 - 1.14, 4/17 - 0.6, 7/17 - 0.5, 10/17 - 0.9, 3/19 -5.8, 4/19 -10
FOLFOX began 6/24/16 - 11/25/16, FOLFIRI - 5/10/19
10 round FOLFOX, 2 round 5-FU & Leucovorin, 1 round FOLFIRI
MRI & CT 8/16 - NED, CT 12/16 - 10/17 - NED


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