Brain Tumour Foundation Working to Cure Paediatric Brain Cancer


ribbon_gray_brain_cancer03The death of a child is an event no parent can ever truly move beyond. Though grief is a lifelong process, for some a personal tragedy such as this can be a springboard to launch an organisation focused on bringing attention to an important cause.

That was the case for Jill and Mazen Kamen, who officially launched the Kamen Brain Tumor Foundation after losing their 19-year-old son in April to brain cancer.

In 2009 he had been diagnosed with a type of rapidly growing brain tumour called a high-grade astrocytoma that, despite aggressive treatment, eventually evolved into a glioblastoma — the highly malignant brain tumor that also took the lives of Vice President Joe Biden’s son, Beau, in 2015 and former Sen. Ted Kennedy in 2009.

The first phase is shock when your child is diagnosed,” said Mazen. “You can’t believe it. You start questioning the why, the where. It’s like someone has hit you with a Mack truck. You have to go through that. But you also have to regroup yourself very quickly, because now you have a long, tedious road ahead. And you really have to do your homework very quickly and efficiently, if you can, to face this.”

Glioblastoma Multiforme is the most common and deadliest of the glial tumours because the cells reproduce so rapidly. The tumour grows by turning normal brain cells into stem cells, which continuously replicate and regrow. So even if a tumour is surgically removed, it is difficult to extract every cancerous cell; any left behind will result in the growth of a new tumour. The 5-year survival rate for children with glioblastoma is 25%.

While there are more new cases of leukaemia each year than new cases of brain cancer, in 2014 brain cancer surpassed leukaemia to become the leading cause of death for those under the age of 19, a result of the great progress that has been made in leukaemia treatment over the past five years. In September the Centers for Disease Control and Prevention issued a report highlighting the need for greater investment as well as new approaches for funding and conducting paediatric brain tumor research.

Dr. José Baselga, chief medical officer and physician-in-chief at Memorial Sloan Kettering Cancer Center in New York, says it is organisations such as the Kamen Brain Tumor Foundation that will be instrumental in driving the cure.

“The science is here, so we are pushing hard,” he said. “We have a very clear image of how to attack this disease.” But, he says, the funding is minimal. “Only 4% of the NIH budget is devoted to Childhood Cancers. To have a foundation that is committed … They’ll find sources; they’ll create a community of people that will support this research.

Deadly Statistics

Currently, there are 28,000 children in the United States living with a malignant brain tumour, and another 4,600 are projected to be diagnosed each year. Yet, since 1985 there have been only 4 FDA-approved drugs to treat the more than 120 different types of brain tumours, according to the National Brain Tumor Society. And none of these are specifically aimed at treating paediatric brain tumours. Between 1998 and 2014, claims the NBTS, 78 investigational brain tumour drugs were entered into the clinical trial evaluation process, and 75 of them failed.

Fortunate to have contacts in the medical field — Mazen is a cardiologist at New York-Presbyterian Hospital and Jill a critical-care nurse by training — the Kamens immediately began investigating treatment protocols. “You need to have at least three or four opinions from major centers, and sometimes you get conflicting opinions,” said Mazen. “Not only about the pathology of the tumor but also the treatment. You say, “What do I do? Who should I go with?’ Ultimately, it’s your gut feeling.

Over the seven years, the Kamens traveled the map, beginning with treatment at Massachusetts General Hospital in Boston, then on to Duke University Medical Center to consult with neuro-oncologist Dr. Henry Friedman, the same doctor who treated former Sen. Ted Kennedy. The Duke team collaborated with Memorial Sloan Kettering in New York to devise a chemotherapy and radiation protocol that could be administered at MSK so their son could be close to home.

Our son had a mutation,” said Mazen. “The question is, what made it mutate? … What we found is that even though you’ve found the mutation in the tumour, there’s no drug to treat it.”

Frustrated with the lack of investment in research and drug development devoted to paediatric brain tumour gliomas, the Kamens decided to take action and launch their foundation. Its mission: to fund cutting-edge research to find better and safer treatment options and to provide guidance and support for families who have a loved one dealing with this devastating illness.

We want to get the word out there that we have been through this experience firsthand. And because we have inside knowledge of the medical community, we feel that we can lend that part of our experience to help others,” said Jill.

Their scientific advisory council consists of a number of experts from leading medical institutions, including Memorial Sloan Kettering Cancer Center, New York Presbyterian Hospital’s Weill-Cornell Medical Center and Duke University Medical Center.

The Kamens claim the main thing that distinguishes their foundation from other brain tumor foundations is their focus on pediatric brain cancer specifically, as well as their close ties with pharmaceutical and biotech companies working in the fields of immunotherapy and target gene therapy.

Moving Closer Toward a Cure

Traditional therapies for brain cancer — surgery, chemotherapy and radiation — haven’t been very successful,” says Memorial Sloan Kettering’s Dr. Baselga, adding, “We have a tremendous need to develop new therapies, especially with children. Surgery is difficult because tumours infiltrate, so it’s very difficult to obtain clear margins, and radiation can be risky.”

We have to be very careful, because these children are developing their brains and the consequences of giving full-dose radiation could be lifelong lasting, so we cannot sometimes give full therapy,” he said. “And then chemotherapy — you know, the brain is protected. The brain is designed so that toxins would not get there. So it is very challenging to have chemotherapy get to the brain with a good dose.

Instead, Dr. Baselga said researchers and scientists are making strides in what he calls precision medicine, an emerging approach for disease treatment and prevention that takes into account individual variability in environment, lifestyle and genes for each person. Rather than a one-size-fits-all approach, doctors and researchers will be able to predict more accurately which treatment will work for a particular person.

Today we can sequence,” he said. “We can look at the genes that are abnormal in brain tumors [and] develop therapies to attack those genes.

The therapies he is referring to are genomic, epigenetic and immune therapies. “This in childhood brain cancers is going to be very promising. We are teaching the immune system how to recognize the tumor cells as something we don’t want. We are teaching the T cells, the lymphocytes, multiple cells to be more proactive in cleaning up the cancer cells in the brain. Epigenetic therapy attacks the way genes are being expressed.”

A Family of Visionaries

Launching a foundation would be a daunting task for most, yet for the Kamens it’s a natural calling. Mazen is the nephew of Elmer and Mamdouha Bobst — philanthropists who in 1968 established the Elmer and Mamdouha Bobst Foundation in New York. Throughout the years, the Bobsts donated millions to cancer research, education and other causes, including New York University, NYU Langone Medical Center, Princeton University, the Animal Medical Center, Memorial Sloan Kettering Cancer Center and the American Cancer Society. In addition, the Bobsts donated $11 million in 1973 to complete New York University’s library on Washington Square, which bears Elmer Bobst’s name, along with $10 million to create the Mamdouha S. Bobst Center for Peace and Justice.

“I was blessed and fortunate to have grown in such a family of visionaries. They have given me a lot of advice throughout my life. The most important thing is to help each other. My uncle Elmer always used to remind me of a saying: ‘Service is the rent we pay for the space we occupy on Earth,'” said Mazen. “So I think if we are fortunate enough to be in a position to give, then we ought to do that.”

With regard to finding better and safer treatment options for children with brain tumor gliomas and providing support for their families, he added: “This is a cause we will be pursuing for the rest of our lives.”

This story is part of NBCU’s Share Kindness. Follow the series on Facebook, Twitter and Instagram. #ShareKindness

 

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About LFCT

This is a blog about CHILDHOOD CANCER and CHILDHOOD CANCER AWARENESS Little Fighters Cancer Trust is a non-profit organisation that offers support and aid to Children with Cancer and their families. When a child is diagnosed with cancer it affects the whole family. One of the parents, usually the mother, must give up their job to care for the child and this creates financial problems for the family. In South Africa especially the majority of these families are not well-to-do; many of them are rural. A diagnosis of cancer can wipe out any family’s finances, let alone a poor family. The costs of special medications, special diets, hospital stays, transport to and from the hospital or clinic and accommodation and food costs for the mother who spends most of the time at her child’s bedside are astronomical. These are the people and problems that fall through the cracks, and these are the people that Little Fighters Cancer Trust has pledged to help in any way possible. LFCT takes a holistic approach to assisting the Children with Cancer and their Families, with the main aim to be the preservation of individual dignity and pride. Little Fighters Cancer Trust also focuses on promotion and advocacy of National Childhood Cancer Awareness in an effort to increase awareness of Early Warning Signs of Childhood Cancer. This would result in earlier diagnosis, giving the Child with Cancer more of a chance at Treatment and Survival. See "About" for more Background info

Posted on 3 January, 2017, in Blog, Research and tagged , , , , , , , , , , , . Bookmark the permalink. Leave a comment.

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