Showing posts with label cancer. Show all posts
Showing posts with label cancer. Show all posts

Finding the resources and information you're looking for is a daunting task. Discovering good, sound and reliable sources can be even more difficult — especially on the Internet.

For those of you living with a past or present diagnosis of cancer, being well informed is one of your best defenses. Some of you have asked recently about finding research updates, the latest in treatment options and how to know what's best for you.

Here are some ideas on how to find the information and education resources that you're looking for:

Get personalized assistance — Go in person to your clinic or health care center and ask if they have a patient library or resource center. Most often the library or education center is staffed with a librarian and educators who can assist in your search for research updates, information and resources. Mayo Clinic Cancer Center in Rochester, Minn., has a Cancer Education Center located on the lobby level of the Gonda building that's open every day (Mon. - Fri.) and can assist with your personal information and educational needs. For more information call 507-266-9288.

Find reliable sources online — Here are a few ideas to help you get started.

Mayoclinic.com — search on the cancer topic you are researching and receive the latest evidence-based updates, see also the links at the bottom of each page for references related to the content.For information and education resources that you can download, go to the National Cancer Institute (NCI) Publications Locator (www.cancer.gov) or the American Cancer Society (www.cancer.org).For information about cancer clinical trials, see our Mayo Clinic site (go to the Resource tab on this page and link to cancer clinical trials) or the NCI site and search for the Clinical Trial Homepage.For excellent research updates see Mayo Clinic Cancer Center (www.cancercenter.mayo.edu), the American Institute for Cancer Research (www.aicr.org), the American Cancer Society (www.cancer.org), or the American Association of Cancer Research (www.aacr.org).

Subscribe to a cancer journal or newsletter — a few suggestions include:

Mayo Clinic "Living with Cancer" newsletter (link to subscribe is on this page)"Coping with Cancer" magazine and website (www.copingmag.com/cwc/index.php)"CURE (Cancer Updates, Research & Education)" (www.curetoday.com)"CR" magazine — from the American Association for Cancer Research (www.crmagazine.org)

Feel free to share other excellent resources that have helped you in your search for information as a cancer survivor.

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Guest blogger and breast cancer survivor MaryEllen Sheppard is our writer this week. She's graciously allowed others to share in her journey.

Photo of MaryEllen Sheppard

A video series about her experience, "MaryEllen's Journey — A 5-part breast cancer video series from Mayo Clinic," can be found on the Resources tab on this page. The following is her perspective:

"Living with cancer." I'm struggling with what to write because, fortunately, the phrase doesn't apply to me. My heart and prayers go out to you for whom the words do apply. However, I had cancer. I'm not living with it today. In my mind, there's a huge difference between the two.

Today, after successful surgery and treatment, I get to drop the "with cancer" part and just focus on the "living" part of the equation. Not only do I get to change the focus, I believe I must change it if I'm going to have the kind of future I expect for my family and myself.

Don't get me wrong, cancer's presence is evident. When I look at my chest I see the changes in breast contour and firmness resulting from the lumpectomy and radiation. I see reddened skin from an allergic reaction to surgical tape. The scars from surgery and the placement of a port, although better each day, still seem almost angry in comparison to my pale chest.

This visual reminds me of any number of brick walls marked with graffiti signifying which gangs have laid their claim. Only in my case the territory invaded was my chest and the words tagged and left behind read, "Cancer was here."

What is important, however, is while the evidence is indisputable that cancer claimed its territory in my body, because of the medical expertise of Mayo Clinic and the larger medical community, it didn't claim my life. Equally important, due to the compassion shown by so many, many people, cancer also failed to claim my joyful spirit.

I had cancer. However, like other major challenges I've faced, I'm choosing to learn from the experience and make changes based upon the lessons learned. I'm holding on dearly to the belief this is my life and cancer can't have any more of it. I'm surrounding myself with friends and family. I'm exercising and eating right. I'm doing my best to ensure there is no more territory ripe for the taking. In other words, I'm not living with cancer ... I'm living!

(As always, you're invited to share your comments. And you can find the video series, "MaryEllen's Journey — A 5-part breast cancer video series from Mayo Clinic," on the Resources tab above.)

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What is resilience? For you as a cancer survivor, it might be defined as the ability to recover, the strength to move forward, and the awareness of the needs of your own body.


Resilience is a strength that comes from within and is self-motivating. Research has shown that cancer survivors, when questioned, many times identify their own inner strength as one of the primary sources of strength as they experience and recover from a cancer diagnosis and treatment.


Many of you can identify with this concept, although it may be hard to put into words at first. Here are a few thoughts to consider as you reflect on your own resilience:

How do you bounce back from difficult situations? What are your coping mechanisms?How do you gain strength and courage to move forward? What motivates you?Are you able to ask for help when you need it? What is your support system?What inspires you and makes you feel whole as a person?

I have met so many survivors who have this amazing ability to survive and thrive despite the physical and emotional stress of cancer. Please share your thoughts on this topic. I would love to hear your opinion on what you feel is resilience and how this inner strength has helped you in your experience.

As a cancer survivor, you may be at risk for the occurrence of a second cancer. After treatment is completed it's great to have a break from all of the medical appointments. However, it's important to keep in mind prevention strategies and screening practices for the future.

As a cancer survivor, your risk for developing another cancer may be higher than the average person. This risk may be due to:

Chemotherapy drugs — Some may put you at risk for developing secondary leukemia. Radiation therapy may put you at risk for developing second cancers that are solid tumors. People at increased risk are those who have received high doses of radiation over a large area.Genetic mutations — Some people have inherited gene changes or mutations that increase the chances of getting a second cancer. If you feel that your family has a higher than average incidence of cancer, seek out a genetics specialist to review your family history and evaluate your risk.

What's important to keep in mind?

You may need more frequent or earlier screening than the recommended practice. Ask your health care provider what's recommended for you personally. Understand your risk for a second cancer. If you had treatment for cancer ask your cancer treatment team what your risk is for developing a second cancer. Be aware of changes in your body. Pay attention to new or unusual symptoms including: skin changes, swollen lymph nodes, unusual bleeding, pain, and excessive fatigue. Practice healthy habits for cancer prevention. Don't use tobacco, protect your skin from sun exposure, limit alcohol intake, incorporate exercise into your routine, and eat a healthy, low-fat diet (fruits, vegetables and whole grains).

Celebrate your life by remembering your risk and understanding what's best for your future. If you're not sure what you need, ask your cancer treatment team or primary care provider to help you plan for your future screening. Many of you have mentioned that you're dealing with a second cancer. Use this blog to share your experiences with each other.

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A while back, we had a discussion about grief and dealing with a terminal diagnosis. Many of you shared your perspectives on having a terminal diagnosis, the grieving process or the death of someone you love. It seems like another discussion on preparing for death might also be important.

Unfortunately, the word "cancer" can bring unwanted fear and anger — emotions that either you or those around you might experience. We all know that we will die some day. It's just that the exact circumstances (when, where and how) are unknown. However, rather than deal with this idea with fear, why not treat this as a time to think about living and dying with the idea of compassion and kindness for yourself and your family.

It's true that most people don't want to discuss dying, but if you're interested in finding some peace for yourself, you might consider a couple of these ideas:

Reflect on the positive aspects of your life; find strength in your deepest values.Keep in mind what is most important to you (in life and after you are gone).Write or tell stories of your fondest memories for your friends and family to reflect on now and later.Inquire early about hospice care. Getting hospice involved earlier rather than later can make such a difference. Hospice care has a holistic approach and can assist you and your family with the entire process of approaching your last days and months in a positive manner.Talk about, or write down what you want to happen after you are gone — this might include funeral planning, memorial ideas and any special requests related to the giving of meaningful personal items to others.

My wish for this discussion is to give you the freedom to reflect on the idea and talk with others about what you need.

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Mentor, navigator, advocate ... these are just a few of the people that you may have been touched by as a cancer survivor.

Most times, the people who fill these roles have faced cancer on a personal level as well. They've walked in your shoes and may have similar experiences to share. The art of caring, listening and supporting is so valuable.

Helping others make it through the experience of living with cancer is an incredible gift. They help you navigate your way through diagnosis, treatment and the time after treatment ends, which can be the hardest period.

People in these roles often want to give back by providing support and guidance to others who may be just at the beginning of their cancer experience. This is an empowering experience where the person helping oftentimes gets back as much as they give. For the person receiving the support, it's just so good to be with someone who knows exactly how they're feeling.

At Mayo Clinic Cancer Center, we are so fortunate to have American Cancer Society Navigators and volunteer survivors who work in the Cancer Education Center, Pink Ribbon Mentors who support breast cancer survivors, a strong group of men who organize the Prostate Cancer Support Group, as well as countless other advocates and community support.

Please share stories of how you've been touched by people in these supportive roles. Whether you were on the giving or receiving end, both are equally important!

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Last year, we had a blog discussion on "How cancer changes you" and so many of you wrote in to share your experiences. With this post, I want to delve deeper into the positive side. I realize it might be asking a lot to do this; however, while having cancer is a generally negative occurrence, some positive things may come from it.

I'll share a story of a woman I met who was diagnosed with breast cancer. After her initial treatment, she decided to reduce her work schedule and pursue her love for painting. She traveled to places she loved and created incredible watercolor paintings reflecting on the beauty of each place.

She stayed active in her work life, but was able to balance it with her dream of painting again. She told me she wouldn't have done this if it hadn't been for her cancer diagnosis. Previous to her diagnosis, she was extremely focused on her career and had put her love for painting on hold.

I'm sure this story isn't unique. Many of you have made positive changes in your life because of your cancer diagnosis. I've heard so many stories of love, courage and strength. At times, it's hard to be positive, as having cancer isn't exactly easy and the physical feelings of the body usually have a strong influence on the mind and outlook.

I would love to hear about your personal experiences. How did you transform the negative to positive? How did this experience change your life?

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In recent years, genetic testing to predict your cancer risk has become more available. As researchers learn more about how genes can predict your cancer risk, it's important to consider all the options.

If you're in a high-risk family, you may be considering genetic testing. The most common cancers that have a genetic component include breast, ovarian, prostate and colon cancers (along with many others as well).

Before you undergo genetic testing, gather as much information as you can about your family and medical history. Talk with your doctor or a genetic counselor about your personal and family medical history. This will help you better understand your risk. Discuss any questions or concerns you have about genetic testing. Also, talk about what your options will be, depending on the results of the test.

If a positive genetic test is discovered, you'll be able to talk with an expert about your specific risk. Some of the benefits of genetic testing include early interventions to decrease risk of actually developing cancer, such as:

More frequent screening tests (detecting cancer earlier with increased survival rate — colon cancer is a good example)Prevention strategies including positive lifestyle changes (such as diet and exercise)Informed decisions can be made for pro-active interventions (for example a decision to have prophylactic mastectomy or removal of ovaries for women with high risk to develop breast or ovarian cancer)

The field of studying genes for predicting cancer is evolving constantly. We are only at the beginning stages of understanding how genes predict our cancer risk and many other aspects of health.

Please share your thoughts on this topic and your personal experiences. blog index

Relationships and the give and take that is part of the process of being in a relationship are present in our everyday lives.

As I reflect on what's written by so many of you, this seems to be a key component to thriving as a survivor. Your personal quality of life is directly affected by the quality of your relationships with others.

This includes your family, your partner or spouse, your work colleagues, your friends, and also your health care team. This connection of one to another is how each day moves forward.

A few of the key components to a relationship are communication, trust, flexibility, honesty and time. If you're not getting what you need from a relationship, it might be time to act on it. Here are some ideas for getting the most from your relationships:

Communicate your needs, wishes and desires — be specific.Be honest about what to expect from others — this includes everyone from your family to your health care provider. Give yourself time to heal and adapt to the changes that you may have in your life.Keep in touch — send a note or call a friend who you treasure and haven't seen for a while. Make a date to reconnect.Be open to new relationships — surround yourself with positive people.Give back when you can — take time to thank those people in your life who have made a difference. A simple phrase such as "thank you for being part of what's good in my life" can bring a smile to them and help them realize how much the relationship means to you.blog index

Let's explore the concept of pain together. You can experience different types of pain, including pain from the cancer tumor or location of the tumor, or from side effects of treatment (radiation, surgery, and/or chemotherapy).

From my perspective, many people are reluctant to talk about pain with their cancer doctor either because they think it is something they must live with, or they do not want to "bother their doctor" with the question of pain relief.

Pain relief is extremely important and can directly affect your quality of life, ability to move forward in your recovery, as well as your emotional and psychological well-being.  Talk to your health care team about your pain.  Most cancer centers will have a pain clinic where you can meet with a pain specialist to address your individual concerns.

Investigate other ways to balance your medical treatment plan for pain relief by exploring alternative therapies including:

AcupunctureAromatherapyBiofeedbackHypnosisMeditationMassageMusic therapy

Much progress is being made related to pain relief for people with cancer, however, more remains to be accomplished.  Please share your perspectives on this topic together.

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A few weeks ago, I asked for your feedback and ideas for topics and discussions for 2011. Thank you so much for your comments, ideas and suggestions. It's clear some of you aren't finding what you're looking for. Here are a few ideas on how to find Mayo Clinic's information on cancer treatments, research and support.

At the moment, you're on the Expert Blog of the Cancer guide at mayoclinic.com/health-information/. If you look all the way to the left (above my picture) you will see the tab called Basics. That's where you'll find more about cancer in general — everything from symptoms to treatment and prevention.

Next, you'll see a tab called In-Depth, where you'll find a variety of information (I highly recommend you check it out) from the latest on treatment and drugs, alternative medicine, coping and support. The Multimedia tab is next. This one is great for people who like visuals — you'll find images, videos and slide shows related to the cancer. Expert Answers is the next tab. You'll find great snippets of information from Mayo Clinic cancer experts written in a question and answer style.

To the right of that is the Expert Blog tab. Then, next to the Expert Blog tab is a tab called Resources. You'll find many helpful links to other great resources within Mayo Clinic and external links to important support resources. The Resources tab is where you'll find the link to our Cancer Clinical Trials site to find out more about treatment trials and clinical research opportunities at Mayo Clinic. The last tab called What's New features the newest cancer information.

I hope you'll find this information helpful as you navigate on our site. Depending on how you found the blog, you may or may not be that familiar with the site. We're here to help in your survivorship journey. Feel free to send me any comments or suggestions that you might have.

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This is a heavy topic to discuss; however, many of you have mentioned that you're dealing with a terminal diagnosis.

Grief is a strong, overwhelming emotion, regardless of whether your sadness comes from the loss of a loved one or from a terminal diagnosis that you or someone you love has received. You might find that you feel numb and disconnected from your daily life, unable to carry on with your regular routine as you're dealing with the emotions and sadness of grief.

Grief is the natural reaction to loss. Grief is both a universal and a personal experience. Individual experiences of grief vary and are influenced by the nature of the loss. It's important to remember while you're grieving that you can't control the process and to prepare for varying stages of grief. Some emotions you may experience during the grieving process include:

Denial AngerBargainingDepressionAcceptance

Grieving doesn't always follow the stages above, but you may experience many of these feelings as you deal with the reality of a terminal diagnosis. A host of emotions are involved and normal. You might experience a sense of shock, sadness, guilt and fear along the way. Talking with others is sometimes helpful as you try to recover from the shock and adjust to a diagnosis of a terminal illness.

I want to have an open discussion about grief through this blog so that you might help each other with some of the feelings and emotions. It's not an easy discussion to have, so I admire your willingness to share.

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The financial burden for cancer survivors is significant. In a recent study, more than 30 percent of people living with cancer said they had practical concerns regarding financial issues. On top of monthly or yearly insurance premiums, extra costs such as co-pays, medication (chemotherapy or treatment) expenses, travel costs and lost wages are all part of the equation as you deal with a cancer diagnosis, treatment and survivorship.

Some practical ideas that may help as you navigate your way through these issues include:

Talk with your health care team on an ongoing basis about treatment costs. If they recommend a new medication or prescription — ask about your out-of-pocket costs. Many times, your cancer treatment center's business office and pharmacy can give you an estimate of costs before hand.Meet with a social worker to review potential financial resources available to you. This might include charity care, prescription assistance programs, gas cards, low cost (or no cost lodging) and other resources.Call the American Cancer Society (1-800-227-2345) to connect with resources that are available to you as a cancer survivor. If you are unable to work because of your cancer diagnosis; talk with your employer to plan for medical leave, or call the Social Security office (1-800-772-1213) to discuss your options for disability benefits.

Feel free to share ideas, pearls of wisdom and any resources that you have found helpful.

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Relaxation therapies may help alleviate certain symptoms of cancer, relieve side effects of treatment, and improve your sense of well-being.

Many relaxation methods, such as massage therapy, meditation and guided imagery may be helpful in managing stress and anxiety. In addition, research studies show that relaxation techniques can lower blood pressure, reduce pain, and ease some side effects of chemotherapy.

Having cancer is stressful, so it may not be possible to eliminate all sources of stress. But you should consider the sources of stress that you can reduce. For example, ask for help with household chores, social responsibilities or work demands. Seek out effective strategies for coping with stress or simplify your life by saying "no" to the extra demands as much as possible.

Common relaxation techniques include:

YogaTai chiListening to musicExerciseHypnosisGuided imageryMassage therapy

Relaxation techniques involve refocusing your attention from the stress to something calming.

For me, it's taking a daily hike and being mindful of the changes in nature around me. It might be the sound of the birds chirping, new leaves on the trees, the beauty of the clouds against the blue sky, or a neighbor, cat or dog that welcomes me along the way.

I return refreshed and ready to take on the rest of the day. Choose a relaxation technique that works best for you and incorporate it into your daily routine. Share with others through this blog what has worked for you.

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“This book is a ‘biography’ in the truest sense of the word,” he claims at the outset. It is “an attempt to enter the mind of this immortal illness, to understand its personality, to demystify its behavior.” He ventures even farther into the realm of the impossible when he promises to address these two questions: “Is cancer’s end conceivable in the future? Is it possible to eradicate this disease from our bodies and societies forever?”


With objectives so vast, and with such a beautiful title, “The Emperor of All Maladies” is poised to attract a serious and substantial readership. And it is an informative, well-researched study. But it is in no way a biography of anyone or anything, and Dr. Mukherjee winds up acknowledging as much before his book is over.


He points out that there is both folly and scientific partisanship in treating “cancer, a shape-shifting disease of colossal diversity,” as “a single, monolithic entity.”


Likewise, questions about whether cancer can be eradicated eventually run up against hard reality. “Cancer is a flaw in our growth, but this flaw is deeply entrenched in ourselves,” the book says. “We can rid ourselves of cancer, then, only as much as we can rid ourselves of the processes in our physiology that depend on growth — aging, regeneration, healing, reproduction.”


How did Dr. Mukherjee allow his otherwise sophisticated book to be presented so reductively? It’s an all too fitting flaw, since the same kind of oversimplification has long been the bane of cancer theory. “The Emperor of All Maladies” provides a survey of the different ways in which cancer has been understood in different eras, from the Greeks’ idea that it was caused by black bile, one of the four liquid humors, to the 19th-century conviction that the most drastic and disfiguring surgery would lead to the best cure. He also writes about the fund-raising, Nixon-era idea of waging war on cancer as if illness were an enemy to be faced in battle.


The biographical aspects of “The Emperor of All Maladies” have more to do with the personalities of anti-cancer combatants than with concocting one for cancer itself. This book pays considerable attention to pioneering figures like William Stewart Halsted, an advocate in the 1870s and 1880s of extreme breast cancer surgery; Sidney Farber, who in the 1940s made great breakthroughs in treating childhood leukemia with dangerously toxic chemicals; and Min Chiu Li, who in the 1950s lost his job at the National Cancer Institute for providing chemotherapy to patients whose symptoms had receded, even though this extended therapy meant the first chemotherapeutic cure of cancer in adults.


In a maneuver as transparently glib as that of calling his book a biography, Dr. Mukherjee also inserts occasional glimpses of his own patients, whose experiences are markedly overdramatized. (“It was now 9:30 in the morning. The city below us had stirred fully awake. The door shut behind me as I left, and a whoosh of air blew me outward and sealed Carla in.”) But none of this personal material is as compelling as the story of how cancer research has progressed through so many different phases.


Here Dr. Mukherjee’s writing is at its most candid and grim. The overarching point made by his narrative is that the whole subject of cancer is dauntingly complex. Even the statistics about mortality rates are tricky, since so much of researchers’ thinking about the prevalence of cancer depends on how they measure progress. And the unmistakable effect of our progress in curing other previously fatal diseases is to make cancer, which is most often found in older patients, look more prevalent than ever.


“The Emperor of All Maladies” is at its most honest in describing the push-pull dynamics of scientific progress. Dr. Mukherjee links a decline in extremely punishing chemotherapy regimens to the fact that patients became less passive. (He credits much of this forcefulness to AIDS activists.) He describes the conflicting interests of surgeons and chemotherapists. He writes most promisingly about the effects of genome mapping on scientists’ ability to understand how cancers progress, and he cites the similar ways in which different cancers create genetic pathways within mutating cells. He is confounding yet fair in writing that “this is either very good news or very bad news.”


Late in “The Emperor of All Maladies” Dr. Mukherjee provides especially apt metaphors for a subject so difficult to grasp. He quotes the Red Queen from Lewis Carroll’s “Through the Looking Glass” to describe the alacrity with which research must move: “It takes all the running you can do, to keep in the same place.” He describes one patient’s maneuvers to keep up with her illness as “like watching someone locked in a chess game.” And he says that the patterns in cancer research repeat themselves just as history does. Among the constants in this struggle are “the hypnotic drive for universal solutions” and “the queasy pivoting between defeatism and hope.”

He had glioblastoma, a brain tumor that fights off every known therapy. The same disease killed Senator Edward M. Kennedy last year. Mr. Sugrue’s cancer was diagnosed in April 2009 and bombarded with the usual weapons: surgery, radiation and chemotherapy. Within months, the tumor was growing back. That was when he signed up for the Avastin study.


About 10,000 Americans a year develop glioblastoma. Nearly all find that the standard treatments seem to work — for a while. And then the clock starts to run down. With treatment, the median survival is about 15 months. Only 25 percent of patients make it to two years.


The disease is the focus of much research, and will almost certainly be for years to come. Hundreds of studies are being conducted in glioblastoma and other brain cancers. Among other things, they involve vaccines, drug combinations and special drug-delivery techniques. Progress is measured in small steps — a few more months of survival, more patients managing to survive two years. On paper the gains may seem minute, but for patients the added time may translate into a graduation or wedding that might otherwise have been missed.


There are two enormous obstacles to treating glioblastomas. First, no drug is highly effective. Second, even if there were such a drug, getting it to the tumor would be difficult. Many drugs cannot squeeze through the blood-brain barrier, a system of tightly packed cells lining capillaries in the brain. The barrier makes all brain tumors hard to treat.


The study that Mr. Sugrue entered, for people with recurring glioblastomas, is being conducted by Dr. John Boockvar, a brain surgeon at NewYork-Presbyterian/Weill Cornell. Doctors first inject a substance called mannitol, which temporarily opens the blood-brain barrier, and then flood the tumor zone with Avastin. Avastin blocks the growth of new blood vessels, which tumors need. The drug is approved for glioblastoma, but tumors can become resistant to it.


Normally, Avastin is dripped into a vein. But Dr. Boockvar and his colleagues wanted to try hitting the cancer with a much higher dose by guiding tiny tubes called microcatheters through blood vessels to the tumor site and then unleashing the drug.


Mr. Sugrue was the second patient to be treated, with a small dose. Since then, the study has shown that higher amounts — seven times the dose he received — can be safely used.


A report on the first 30 patients was published online last month in The Journal of Neurosurgery. Tumors shrank in some, particularly those who had not had Avastin before. But one patient suffered a stroke from the treatment, which caused weakness on one side. And it is still too soon to tell whether this approach can prolong survival.


“We started a year ago,” Dr. Boockvar said, adding that the early patients were quite ill and had only one dose of Avastin. “We’ve lost about 15, or half the patients. The rest are alive and kicking.”


His team has begun new experiments using mannitol and microcatheters to deliver other drugs directly into the brain. In the future, certain drugs may be combined with Avastin.


Dr. Keith Black, chairman of neurosurgery at Cedars-Sinai Medical Center in Los Angeles, and an expert on breaching the blood-brain barrier, said it was not clear that Avastin would work well enough to improve survival very much, even when infused right into the brain. Better drugs are needed.


“We can get drugs in, but there’s a belief in glioblastoma, for example, that even if you push the limit of the drugs you still won’t increase the survival all that much,” Dr. Black said. “It’s kind of like having the Trojan horse before we have the soldiers to put in it.”


He said vaccines looked promising for some patients with glioblastoma. In addition, research with animals suggests that Viagra or Levitra — the drugs for erectile dysfunction — can open the blood-brain barrier, particularly around tumors, and let chemotherapy in. In theory, the drugs could be taken in pill form, unlike mannitol. Dr. Black said he was planning to study the idea in people with various types of brain tumors, including those that had spread from other sites, like the breast or lung. Cancer from other organs invades the brain in about 100,000 Americans a year.


The study that Mr. Sugrue entered is still going on. And so is Mr. Sugrue. He lives in Stamford, Conn., with his wife, Donna, and their teenage children, Molly and Tim. Molly, a high school senior, is about to apply to nursing schools. Mr. Sugrue is still receiving intravenous Avastin regularly. (He had only one dose infused into his brain.) There is no sign of tumor recurrence.


But it has not been an easy year. An infection in his incision required many operations. He has lost some peripheral vision and no longer drives. He needs physical and occupational therapy. Though he does some work, he has not been able to return full time to his job at a hedge fund. But he never lost his quick wit or sense of humor, his wife said, adding, “What he went through would have killed a lesser man.”


If he had it to do again, would he enter the study?


“Absolutely,” Mr. Sugrue said in a telephone interview last week. “In fact, I’m going to ask Dr. Boockvar if there are any more trials out there.”

There is only “moderate’’ evidence that the newly approved prostate cancer drug Provenge helps patients, according to an analysis done for Medicare that was made public on Wednesday.


The analysis is part of a controversial review by the Centers for Medicare and Medicaid Services to determine whether to pay for Provenge, which costs $93,000 per patient and extended lives by about four months in clinical trials. Medicare advisers will meet next Wednesday to discuss the drug, which was developed by Dendreon, a Seattle-based biotechnology company.


Provenge is the first so-called therapeutic cancer vaccine – meaning it works by training the patient’s immune system to attack the tumor – to win F.D.A. approval. The treatment is made for each patient from his own blood. Sales have been small so far because Dendreon’s manufacturing capacity has been limited.


While Medicare generally pays for drugs that are approved by the Food and Drug Administration, its debate over paying for Provenge has raised concerns among some cancer patients, doctors and investors who say the government is sending a warning shot that it will not automatically pay for high-priced medicines.


“Not only is C.M.S.’s action contrary to Congress’s intent to ensure beneficiary access to drugs and biologicals used in an anticancer chemotherapeutic regimen, but it threatens to stifle future innovation and cancer research for years to come,’’ Dr. Al B. Benson III, president of the Association of Community Cancer Centers, said in a comment submitted to the Centers for Medicare and Medicaid Services.


But others say the health care system cannot afford to continue paying high prices for all therapies, particularly cancer drugs that extend lives by only a few months.


With expensive medicines there is already a sort of dual approval system, especially with private insurance companies. First a drug must get F.D.A. approval and then a manufacturer often must go through a lengthy process of persuading insurers to pay for the drug.


Medicare is not supposed to consider price when determining whether to cover a drug, however.


Some analysts have assumed that Medicare will pay for Provenge when used for the patients specified in the drug’s label – those with advanced prostate cancer that is resistant to hormone-deprivation therapy but who are experiencing no or minimal symptoms.


The Medicare review might be more designed to limit off-label use of the expensive drug, such as for patients who already have symptoms. The review for Medicare said there was insufficient evidence to judge whether Provenge would work if used off-label.


The F.D.A. declined to approve Provenge in 2007, setting off protests by patients and Dendreon investors. After Dendreon completed another trial, which reaffirmed a survival advantage for the drug, Provenge was approved this April.


But the analysis for Medicare said that there were issues in how the trials were designed that made it difficult to assess how effective Provenge really was. One big issue was that the placebo used in the control arm was not really inert.


Robyn Karnauskas, a biotechnology analyst at Deutsche Bank, said in a note to clients Wednesday that the assessment of moderate evidence in support of Provenge boded well for reimbursement. “Historically, moderate means that CMS will reimburse the product for its on-label indication,’’ she wrote.


Dendreon’s shares rose more than 5 percent in trading after the close of the market.


The assessment was done by a technology evaluation group at the Blue Cross and Blue Shield Association under contract to the government’s Agency for Healthcare Research and Quality.

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Too much body fat may increase the risk of his triple-negative breast cancer, a rarer and more aggressive form of the disease, a new study claims.

According to the triple negative Breast Cancer Foundation, this type of breast cancer is diagnosed when a cancer does not have three "receptors" associated with breast cancer tumors: estrogen receptors, progesterone receptors and human epidermiko growth factor receptor 2 's. The triple negative breast cancer chemotherapy response, but more targeted therapies usually receiver do not work.

The new study, published in the Journal cancer epidemiology, prevention, and means scientists analyzing data for the 155,723 women, taking part in a study on the effects of menopausal women, hormone replacement therapy. Scientists focused on the body mass index (BMI) levels and exercise of 307 men in the study were diagnosed with triple-negative breast cancer, and women were 2,610 estrogen receptor positive breast cancers.

Researchers discovered that women with a higher BMI was 35% higher risk of breast cancer is negative, and triple-a 39% increased risk of breast cancer, estrogen-fed. Body fat has been shown to produce more estrogen.

Overall, the scientists say that the effect was "moderate", but the results can provide new ways for women to reduce the risks of breast cancer is triple negative.

In 2008, the World Health Organization (who) data says cancer killed 7,6 million people worldwide. Breast cancer deaths accounted for 460,000. fifth in a row, behind lung cancer, stomach, liver and colon. And depending on the survey, in 2008, of 1.5 billion adults, aged 20, was overweight. 200 million men and approximately 300 million women were obese.

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Getting a good amount of sleep (for most people, between 7 and 9 hours of sleep) has been advocated for a number of health reasons. Sleep is the time when the body Gets to reload itself and is the time when the brain Gets the time to get back to good working condition (several studies have shown that when a person does not sleep the suficienteo brain becomes slower in operation, and in extreme conditions, if the brain has not get rest for 2 days or more, get off to ensure that some amount of sleep is available). In addition, getting an insufficient amount of sleep is also associated with an increased risk of health problems like diabetes, obesity, heart disease and so on.
Researchers are always the quest to find the links between diseases and various factors that may contribute to this type of problem, through statistical methods (since these statistical methods enable the discovery of links between cause and effect and provide an entry point for most clinical research). In a similar such research, researchers found that getting less than six hours of sleep had led to an increased risk of developing Colorectal adenomas (link to article):



Researchers at the University Medical Center hospitals (UH) Case and Case Western Reserve University School of Medicine found that individuals who averaged less than six hours of sleep during the night had an increase of almost 50 per cent of the risk of Colorectal adenomas in comparison with people sleepingat least seven hours a night.
Adenomas are a precursor to cancer tumors, and treated, they can turn malignant. "A short period of sleep can now be seen as a new risk factor for the development of the development of colon cancer," said Li Li, principal investigator of the study.
Patients with adenomas were found in general have communicated to sleep less than six hours compared to patients without patients adenomas (control).

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