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Straight talk about what works & what doesn'tDr Vasilev gynecologic oncologist

 
 
 
 
How Is Cancer Treated? PDF Print E-mail
In order to make intelligent choices about treatment, you need to know the basics of standard mainstream proven treatment.  At the moment it is your best chance of beating Cancer.   However, don't forget to look around this site for integrative options which include promising, plausible or proven alternative and complementary therapies which may increase your chances of cure and help reduce cancer related symptoms and/or treatment side effects. 

The three primary methods to treat a cancer are surgery, radiation and chemotherapy. In treating gynecologic cancers sometimes all three are used, and often two are combined depending upon the cancer and how far it may have spread at the time of diagnosis. Immunotherapy has a far lesser role and is mostly in experimental phases, although there has been a resurgence of interest in more recent findings.

There are also four treatment goals in cancer management. First and foremost is prevention. Failing that goal, the rest are cure, prolongation of life, and palliation. Palliation means that treatment is given to help alleviate a symptom of the cancer rather than trying to cure the cancer. This might mean elimination or reduction of bleeding from a uterine cancer (e.g. hysterectomy) which has already spread or reduction of pain from treating an area where cancer is pressing on or involving nerves (e.g. radiation or chemotherapy).

SURGERY
Surgery alone can cure many gynecologic cancers, IF and only IF, the cancer is still contained in the area that it started; this is otherwise known as localized disease and usually means it is in an early stage. The organ the cancer started to grow in, like the uterus or ovary, must be easily removable with no sign of the cancer spreading beyond that organ into surrounding supportive tissues. The chance of cure with surgery alone is best then the type of cancer (how it looks like under the microscope) is not one that microscopically spreads early by the blood or lymphatic system. The best example of this situation is the common form of uterine or endometrial cancer.

lymph nodes in the area of the organ involved by cancer are usually removed during surgery. This is done for the purpose of staging. Very simply, a way to determine if the cancer has spread beyond the organ it started in. Again, if the cancer is fairly small inside the organ it started in, and the lymph nodes removed have no cancer cells found in them (i.e. no metastases), surgery alone can result in a cure. In many cases, surgery is preceded by or followed by additional treatment in the form of radiation or chemotherapy or both. This is called neo-adjuvant (before) or adjuvant (after) therapy. The role of surgery in these cases is to more accurately determine if the cancer has spread and remove the bulk of the tumor.

RADIATION THERAPY
Radiation therapy is otherwise known as X-ray therapy and is delivered to the patient several different ways. Generally, this form of treatment is given when an entire area or region of the body must be treated. For example, when a surgery for endometrial cancer uncovers the presence of cancer cells in the pelvic lymph nodes, the entire area or region of the pelvis is treated. This relatively large area is usually treated with external radiation treatment, otherwise known as teletherapy. This means that X-ray beams are given to this pelvic area. This external X-ray treatment only takes a few minutes a day while the patient lays on a table and is repeated every day Monday through Friday. This is repeated approximately 20-25 times and MUST follow this schedule without skipped days, otherwise the result is not as good. On occasion a day or two of delay is unavoidable due to severe side effects. X-rays pass through the skin and are focused on the area requiring therapy which is located much deeper. At that area of interest, the maximum amount of energy is deposited. This results in damage to the genetic structure of cells, killing them before they can reproduce. Unfortunately, some cancer cells are more resistant than others and can repair themselves more readily than others. However, upon daily radiation, most are eventually killed. Normal cells in surrounding non-cancerous areas are also affected but have better mechanisms of repair. Radiation doctors and physicists take all of this into account in planning treatment dose and timing so that the treatment is most likely to kill the cancer cells and limit severe damage to normal cells in the area.

The rad (Radiation Absorbed Dose) is measurement of the amount of radiation dose delivered to the cancer cells. You should be aware that the newer term for this is the CentiGray (cGy), which is equivalent to the rad. Both are used in medical jargon. Typically, 200 rad is delivered per day (same as 200cGy). One hundred rad or cGy is referred to as a Gray(Gy). Therefore a typical weekly Monday through Friday regimen of 200cgy per day for 5 weeks often totals to 5000rad or cGy (same as 50 Gy).

Another common way radiation therapy is administered is by way of using implants, and is called brachytherapy. You may hear or read about other terms for this, including intra-cavitary or interstitial implant, radium implant, cesium implant, high dose rate insertion, or needle implant. In addition, some implants are named after the physician who developed the technique, notably the Syed interstitial implant. These various kinds of implants are all placed into the cancer itself or right next to it, and a radioactive element (Cesium or Radium) is placed into the implant (called after-loading). The implant is then left in place for several hours (called high dose rate) or several days (called low dose rate) and then removed. Brachytherapy is used to deliver very high doses of radiation to a smaller area involved by cancer while limiting damage to surrounding organs and tissues, like the bladder and rectum. While this form of radiation delivery is sometimes used alone, it is more often used in combination with the external form or radiation (teletherapy) to complete the total dose to an area affected by cancer. The amount of each is determined using very specialized radiographic and computerized techniques (called simulation), in order to optimize the probability of eliminating the cancer cells and minimizing radiation damage to normal surrounding organs. The total amount of radiation given is limited by the tolerance of the normal organs and tissues in the cancer afflicted area. The total dose to an area cannot exceed the tolerance of normal organs or severe complications will result. On the other hand, unless the radiation dose is optimized to a cancerous area, there is a danger that the treatment will be incompletely effective. Again, this is all taken into very serious consideration during the treatment planning and simulation process. For any given general situation, standard doses have been developed which then require consideration of the specific patient’s anatomy and other health factors. There is always a risk vs. benefit trade off. Specifically, it is the probability of cure vs. the risk of complications.

CHEMOTHERAPY
Chemotherapy is the administration of anti-cancer drugs, usually by an intravenous injection or infusion. Second most common administration is by pill. Since the drugs travel by bloodstream to almost all parts of the body, this type of treatment can affect cancer in almost all parts of the body. Because of this, chemotherapy may also result in temporary loss of hair or other “systemic” side effects. Although these side effects are common they are not inevitable and vary depending upon the drugs used.

Almost all chemotherapeutic agents act by interfering with cell division. Since cancer is the result of uncontrolled cell division, if cancer cells can be prevented from dividing then the cancer cannot grow. Normal cells also must divide to replace those lost through wear and tear as well as to repair tissue injuries. These normal cells are also affected by the chemotherapy. Those which divide fastest are the ones most affected, hence hair loss and some intestinal side effects. Both of those areas have cells which normally divide rapidly. Chemotherapy is also referred to as cyto-toxic therapy. This is simply another way of saying cell-toxic therapy. Administration of all chemotherapeutic agents can lead to some form of side effects. Often these side effects are specific to the drug which is being given. Some can affect the heart, many can affect the kidneys, and some can damage nerves. Almost all of these drugs are toxic to the bone marrow which produces the white (infection fighting) and the red (oxygen carrying) blood cells and the platelets(help blood clotting). Chemotherapy drugs are toxic to bone marrow and cause a drop in the white cell and platelet count after each chemotherapy administration. red cells are not affected as much, but tend to drop over time after multiple chemo treatments. The lowest white cell and platelet count, which usually occurs about 7-14 days after treatment, is called the nadir count. This low count can persist for 3-10 days, but usually the white blood cells and platelets “recover” or come back up in time for the next treatment. After multiple administrations the recovery can be slow, resulting in delays of treatment unless certain bone marrow supportive drugs are given to help accelerate recovery, thereby minimizing delays.

If the white cell count gets too low, then infections can occur which may be fatal. If the platelet count gets too low then spontaneous bleeding can occur in various parts of the body. Sometimes this bleeding may be detectable (rectal or vaginal bleeding) but sometimes it can occur in enclosed organs like the brain, resulting in a stroke. Over a period of time there may also be a drop in the red cell count which could cause symptoms of fatigue. For this a transfusion may be required, or bone marrow support drugs can be given to keep the red blood cells count up.

Many drugs can cause nausea and sometimes vomiting. However, the medications used to prevent this have improved immensely to the point that some patients experience minimal to no nausea. Since chemotherapy affects the lining of the mouth, stomach and intestine, irritation and sores can occur in any of these areas causing pain, possible bleeding and diarrhea. A disturbing side effect is nerve sensation changes at the fingers or toes from taxanes, cisplatin, or altretamine. In the worst cases, this can alter the ability to use hands for fine movements. While this often resolves at least partially, it can persist for long periods of time or indefinitely. Some of the drugs can affect the kidneys and bladder, but prevention via administration of lots of fluids or medications is usually very successful. Some drugs affect the skin, and often increase sensitivity to sunlight. In the case of Doxil (a common drug used in ovarian cancer), skin rashes may develop. While other side effects can occur they are usually more rare. However, a full discussion with your treating physician should address what might be expected with the particular drug treatment that is planned.

Chemotherapy might be administered to you under the supervision of either a medical oncologist or a gynecologic oncologist. Both are certified to safely administer chemotherapy and handle the complications thereof. Medical oncologists administer chemotherapy to patients with many kinds of malignancies, while gynecologic oncologists restrict their practice to gynecologic cancers only. Therefore, in seeking opinions, it is important to know what the level of expertise is in managing you particular kind of cancer. Some medical oncologists take a special interest in gynecologic cancers, otherwise it is a prudent idea to seek the opinion of a board certified or fellowship trained board eligible gynecologic oncologist for the overall treatment plan.





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Last Updated ( Sunday, 10 February 2008 )
 
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  • Removing ovaries to be safe - good idea???? 20:00 - 20.11.2008

    Dear AllA while ago I posted asking if US could DX ovca at early stage, and got SO MANY wonderful replies, for which I was extremely grateful.I've now gone on to have some investigative work done, and a detailed TVS has shown that I have a cyst on my right ovary which is not functional, but is almost 50:50 either benign or borderline.There doesn't seem to be any invasion of the ovary tissue from the cyst, and it is poorly vascularised, both of which I believe are optimistic signs. I read (on an Internet search) that around 7% of borderline cysts progress to becoming malignant. However, because my husband has Stage IV kidney cancer and 'staying alive' is, right now, our main concern (!!!!), I am thinking of simply having a double oophrenectomy (sp?!) (I'm 55, and my bloods show I'm now perimenopausal, so my ovaries are due for retirement anyway!), and being done with it (I hope....!)  I'm not clear whether suregery would include the fallopian tubes as well. Everything else in my pelvis is showing OK, so far as I understand. (Plus, no family history of ovca etc)Has anyone else been in a similar situation, and what was your decision, and your experience? My husband is worried at the thought of me having surgery (he had his kidney out this year, so knows abdominal surgery isn't a walk in the park!), though the TVS gynae says it could be done with keyhole.However, I also wonder whether it's best NOT to do keyhole, as is there not a risk that the ovary will rupture during removal, and then, if there IS any malignancy (or even proto-malignancy) in the cyst, that may get loose into my body and nest somewhere else!All information on this will be MOST gratefully received.I am very glad I did go ahead and get all this further checked out. I know US has its limitations, but even so, I think it's paid off this time by spotting 'something'.All the very, very best to all of you fighting ovca, and I hope, hope you win your battles.Julie.       

  • Abnormal cells after LEEP 20:00 - 19.11.2008

    I had the leep procedure done in the end of march and I recently had an abnormal pap.Before i had this procedure I was told I could have some difficulties with having children in the future. Well I went in for a pap and she told me everything looks great and now I recieved my results back and it came back abnormal. For once in for all i thought maybe i could have children without worring..but now im going back in on monday and im 24 and i almost want to be selfish and have a child now before its to late and things just get worse. Has anyone experienced a leep and abnormal paps and have had children after?I never thought i would have to think about this at my age but not having  children in the future years and waiting for it will kill me. someone please help me with a story of their own.Danny

  • Cone Biopsy 20:00 - 16.11.2008

    So the background info is that I had an abnormal pap in 2006, was diagnosed with HPV, and had a colposcopy in 2006 that showed low grade dysplasia.  They wanted me to have 6 month paps and would watch and wait I suppose.  From there, I wasn't impressed with my doctor and switched to a different clinic.  I had my records from the previous clinic sent to this one so there wouldn't be any confusion as to what was going on or why I was so persistent to have a repap right then which was 6 months after my previous one.  So, afterwards I recieved a lovely letter in the mail stating that the results were normal for my condition.  I probably should have asked what exactly that meant.  But, I was thrilled with the thought of not having another colpo.  Six months later I was back again for another pap.  Thinking the last one was "normal for my condition" I didn't freak out at all until I got the call saying I needed to schedule a colposcopy because there had been changes.  I'm not really thrilled at this point where I have a month to anxiously wait to have my colpo.  I had the colpo last week and it really wasn't as bad as the first.  Not really any pain except when she took the biopsy.  My Dr. was really good at explaining what she was doing etc. and drew me a picture of what she saw.  So I freak out for a week waiting for the results.  For some reason they didn't have my records from the previous clinic I went to and my Dr. wanted to look at them to make comparisons I suppose.  I was able to track down my records but found out she didn't really need them at this point.  I talked to the Dr. Friday night at around 6pm while I was driving in the rain and couldn't see a thing.  Not the best time to chat since I was a little preoccupied with not driving off the road.  What I got out of the conversation was that my results came back high grade and something about glands.  She wants to do a cone biopsy and I have the option of either doing it in the office with the LEEP or the operating room with the laser.  She did explain the difference between the two but I was so distracted with the rain and driving and the high grade and glands part that I can't remember the difference between the two.  I talked to her nurse today which was no help at all.  She said she was new and didn't have answers to any of my questions but would have someone call me tomorrow.  So I guess my question is...what is the difference?  What does high grade and glands mean?  Do I have cancer?  Will I ever be able to have children?  I don't do well with things that aren't in my control and at this point I'm seriously freaking out.  Any answers or suggestions?  Sorry for the lengthy detail.

  • mouth sores from Doxil 20:00 - 15.11.2008

    I was just wondering if anyone has any cures that have worked for mouth sores from Doxil.  My mom has them very bad.  Her oncologist has given her varies treatments but nothing seems to work, not even the "magic mouthwash"  My mom is a fighter, but this is really kicking her but.  She started getting them with her 3rd treatment, were they were so bad that they even ran down her throat.  Now on her 4th treatment she has them again, luckly not down her throat, but has them really bad, that she can barely even speak.  Please help, she will pretty much try anything just to get rid of them.Sandra  

  • need advice 20:00 - 14.11.2008

    I am recovering from a cone biopsy and scraping of cervix. I am 1 week post op. My wonderful MD called me on thursday 11-13-08 to let me know that my results from the biopsy came back and did show severe displasia of the cervix, which i knew, that was why we did the procedure. He also told me that the scraping that was done further inside my cervix also came back with displasia.  So i am left with not many options. Eaither go for another cone, or have a hysterectomy. I think this has put me in a depression. I feel down, tired, and dont want to talk to anyone. I have one child and probably would not have had anymore, but it is tearing me up to have this taken away from me. I know i have to have it done. I feel like i am not worth anything anymore.                thanks  dancie

  • Radiation or not 20:00 - 13.11.2008

    I am post-op, a month ago I had a hysterectomy  for cervical cancer 1a2, for my two week fallow up my doctor said that the tumor that was removed was bigger than what they thought and I might need radiation if it was bigger than 1/5 of an inch.  My tumor was 3mm by 3.2mm before the surgery. I can not Imagine being much more. Does anyone know what is the cut off mesurement for not reciving anymore treatment after a hysterectomy?

  • after chemo radiation 20:00 - 12.11.2008

    hi! I had treatment of chemo radiation in July. Some side effects i am experiencing still are swelling of the abdomen/ lower back ache/ some spotting - i also started HRT but wonder if anyone else experienced these things ? i am due back to cancer agency next week for check up.

  • Signet Ring Adenocarcinoma 20:00 - 12.11.2008

    Hi, Any information on Signet Ring Abenocarcinoma ?  

  • scared 20:00 - 11.11.2008

    Hi, I am a 23 year old female. Over the past month or so I've developed some symptoms that are concerning me...For the past 2 years or so, I've had very painful intercourse upon deep penetration - I get a shooting pain throughout my pelvis....then about 1 month go, I started to experience burning upon urination & increased frequency...I made an appointment to go see my family doctor (to rule out infection, etc) & get a pap, in between the time of scheduling my appointment & going to see my doctor, I developed a dull aching in my pelvis, mostly in the lower right quadrant. I tell him this informtion, he does a urine test, pregnancy test - all negative. during my pelvic examination, he presses down on my lower right quadrant, & it just about sends me off the bed, I had pushed down on my pelvis on my own standing up & didn't really have much discomfort. Over the next few days I've been experiencing lower back pain & shooting pain into my right groin area. The doctor's next suggestion is to go for a pelvic ultrasound....however, I have to wait until January for an appointment- in the meantime I am beside myself worrying I have cancer! I will note that my periods have remained normal, & I have had no abnormal bleeding

  • Signet Ring Adenocarcinoma/Ovarian Cancer 20:00 - 11.11.2008

    My BFF is 39 and was just diagnosed with Signet Ring Adenocarcinoma/Ovarian Cancer. Her first Chemo treatment is today.Does anyone have any experience with this type of Cancer or any suggestions that can help us better understand it?Any information would be really appreciated!Thanks,Juli