Mother is carboplatin-refractive, what else can we do?
My mother, age 76, was diagnosed with Stage 3C Ovarian Cancer in October 2015. It was too advanced, diffuse to operate so she did the traditional Carboplatin/ Taxol chemo for a series. In January, the dr said that while the tumor shrank, it was complicated to operate and she'd risk a colostomy, which scared her. The dr said she could do just one chemo drug (Carboplatin) to make it easier on her (the chemo was really rough on her). The hope was the tumor would shrink more and surgery would be possible after another round. (I was skeptical because I couldn't understand how removing one drug would continue to shrink the tumor)
In April, the dr said that the Cancer is inoperable, it would be dangerous, he would lose his license to operate. He told her she is Platin-resistant and it was a very aggressive form of cancer. She is seeking care at MD Anderson in Houston, TX but they live in Santa Barbara, CA where she is receiving the chemo.
She is now on Doxil (spelling?) and is scheduled to return in July for a scan. They added Avastin and she's also trying Cannabis Oil- why not?
It seems she is getting pain more frequently (she won't take pain medication) and I'm concerned the tumor is worsening and I don't think we should wait until July?
The drs have talked about clinical trials for Immunotherapy? Does anyone have information on getting in these trials? She was told to exhaust these normal courses of chemo first, but I don't understand why the first two series are sufficient and we can move on to the next line of defense? I understand there are trials at Stanford and that would be logistically-doable.
Please, any suggestions? Navigating the healthcare, especially where you must be your own advocate, is challenging and I appreciate the support of this community.
Comments
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lisagpaine, such a good
lisagpaine, such a good daughter to be looking what can be done for her mother - it is touching.
It sounds like your mother is having a tough time, has she called to talk to them about the increased pain? Maybe that would push up the scan from July?? I think I have read some of the women here have, or on, doxil. They might be able to chime in but you might find information by doing a search for it.
Hopefully your mother is letting you help her. You MUST have someone who will be your advocate if you can't do it for yourself. You will have to demand that they do more and push for answers.
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Lisa - Second section with web link references will NOT post !
Hey Lisa - Maybe later this site will take the rest of my letter to you, but I've said enough to give you the impetus to "charge ahead", follow your instincts and question everything this current surgeon says. A second opinion would be a necessity if this were me.
Loretta
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Lisa-Trying one link at a time- AVASTIN info
http://www.netdoctor.co.uk/cancer/medicines/avastin.html
“Avastin (bevacizumab - What is it used for?
...Advanced ovarian, fallopian tube or primary peritoneal cancer.
…How does it work?
Avastin infusion contains the active ingredient bevacizumab, which is a type of medicine called a humanized monoclonal antibody. It is used to treat cancers of the large intestine and rectum (colorectal cancers) and breast cancers that have spread to other parts of the body. It can also be used to treat advanced lung cancer and advanced kidney cancer…
Bevacizumab is given in combination with chemotherapy treatment that directly attacks and kills the cancer cells… To treat ovarian cancer it is given in combination with carboplatin and either paclitaxel or gemcitabine…
Side effects
Medicines and their possible side effects can affect individual people in different ways. The following are some of the side effects that are known to be associated with this medicine. Just because a side effect is stated here does not mean that all people using this medicine will experience that or any side effect.
- Raised blood pressure (hypertension).
- Diarrhea.
- Abdominal pain.
- Feeling weak or tired.
- Decreased number of white blood cells, red blood cells or platelets in the blood (see warning section above).
- Feeling of numbness or tingling in hands or feet.
- Slow wound healing.
- Infections.
- Bleeding.
- Headache.
- Nausea and vomiting.
- Constipation.
- Fever.
- Pain.
- Aching muscles or joints.
- Watery eyes.
- Sore mouth.
- Loss of appetite.
- Change in taste.
- Shortness of breath.
- Blood clot in a vein of the leg or in the lungs (deep vein thrombosis or pulmonary embolism) - see warning section above.
- Blood clot in an artery, causing a heart attack or stroke - see warning section above.
- Heart failure.
- Formation of holes (perforation) in the wall of the stomach or intestine.
- Formation of abnormal tube-like connections between organs that are not normally connected or between an organ and the skin (fistulae).
- Protein in the urine, which may be linked to kidney problems.
- Skin reactions such as dry or peeling skin, skin discoloration or hand-foot reaction.
The side effects listed above may not include all of the side effects reported by the medicine's manufacturer…
How can this medicine affect other medicines?
You should tell your doctor or pharmacist if you are taking any other medicines, including those bought without a prescription and herbal medicines, before you start treatment with Avastin. Similarly, you should also check with your doctor or pharmacist before taking any new medicines while you are still receiving treatment with Avastin, so they can check that the combination is safe.
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Lisa~Looks like time 2 check out Stanford~Might B time 2 move on
(My entire letter to you will not post, so I will break it up and see if the first part will post. Once again I am getting "blocked" by SECURITY. Can't tell you how many times they have attempted to "solve" this problem, but ever since they have "improved" the site, things aren't working as they used to. They have at least a dozen messages from me, and have made attempts to stop this from happening, but HERE WE GO AGAIN." I'll try again later to post the web link addresses I wanted to share with you. But here is the text of my letter.)
First of all, I’ll call you “Lisa” and say hello –
A few questions come to mind immediately as I read your letter. And I totally agree that the patient must be their own ADVOCATE, RESEARCHER, Physician’s Assistant and CAREGIVER AND/OR PATIENT all at the same time.
Secondly, at the age of 74, in November of 2012, I was diagnosed with Peritoneal Carcinomatosis, (numerous large tumors in my peritoneal fluid in my abdomen). I sought a SECOND OPINION at the University of Pittsburgh Medical Center with Dr. David Bartlett. There I had a PET/CT scan and exploratory surgery. Cancer would also be found in my ovaries. But understand that I was already Stage IV from the time of my initial CT scan in November. But since the treatments are the same for both Peritoneal Carcinomatosis and Ovarian cancer, I'm being treated as though I only had Ovarian cancer.
The findings were that the tumors were too large in size and too many to perform Cytoreductive Surgery (CRS) (debulking in layman’s terms). Their recommendation – have a series of chemotherapy consisting of Carboplatin and Paclitaxel (Taxol) and then they would take a second look.
So I completed the 6-session chemo combo treatment and it was ROUGH! But the findings were that the tumors were reduced in size to the point that surgery was possible. Now I will tell you that I had learned of a new “heated chemo treatment” known as HIPEC. It is done at the end of the surgical removal of (in my case) the spleen, gallbladder, ovaries, fallopian tubes, omentum and sections of my intestines. I had already had an appendectomy at age 12, or my appendix would have been removed as well. My surgery was performed on July 1, 2013. And the surgery wasn’t a piece of cake either. I had an infection that caused my incision to break open from right above my waist line to the pubic area. I was in the hospital there for a total of 42 days.
Now I will tell you that the infection was the culprit that extended my hospital stay. But ultimately it was cleared up. I have no complaints except for one “nurse’s aide” which I will call “Nurse Cratchet”! I won’t go into detail, but she should have been on duty somewhere patients were not trying to recuperate. She was grouchy and mean-spirited. And I might add, I gave her a nice write-up as to her quality of service. She should have been FIRED. I told the head nurse that I never wanted that lady in my room again. So sometimes you have to be the BOSS as well!
Then in 2014, three tumors were found to have attached themselves to the Caudate Lobe of my Liver. Now that’s not IN the liver, but bordering it in a sense. I had successful “Cyberknife” targeted radiation that was totally successful.
Then in June of 2015 that I began to have indications of intestinal blockage. (My stomach was distended and I had pains akin to childbirth. For all us mothers, most will never forget that pain or at least I NEVER WILL!
At that point, my oncologist did another CT scan, and said, “You’re going to have to make a decision at this point.” Now, he never made the decision, only gave me the options. That’s the way we agreed upon things from the very beginning. He kept nothing from me. He said, “Either you can choose to go on Hospice, or we can do another round of the same chemo. You had good results with the last series and it’s been 2 years. I think the chemo regimen would probably work well, and would give you many more “months” of survival.” I prayed about it, and decided to take the chemo route. So I started a second round on June 11, 2015 and completed it in Sept. of 2015. It did reduce the size of the tumors, but not the number. I tell you all that to let you know that women my age are still capable of having both surgery and treatments that can extend their life span and quality of life. Sounds like the doctor just wants to "let nature take its course", and he isn't about to "lose his job!"
Now Lisa, are you telling me that your mother is going to seek treatment at MDAnderson in Houston, TX, or has she already been seen there, and now returned home to Santa Barbara, CA to undergo the chemo treatment of “Doxil” plus Avastin? You can see references and remarks below my name. However, in my own research, I have not found AVISTAN to be anything remarkable. Personally, I am “averse” to Avastin and would never take it since I know of a couple of patients that have bled to death and AVASTIN was known to have adverse side effects that their relatives said caused it. You can decide for yourself if all the potential side effects of this drug are things you want your mother to be subjected to and yet it provides no promises for help with Ovarian cancer.
Lisa, as for your question about clinical trials for Immunotherapy, here is a link that should be helpful for you. Presently I am reading many articles involving immunotherapy because it is proving to be effective in more than one type of cancer.
Now Lisa, I am not liking this statement made by the doctor. “In April, the dr said that the Cancer is inoperable, it would be dangerous, he would lose his license to operate. He told her she is Platin-resistant and it was a very aggressive form of cancer.”
This would be enough for me to seek another opinion. Mom is not married to that doctor, is she? Some surgeons are more aggressive than others, and take on patients that some are too timid to touch. Why not seek a second opinion NOW at Stanford since you say that is doable?
And as for the colostomy, my surgeon mentioned that it might be part of my operation, but once he examined me more closely during the actual surgery, he ruled out both HIPEC (Heated Intra-peritoneal Chemotherapy) and a colostomy. Since I had prayed about it, I wasn’t overly upset about it. After all, the surgery wasn’t able to “eliminate” the many tumors in my abdomen, but they were able to remove “non-essential” organs to which the cancer would eventually spread. This has given me more quality of life than I would otherwise have.
Why not call up Stanford and see what it takes to have a consultation with one of their best surgeons? I have Stage IV Ovarian cancer, and I am no “spring chicken”, and I was a candidate for Cytoreductive Surgery after my first series of Carboplatin/Paclitaxel (Taxol) treatments. The tumors were eliminated but were reduced to a size that my UPMC surgeon could work with. Moreover, I had consulted with another surgeon before going to UPMC. But I ruled them out when they said they didn’t like to perform surgery on anyone over 60! Of course, they said, “You can send us your records though.” They weren’t in any particular hurry, but I WAS! And so UPMC made an appointment for me for a SECOND OPINION within 3 weeks from my initial diagnosis of “Peritoneal Carcinomatosis.” So, personally, I wouldn’t take that doctor’s word as FINAL. After all, you said your mom is Stage III. Yes, it will move faster, if no effective treatments can be found to slow the progression. But frankly, I think you need to “turn a corner” and find another place more hospitable to the needs of your mother. At least you will have satisfied your own conscience that you’ve done everything possible to have help for your mother.
At this time, I don’t understand enough about Immunotherapy to put it in a few words, but when I do more research on it, I will be sharing it with “sisters” here. I'll be discussing the possibility of immunotherapy for me as well, if my oncologist says I can be added to their trial. There are certain criteria for all clinical trials you know.
All the best to you in your endeavor to find help for your Mom. I know what it’s like to be both a caregiver, and a cancer patient myself. If you click on my picture, up will come my “about me” page and you will find that I’ve been around the block already, and thank God, I’m living with a miracle. And as for me, I’ve already lived longer than I imagined and like I say, I’m not gonna’ leave this earth one day sooner or one day later than my allotted number of God-given days. But God expects us to use the “good sense” He gave us, and I think you are doing just that. May He bless you in your efforts to find something that will give your mother more quality of life and more days to be with the family that she loves. I know you will say, “AMEN” to that.
Sincere prayers for you in your search for help,
Loretta Marshall
Peritoneal Carcinomatosis/Ovarian Cancer Stage IV, diagnosed November 2012
p.s. (My note: This is a heartbreaking letter from a widow whose husband was treated with Avastin.)
http://csn.cancer.org/node/213333#comment-1029056
Grandma Jo,
I'm so sorry that you're going through this with your daughter. It has to be so very hard to watch your child suffer. I hope you cherish every day you have with her. You sound like a great mother. Cancer is such a horrible disease and it can change your life overnight.
I lost my husband of 46 years last March 25th. I can hardly believe it's almost a year since I held him in my arms.He had been diagnosed in January with lung cancer & lesions in his brain & spine. He had 2 weeks of radiation to his brain & spine which showed good results. Then he had his first chemo treatment with 3 chemos one of which was Avastin. He started coughing up blood before his next treatment, so they did a CT scan and said things looked good, but his next chemo would be minus the Avastin.
Well it was too late. The damage from Avastin had already been done and he hemorrhaged in the bathroom one night. It was traumatic & I couldn't do anything except call 911. They worked on him for 45 min. but it was too late. I question the Avastin because on the info it said "can be a RARE side effect--hemorrhaging. Since it did say rare, guess we had faith that it wouldn't happen. But it did!
Sorry I'm rambling. Please be strong and give your daughter a hug for me, okay?
Friends, Carole"0
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