Tuesday, December 13, 2016

City of Hope Patient Forum this Saturday and IVIG and immunoglobulins in CLL (chronic lymphocytic leukemia)


Dr. Ben Kennedy

On Saturday, December 17th, we’ll be at the 2nd Annual Post-ASH CLL Patient Forum at City of Hope Medical Center in Duarte, CA. If you can make it, we’d love to see you there. You can access the flyer below and pre-registration is requested. We look forward to seeing you there!

Flyer: 


Pre-registration: 


Today we are posting an audio interview (and accompanying transcript) with Dr. Ben Kennedy who I spoke with during the 2016 CLL Horizons meeting in Belgrade Serbia a few weeks ago. We talked about how CLL affects our immune systems in addition to being a blood cancer. 
You can access that interview here.  


The next issue of The CLL Tribune will be coming out the week after Christmas. We’re busy editing, and doing the layout and putting on all the finishing touches. We’ll also be sharing the poster from ASH that many of you contributed to in our Q1 2016 Reader Poll. Stay tuned!

Newly-Forming CLL-Specific Support Groups

We are organizing some CLL-specific support groups in a variety of cities. Some of you may have attended a CLL educational meeting in that area, or just be interested in joining a support group. Click on the City to sign up and tell us about your preferences as we work to get them started. We appreciate those who expressed interest and have already completed the survey.


In the meantime….
Stay strong.
We are all in this together.
Brian Koffman, MD

12/12/16

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Thursday, October 27, 2016

See you in San Francisco Oct 29, 2016 to help launch a bay area CLL Society Support and Education Group

I am a big believer in the importance of CLL specific support and education groups, run for and by patients and caregivers.

As a result the nonprofit 501c3 CLL Society, has been active in setting up or supporting several such groups in 2016 and laying the framework for many more in 2017.

We have done this by using amazing team consisting of well experienced and trained members of our local support groups, all patients themselves.

I have happily handed off this important effort to my fellow CLLers, but I did reserve the meeting this Saturday, Oct 29, 2016 near the San Francisco airport to attend myself.

If you want to hear why I believe being a member of the right support group has been and can be both a life saving and life affirming move, please come by and say hello

Details are below. Click of the photo to zoom in. I will be speaking on support groups immediately following the end of the B-Connected Live Event. The B -Connected Events are unbranded programs and present the basics about CLL without promoting any particular drugs and also share the patient's and /or caregiver's perspective.

Hope to see you there. I will be hanging around after if you want to chat.

Stay strong

We are all in this together

Brian




SaveSave

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Monday, April 11, 2016

Patient Survey, New CLL support groups, Life at the Beach, and Living Well with CLL (chronic lymphocytic leukemia)

Friends, 
It’s been a very busy year and this week I spent a few days away from my patients and my online and live support group efforts just walking, reading, and resting at a nearby state park on the beach. It was wonderful! 
As I prepare to speak at a symposium at the 2016 European Hematology Association Congress in Copenhagen in June, I am asking you to please consider completing our Reader Poll [https://asktellq12016.questionpro.com/] on how we patients and caregivers make decisions about therapy. It takes less than 5 minutes to complete. Many thanks to the 190 folks who have already done so!  We’ll present the aggregated results in a future issue of The CLL Tribune.
In our live support group efforts, we are forming 2 new patient and caregiver support meetings: Charlotte, NC and Tampa FL.  
• If you live in Charlotte, NC and are interested, please complete the online survey to indicate your preferences for days and times. [https://charlottegroup.questionpro.com/]
• If you live in Tampa, FL and are interested, please complete the online survey to indicate your preferences for days and times. [https://tampa.questionpro.com/]
We look forward to getting started. For those interested in getting a CLL support group going on the west side of the LA Basin, or in attending our Orange County group that meets at UCI, or the group that meets at City of Hope, please send us an email at support@CLLSociety.org and we will provide you with the necessary information.
Find out about other’s experiences with support groups in the Support area of the Living Well with CLL section of the website. [http://cllsociety.org/living-well-with-cll/support/] Teresa Altemeyer wrote a great article in the latest issue of The CLL Tribune about The Value of Support Groups – A Personal Perspective about how she was asked by her CLL specialist to facilitate a support group in Indianapolis, Indiana and the positive effect it had on her life. Check it out. [http://www.cllsociety.org/newsletter/quarter-1-2016-volume-2-issue-1/living-well-with-cll-quarter-1-2016-volume-2-issue-1/value-support-groups-personal-perspective/]

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Monday, April 4, 2016

Busy Few Weeks and a Therefore Rather Ironic Article on Fatigue in CLL (chronic lymphocytic leukemia) by Dr. Estrov

Hi Friends,

It’s been a busy few weeks.

Last week was exciting as we marked the first year since we launched our website, published our first 2016 issue of The CLL Tribune, and fielded a short survey in our Reader Poll on how we patients and caregivers make decisions about our therapy. I hope to present the results at a symposium at the 2016 European Hematology Association Congress in Copenhagen in June, so I am asking you to please complete it. It takes less than 5 minutes. Many thanks to the 78 folks who have already done so!

Two weeks ago in Anaheim, I spoke in front of more than 550 patients and caregivers on behalf of LLS at their southern Californian Blood Conference. My topic was “How to be your own advocate”. It was a great privilege, in every way, to be able to give such a talk after 10 years of dancing with my CLL.

On April 2nd, the CLL Society had an active table sharing CLL information and resources at the LRF Lymphoma Workshop in Manhattan Beach.

Both meetings had superb CLL breakout sessions, in Anaheim by Dr. Tanya Siddiqi of City of Hope, and in Manhattan Beach by Dr. Herbert Eradat of UCLA. Thanks to them both for donating their time.

At both meeting we collected signatures for those interested in getting a CLL support group going on the west side of the LA Basin. It you missed the meetings and are interested, please send us an email at support@CLLSociety.org and we will make you aware of our interest survey when it launches.

This week in the 2015 Conference Coverage section of the CLL Society website, we have posted an interesting article written by Dr. Zeev Estrov from MD Anderson Cancer Center describing the abstract they presented at ASH 2015 focused on exploring treatment options to address CLL fatigue. 

You can see a summary and view our interview on the website.

We are also gathering interest in forming 2 new patient and caregiver support meetings: Charlotte, NC and Tampa FL.

If you live in Charlotte, NC and are interested, please complete the online survey to indicate your preferences for days and times.

If you live in Tampa, FL and are interested, please complete the online survey to indicate your preferences for days and times. We look forward to getting started.

In the meantime….

Stay strong.

We are all in this together.

Brian Koffman, MD
Volunteer Medical Director of the CLL Society


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Tuesday, December 15, 2015

Starting a CLL (chronic lymphocytic leukemia) Society Support Group in LA area

Dear friends and fellow CLLers,

If you live has been touched by CLL, then you realize how valuable a CLL specific support group can be.

And some of us live in Socal and know how long it takes it get anywhere, anytime, any day.

Regardless, let’s try to find a way to make a CLL specific support group work for as many of us in the LA area as possible. It will be worthwhile and the CLL Society will support you to ensure success.

We have a very short online survey to help figure out the best options.

Please click on or paste into your browser: https://cllsocietysupport1.questionpro.com and answer the questions.

We will collate this brief single page survey about dates and times and locales and get back to you.

Everything is confidential.

Feel free to contact me with any questions

I would like to start meeting in February or March at the latest. Our group in Orange County started with 3 only members more than 8 years ago and is one of the reasons that I am alive today

Thanks

Stay strong.

We are all in this together.

Brian

Brian Koffman

Volunteer Medical Director, CLL Society Inc.

http://cllsociety.org
http://bkoffman.blogspot.com

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Friday, November 6, 2015

CLL Society, LLS And City of Hope for CLL Specific Educational Forum and the chance to launch an Ongoing CLL Support Group

This will be a super meeting right after ASH and will be a chance to get a LA support group going. Click here to register: https://cllforum.questionpro.com



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Thursday, January 15, 2015

There is One Less Doctor/Patient with CLL (chronic lymphocytic leukemia) Alive Today

More bad news.

After a 10 year struggle, a young friend (in his mid 40s) with very young children, a fellow MD with CLL, just passed away from complications of his leukemia.

Being a doctor, even a very thoughtful Harvard trained doctor, and being treated at world class medical centers, and making all the smart decisions, and getting randomized to the "right" arm of the trial, and getting the best possible therapies and living a clean lifestyle, and being a hardworking, good person, and having the love of your family and friends and the respect of your colleagues and the prayers of many, none of it provided a free pass.

This is the second doctor/patient that I personally have known that succumb to this disease.

When it comes to CLL there is no immunity. Double entendre definitely intended.

I hate this cancer.

Mostly I am just so sad for his wife and his children and the rest of his family.

And angry (but I am not sure at what- the cancer I guess).

My prayers goes out to his loved ones.

I am also so motivated to do what can be done to increase all our odds of avoiding a premature death. It's possible. It's close. But we are not there yet.

I and several other CLL survivors from our Orange County CLL support group will be at the LLS Blood Conference Feb 7 in Anaheim.

Please click here to learn more.

On behalf of LLS, I extended an invitation to Dr. Tom Kipps of UCSD and Dr. Steve Rosen of City of Hope and was thrilled that they both accepted to speak. It will be super meeting, so don't miss it.

Please register and when you are there, please drop by our table for the CLL Society Inc. the new nonprofit 501c dedicated to the unmet needs of the CLL community. Learn how with your help, we plan to make a real measurable difference in the years to come and do what we can so that everyone has the best possible odds.


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Wednesday, January 22, 2014

Dosing of Ibrutinib and Other Oral Agents

"Poison is in everything, and no thing is without poison. The dosage makes it either a poison or a remedy."

PARACELSUS

Recently there has been some discussions among those of us who hang out at online at CLL forums such as ACOR and CLLSLL Yahoo Groups about the dosing of ibrutinib.

I am a strong believer in the power of these online communities to help us cope with our disease.

The problem inherent in peer to peer counsel is not the inaccuracy of the advice given as that also sadly too often occur in professional to patient counsel. The problem is more the lack of authority afforded any particular response. That said, if respect is earned, several regular contributors have earned my respect with their well reasoned and researched frequent comments online.

Often, especially with cutting edge therapies, the patient community is better informed about their rare disorder than the community healthcare professional who must handle the full spectrum of illness his or her chosen specialty demands.

For more on this subject see this article in BMJ  provocatively titled: What happens when patients know more than their doctors? Experiences of health interactions after diabetes patient education: a qualitative patient-led study

Case in point: Dosing of ibrutinib.

The only approved dose for ibrutinib is four tablets a day for mantle cell lymphoma (MCL), which by the way is usually a nastier disease than CLL. The Imbruvica dosing is right on the package insert.

So the community oncologist dutifully looks up what the dose to use for CLL, and finding no FDA sanctioned guidance, recommends using the MCL dose. After all,  the somewhat arbitrary dose of rituximab is the same across a wide spectrum of illness.  Arbitrary because, according to legend, the original dosing was based upon how much rituximab was available, divided by how many trial patients needed it. That worked out to be 375/Mand the rest is history.

The circumstances are less arbitrary with ibrutinib. We know that ibrutinib works by irreversibly blocking BTK through covalent binding to cysteine-481. We know that the sweet spot for getting that site fully saturated is somewhere between two and three 140 mg. capsules a day.

Moreover we know that mutation of cysteine-481binding site is an important cause of late resistance. Ibrutinib no longer fits, and the BTK pathway, and thus BCR signaling continues unabated. Not a good thing.


One sure way to increase the odds of that sinister development is to start with a low dose of ibrutinib that only partially blocks the site, but allows a significant population of lymphocytes to continue to express BTK. That is the last thing we want in cancer therapy. What we want is a SHOCK AND AWE approach to cancer. We don't want the cancer cells retreating, regrouping, and later coming back to get us by probing our weak points.


Worse yet, the up and coming second generation BTK inhibitors also seem to bind at the exact same site, so if we become resistant to oneBTK inhibitor, we may be resistant to them all. A strong incentive to get the full dosing the right from the start.


So when a doctor suggests slowly going from one to two to three or more capsules a day, it is OK for a patient to say: Can we please get a second opinion from someone with more experience with the particular drug? (Of course, there is always the possibility of the individual's extenuating circumstances that we just don't know).


Some drugs for good reasons such as allopurinol in gout needs very slow upward titration to prevent increased painful flares, but ibrutinib and most of the other TKIs should almost never be dosed that way.

Bottom line: The standard dose for CLL is three 140 mg. capsules once a day, for MCL four 140 mg. capsules once a day. Sometimes those doses can be adjusted due to adverse events or hepatic disease or concomitant medications that effect its clearance (more on that topic, specifically on the CYP3A4 pathway in another post). Short of end stage renal disease or dialysis where there is no data to go by, no dose adjustments are needed as less than 1% of the drug is excreted unchanged by the kidneys.


The right dose is more than important, it is mission critical.

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Thursday, November 14, 2013

It's All Too Much: The Loss of a CLL Friend and the Approval of Ibrutinib for Mantle Cell Lymphoma

The world of CLL is unrelenting and demanding.

I tried to step away for a few days, but news, good and bad, swirled into the center of my vision, and if that didn't get my attention, it then whacked me off my seat with its wild and blunt force.

Like my six month old granddaughter saying with her fusses and her smiles, PAY ATTENTION TO ME, CLL craves to be the center of the universe.

We lost another CLL warrior today. A member of our Orange County support group, Susie Vercruse passed from complications from a stroke. This was not likely a direct CLL issue, as even with counts of a million or more lymphocytes, we don't get the dangerous hyperviscosity (the blood gets too thick) seen in other blood cancers than can lead to blood clots, but that doesn't ease the pain. I will miss her easy smile and friendly positive ways. Very sad.

And yesterday we gain a new warrior in our CLL battles. Well sorta. 

Ibrutinib or should I say now say Imbruvica was approved for relapsed and refractory mantle cell lymphoma (MCL).

This is very good news. It was as a friend in Houston said: a clean approval: No black box warnings concerning use with blood thinners (an early concern in some trials). 

The label says:

Five percent of patients with MCL had Grade 3 or higher bleeding events (subdural hematoma, gastrointestinal bleeding, and hematuria). Overall, bleeding events including bruising of any grade occurred in 48% of patients with MCL treated with 560 mg daily.
The mechanism for the bleeding events is not well understood.
Consider the benefit-risk of ibrutinib in patients requiring antiplatelet or anticoagulant therapies.
Consider the benefit-risk of withholding ibrutinib for at least 3 to 7 days pre and post-surgery depending upon the type of surgery and the risk of bleeding 


Importantly patients only have had to fail one prior drug before they can have access to Imbruvica (get used to that name). Often new and expensive treatments are held in reserve only for those who have failed all other therapies, not just one.

Also there are no restrictions as far as I can see on how it used, alone or in combination, unlike the more limited recent approval of obinutuzumab.

MCL is much rarer than CLL, less than 3,000 cases a year in the USA, and is generally a much nastier and faster moving cancer than most CLL, with until very recently, fewer good treatment options.

Both obinutuzumab and ibrutinib could benefit a ton of patient of patients "off label", which is an ethical and legal way that many cancer and other drugs are often used.

Of course, cost will be a big issue. At an estimated more than $90 a pill for Imbruvica, the annual price tag for those of us with CLL would be just a tad under $100,000 a year. It is a full third higher in MCL as they take four 140 mg tablets daily. To their great credit, I have read that Pharmacyclics will be offering some medication free to help patients while the insurance is being worked out and will offer co-pay support for others longer term.

These days, this is the typical cost of many new cancer drugs, and is actually lower than some. Some orphan drugs used to treat very rare disorders can cost $200,000 to $400,000 a year, making ibrutinib look like a bargain.

Still 99% of us will not able to pay for that, and insurance will likely balk or in the best case scenario, take a good arm wrestle to consent to lay out that kind of cash.

We need to hope from a very broad approval for Imbruvica for CLL, speedily to minimize these issue.

It is a brave new world we are entering, and there are no easy answers. Drugs are very very expensive to get to market and for every single chemical that succeeds in making it to market, scores and scores never make it to the pharmacy. 

We can't afford it and we can't afford not to do it. 

I will post more helpful interviews real soon from iwCLL 2013 (I promise), but as John Lennon said: Life is what happens to you, while you are busy making other plans.

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Tuesday, July 2, 2013

CLL Support Group on July 3, 2013 at 4 PM at the Moore Cancer Center

Please join me tomorrow at UCSD at 4 PM on the 2nd floor of the Moore Cancer Center in the "Commons" for my talk to the CLL support group based on my experience as a doctor turned patient dealing with cancer.

I plan to start with a brief overview of CLL, discussing in general terms diagnosis, lab tests, prognostic factors, symptoms, complications, management, and how treatment is changing. The last half of my talk will be about my personal experiences as a patient ending with my participation in OSU clinical trial with ibrutinib.

It will feature video clips from my interviews with Drs Kipps, Wiestner, Byrd and Pagel at past ASH meetings.

After my 45 minutes, we all have a chance to meet and exchange stories and information.

Hope you can make it.

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Thursday, December 20, 2012

ASH 2012: Interview with Web Savvy Patient, Andrew Schorr

Andrew Schorr is a journalist, an advocate, and a very web savvy patient who has stared down CLL for about 16 years and it now winning his fight with myelofibrosis.

Through his helpful website, patientpower.info, he has provided a treasure trove of information for patients looking for answers.

Now he gets to be on the other side of the microphone in the hall outside the press rooms at ASH 2012. We learn from the interviewer turned interviewee about his strategies to navigate his disease. He outlines through his personal story and his decision process, the critical need for getting support from others with the disease, the primacy of expert advice, and the important role of clinical trials in saving his life.

In future posts, we will both share the interview he did of me about my ibrutinib trial.

Andrew and I have moved in the same CLL circles for several years now and I hope we keep doing it for many more to come.

Here is the interview:



Below is a photo of some of my local support group and our significant others at our holiday get-together. We don't look too bad for a bunch of patients with an incurable cancer, do we?

I would be lost without them.  If you have CLL, and don't have  support group, get one or join ours if you are local.


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Wednesday, September 9, 2009

The Beach and Beyond

I took time out from idyllic camping at Doheny State Beach right on the sand to attend the CLL support group.

It was not easy to leave the no worries, life is simple, mindset of the beach to drive up Pacific Coast Highway to visit my friend Joe and the rest of the CLL gang.

I even brought Joe salt (Himalayan) and fresh bread (from my favorite organic vegan bakery, Avanti Cafe) to bless his new home: Bread... that this house may never know hunger. Salt... that life may always have flavor. You can add a broom to sweep the troubles away, but enough already.

The meeting was as always, solid and authentic, well worth the travel, but sadly only 3 of us were able to make it. Maybe it was because it was hard after the holiday weekend. I guess it is good that we are all so busy with more than our CLL, still I miss the rest of the gang. This is important stuff. The support group is crucial for my well being and for helping me to clarify to my decisions. It is also a chance for all of us to, (pardon my Californian 60's speak): Share

Meanwhile back at the campsite.

The beach was cooled by onshore breezes to a perfect toasty warm, but the waves were flat, so no Surfing USA, just swimming and bogie boarding in the shore break. And of course staring at the dancing flames in the campfire, and reading and vegging out. One advantage to being a raw foodie is no cooking pots to clean.

I remain confident that I have excellent options and no emergent dangers, and so look forward to many more chances to surf. No bucket list for me. Not for a long time.

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