Metastatic Breast Cancer Project - Great research
Comments
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Just got my saliva kit the other day. So glad I searched and found this thread on BCO! As far as records, I think WTF. I'm so excited that MBC is really starting to get its due in research and happy to do my part to hopefully help save ours and future lives. #researchnotribbons
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Got my kit!! you're right...lots of saliva!
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I got home today to find that I got my spit kit!! I'm a bit disappointed that we Canadians have to pay the postage, I'm going to find out how much it is and I'll post here.
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I had a question. Got my kit, did the spit thing (glad you mentioned how much you needed to spit, Caryn, or I would have thought I was doing something wrong).
Now I'm ready to mail it back and am wondering how they're going to know its from me. There's no identifying label where my name "Mrs.M." goes, not on the vial or the box so how does that work?
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There seems to be a number sequence on my tube, they did say that no one would have access to our information, so I assume that our files would have the same numbers as our tube.
I'm glad to read that I don't have to send it in until July. I already have a dry mouth, I don't know where I'm going to get all that saliva from. GG
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Thanks, GG. I didn't think to look at that tube. My brain knew there had to be some logical tracking system but I couldn't figure it out on my own.
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MCB posted on their closed Facebook page to get a fresh lemon and put one drop on your tongue to stimulate the saliva. I did that and it helped a lot. Even cutting open the lemon and smelling it help the salivary glands get going.
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Thanks for that tip Lindalou. I really had no idea how I was going to get any saliva.
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Hi Everyone,
I've asked Corrie from MBC to repost her saliva lemon instructions and I will post it here as soon as I get it. It should only be a day as she responds quickly.
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This is from Corrie Painter with MBC Project regarding dry mouth and saliva collection. The lemon worked for me.
Linda
Hi Everyone. I want to thank everyone who helped us with the brochure, we handed out over 500 last weekend at the LBBC Thriving Together Conference! I also want to thank those of you who took the time to come meet with us, and to sit with us to help out.
One of the major pieces of feedback that we received from patients who have already received their saliva kits, are that they are really struggling with dry mouth. I asked the manufacturers of the kit to come up with a set of instructions to address this. They sent me a lengthy reply, and I'd love to trim it down, and make sure that it 1) Makes sense to patients and 2) WIll help people better understand how to contribute saliva. Can you provide feedback on this:
We understand that dry mouth can sometimes be difficult, but donors with dry mouth can still use the OG-500 kit. Typically we find that through a little stimulation the donor can provide enough saliva. A small amount of sugar tongue will help and we also find that a drop of lemon juice onto the tip of the tongue is very effective in producing saliva. We have heard from other researchers that rubbing your cheeks near the jaw bone will help to stimulate saliva.Try this: have the donor sit quietly without speaking (which can often produce bubbles and make collection more difficult) and place a drop of lemon juice on the tongue. Have them close their mouth and move their tongue around to stimulate and collect saliva. Once they have collected as much as they can in their mouth, release it into the kit. You can ask them to do this a couple times until they reach the "fill to" line We do not recommend leaving un-stabilized saliva in the kit past 15-30 minutes so if they want to collect later (such as an hour later, I wouldn't reccomend a full day) they will have to cap the kit and store it upright with the funnel still attached and return later on to finish spitting
THANKS! -
Hi all!
I went to mail my spit kit today & the postage with a tracking number is $16+ from Canada. I'm not really very happy about having to pay that especially with shipping being free in the US.
Also they will not ship it out without having my name & address on the form, so much for anonymity, I guess I can't blame US customs for wanting this, but I guess I'm just disappointed in the process.
Editing to add that I just rec'd an email from MBC project, they said they will be contacting all Canadian participants regarding a corrected mailing box which will be postage paid. You can also request a box without the MBC identifiers on it as you will have to fill out a US customs declaration with your name & address on it. I haven't yet heard back as to what we are to fill out the declaration with regard to contents.
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All,
You may want to read this. The Metastatic Breast Cancer Project is mentioned in this interesting article featured in the New York Times magazine several weeks ago.
http://www.nytimes.com/2016/05/15/magazine/excepti...
Tina
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Tina, very interesting article, thanks for sharing. Such a hopeful message
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Received my kit today!
Tina
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Happy spitting, Tina!
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Hi all,
This is the MBC Project poster that was presented at ASCO recently.
If you are not familiar with the Metastatic Breast Cancer Project please read this overview. Click the image below to view the full-size infographic.The MBCproject.org is a collaborative effort between researchers, doctors and patients launched at the Broad Institute of MIT and Harvard as well as Dana Farber Cancer Institute.
The MBC project is focused solely on metastatic breast cancer. Our goal is to generate a comprehensive set of data that will be stripped of personal information and shared with the entire research community so that all scientists can take part in the discoveries made possible by direct patient engagement. To join the project, please press the "Count Me In" button on our website www.mbcproject.org.
If you are a stage 4 breast cancer patient, we strongly encourage you to join this project. We also strongly encourage everyone to be a supporter by share this
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just got my spit vial.
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Thanks for sharing the poster, Lindalou.
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Thank you, Linda
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Thanks, Linda. Clearly, the direct-to-patient approach may be the wave of the future.
Tina
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Just mailed my saliva sample. No problem filling the vial. I seem to be full of spit!
Tina
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I asked my onc at my Mon appt if I should do this & he said, Yes! My center is also involved with it so..signing off :-)
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It must be exciting to know that your center is involved in the study. I received an email the other day saying that my saliva sample has been received. The people on the project will now contact my doctors and hospital to request my records.
I hope and pray that the researchers are successful in finding breakthroughs.
Lynne
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Lynne, we're on a similar timeline. I also just heard that they received my saliva. Funny, but everytime I hear from them, I feel a sense of exhilaration and hope. I truly believe (like feel in my gut) that this project will result in some very important discoveries. I just hope and pray whatever they learn can translate quickly into new tx options.
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Lynne and Deanna - I'm in the same group as both of you with the project.
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So impressed with this project and their communication! Here's an update. Please consider registering if you haven't already!
Thank you again for signing up for the Metastatic Breast Cancer Project (mbcproject.org). This email is being sent to you, as one of over 2,400 women and men with metastatic breast cancer who have signed up for the MBCproject over the past 9 months. Thanks to ALL of you for your enthusiasm and support — and for your willingness to be a driving force in this project. We have been amazed by the tremendous outpouring of support.
Today, we're writing to you to tell you about the progress we've made to date, and what to expect from the MBCproject over the next few months. We appreciate your patience as our project continues to grow, and we are excited to share the next steps with you.
The Numbers
In the 9 months since the project has launched, we have had over 2,400 of you come to our website at mbcproject.org and click "Count me in!" to enroll in the project -- an incredible response! By now, all of you should have received an email with a link to our online consent form – so far, more than 1,300 of you have signed the consent form giving your permission to us to obtain and analyze copies of your medical records, portions of your leftover tumor samples, and your saliva.
We've sent saliva kits to everyone who has signed the consent form (for US and Canada participants for now — we hope to add more countries in the future). To date, we have received back more than 650 saliva kits. And, we are beginning to request more medical records and tumor samples – we have already received hundreds of records and tumor samples over the past few months.
What have we learned so far?
Of the 2,400 people who have enrolled in the MBCproject, more than 95% of you answered the 16-question survey about your cancer and treatments. This information is hugely informative. Here's what we've learned from you:
- Average age of those who have signed up: 52 (ranging from 24 to 91)
- Average age at diagnosis: 45
- Average age at time of metastatic diagnosis: 49
- Average time between initial diagnosis and metastatic diagnosis: 4 years
- Number of patients diagnosed with metastatic disease from onset ("de novo" metastatic disease): >800
- Number of patients who have been alive with metastatic diagnosis for 10 years or longer: >160
This is really important information for metastatic breast cancer research — and helps us frame how we are going to ask and answer key biological questions in this disease.
And this is just the very beginning of what we're learning. You've also told us a great deal about your cancer types and treatments — including which treatments worked well for you and which didn't. We've also heard many of your stories, about what's important for you to learn about, and even about issues that we didn't think to ask about in the first place.
We've been sharing much of this information online on Twitter (@mbc_project), on our Facebook page (https://www.facebook.com/The-Metastatic-Breast-Cancer-Project-852059048224675/), and on our blog at http://mbc-project.blogspot.com. We have lots more to learn from your responses - and we will continue to post what we learn on our blog as well as on Twitter and Facebook.
MBCProject in the news
Many people are taking notice of the project, and are inspired by our partnership with you and our patient advocates. We've been excited to have been featured in a number of recent press articles and blog posts, including two articles in The Wall Street Journal (Researchers Take Aim at Metastatic Breast Cancer and New Studies Rely on the Internet for Help Treating Cancer Patients), The New York Times Magazine (Learning from the Lazarus Effect), Fast Company (#Cancer: Researchers are conducting huge studies using Twitter, Facebook) and the Broad Institute blog (Power to the Patients). In addition to this, we are proud to announce that the White House has listed us as one of 40 initiatives that will accelerate precision medicine (Obama Administration Announces Key Actions to Accelerate Precision Medicine Initiative).
We also recently presented the project at the American Society of Clinical Oncology (ASCO) Annual Meeting, where it was extremely well received by both the oncology community and press. You can find a copy of our ASCO poster, as well as slides and video from the press conference on our blog at http://mbc-project.blogspot.com/2016/07/mbcproject-updates.html.
In March, some of you were able to join us in person to discuss the project, and are featured in this video. If you haven't yet seen it, please watch and share this video about why the MBCProject is so important to patients and researchers alike (The Metastatic Breast Cancer Project).
What are the next steps?
In the coming months, we'll continue to collect medical records and tumor samples from everyone who has signed the online consent form and sent in their saliva kit. Genomic sequencing studies on tumor tissue and saliva samples are already underway, and we hope to have our first data analyzed by the end of the year.
We are also in the process of bringing on additional advocacy partners to build our partnerships and expand our reach, and are will continue to work with our current partners and participants to continue to grow. Our advocacy partners include The Metastatic Breast Cancer Network, The Metastatic Breast Cancer Alliance, Avon Foundation, Living Beyond Breast Cancer , Inflammatory Breast Cancer Research Foundation, Young Survival Coalition , SHARE , Male Breast Cancer Coalition , Theresa's Research Foundation, Triple Negative Breast Cancer Foundation, The IBC Network Foundation, Advocates 4 Breast Cancer , METAvivor, MET UP, Tigerlily Foundation, and several more collaborations that are in the works. We feel strongly that the success of the project is because of our combined efforts with you, our patient-participants, and with our advocacy partners, and are continuing to strengthen those relationships.
What can you do to help?
We have been contacted by many of you who are eager to help us accelerate the project. Here are 3 things you can do to help:
1) If you have not yet signed the consent form and if you are willing to share copies of your medical records, portions of your leftover tumor samples, and your saliva, please sign the online consent form that we emailed you. (If you need to find the email, the subject is "Next step for the MBCproject: Sign the consent form". If you've already signed the consent form, you should have an email from us with the subject "Thank you for providing your consent"). If you can't find the link to your consent form, email us at info@mbcproject.org and we can send you a new one.
2) If you've already signed the consent form and have received your saliva kit (for people living in the US or Canada), please send in your saliva kit. If you lost your kit or need a replacement, email us at info@mbcproject.org and we can send you a new one.
3) Help spread the word. The MBCProject is a patient-driven research movement. Our biggest enrollment days have been a direct result of your outreach to other patients. We are deeply moved by your contributions and enthusiasm, and we know that the project will continue to grow through patients like you reaching out to other patients. If you'd like to help spread the word, please let other patients with metastatic breast cancer know about mbcproject.org by posting on social media or simply telling others in your community. Many of you have also asked how you can volunteer to further engage patients and expand the project -- if you'd like to do more, please email us at mbcvolunteers@broadinstitute.org.
For more information
Thank you again for your participation and support. We hope to provide quarterly updates through this email list, and would love your feedback on what aspects of the project you are interested in learning more about. In the meantime, you can find more frequent updates on our blog, twitter feed, and facebook page. You can also find additional information about the project on our FAQ page (https://www.mbcproject.org/faq).
If you have any questions, feedback, or ideas for the project, please feel free to reach out to us at info@mbcproject.org or call 617-800-1622.Warmly,
Nikhil Wagle
Corrie Painter
Elana Anastasio
Michael Dunphy
and the rest of the MBCProject team -
Hello All,
Today, The Broad Institute released a new You Tube video featuring 3 women from the project.
Search, Metastatic Breast Cancer project: Patient- Driven Research.
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Great piece, LInda! Here's the link.
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Thanks Deanna, I could post it on Bone mets thread but for some reason couldn't do it here. Thanks for posting the video.
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Thanks Deanna and Linda for your posts! I work for a company that manages 60 conferences a year for research scientists - all fields. I'm the "social media guru" and will post this to our FB, etc. pages.
I haven't checked here lately and missed your post from July 26, Deanna, so I'm going back to read it, too. Hugs all.
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