Experiences with

Vinorelbine

So far she has received anastozole, nolvadex for the early stage, and for mbc fulvestrant +ibrance, paclitaxel, capecitabine, she is currently on vinorelbine iv. He has metastases on the liver and bones, so far he is stable.

I was put on xeloda, vinorelbine, enhertu and eribulin. In the past two years, by markers reacher nearly 5k and last Oct. I was in the ER.

He said I could do another round of Enhertu and I just said, look, just over a year now and I have gone through xeloda, vinorelbine and now enhertu. Markers back then were at 70. Last pet was in June. He asked for the scan well over a month ago. Finally today, he wrote on it stating it was urgent.

They gave her a choice between Vinorelbine and Carboplatin. She is reluctant to have chemotherapy because of the side effects. I would love to hear from the following people about their experiences: *Those decided not to have chemotherapy and how you are doing now?

Hi, could anyone tell me if this amount of chemo sounds right as all posts I read are more, I have stage 2b nsclc adenocarcinoma, plan is 6 weeks radiaton with week 1 cisplatin and vinorelbine, week 2 vinorelbine, week 3 just radiotherapy, week 4 same as week 1, week 5 same as week 2, week 6 just radiotherapy

On quick search it loks like Vinorelbine and Enhertu may be options? Thanks in advance ... 😢

So after a lot of stress and going from stage 2b to stage 3 my first week of chemoradiotherapy has finished, weekend off before vinorelbine capsules Monday and back on the radiotherapy. Didn't expect to feel so rough after first week and looking for advice please.

To be precise I have T3 N2 MO, I have been prescribed the following treatment plan : Approximately 6 weeks (5 days a week) of Radiology, followed by 3 courses of Chemotherapy (with the following drugs Cisplatin, and Vinorelbine) followed a year or so of Immunology.

Has anybody found that they feel fine when taking the drug, but get painful bones in the week off? This could be a cancer flare up, or something else? I am taking it orally.

rising again and it reached 2.47 ng/mL, we're now torn in between: 1) his MO recommended Xtandi, which costs ~ 1300$ and that's around 4.5X of his monthly income and the national health service in Egypt is not administering it. 2)instead, the national health service suggested a mix of Mitoxantrone & Vinorelbine

assigned to ribociclib (600 mg daily, three weeks on/one week off) plus an aromatase inhibitor – letrozole or anastrozole – and goserelin and 110 patients were assigned to a physicians’ choice combination chemotherapy regimen (docetaxel plus capecitabine, paclitaxel plus gemcitabine, or capecitabine plus vinorelbine

Oncologist has suggested oral chemotherapy treatment using Vinorelbine (navelbine) capsules as a middle, gentler path than intravenous route but hopefully more beneficial than no treatment. Does anyone have any experience of this treatment please before I decide to go ahead. Thank you so much

Or experience of taking oral Vinorelbine?

Now my doctor says we’ll start Vinorelbine next week….I think it has another name that starts with N,,,,(Navilbeane?)…I haven’t heard it mentioned on this site…has anyone been on it? Thanks in advance…

Hello Is anyone on here taking cape and vinorelbine for 2nd line of treatment? Just wondering how you’re doing on it xx

He says I can go onto Vinorelbine if Verzenio doesn't work. Has anyone gone on Verzenio after progression on Ibrance and if so, how did you do?

Anyone else had good results with cape and Vinorelbine together, I’m hoping for a five year miracle. Much love to you all

Epirubicin - once weekly continuous or 3 weekly Vinorelbine - oral day 1 & day 8 - 3 weekly cycle. I’m currently considering my options and Steve and I will visit Steph again on Thursday.

However, she has also offered me two other options to consider Epirubicin or an oral drug called Vinorelbine. I am very scared of IV chemo so I’ve been given up to a week to digest things and reach a decision on what to try next.

After only 3 months on Abraxane the scan showed progression on several places on bones! My oncologist said it is a “mixed reaction” some tumors have shrunk, but some of them have increased in size and few new ones! He talked about several options and we decided to go with Vinorelbin weekly! Fingers