Friday, July 18, 2014

Cancer Patients Choosing Hypnosis Over Counseling

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(Photo Credit: KDKA)
(Photo Credit: KDKA)
(Source: KDKA-TV)Dr. Maria Simbra
Dr. Maria Simbra is an Emmy award-winning medical journalist, who...
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CBS Pittsburgh (con't)
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PITTSBURGH (KDKA) – Dealing with cancer is difficult both physically and emotionally, especially when the treatments start, but some cancer patients are now using a new tool to help them get through it.
Being diagnosed with breast cancer can be frightening.
“Having a diagnosis of any kind of cancer, I imagine, is devastating, and your mind races,” breast cancer patient Althea Queen, of Natrona Heights, said. “When it came time for chemotherapy, I had a hard time wrapping my mind around that.”
Counseling is often offered to help with stress and anxiety. But, Althea wanted to try something different.
“And I said, I’m beginning to wonder if I shouldn’t find a hypnotist to help me with what my mind was going through,” she said.
Another approach is hypnosis and cognitive behavior therapy (CBT), a problem-focused, action-oriented approach. A recent study shows it could help women with breast cancer deal with feelings of fatigue.
“Feeling anxious and worried can lead to fatigue,” Dr. Guy Montgomery, with Mt. Sinai Medical Center, said. “That’s one of the steps we’re working with patients to be more in control of those kinds of emotions.”
A researcher at Mt. Sinai Medical Center in New York did a study of 200 patients getting radiation treatments. Half got meditation, half got CBT and hypnosis.
Fatigue was checked at specific points before and after treatment up to six months out. Those who got CBT and hypnosis had comparatively less fatigue up to four weeks after treatment.
“They learned the skills that they needed to help themselves feel better over time and hopefully,improve their quality of life,” Montgomery said.
Here in Pittsburgh, Bonnie Shields is a social worker who offers hypnosis to help cancer patients. She demonstrated on a colleague.
“Their eyes begin to flutter,” she said. “That’s a sign that they’re wanting to go into trance. I invite them to take deep breaths and then to close their eyes.”
She believes it helps people reduce anxiety, stabilize mood and make decisions.
“I may count to three. My voice will get louder, and then they’ll hear me in a different way than when they were in a trance,” she said.
“Hypnosis is not something that’s a Vegas act or mind control,” Shields said. “We cannot undergo hypnosis and achieve a trance unless we’re willing to do that.”
Althea’s experience with CBT and hypnosis was positive.
“It’s nothing that you can’t remember,” she said. “It’s a feeling of deep relaxation. It keeps your mind from being crowded with unnecessary things.”
“This is a life-changing thing, and it will never really be over. It’s giving me a tool to cope with the changes it brings.”

Wednesday, July 9, 2014


The Metastatic Breast Cancer Conversation

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BREAST CANCER

There are many interesting people in the breast cancer movement, and Shirley Mertz ranks among one of the most interesting. A former high school principal, Shirley leads the Metastatic Breast Cancer Network and serves as a Susan G. KomenAdvocate in Science, bringing the patient's perspective to Komen's research granting decisions. Shirley has also had metastatic breast cancer for the last 11 years, living like so many with a schedule of regular checkups where she learns whether the latest treatment is working and, if not, which treatment to try next.
It's a cycle she calls "Scan, treat, repeat..." and like so many, she thinks breast cancer organizations can do better. So Shirley advocates on behalf of those living with metastatic breast cancer to support patients and work for better outcomes in the clinic.
I was pleased to share the dais with Shirley last week at a media briefing about metastatic breast cancer, hosted by Pfizer. We were joined by Dr. Marc Hurlbert, executive director of the Avon Foundation for Women Breast Cancer Crusade, by Sally Susman and Dr. Cynthia Huang of Pfizer, and by Amy Robach, the ABC News morning anchor whose recent breast cancer diagnosis has made national headlines.
The conversation was frank. Metastatic breast cancer -- that is, cancer that's spread from the breast to other organs -- causes the majority of the 40,000 breast cancer deaths annually in the United States. The five-year relative survival rate for metastatic disease is only 24 percent, although there are women, like Shirley, who may live with the disease for many years.
Metastatic breast cancer claimed the life of our namesake -- Susan G. Komen -- who was diagnosed with breast cancer in 1977 and died three years later. In Suzy's time, people crossed the street to avoid her, unsure of what to say and perhaps even afraid they would "catch" her cancer. Breast cancer wasn't discussed in polite company, even in the 1980s. There were few breast cancer centers, little in the way of treatment options and a stigma and shame around breast cancer itself that kept many women feeling isolated and alone with their disease.
Unfortunately, many living with metastatic disease feel that same isolation today. They deal with friends who don't quite know what to say, anxious family members and even with those who suggest that maybe these patients aren't "fighting hard enough" or didn't do something to prevent their disease. There are often significant psychological, physical and financial pressures along with the fear that the latest treatment will stop working.
"Since there is no cure, we are always in treatment," Shirley told us.
We can and must do better for the tens of thousands of women and men living with metastatic breast cancer in the U.S., and for those who will be diagnosed with it. Fortunately, breast cancer organizations have heard this call and are stepping up.
Last fall, 16 breast cancer organizations, including Komen, came together to form theMetastatic Breast Cancer Alliance (MBCA). Four new organizations have joined the fold since then, working in partnership to address the most pressing issues in metastatic disease. Dr. Hurlbert serves as MBCA chairman.
Komen has funded $91 million in scientific research into metastatic disease in just the past eight years alone. Very importantly, we're also working to cut through the isolation and stigma of metastatic disease by funding outreach programs in hundreds of communities across the country. These programs provide insurance co-pays, medical supplies, rent, groceries, transportation to treatment and other services, offering real-time help for people dealing with the profound physical, financial and emotional challenges of this disease.
As I participated in this event last week, it affirmed my belief that organizations like Komen, Avon and others can and must work together on issues such as metastatic disease in an even more collaborative and focused way. The formation of the Metastatic Breast Cancer Alliance is one step but, again, we can all do more.
Cancer organizations large and small can jointly fund high-reward research. We can develop and fund more widespread metastatic programs. And we can jointly develop programs to address disparities in treatment that lead to worse outcomes for many women of color and medically underserved individuals.
My pledge as president and CEO of Komen is to seek greater collaboration among cancer organizations, research organizations and industry in order to ensure we do everything in our power to end the most lethal forms of breast cancer.
We can do this, and we must do this. Because lives literally hang in the balance.

Tuesday, July 8, 2014

Who Is On Your Cancer Support Team?

 
Contributor: Josette Snyder, RN, MSN, AOCN
Learning that you have cancer can make you feel terribly isolated. Suddenly you find yourself in a new, unfamiliar world. But you are not alone.
Take a few minutes to think about the many people who surround you and want to help support you through your treatment into survivorship. Who is on your team?

Your physicians

Your physicians are the experts who are in charge of your treatment plan. They will discuss the risks and benefits of your treatment plan, answer your questions, and provide information.
Don’t forget that your family physician also is a member of your physician team. Your general practitioner is an important resource for you and your family, by providing an empathetic and credible source of information, support and advice.

Your nurses

Nurses are the ones you can go to with questions about the day-to-day issues and the practical matters of dealing with cancer treatment.
This is someone who can tell you what to expect, how to stay comfortable and how to manage cancer-related pain and other symptoms or treatment side effects. Your nurses also can be an important sounding board for your concerns and fears.
Your nurses are very knowledgeable about the details and nuances of navigating the cancer terrain because they are always talking to patients. With their accumulated wealth of patient information, your nurses are a powerful ally in your cancer experience.

Your social worker

Your oncology social worker is a licensed professional who can address the counseling, support and advocacy needs of patients with cancer and their families.
The counseling your social worker provides can help you or a loved one adjust to the cancer diagnosis, communicate with your children, family or doctors and cope with the changes in self-image and sexuality, among other issues.
Support can include referrals to resources for nutrition, complementary therapies, spiritual guidance and home health care. Your social worker also is your advocate, and can help you navigate the health care system, get prescriptions and access transportation to treatment, among a number of other services.

Your family and friends

Your family and friends represent a wealth of support, in the emotional as well as the practical aspects of your cancer journey.
They are the people you confide in, the people you vent to, the people to whom you can express your fears and frustrations. They can be a source of comfort, joy and reassurance.
In a very practical sense, your friends and family also can be of enormous help with the logistics and the myriad of tasks associated with your cancer treatment. They can drive you to doctor’s appointments, watch your children when you need to rest, make meals that you can freeze for later, or create a Facebook group so you don’t have to constantly tell your story.
You might find it difficult accepting help from others.  But by letting your loved ones help you, you can give them an active role in fighting your cancer, rather than leaving them stand on the sidelines. These acts of kindness will strengthen your relationships and bind you closer together. You will always remember how your loved ones helped you in your time of need.

Other cancer survivors

Connecting with other people who have been through a cancer diagnosis and treatment can be a tremendously helpful and empowering experience.
You might be able to understand your own feelings by learning how others responded to cancer. You also may be better able to cope with special challenges of cancer by learning how others managed similar problems.
How to connect with cancer survivors? One way might be within easy reach: You may have a relative or friend who has been through cancer and has an interest in sharing their experiences with you.
One resource I highly recommend to my patients is the 4th Angel Mentoring Program. 4th Angel offers free, one-on-one, confidential outreach and support via telephone from a specially trained cancer survivor.
The American Cancer Society also has a number of support programs, including online support groups, rides to treatment, patient lodging assistance and cancer education classes, among other offerings.

Oncotype DX Test


The Oncotype DX test is a genomic test that analyzes the activity of a group of genes that can affect how a cancer is likely to behave and respond to treatment. The Oncotype DX is used in two ways:
  • To help doctors figure out a woman’s risk of early-stage, estrogen-receptor-positive breast cancer coming back (recurrence), as well as how likely she is to benefit from chemotherapy after breast cancer surgery.
  • To help doctors figure out a woman’s risk of DCIS (ductal carcinoma in situ) coming back (recurrence) and/or the risk of a new invasive cancer developing in the same breast, as well as how likely she is to benefit from radiation therapy after DCIS surgery.
The results of the Oncotype DX test, combined with other features of the cancer, can help you make a more informed decision about whether or not to have chemotherapy to treat early-stage hormone-receptor-positive breast cancer or radiation therapy to treat DCIS.

Who is eligible for the Oncotype DX test?

You may be a candidate for the Oncotype DX test if:
  • you’ve recently been diagnosed with stage I or II invasive breast cancer
  • the cancer is estrogen-receptor-positive
  • there is no cancer in your lymph nodes (lymph node-negative breast cancer)
  • you and your doctor are making decisions about chemotherapy.
Most early-stage (stage I or II), estrogen-receptor-positive breast cancers that haven’t spread to the lymph nodes are considered to be at low risk for recurrence. After surgery, hormonal therapies such as an aromatase inhibitor or tamoxifen are prescribed to reduce the risk that the cancer will come back in the future. Whether or not chemotherapy is also necessary has been an area of uncertainty for patients and their doctors.
If you’ve been diagnosed with early-stage, estrogen-receptor-positive breast cancer, the Oncotype DX test can help you and your doctor make a more informed decision about whether or not you need chemotherapy. (Some research also suggests the test may help postmenopausal women with estrogen-receptor-positive breast cancer that has spread to the lymph nodes make chemotherapy decisions. Talk to your doctor if you are in this group.)
You also may be a candidate for the Oncotype DX test if:
  • you’ve recently been diagnosed with DCIS
  • you’re having lumpectomy to remove the DCIS
DCIS is the most common form of non-invasive breast cancer. DCIS usually is treated by surgically removing the cancer (lumpectomy in most cases). After surgery, hormonal therapy may be recommended if the DCIS is hormone-receptor-positive. Radiation therapy may be recommended for some women. Doctors aren’t always sure which women will benefit from radiation therapy.
If you’ve been diagnosed with DCIS, the Oncotype DX test can help you and your doctor make a more informed decision about whether or not you need radiation therapy.

How does Oncotype DX work?

The Oncotype DX genomic test looks at groups of genes and how active they are, which can influence how a cancer is likely to grow and respond to treatment. A genomic test is different from a genetic test. A genetic test looks for mutations (unusual changes) in genes that are inherited, or passed from one generation to the next.
The Oncotype DX test uses a sample of breast cancer tissue to analyze the activity of 21 genes. Genes control the behavior and activities of all cells, including cancer cells. When cells are behaving abnormally, it often can be traced back to unusual activity by certain genes.
Looking at these 21 genes can provide specific information on:
  • the likelihood that the breast cancer will return
  • whether you’re likely to benefit from chemotherapy if you’re being treated for early-stage invasive breast cancer
  • whether you’re likely to benefit from radiation therapy if you’re being treated for DCIS
So, the Oncotype DX test is both a prognostic test, since it provides more information about how likely (or unlikely) the breast cancer is to come back, and a predictive test, since it predicts the likelihood of benefit from chemotherapy or radiation therapy treatment. Studies have shown that Oncotype DX is useful for both purposes. The American Society for Clinical Oncology (ASCO) and the National Comprehensive Cancer Network (NCCN) now include the Oncotype DX test in their treatment guidelines for early-stage breast cancer. Because the Oncotype DX test for DCIS is relatively new, it’s not yet included in the ASCO or NCCN DCIS treatment guidelines.
Oncotype DX test results assign a Recurrence Score — a number between 0 and 100 — to the early-stage breast cancer or DCIS. You and your doctor can use the following ranges to interpret your results:
  • Recurrence Score lower than 18: The cancer or DCIS has a low risk of recurrence. The benefit of chemotherapy for early-stage breast cancer or radiation therapy for DCIS is likely to be small and will not outweigh the risks of side effects.
  • Recurrence Score between 18 and 31: The cancer or DCIS has an intermediate risk of recurrence. It’s unclear whether the benefits of chemotherapy for early-stage breast cancer or radiation therapy for DCIS outweigh the risks of side effects.
  • Recurrence Score greater than 31: The cancer or DCIS has a high risk of recurrence, and the benefits of chemotherapy for early-stage breast cancer or radiation therapy for DCIS are likely to be greater than the risks of side effects.
You and your doctor will consider the Recurrence Score in combination with other factors, such as the size and grade of the cancer, the number of hormone receptors the cancer cells have (many versus few), and your age. Together you can make a decision about whether or not you should have chemotherapy or radiation therapy.

How is Oncotype DX different from the MammaPrint test and the Mammostrat test?

You may have heard about two other tests that analyze breast cancer genes to predict recurrence:
  • the MammaPrint test
  • the Mammostrat test
While all three tests are somewhat similar, there are differences:
  • The Oncotype DX test is used to estimate a woman’s risk of recurrence of early-stage, hormone-receptor-positive breast cancer, as well as how likely she is to benefit from chemotherapy after breast cancer surgery. The Oncotype DX test also is used to estimate a woman’s recurrence risk of DCIS (ductal carcinoma in situ) and/or the risk of a new invasive cancer developing in the same breast, as well as how likely she is to benefit from radiation therapy after DCIS surgery. The Oncotype DX test analyzes the activity of 21 genes and then calculates a recurrence score number between 0 and 100; the higher the score, the greater the risk of recurrence.
  • The MammaPrint test is used to estimate a woman’s recurrence risk for early-stage breast cancer. The breast cancer can be hormone-receptor-positive or hormone-receptor-negative. The MammaPrint test analyzes 70 genes to see how active they are and then calculates either a high-risk or a low-risk recurrence score. MammaPrint results can help a woman and her doctor make a more informed decision about whether to use chemotherapy to reduce recurrence risk.
  • The Mammostrat test is used to estimate a woman’s risk of recurrence of early-stage, hormone-receptor-positive breast cancer. The Mammostrat test measures the levels of five genes in breast cancer cells. These measurements are used to calculate a risk index score. The higher the risk index, the more likely the cancer is to come back. Women are assigned to a risk category (high, moderate, or low) based on their risk index score.

Insurance coverage and financial assistance

The Medicare program and several other major insurance companies have agreed to cover the Oncotype DX test. According to Genomic Health, about 90% of insured people in the U.S. are members of a plan that covers the test. If you discover that your plan does not cover the Oncotype DX test, talk to your doctor: he or she may be able to work with your insurance company to get coverage. If you have a low Recurrence Score and you and your doctor decide you do not need to have chemotherapy or radiation, your insurance company can save much more than the cost of the test.

Genomic Health also has started the Genomic Access Program to assist you with verifying insurance coverage and obtaining reimbursement. If you do not have or cannot secure insurance coverage, the Genomic Access Program still may be able to help. Various forms of financial assistance and payment plans are available for people facing financial hardships or those who are uninsured or underinsured. The Oncotype DX test costs about $4,000. For insurance- and payment-related questions, call 1-866-ONCOTYPE (1-866-662-6897).

US regulators fast-track novel leukemia therapy

AFP 
Nurses walk in a corridor on September 20, 2013 in a hospital in France
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Nurses walk in a corridor on September 20, 2013 in a hospital in France (AFP Photo/Philippe Huguen)
Washington (AFP) - US regulators on Monday put an experimental immunotherapy agent on the fast track to market approval, after 89 percent of leukemia patients in early trials saw their cancers disappear.
The personalized immunotherapy known as CTL019 was developed by the University of Pennsylvania and was designated a "breakthrough therapy" by the US Food and Drug Administration.
That means the experimental therapy will benefit from a speedier than average review process and will get extra attention from the FDA toward development for market.
It is the first cancer immunotherapy to receive the breakthrough designation, and only the fifth biologic agent so far.
The approach works by extracting a patient's T-cells, then genetically programming them in the lab to target cancer cells that produce a protein called CD19.
The altered T-cells are then re-injected into the patient's body, where they multiply and attack cancer.
Researchers reported last year that of 27 patients, including 22 children and five adults, with acute lymphoblastic leukemia, 89 percent had a complete response to the therapy, meaning their cancer became undetectable.
The first child to receive the treatment, Emily Whitehead, in May marked two years of being in remission, and the first adult patient has been in remission for one year.
"Our early findings reveal tremendous promise for a desperate group of patients, many of whom have been able to return to their normal lives at school and work after receiving this new, personalized immunotherapy," said the Penn research team's leader, Carl June.
The university in 2012 teamed up with pharmaceutical company Novartis to develop and license personalized chimeric antigen receptor (CAR) T cell therapies for the treatment of cancers.
In addition to the ongoing trials for acute lymphoblastic leukemia, trials using CTL019 began in the summer of 2010 in patients with relapsed and refractory chronic lymphocytic leukemia.
It is also being tried in patients with non-Hodgkin lymphoma and myeloma.
More research is also under way into CAR therapies for mesothelioma, ovarian, breast and pancreatic cancers.