Discuss your experiences with the benefits, risks, and side effects of immunotherapy treatment for breast cancer.
Posted on: Mar 3, 2020 11:10AM
I start Abraxane and Tecentriq tmrw. I think I know the answer, but want be sure before I shave my head lol, I will lose my hair correct? Never had immunotherapy before so just wanted be sure. Thanks in adv
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Mar 3, 2020 01:02PM dlittkemann wrote:
Will do. Just curious if anyone knew on boards before I see them.
Mar 7, 2020 01:05PM LoriCA wrote:
I can't answer for Tecentriq, but Abraxane is protein (albumin)-bound paclitaxel, the same chemotherapy drug as Taxol, but protein-bound instead of using a solvent. Because Abraxane doesn't use a solvent like Taxol does, it is supposed to be easier to tolerate. Taxol is paclitaxel and Abraxane is nab-paclitaxel. It does cause hair loss. You may not lose all of your hair, but you will certainly lose some, if not most, of it. It can also cause neuropathy so you may want to look into icing your feet and hands.
Mar 7, 2020 01:23PM JCSLibrarian wrote:
I started Abraxane December 2018. I lost my hair three weeks later. It took a while longer, but also lost eyelashes and eyebrows. The side effects were minimal other than the hair loss. About three months ago the neuropathy started. PA said to take Vit B6. I am currently on a chemo break and the hair has started to come back.
Mar 7, 2020 01:32PM dlittkemann wrote:
Thank you all for replies. I see you are also triple negative JCS. So why on chemo break? Did the treatments work so far
Mar 8, 2020 09:48AM JCSLibrarian wrote:
MO has done scans every three months since the diagnosis. The only bad one was the very first PET scan. I asked him to treat me with curative intent. He thinks we “may” have “got it.” I am taking a break to see what happens and to get all my counts back to the more normal range. There will be yet another set of scans the end of this month to see how things are going. Fingers crossed! I feel great and believe things worked for me. It may come back, but I refuse to spend much of my time worrying about it.
Mar 8, 2020 10:25AM - edited Mar 8, 2020 10:32AM by dlittkemann
JCS I am so happy for you and pray it continues to work! I have bone mets, spine and pelvis area. Praying this works and keeps it at bay for a long time. I have a 5 year old and I need to be here for himat least til he's independent (praying) and pls let me know how your end of month scans are! I don't know many TNBC w mets so happy to have found you :-) (((hugs)))
Also have you been getting weekly treatments since diagnosed? I feel ok. Lack of energy and aches here and there. Overall ok but I’ve only had one treatment thus far. Hoping at my 3 mos scan they will tell me it’s working.
Mar 8, 2020 01:25PM JCSLibrarian wrote:
I did the three weeks on/one week off with Abraxane for slightly over a year. I was more tired than usual during treatment, but no other QOL side effects. I did start neuropathy in my feet about four months ago. My MO said that having metastasis to the bones was very doable long term. He is more concerned about organ involvement. Thetnbc part does worry me some.
You must be somewhat younger than me as my kids are in their 30’s. So unfair to have to deal with this while so young. I do hope your treatment goes well and you stay healthy as can be expected with this diagnosis for years to come. Let’s stay in touch.
Mar 8, 2020 01:50PM dlittkemann wrote:
That’s what I’m doing too w the addition of Tecentriq (immunotherapy). Thanks for such encouraging words re bone mets. I appreciate that so much. I’m 45. Just turned in Dec. Definitely want to stay in touch. Thanks for the reply. Appreciate it so much and happy you are doing so well :-)
Mar 11, 2020 10:53PM - edited Mar 11, 2020 10:54PM by Deedi
Dlittkemann. I hope your treatment today went well. I was on the tecentriq and abraxane for six months and tolerated this combo well I hope the treatment works for you. I wish I could have stayed on it for a while longer I did lose my hair but of course everyone is different. I would ask you oncologist.
Jcslibrarian. Did I read your post correctly. That you are taking a break and that you think you might have “got it" with abraxane. That is so exciting! I am So happy for you I am grateful My cancer has been holding in my mediastinal nodes with only slight growth (mm)with each scan for about 16 months now. you are my new inspiration! Good luck on your scans! I will keep my fingers crossed.
Mar 19, 2020 04:29PM dlittkemann wrote:
...well 3 treatment and no hair loss yet. When on taxol and ACT red devil it was all gone in 2 weeks. Hoping I don’t lose it all but if I do,I have two nice wigs. Have to look at positive side. Lol ;-)
May 21, 2020 05:59PM Naesha wrote:
I am new to this group. I will be starting the Abraxane starting next week. According to doctor, this should be tolerable than the AC,Taxol and Carboplatin. I was on oral chemo Xeloda but looks like it did not help much and my cancer is back again. So this time my ONC is using the Abraxane, once in 3rd week. So I asked for the prevention of hair loss and cold cap was suggested. Has anyone used cold cap to prevent hair loss. I lost all my hair during AC and Taxol. I think i do not want to go through the same hell. Thanks god i did my microblading after the treatment so i am less worried on eyebrows. But hair loss is something that plays a big role for me to get easily demotivated and lost my track.
Can any one of you share the exp.
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