Thursday, September 27, 2012

Distinct | First Comprehensive Genetic Analysis Of Breast Cancer Could Change Treatment

JUDY WOODRUFF: Next, new investigate that's varying the bargain of cancer.

Scientists say they have found new insights in to 4 genetically noteworthy types of breast cancer, potentially altering the way doctors a day provide the disease.

The commentary were published yesterday in the biography "Nature" as segment of a thorough genetic review of breast cancer.

Among other discoveries, researchers say that a singular but lethal form of breast cancer bears a genetic likeness to the kinds of tumors found in lung and ovarian cancers.

Doctors moreover schooled that the two many familiar forms of breast cancer, both of that rest on estrogen to fuel their expansion and have been treated with colour likewise in the past, are obviously genetically noteworthy from a another.

Well, for more on this, I'm assimilated by Dr. Harold Varmus. He's executive of the National Cancer Institute. The hospital helped to lead the work as segment of a incomparable plan to chart genetic changes in cancer.

Dr. Varmus, appreciate you for being here.

DR. HAROLD VARMUS , National Cancer Institute: My pleasure.

JUDY WOODRUFF: So, discuss it us what is poignant about what you found about these 4 types of breast cancer.

HAROLD VARMUS: Well, these 4 types have obviously been well known for a few time formed on work completed scarcely a decade ago that was vigilant on characterizing that genes were off and on in breast cancer types.

And to the astonishment of many, it was probable to form 4 considerable groups that many breast cancers could fit into.

What these studies uncover -- and they are segment of a ample incomparable bid that the Cancer Institute and the Human Genome Institute are carrying out on many various types of cancer -- is that by using a accumulation of new techniques to coming after the genome, to tally the number of copies of genes, to look at that genes are being read out and that proteins are being made, that you can start to look at the heterogeneity of these 4 groups and conclude specific commonalities inside of the groups that give us -- will give us a few perception in to that therapies are many apt and what type of new therapies might be envisioned.

JUDY WOODRUFF: So, is this revelation you that the genetic markings are more critical than only about any other eminence to these breast cancers?

I mean, you mentioned...

HAROLD VARMUS: Well, in general, all cancers have been traditionally characterized by the way they be present beneath the microscope and the viscera in that they arise.

But as you pick up more and more about cancer of every type, inclusive breast, what you pick up is that the drivers of cancer are primarily mutations and changes in chromosome group or figures of copies of genes, and that those are the instruments that expostulate a cancer and thus turn ways of classification cancer, ways of conceptualizing new therapies that especially aim those changes, and markers for knowing either or not these cancers will reply to established existing therapies.

JUDY WOODRUFF: So, was this a intolerable square of information?

HAROLD VARMUS: It wasn't shocking, no.

We have been going by many kinds of cancers, and many more are to advance inside of this considerable study.

And what we're perplexing to do is to emanate a warehouse, a collection of information. The plan is called the Cancer Genome Atlas.

It's an atlas, a warehouse, a storehouse, a database that everybody is giveaway to look at, since all this data is being made publicly available.

If you go to the website and look at the Cancer Genome Atlas, you will see the information. You can -- all these credentials are openly available to everyone.

And the indicate is that you know that every time you draw close a cancer with these technologies and look at many hundreds of particular cancers of a specific normal grouping, similar to pancreatic cancer or liver cancer or gastric cancer or breast and other cancers that have been published, that we're going to see engaging patterns.

Every cancer looks different. All cancer has similarities to other cancers. And we're perplexing to divert those differences and similarities to do a improved job of presaging how things are going to work out and creation new drugs.

JUDY WOODRUFF: And how will that affect the treatment of these cancers? I mean, do you already know how that might happen, or is that just...

HAROLD VARMUS: Well, you have an idea.

First of all, there is the long-range perspective that, as you comprehend precisely what's wrong, you will make targeted therapies that are specific for cancers that have specific kinds of genetic aberrations.

But even in the more evident future, it's going to be probable to put together the understanding, the outline of the genetic changes in a cancer and the responses to existing therapies. And that's the square that you still miss.

And a way in that I think that patients who have cancer right away and are being treated with colour right away can make a leading grant to the development of more efficient and more precise treatment, using existing therapies.

JUDY WOODRUFF: So, this -- you're adage this could make a disparity in the really nearby future?

HAROLD VARMUS: In the next few years. It is not going to change use overnight.

Some of the ideas that are in this paper, the connection you referred to between a few of the genetic changes seen in a specific quite serious from a breast cancer and ovarian cancer, for example, suggest that those cancers have an unstable in their genome that may be addressed with a few existing therapies. And those therapies are being tested right away in those breast cancer patients.

But what waste to be figured out is how you obtain the clinical data together with the genetic data in the type of database that you can all use to start to envision who is going to reply to that drugs.

JUDY WOODRUFF: And why is that as hard as it is? What would make that easier?

HAROLD VARMUS: Well, in segment since it's hard to obtain the clinical data in to a form that may be put in to a database that is interpretable.

Some of this is a matter of learning how to rub-down the data so you make the correlations that are indeed helpful.

The second is that you must be beat a hostility to provide personal clinical data and genetic data to a database that will help others, to provide the right kinds of acceptance forms and privacy protections that enable this all to happen.

And I would titillate patients who have cancer right away to think of themselves as data donors who can gain not only others who will have cancer later, but themselves over the next few years.

Because cancer patients are living longer and improved lives, interjection to improved sign control, more efficient therapies, and a deeper bargain of cancer that has advance about by investigate over the final decade.

JUDY WOODRUFF: So, finally, only to enlarge this out, what are your hopes, Dr. Varmus, for this incomparable genetic study of all kinds of cancer?

HAROLD VARMUS: Well, I think that you are going to have a ample deeper high regard of what kinds of abnormalities in cancer cells and in the surrounding cells that feed and reply to cancers are vulnerabilities that will enable us to make improved predictions of that kinds of drug will work to provide these cancers.

They moreover turn markers that enable or enable early detection. They turn signposts for considering about what the environmental causes of cancer might be and for considering about how you can stop cancers more effectively.

But this is not only all about treatment. And you must be think imaginatively about how you stop cancers, that is the best goal.

JUDY WOODRUFF: It must be really exciting for you.

HAROLD VARMUS: Well, it's a tough complaint that you think we're creation great progress against these days. And it is an confirmation of the significance of medical investigate to the nation.

JUDY WOODRUFF: Dr. Harold Varmus, you appreciate you really ample for being here.

HAROLD VARMUS: Pleasure. Thanks.

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