Chemo first, then Mastectomy
Comments
-
Hi, Everyone ~
Ok, I saw the onco today (Jan 19), and we are definitely doing chemo before surgery. And, joy of joys, after poking around my armpits, he said he wasn't concerned about nodes and said nothing about SNB! Yay!! Now I can put the fear of nipple injections behind me!Onco did order a PET scan and an echocardiogram. The echo must be standard procedure since he didn't even listen to my heart, and I have no (known) problems with it.
The PET has gotten me a little shaken since I learned that cancer can spread even if there's no node involvement. I won't have that scan until Friday the 23rd, so there will continue to be much swallowing of Xanax until I have those results.
I will be getting a port Jan 22nd; I've been assured I'll be sedated for that, so I'm not too nervous about that.
So, if everything goes as planned, I should be starting chemo next week. While it's not something I look forward to, I am glad that we will finally be doing something!
Blessings to you all,
Artemis -
Artemis,
I got my port inserted about 2 weeks ago. The sedation for the port insertion did wonders for me. I felt rested, refreshed and took time to enjoy that sensation before I started thinking again about BC. It sounds like your stomach is in knots needing Xanax. I know what you mean being glad when the time for action finally comes,
Go to your "happy place".
-
I am having a SNB day after tomorrow and now I am scared out of my mind reading about them putting a needle in my nipple. My breast surgeon showed me physically that they would insert the needle right up next to the outside of my nipple. He also told me that I would not be put "under" for this part of the procedure as then I would be under anesthesia longer than he wants me to. HELP! I can't take a valium either that morning since they are putting me under.
Ok, back to the original thread. I responded days ago but that was before I had a treatment plan in place.
Like Deb and some others I am having chemo first. 4 rounds of AC then 4 rounds of Taxol. The idea is to shrink my tumor from 4CM to something small enough to where I can get a lumpectomy.
The reason for the SNB prior to chemo is to know if I have cancer in my lymph nodes before chemo kills them. At least that is my understanding. Also the radiologist insisted on this procedure first so that she would not have to radiate my underarm area for no reason at all if my nodes are negative.
After surgery I will have 6 weeks of radiation.
I think there are great reasons to do chemo first as others have stated above.
-
A little hope Ladies...can't remember if I posted this here.......but will do so again....my tumor was 3cm....After 3 A/C treatments the onc said it had shrunk 90%........last Thursday when I went for my second weekly Taxol treatment of 12, the mid level assistant told me she couldn't even find the lump in my breast or under my arm......I"m withholding being too excited until I see my regular oncologist as this was the first time I have seen the mid level asst.........but still 90% after 3 treatments is awesome!!!!!!!! I too am getting a lumpectomy so this makes me very happy!!! So do the chemo first......it works wonders.
luv, hugs and prayers
Debbie
-
Awesome news debbie! I know how you feel I too had really good results with neoadj chemo, but I still went for the mastectomy. Good luck with your surgery!
-
Hi ejlj
I seriously considered a mastectomy.....but after doing alot of research on mastectomy versus lumpectomy, looking up info on implants, decided against it.....my chances are the same with a lumpectomy and with the amount the tumors have shrunk, I figure it wouldn't be too disfiguring.....I just don't want to have to go thru the expanders, the fills, etc.....and possibly have to go in at a later date to have them removed and new ones put in, etc......while the possibility of nice boobs at 53 sounds nice, it just doesn't seem worth it to me...especially since I can get by with less invasive surgery........Granted not everyone can, and I fully understand everyones decision to get what they want, this is just my own personal opinion and based on my own case.........
Luv, hugs and prayers
Deb
-
Hi, lovemy3girls ~
Thank you for your lovely and encouraging post. I will make a mental note to fully appreciate the sedatives for the port placement, and I hope I get a bit of the refreshment and relaxation that you did.
Artemis -
Hi Debbie
This is Annette from Scotland. I saw my consultant and got the diagnosis. It was pretty much as I expected and I am soooo very glad I stumbled intp this forum as I was totally clueless about this vile thing no more than 2 weks ago.
Anyway, like 80% of you its invasive ductal carcinoma, high grade - it's termed "poorly differentiated" here in the UK. Tumour is 4cm and appeared most suddenly so is growing very fast, looks from the ultrasound that they nodes are clear, but I am undergoing sentinel node biopsy on Feb 12th. This willl be done under a general anaethetic. This seems to a very new technique and I am really lucky to bein such goods hands. I am waiting on pins though, to see the onc - he is the same doc who treated my late brother (died july 06, cancer of the gullet) So clearly I am a sea of conflicting emotions. I am to be assessed on Friday for surgery, bloods etc,
The plan is to undrgo chemo to shrink the tumour, then lumptectomy if it responds to treatment, followed by radiology. Alternative is mastectomy followed by chemo and the consultant favours the former. Also getting CAT abdominal ultrasound etc - the full works.
Breast care nuse reconds that I'll have "a crappy year" and to prepare for it.
Wish I could express my feelings. I have so many, everything to getting a dentist appt before treatment to how to manage financilly and practically - I live alone and have debts, like everyone else. I also was made redundant on 3rd Jan and have had no income since then. Waiting on sick pay, I think I'll get some kind of cancer premium, but have no idea how much it will be.
I know that everyone will say to concentrate on getting better - it's what I would say.
I cannot believe that at this age I am unemployed - have never been in the past - have the word that we are all frightened to say. I am putting on the bravest face for the family - we have all been through too much for me t put any more burden on them than I have to.
Tomorrow I will take on life assurance to pay for my funeral, whenever it comes - and make my will, try to get my teeth checked - need a filling or 2 - and see my GP to get a certificate for a year to ensure that I will get sick pay. I have slept most of the day - I am really fatigued. Having the family around for dinner tomorrow.
I will feel better once I have got my affairs in order I think.
Thanks for letting me unload guys.
Any advice would be greatly appreciated.
Love and lolllipops
Annette xx
-
hi all, i am also doing chemo first in hopes to shrink my tumor. My doc gave me the choice but what clenched it for me they said they would not have given me the chioce if one was a lesser treatment. they said cure rates were equal enough to do either. so while i am still strong and not trying to recover from surgery lets do chemo first and start kicking butt.
-
oh annettte, so sorry you had to join us here, but am glad you found us. Have any of your tumor receptors come back yet? Once I had a plan of action, I felt much better. The unknown is the worst. The emotional fatigue is crippling, sometimes more than the physical! I wish you well. keep us informed as to your progress. Tina
-
rsben-did you start yet and do you know if it's working? As Debbie said it's really "awesome" when you know it's working!
-
That's what I did and I am thankful everyday for my decision. Recovering from surgery chemo sick must be a nightmare + this way you don't have to worry about fixing your hair with limited mobility post op
. Good Luck! -
hi mom_of_2-any word on if you'll need more chemo or not yet? Been thinking of you and hope your doing well.
-
ejlj
No word yet. Just got back from Herceptin infusion and made sure everyone knows I am waiting. Even though I will be devastated if I need adriamycin...the waiting is worse. Might sound strange but I'd rather just get my crying out of the way and move forward with chemo if needed.
Bi lat recovery going well and hoping I am past point of infection, seroma, rejection etc. 2nd fill (maybe final) Thursday and hoping for a good report. I'm ready to schedule implant swap. If I don't need more chemo is it better to wait a certain period for healing sake? AND my PS uses Mentor MemoryGel...do you know anything about them?
Thanks for checking in.
Kris
-
mentors a great company. our rep does alot for our patients, great implants as well, but so is naturelle. I kinda think you should get the verdict on the adriomycin before proceeding with the swap. the only reason i say this is because i had adriamycin (with cytoxin) after my surgery and i ended up with an infection that was impossible to deal with during treatment. I ended up in the hospital and on IV antibiotics and then on antibiotics for weeks by mouth and had to have the d@#! drain put back in, then yet another infection, that's when they popped my expander! and more antibiotics! Not Fun! Then again, I had a mastectomy and not just an exchange, nonetheless it's still an invasive procedure. How are feeling after the herceptin?
-
Definitely no decisions until I find out about more treatment. I don't think PS will touch me for at least a month after chemo ends. I know surgical oncologist wouldn't do mast until I was a month out and because of coordinating both surgeons I waited 6 wks. Do you think that is enough time? After everything I have been through I do not want to be impatient and mess anything up.
Whats the difference between smooth and textured implants? Is one better than the other?
I'm lucky and don't really have any side effects from herceptin other that the long day making me tired!
-
6 wks sounds pretty good-definately err on the side of caution. Listen to your gut about that one. Did your surgeon give you a choice as to whether you could choose smooth or textured? We usually do not give a choice-it's pretty much up to surgeon preferance. "they say" that there is less chance of capsular contracture with the textured implants, MAYBE by 2-4%(very small) That would be a question for you PS-"what's your capsular contracture rate?" Our surgeon pretty much only uses smooth and we don't see that complication very often. hope that helps! I'm glad your tolerating herceptin well. I get wiped out as well, but can't tell if it's from the herceptin or just emotionally draining.
-
ejlj
Thank you so much....your info gives me a good starting place with my PS tomorrow. My husband I saw the change in our vocabulary the first time we walked into the cancer treatment center...8 months ago I barely knew the word "cancer" let alone "capsular contracture rate"! Amazing the path out lives have taken.
Have a good day...and thank you again from the bottom of my heart for your support...Kris
-
ejlj- first tx was 1/16 have another friday, don't know if it is working, if how crummy i feel is any hint then it is.
-
ejlj and Fairy49
Just got home from PS and feel much better. No infection! We talked about what to look for and fact that infection will always be possible because implants are foreign bodies. Had second and final fill...I am at 420 cc and spilling out of daughters 34C. I'm going for the "perky yet natural" look! They are setting up swap for a month out and hopefully won't have to cancel to get further treatment.
Thanks for listening...Kris
-
I'm new here, 28 years old, and newly diagnosed and I am here looking for info on having chemo first, which is what my docs recommend. Thank you so much all of you for sharing your stories and information. It's helping me feel more secure in this decision to do chemo before the surgery. I'm still getting all those pre-chemo tests and scans done, but I should be starting within a few weeks. I'll definitely be coming back here to learn from all of you.
-
Hi Bellydancer,
I decided to go with chemo first. So far I am glad I did because my tumor has responded and shrunk significantly. My lymph nodes responded also and are no longer swollen. The A/C treatments got progressively more difficult to tolerate, but now they are behind me. I have 8 weekly taxol and herceptins to go I am rebuilding my strength with Tai Chi and walking to prepare for surgery. After all the testing, I was ready to get on with it and do something. Knowing the tumor is shrinking has set my mind at ease somehat.
Keep the faith!
-
I did chemo first to try and shrink the tumor(s) but ended up getting a mastectomy anyway because it was then detected that I also had DCIS in the same breast. The chemo did shrink my tumor to nothing though after 3 treatments (of 6 TCH), the u/s I had subsequently showed nothing detectable as cancer at all! I also had a breast MRI before this decision was made. I am glad I did chemo first as it made the surgery seem like a piece of cake. Chemo is hard but doable though....
-
My tumor was so large that they could not do the surgery first. I had to have the chemo first. I did respond well, the tumor shrunk to almost nothing, as did the lymph nodes. I really didn't "choose" that course of action. I just went along with everything my oncologist said was to be done. Being that this was the same oncologist that saved my sister's life from stage 4 colon cancer, I was not going to question his decision. Turned out to be the best anyways. Chemo for me was very hard. But as kimbly said, it was "doable" and will be behind you. I'd do it again, even knowing how hard it was!
Cora
-
Hi Everybody. Nice not to be alone in this boat. Stupid cancer.
I will probably use some terminology that is incorrect because I'm learning as fast as I can.
I'm not staged yet. I'm 49, I felt a lump in right breast, Feb 26 this year, had it needle biopsied March 10, was positive, 1.7cm. Oncologist called for an MRI, that revealed another nodule in the left breast, ultrasound biopsy couldn't find it, so did biopsy with MRI scan technology. It was positive too - about 0.7cm. It is a distinct and different cancer, not the first lump having spread.
I wanted a PET scan and LNB to figure some things out for myself, but my team kept explaining that a good course of action was immediate lumpectomy surgery combined with LNB then we could check the margins, get me staged, etc. Just had that surgery last Tuesday.
(Side note about the nipple injections, not a pleasant thing, but there is local anesthesia in the injection as well, so it's only the initial surprise that gets ya. They feel like a slight bee sting because the liquid is going right under the skin rather than into deeper tissue. A good breathing technique will get you through it. I had both my breasts done at once - they try to do it quickly. I was glad two doctors were seeing to it simultaneously so I didn't have to wait for 8 consecutive shots! Still - not a picnic.)
Here's what my surgery results revealed: the margins on both sides were not good (that second margin was a surprise, because that's the one that looked smaller and "very well defined" in all the images.) I was pretty disappointed about that, but I know I want to have the double mastectomy now, rather than play around with trying to get all the cancer out. I think my breasts are trying to tell me something.
There is good news (fantastic news, really) - I was negative for cancer in all the biopsied lymph nodes. I hope that means it isn't spread? But I still wish my doctor would recommend some scans to alleviate this worry.
I don't like my oncologist - he doesn't listen or explain things well and is kind of dismissive. And he's what they call my "lead" doctor. I love my surgeon, who takes the time to listen, though I know he's heard the questions a million times before. He remembers things about how I think and what kind of person I am and considers my individuality when I ask his advice about things.
I have to meet with my medical oncologist two days from now (Friday) and discuss options. He has already said that if the LNB proved negative, he would still recommend chemo. I wonder why? He may have been thinking because the original course was lumpectomies instead of double mastectomy? I think I remember him saying chemo first, then mastectomy. Why in that order if I'm not trying to shrink lumps to prepare for lumpectomy surgery?
Can anyone shed some light?
Also, Annette, I feel your money woes and fears. I am currently employed, have decent health insurance, but my firm is downsizing and I fear being left out there uninsurable with a preexisting condition. I may lose my hair from worrying before the chemo gets a chance to attack it!
It's frankly another reason I am opting for mastectomy instead of keeping battling what's left of these lumps. I may not have the insurance coverage to keep monitoring the situation much longer - I just need to do as much as I can while I can.
Good health to all of you dear ones. Sorry this is so long.
-
Hi. I'm new to this as I just got the biopsy results today. Two lumps in right breast that are far apart so I will need a masectomy. However, my breast surgeon recommended chemo before surgery. I am confused. Since I'm going to need a masectomy anyway, shouldn't I surgically remove the cancerous tumors ASAP then do chemo? Anyone out there have more than one tumor, need a masectomy, and still do chemo first? What are the pro's/cons of that ? (at this point she doesn't suspect involvment in the nodes but I'll be having a MRI and bone scan done.)
-
Evelyn, sorry about all the troubles you are going through. But it sounds like you are getting good care, etc. Hope the questions you have about chemo, etc., will be answered. It may be that having the cancer in both breasts raises some flags about possible spread. It only takes one cell floating around to cause later problems, and chemo would help minimize those chances of spread.
Janet, you did not mention how large the tumor was. I had chemo first, then the mastectomy. My whole breast and underarm were involved. They said there was no way they could do surgery first withut having the tumors shrunk down first. I also had the MRI and bone scan done before starting chemo. Had the PET scan after chemo and surgery.
-
I have already had rad on both sides with lumpectomies and now will face bi-lateral with probably s-gap reconstruction. No word as yet about chemo, so i'm interested in anyone who has been in that situation as well. Which comes first? I also don't have the staging info yet.
-
Thanks for responding, Nelia48. So you don't think it's strange to start with chemo even if they know beforehand that you'll have a mastectomy? One of my tumors is 2 1/2 cm and the other is about 1 cm. How are you doing today? I just scheduled the MRI and Bone Scan... I'm worried, the odds haven't exactly been working in my favor lately. (I can't even believe I'm saying this stuff about myself)
-
I had chemo before mast and feel better that my tumors including the 5cm in my lymphnodes were all shrunk down to almost nothing. Pathology had trouble finding the original tumors. Good luck ladies with your decisions and treatments.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team