Sales Revenues at the Potential Expense of Patient Safety: The Example of You&i TM – The Cancer Letter Publications

By | aprile 21, 2018

Sales Revenues at the Potential Expense of Patient Safety: The Example of You&i TM – The Cancer Letter Publications

mi vengono un sacco di epiteti ma nessuno positivo…

Link articolo originale

Archivio di tutti i clip:
(Notebook di Evernote).

Sales Revenues at the Potential Expense of Patient Safety: The Example of You&i TM

Mark J. RatainThe University of Chicago and Value in Cancer Care Consortium

Lisa S. ChenMD Anderson Cancer Center

Allen S. LichterValue in Cancer Care Consortium

R. Donald HarveyEmory University School of Medicine

Sonali M. SmithThe University of Chicago

Leonard B. SaltzMemorial Sloan-Kettering Cancer Center and Value in Cancer Care Consortium

William G. WierdaMD Anderson Cancer Center

 Varsha V. GandhiMD Anderson Cancer Center

 Michael J. KeatingMD Anderson Cancer Center
brutinib is a selective and irreversible inhibitor of Bruton’s tyrosine kinase (BTK) that entered phase 1 clinical trials in 2009 based on preclinical efficacy in models of B-cell malignancy and autoimmune disease.[1, 2] The initial phase 1 trial showed clear efficacy in a number of lymphoid malignancies at doses as low as 1.25 mg/kg/d. Furthermore, full receptor occupancy was demonstrated at 2.5 mg/kg/d. Despite these pharmacological and early clinical findings, development of ibrutinib continued at doses of 420 mg qd and 560 mg qd, levels 3-4 fold higher than suggested by the pharmacological data. In addition, the absorption of ibrutinib is enhanced by administration of food, which may explain why even the lowest dose showed efficacy in some patients.
Ibrutinib is unique in having received four Breakthrough designations on the basis of its efficacy data. It was first approved in November 2013 for the treatment of mantle cell lymphoma at a dose of 560 mg qd, administered as four 140 mg capsules. Three months later, ibrutinib was approved for chronic lymphocytic leukemia (CLL) at a dose of 420 mg qd, again administered as multiple 140 mg capsules. Between July 2014 and August 2017, ibrutinib was approved for five addition indications, but it was not until December 2017 that its 70 mg capsule, necessary to permit safe administration of 70 mg qd in patients with B-cell malignancies receiving posoconazole or patients with moderate hepatic impairment, was approved.
Most recently, the manufacturer received approval of a new tablet formulation of ibrutinib in four different strengths: 140 mg, 280 mg, 420 mg, and 560 mg. Of note, these tablets of varying potencies are priced the same. It may initially appear to be appealing to have higher strengths as a single tablet, as opposed to 1-4 capsules per day. However, this new formulation is associated with removal of the 140 mg capsules (priced at about one third the cost of the new 140 mg tablet) from the market, as well as a marketing and pricing scheme that raises concerns regarding patient safety and access for lower socio-economic groups.
The current ibrutinib label is very complex, as it identifies five potential dosages to be administered over an 8-fold range (70 mg, 140 mg, 280 mg, 420 mg, and 560 mg). The specific dosage to be prescribed depends on the indication, the patient’s prior toxicities, concomitant medications, occurrence of ibrutinib intolerance, and current hepatic function. These criteria are all dynamic, often not based on pharmacologic data, and thus frequent dosage adjustments may be required, both upwards and downwards. For example, many patients for whom ibrutinib is indicated (e.g., CLL, chronic graft-versus-host disease) are at increased risk of infection, and will require concomitant (and likely temporary) antifungals (e.g., posoconazole, fluconazole) or macrolide antibiotics (e.g., erythromycin). Furthermore, patients with concomitant cardiovascular disease may intermittently require calcium channel blockers (e.g., diltiazem, verapamil). Finally, these patients are also at risk for developing hepatic dysfunction, either due to disease (e.g., hepatic graft-versus-host disease) or other intercurrent illness. All of the aforementioned scenarios require rapid dosage reduction to as low as 70 mg qd, and potentially reinstitution of the prior dosage if and when the intervening event is reversed.
While the prescribing information is complex, prescribers and patients have had the flexibility of taking anywhere from one to four 140 mg capsules, readily permitting dose reduction to all but the lowest labeled dose (70 mg). However, the new formulation and its associated marketing scheme (You&iTM) greatly impact the ability of the prescriber and patient to follow the prescribing information, resulting in the potential for a greatly enhanced risk of toxicities relative to that observed in the clinical trials which utilized multiples of the 140 mg capsules.
Delays in therapy at the new dose will be at least 2 days and usually more, because new drug will have to be secured by mail order,and will require significantly more participation by physicians and mid-level providers. Specifically, the new marketing and pricing scheme ensures that all patients are dispensed a single tablet (or capsule) a day at one of the five marketed strengths. Thus, patients will not be able to titrate their daily dosage on the advice of a physician (e.g., in the context of off-target toxicities and intercurrent illness, such as a fungal infection requiring an azole).
In order to ensure that all patients receive a single tablet rather than multiple 140 mg tablets, the manufacturer has priced all tablet strengths at the same price, so that a physician who wished to prescribe 420 mg as three 140 mg tablets would be unlikely to get payor approval to do so, since the cost would be 300% of the single 420 mg tablet. Furthermore, patients who have been on a daily dose of 140 mg now find that the cost of their 140 mg tablet is more than three-fold higher than the cost of their prior 140 mg capsule.
While flat pricing schemes are not uncommon, it is highly unusual to change from a linear (i.e., per mg) to flat pricing scheme after initial marketing approval, over an eight-fold range of daily dosages. Furthermore, this flat pricing scheme appears to have been motivated by the manufacturer’s awareness of the increasing interest in utilizing lower doses of ibrutinib off-label,[3] based on a study initiated at MD Anderson in June 2016 and recently presented at the 2017 meeting of the American Society of Hematology. In this small pilot study, the dose was lowered from 420 mg to 280 mg, then to 140 mg qd, without any apparent loss of biological efficacy, not surprising given the initial phase 1 study.
The MD Anderson study was initiated based on the molecular pharmacology of ibrutinib. At the molecular level, a single ibrutinib molecule binds covalently to a single BTK molecule, thereby inactivating BTK. Hence a 1:1 stoichiometry is needed to inhibit the BTK target. Once this is achieved, free drug is only required if additional BTK protein is synthesized. Because BTK transcription is driven by NF-kappaB, a downstream target in the B-cell receptor pathway and suppressed by ibrutinib, it is believed that ibrutinib both inactivates BTK and inhibits BTK synthesis. In fact, after one cycle of ibrutinib at the standard dose, both BTK mRNA and protein levels decreased in circulating CLL lymphocytes.[4]Such decline supports the use of a lower subsequent dose of ibrutinib, considering the 1:1 stoichiometry. Results of the pilot protocol (NCT02801578) suggest that after one cycle of the standard 420 mg dose of ibrutinib, the dose may be lowered to 140 mg qd for subsequent cycles without compromising the biological impact.[3] 
While clinical efficacy was not evaluated in the pilot protocol using a lower ibrutinib dose, in the real-world situation, as many as one-third of patients with CLL require a lower ibrutinib dose due to toxicity. This is a common occurrence and has been reported in the US[5], UK[6], Sweden[7], and Poland[8]. The dose decrease occurred after one or more cycles of full dose ibrutinib. Importantly, these patients had identical overall and progression-free survival as those who did not require dose reductions, further demonstrating the clinical utility and appropriateness of dose reductions in patients with CLL.
Given the expected frequency of dose adjustments, the manufacturer (and/or its marketing partner) has developed the You&iTM program to allow patients to exchange their current tablets for those of a different strength. However, this program is inconsistent with rapid dose adjustments, since it requires completion of a form by the prescriber, signature of the form by a You&iTM pharmacist (only available from 8 am to 8 pm Eastern Time, Monday to Friday), shipping of the new strength to the patient, and the requirement for return of the patient’s prior tablets to the manufacturer. In the event of a temporary dose reduction (e.g., 14 day course of antibiotics), the process would need to occur again. This is critical because prior studies have demonstrated that a gap of a week or more without ibrutinib can impact survival.[9] Any putative convenience advantage of taking one pill a day is negated by the marked inconvenience to the patient of having to return pills every time there is a need for a dosage change. Furthermore, in the future, it is likely that many patients will be receiving combinations with other agents. Dosage adjustment in combination protocols is often much more complicated than for single agents.
It is worth comparing the prescribing information for ibrutinib with that of warfarin, which has been called “the most dangerous drug in America”.[10]Warfarin is formulated in nine strengths ranging from 1-10 mg daily. However, prescribers have complete discretion to select the dose strength most appropriate for each individual patient, and may choose to prescribe a 2 mg strength for a patient whose daily dosage requirement ranges from 4-6 mg daily. Prescribers also choose to use every other day dosing on occasion. Needless to say, it would be not be possible to safely use warfarin if the prescriber had to order a new tablet strength for each and every dosage change.
In contrast to warfarin, we do not believe that physicians and patients will be able to prescribe and self-administer ibrutinib in accordance with the prescribing instructions without the ability to prescribe 140 mg tablets regardless of the daily dosage. When dose reductions are required and substitute tablets are not readily available, physicians will need to choose between continuing the higher dose (a major safety risk) or interruption of the dosing for as long as two weeks, which could potentially impact efficacy.[9] 
In this context, we urge the Food and Drug Administration to review the safety of the You&iTM program in the context of the approved drug label, given that it creates a barrier to optimal prescribing for some patients. We further urge the FDA to recognize that the combination of the high price per pill and the flat pricing scheme are specific impediments to safe administration, and that ignoring the marketing approach for ibrutinib is antithetical to fostering optimally safe dosing and administration. We also urge clinical investigators to consider studies of every other day dosing of ibrutinib, given that it is an irreversible inhibitor of its target, and that its target’s turnover rate is relatively low and would likely permit effective dosing on this schedule.[11]Of course, this would also result in a 50% reduction in treatment cost, despite You&iTM.
Advani RH, Buggy JJ, Sharman JP, Smith SM, Boyd TE, Grant B, Kolibaba KS, Furman RR, Rodriguez S, Chang BY, Sukbuntherng J, Izumi R, Hamdy A, Hedrick E, Fowler NH. Bruton tyrosine kinase inhibitor ibrutinib (PCI-32765) has significant activity in patients with relapsed/refractory B-cell malignancies. J Clin Oncol. 2013;31(1):88-94. Honigberg LA, Smith AM, Sirisawad M, Verner E, Loury D, Chang B, Li S, Pan Z, Thamm DH, Miller RA, Buggy JJ. The Bruton tyrosine kinase inhibitor PCI-32765 blocks B-cell activation and is efficacious in models of autoimmune disease and B-cell malignancy. Proc Natl Acad Sci U S A. 2010;107(29):13075-80. Bose P, Chen L, Cruz N, Jiang Y, Thompson PA, Feng S, Kroll M, Jain N, Wierda WG, Keating MJ, Gandhi V. 4307 A Pilot Study of Lower Doses of Ibrutinib in Patients (pts) with Chronic Lymphocytic Leukemia (CLL). ASH 59th Annual Meeting & Exposition. 2017(Session: 642, CLL: Therapy, excluding Transplantation: Poster III). Cervantes-Gomez F, Kumar Patel V, Bose P, Keating MJ, Gandhi V. Decrease in total protein level of Bruton’s tyrosine kinase during ibrutinib therapy in chronic lymphocytic leukemia lymphocytes. Leukemia. 2016;30(8):1803-4. Mato AR, Nabhan C, Thompson MC, Lamanna N, Brander DM, Hill B, Howlett C, Skarbnik A, Cheson BD, Zent C, Pu J, Kiselev P, Goy A, Claxton D, Isaack K, Kennard KH, Timlin C, Landsburg D, Winter A, Nasta SD, Bachow SH, Schuster SJ, Dorsey C, Svoboda J, Barr P, Ujjani CS. Toxicities and outcomes of 621 ibrutinib-treated chronic lymphocytic leukemia patients in the United States: a real-world analysis. Haematologica. 2018. Forum UC. Ibrutinib for relapsed/refractory chronic lymphocytic leukemia: a UK and Ireland analysis of outcomes in 315 patients. Haematologica. 2016;101(12):1563-72. Winqvist M, Asklid A, Andersson PO, Karlsson K, Karlsson C, Lauri B, Lundin J, Mattsson M, Norin S, Sandstedt A, Hansson L, Osterborg A. Real-world results of ibrutinib in patients with relapsed or refractory chronic lymphocytic leukemia: data from 95 consecutive patients treated in a compassionate use program. A study from the Swedish Chronic Lymphocytic Leukemia Group. Haematologica. 2016;101(12):1573-80. Iskierka-Jazdzewska E, Hus M, Giannopoulos K, Madro E, Holojda J, Piotrowska M, Zaucha JM, Piszczek W, Szeremet A, Wojciechowska M, Steckiewicz P, Knopinska-Posluszny W, Osowiecki M, Drozd-Sokolowska J, Kumiega B, Kyrcz-Krzemien S, Halka J, Dudzinski M, Wieszczy P, Robak T, Warzocha K, Jamroziak K. Efficacy and toxicity of compassionate ibrutinib use in relapsed/refractory chronic lymphocytic leukemia in Poland: analysis of the Polish Adult Leukemia Group (PALG). Leuk Lymphoma. 2017;58(10):2485-8. Barr PM, Brown JR, Hillmen P, O’Brien S, Barrientos JC, Reddy NM, Coutre S, Mulligan SP, Jaeger U, Furman RR, Cymbalista F, Montillo M, Dearden C, Robak T, Moreno C, Pagel JM, Burger JA, Suzuki S, Sukbuntherng J, Cole G, James DF, Byrd JC. Impact of ibrutinib dose adherence on therapeutic efficacy in patients with previously treated CLL/SLL. Blood. 2017;129(19):2612-5. Ornstein C. Popular Blood Thinner Causing Deaths, Injuries at Nursing Homes. ProPublica. 2015. Daryaee F, Zhang Z, Gogarty KR, Li Y, Merino J, Fisher SL, Tonge PJ. A quantitative mechanistic PK/PD model directly connects Btk target engagement and in vivo efficacy. Chem Sci. 2017;8(5):3434-43.

Response statement from Pharmacyclics and Janssen
We appreciate the opportunity to share a brief response to the opinions in the article regarding the new single-tablet formulation of Imbruvica®.
We are committed to developing safe and effective medicines and improving outcomes for patients facing some of the world’s most challenging diseases. Our commitment to patient safety is demonstrated through the breadth and rigor of our clinical development program for Imbruvica. This included controlled randomized multi-national studies across a broad range of diseases that resulted in the FDA-approved dosing for Imbruvica.
Starting in 2015, we began development of a single-tablet formulation of Imbruvica as a new innovation to provide patients with a convenient one pill, once-a-day dosing regimen and improved packaging, with the intent to improve adherence to this important therapy. Our new formulation reduces the number of pills patients need to take daily from three to four pills (420 mg & 560 mg, the FDA-approved standard starting doses) to just one pill. The new formulation is available in a new blister pack that was designed to help patients take their medicine as prescribed. Research demonstrates that better adherence to medicines can lead to improved outcomes and that one-pill, once-daily regimens can lead to improved adherence.
We understand that clinicians are free to exercise their independent medical judgment, inclusive of dosing for their patients. However, to best support appropriate and effective treatment, Imbruvica is intended to be prescribed in accordance with the prescribing information approved by the FDA. Furthermore, the FDA-approved prescribing label provides specific guidance on dose modifications due to adverse events and drug interactions.
The new formulation is available to patients without an increase to the annual price per patient for Imbruvica’s FDA-approved recommended starting doses of 420 mg and 560 mg. Now the price of Imbruvica is based on the most widely prescribed and lowest of the two FDA-approved standard starting doses, regardless of disease type and dose. This approach is in line with other approved oral oncology therapies.
The YOU&i™ Support Program was established upon initial FDA approval in 2013 as a comprehensive program that enables patients to learn about access, find affordability support options, and receive additional educational resources to help them along their journey.
We recently introduced a Dose Exchange Program to help facilitate mid-cycle dose adjustments if a healthcare professional (HCP) decides to reduce their patient’s Imbruvica dosage because they have experienced an adverse reaction or are taking certain concomitant medications. The Program is intended to promote patient safety and quality of care by helping to ensure that dose reduction can occur when a HCP believes that it is clinically appropriate. Patients will not have to wait to reduce their dose until the next month due to potential financial constraints. In this safety-based returns program, patients will receive their new dose of Imbruvica through rapid shipment to ensure continuity of care.
Pharmacyclics and Janssen are committed to patient safety and to helping patients lead longer, healthier lives. We welcome further dialogue with the authors and interested stakeholders about this important topic.

The post Sales Revenues at the Potential Expense of Patient Safety: The Example of You&i TM – The Cancer Letter Publications appeared first on Quinta’s weblog.

Source: Stefano quintarelli- Blog

42 thoughts on “Sales Revenues at the Potential Expense of Patient Safety: The Example of You&i TM – The Cancer Letter Publications

  1. Ricardo Omara

    Thanks for a marvelous posting! I actually enjoyed reading it, you might be a great author.I will make sure to bookmark your blog and definitely will come back in the foreseeable future. I want to encourage you continue your great posts, have a nice morning!|

  2. Santos Jira

    I do not even know how I ended up here, but I thought this post was good. I don’t know who you are but certainly you’re going to a famous blogger if you are not already 😉 Cheers!|

  3. Jessie Frederic

    Pretty great post. I just stumbled upon your blog and wanted to say that I’ve really loved surfing around your blog posts. In any case I’ll be subscribing to your rss feed and I’m hoping you write once more very soon!|

  4. windows 8 microsoft office 365 product key

    Microsoft Office or are just looking to refresh your skills for any job or the one you’re already in, you’re in the right spot. Our lessons give you a mix of textual content, video, interactives, and issues to practice what you might have learned, so you can learn the basics and more of Access, Stand out, Outlook, PowerPoint, Publisher, and Word. You’ll also learn tips, tricks, shortcuts, and more to raised use these programs at work and life. Let’s get going!

  5. windows 10 product key free

    Microsoft Office or are just looking to refresh your skills for any job or the one you’re already in, you’re in the right spot. Our lessons give a mix of text message, video, interactives, and troubles to practice what you have learned, so you can learn the basics and more of Access, Exceed, Outlook, PowerPoint, Publisher, and Word. You’ll also learn tips, tricks, shortcuts, and more to higher use these programs at work and life. Let’s start!

  6. Marin Aravjo

    Hi there! I know this is kind of off topic but I was wondering if you knew where I could locate a captcha plugin for my comment form? I’m using the same blog platform as yours and I’m having trouble finding one? Thanks a lot!|

  7. Nike Air Jordan 1

    Hello! This is kind of off topic but I need some help from an established blog. Is it very difficult to set up your own blog? I’m not very techincal but I can figure things out pretty fast. I’m thinking about making my own but I’m not sure where to begin. Do you have any tips or suggestions? Thanks

  8. air max 2014 90

    árboles; no circular debajo de anuncios publicitarios o andamios; no hacer fuego; sujetar con firmeza el volante y reducir la velocidad; no abandonar el coche y buscar refugio en un lugar seguro.

  9. air max 95 essential homme

    “melaEarning His SpursJan Vertonghen in line for new contract after helping Tottenham concede just four league goalscaught nappingTottenham Hostpur boss Mauricio Pochettino reveals mentor Marcelo Bielsa signed him in his sleepJack StatJack Wilshere tops the premier League passing accuracy table ahead of four Gunnersteam newsBournemouth vs Tottenham: Harry Kane and Toby Alderweireld will again miss out but Kyle Walker returns The game ended on a sour note when Moussa Sissoko caught Arter with an elbow after the ball had gone out for a throwing, but after players jumped in to protect their teammates, Sissoko luckily got away with just a warning.”

  10. adidas superstar foundation camo

    Searching I noticed your web site book-marked as: %BLOGTITLE%. Now i’m assuming you bookmarked it yourself and wanted to ask if social bookmarking gets you a good deal of visitors? I’ve been thinking about doing some bookmarking for a few of my websites but wasn’t sure if it would generate any positive results. Appreciate it.

  11. adidas shoes 70s

    Hi there. I was contemplating adding a hyperlink back to your blog since both of our sites are centered around the same topic. Would you prefer I link to you using your website address: %BLOGURL% or website title: %BLOGTITLE%. Be sure to let me know at your earliest convenience. Thanks!

  12. ravens jersey dress

    Hey there! This is my first visit to your blog! We are a group of volunteers and starting a new project in a community in the same niche. Your blog provided us useful information to work on. You have done a wonderful job!

  13. new balance basketball sneakers

    I know this if off topic but I’m looking into starting my own blog and was wondering what all is needed to get setup? I’m assuming having a blog like yours would cost a pretty penny? I’m not very web savvy so I’m not 100% certain. Any tips or advice would be greatly appreciated. Appreciate it

  14. peyton manning jersey broncos

    “y Atl茅tico de Madrid (.atleticodemadrid) on Aug 25, 2016 at 6:20am PDTPA:Press Association2Cardiff’s Principality Stadium will host the Champions League final for the first timeMeanwhile Ronaldo has decided to fly out with his entourage, including agent Jorge Mendes.”

  15. 靻岆媺 鞁犽皽

    google_adset(‘Web_Sub_view_in_200x200′,’C’);최민정은 13일 강원 강릉 아이스 아레나에서 열린 2018 평창 동계올림픽 여자 쇼트트랙 500m 준결승전 1조 경기에서 42초422를 기록해 1위로 결승선을 통과했다.

  16. training adidas climacool

    Woah! I’m really enjoying the template/theme of this website. It’s simple, yet effective. A lot of times it’s very hard to get that “perfect balance” between usability and visual appearance. I must say you’ve done a superb job with this. In addition, the blog loads extremely quick for me on Opera. Excellent Blog!

  17. superstar xeno homme

    Good day! I know this is kind of off topic but I was wondering which blog platform are you using for this website? I’m getting sick and tired of WordPress because I’ve had problems with hackers and I’m looking at alternatives for another platform. I would be great if you could point me in the direction of a good platform.

  18. adidas yeezy boost 350 v2 original price

    Hey! My name is %NAME% and I just wanted to say your weblog is awesome! It really is funny simply because I use to have a blogging site that almost had an identical url: %BLOGURL% mine was only a few characters different. Anyhow, I am a big fan of your website and if you at any time want a guest article please make sure to email me personally at: %EMAIL%. I love writing!


Lascia un commento

Il tuo indirizzo email non sarà pubblicato. I campi obbligatori sono contrassegnati *