Dialysis world news


Rockwell Medical Announces Triferic(TM) Clinical Data Selected for Four Poster ... - GlobeNewswire (press release)

WIXOM, Mich., March 26, 2015 (GLOBE NEWSWIRE) -- Rockwell Medical, Inc. (Nasdaq:RMTI), a fully-integrated biopharmaceutical company targeting end-stage renal disease (ESRD) and chronic kidney disease (CKD) with innovative products and services for the treatment of iron replacement, secondary hyperparathyroidism and hemodialysis, announced today that four individual abstracts for Triferic have been selected by the National Kidney Foundation (NKF) for presentation at their Spring Clinical Meetings, March 26-29, 2015 at the Gaylord Texan in Dallas, Texas.  Triferic is the Company's recent FDA-approved iron-replacement drug for the treatment of iron deficiency in chronic kidney disease patients receiving hemodialysis.

The following abstracts will be presented at the NKF meetings:

  • Triferic Does Not Induce Oxidative Stress In CKD-HD: The PRIME Study; Poster #126 
     
  • Triferic Administered Via Dialysate Maintains Hemoglobin Long Term: Results Of The CRUISE Open-Label Studies; Poster #125
     
  • Pharmacokinetics Of Triferic Administered IV To Healthy Volunteers; Poster #329
     
  • Triferic Does Not Increase Pre-dialysis Hepcidin Or Iron Sequestration: The PRIME Study; Poster #124

The NKF Spring Clinical Meetings 2015 present a unique opportunity for renal health care providers to learn new developments related to all aspects of nephrology.  It is designed for kidney doctors in the private sector and academia, fellows and residents with a special interest in kidney disease, general internists, pharmacists, physician assistants, nurse practitioners, nurses and technicians, social workers, and renal and clinical dietitians. An important objective of the conference is to present the latest insights into chronic kidney disease care.  Participants will learn about new and evolving concepts related to kidney disease through a carefully designed combination of interesting courses, practical workshops, thought-provoking symposia and insightful debates incorporating the latest developments in clinical nephrology.

About Triferic

Triferic is a unique iron compound that is delivered to hemodialysis patients via dialysate, replacing the ongoing iron loss that occurs during their dialysis treatment. Triferic is introduced into bicarbonate concentrate, on-site at the dialysis clinic, and subsequently mixed into dialysate. Once in dialysate, Triferic crosses the dialyzer membrane and enters the blood where it immediately binds to transferrin and is transported to the erythroid precursor cells to be incorporated into hemoglobin. In completed clinical trials, Triferic has demonstrated that it can effectively deliver sufficient iron to the bone marrow and maintain hemoglobin, without increasing iron stores (ferritin). Please visit www.triferic.com for more information.

About Rockwell Medical

Rockwell Medical is a fully-integrated biopharmaceutical company targeting end-stage renal disease (ESRD) and chronic kidney disease (CKD) with innovative products and services for the treatment of iron replacement, secondary hyperparathyroidism and hemodialysis.

Rockwell's recent FDA approved drug Triferic is indicated for iron replacement and maintenance of hemoglobin in hemodialysis patients. Triferic delivers iron to patients during their regular dialysis treatment, using dialysate as the delivery mechanism. In completed clinical trials, Triferic has demonstrated that it safely and effectively delivers sufficient iron to the bone marrow and maintains hemoglobin, without increasing iron stores (ferritin). Rockwell intends to market Triferic to hemodialysis patients in the U.S. dialysis market.

Rockwell's FDA approved generic drug Calcitriol is for treating secondary hyperparathyroidism in dialysis patients. Calcitriol (active vitamin D) injection is indicated in the management of hypocalcemia in patients undergoing chronic renal dialysis. It has been shown to significantly reduce elevated parathyroid hormone levels. Reduction of PTH has been shown to result in an improvement in renal osteodystrophy. Rockwell intends to market Calcitriol to hemodialysis patients in the U.S. dialysis market.

Rockwell is also an established manufacturer and leader in delivering high-quality hemodialysis concentrates/dialysates to dialysis providers and distributors in the U.S. and abroad. As one of the two major suppliers in the U.S., Rockwell's products are used to maintain human life by removing toxins and replacing critical nutrients in the dialysis patient's bloodstream. Rockwell has three manufacturing/distribution facilities located in the U.S.

Rockwell's exclusive renal drug therapies support disease management initiatives to improve the quality of life and care of dialysis patients and are intended to deliver safe and effective therapy, while decreasing drug administration costs and improving patient convenience. Rockwell Medical is developing a pipeline of drug therapies, including extensions of Triferic for indications outside of hemodialysis. Please visit www.rockwellmed.com for more information.

Certain statements in this press release constitute "forward-looking statements" within the meaning of the federal securities laws, including, but not limited to, Rockwell's intention to launch Calcitriol and Triferic following FDA approval. Words such as "may," "might," "will," "should," "believe," "expect," "anticipate," "estimate," "continue," "predict," "forecast," "project," "plan", "intend" or similar expressions, or statements regarding intent, belief, or current expectations, are forward-looking statements. While Rockwell Medical believes these forward-looking statements are reasonable, undue reliance should not be placed on any such forward-looking statements, which are based on information available to us on the date of this release. These forward looking statements are based upon current estimates and assumptions and are subject to various risks and uncertainties, including without limitation those set forth in Rockwell Medical's SEC filings. Thus, actual results could be materially different. Rockwell Medical expressly disclaims any obligation to update or alter statements whether as a result of new information, future events or otherwise, except as required by law.

Michael Rice, Investor Relations; 646-597-6979

Triferic is a trademark of Rockwell Medical, Inc.

...

 
Mycophenolate Mofetil Offers No Advantage in Lupus Nephritis - Renal and Urology News
March 26, 2015 Mycophenolate Mofetil Offers No Advantage in Lupus Nephritis - Renal and Urology News
New study also provides evidence that an early proteinuria decrease is a strong predictor of good long-term outcome.

A 10-year follow-up of the MAINTAIN Nephritis trial showed no advantage of mycophenolate mofetil (MMF) over azathioprine (AZA) for lupus nephritis (LN)maintenance therapy.

The data confirm the relevance of recommendations from the European Renal Association-European Dialysis and Transplant Association and American College of Rheumatology regarding maintenance therapy of LN, namely that AZA and MMF can be prescribed, stated a research team led by Frédéric A. Houssiau, MD, professor of rheumatology at Universite catholique de Louvain, Brussels, Belgium.

The original MAINTAIN trial randomized 105 mostly Caucasian LN patients to maintenance MMF or AZA in 2002-2006. For the 10-year analysis, the investigators examined long-term outcomes, such as survival, kidney function, 24-hour proteinuria, and renal flares.

The researchers found that the time to renal flare did not differ between the AZA and MMF patients, according to results published online ahead of print in the Annals of Rheumatic Disease.

Furthermore, they discovered that patients with an early proteinuria decrease of 0.5g/day or less at 12 months have a very low risk of long-term renal impairment at 10 years. (Proteinuria greater than 0.5 g/day was not predictive of poor outcome, however.)

“At the bedside, the clinician can therefore confidently reassure patients who achieve a durable early response in proteinuria but should not consider a switch to an alternative agent based only on non-achievement of this target,” the researchers said.

Source

  1. Tamirou, F, et al. Ann Rheum Dis 2015; doi: 10.1136/annrheumdis-2014-206897.

...

 
Medicare Part C: The choice of Medicare Advantage Plans - The Glen Rose Reporter

Posted: Thursday, March 26, 2015 11:54 am

This article is the third in a series examining what Medicare does and does not cover. This segment addresses Part C, which allows the insured to choose Medicare Advantage plans instead of regular Medicare.

What are Medicare Advantage Plans?

Subscription Required

An online service is needed to view this article in its entirety. You need an online service to view this article in its entirety.

Have an online subscription?

Login Now

Need an online subscription?

Subscribe

Login

Or, use your linked account:

Choose an online service.

Current print subscribers

You must login to view the full content on this page.

Or, use your linked account:

kAm|65:42C6 p5G2?E286 A=2?D AC@G:56 4@G6C286 E9C@F89 2 962=E9 A=2?[ 2AAC@G65 3J |65:42C6[ 3FE CF? 3J AC:G2E6 4@>A2?:6D] |@DE AC@G:56 E96 D6CG:46D 2?5 C:89ED AC@G:565 3J |65:42C6 !2CED p 2?5 q] %96 !2CE q AC6>:F> :D A2:5 7@C >6>36CD :? D@>6 A=2?Dj @E96C A=2?D A2J A2CE @C ?@?6 @7 :E] $@>6 A=2?D 92G6 2? 255:E:@?2= >@?E9=J A=2? AC6>:F>] $@>6 :?4=F56 AC6D4C:AE:@? 5CF8 4@G6C286 H9:49 DF3DE:EFE6D 7@C |65:42C6 !2CE s]k^Am kAm|6>36CD >2J A2J 2 565F4E:3=6 2?5 H:== A2J 4@A2J>6?ED H9:49 >2J 5:776C 7C@> @C:8:?2= |65:42C6 2?5 7C@> A=2? E@ A=2?]k^Am kAmkDEC@?8m(92E %JA6 !=2?D 2C6 pG2:=23=6nk^DEC@?8mk^Am kAmp ?F>36C @7 EJA6D 6I:DE[ 2=E9@F89 H9:49 A=2?D 2C6 2G2:=23=6 5:776C 3J 86@8C2A9:4 2C62]k^Am kAmkDEC@?8m`]k^DEC@?8m w62=E9 |2:?E6?2?46 ~C82?:K2E:@?D Ww|~X 2?5 w|~ !@:?E\@7\$6CG:46 |65:42C6 p5G2?E286 !=2?Dk^Am kAmp? w62=E9 |2:?E6?2?46 ~C82?:K2E:@?D Ww|~X 24ED 2D 2 =:2:D@? H:E9 AC@G:56CD @? 2 AC6A2:5 32D:D] %96 5@4E@CD[ 9@DA:E2=D 2?5 @E96C 962=E9 AC@G:56CD 28C66 E@ EC62E A2E:6?ED :? 244@C52?46 H:E9 E96 8F:56=:?6D 2?5 C6DEC:4E:@?D @7 E96 w|~]k^Am kAm(:E9 >@DE w|~ |65:42C6 p5G2?E286 A=2?D :?DFC65D 2C6 C6DEC:4E65 E@ @3E2:?:?8 E96:C 962=E9 42C6 D6CG:46D 7C@> 5@4E@CD[ 9@DA:E2=D 2?5 @E96C 42C6 AC@G:56CD =:DE65 :? E96 A=2? ?6EH@C<] p? 6I46AE:@? E@ E9:D CF=6 6I:DED 7@C 6>6C86?4J 42C6[ @FE\@7\2C62 FC86?E 42C6 2?5 @FE\@7\2C62 5:2=JD:D] v6?6C2==J[ E96 :?DFC65 :D C6BF:C65 E@ ?2>6 2 AC:>2CJ 42C6 A9JD:4:2? W!r!X H9@ H:== 24E 2D 2 82E6<66A6C 7@C D6CG:46D] %96 A2E:6?E H:== ?665 2 C676CC2= 7C@> E96 !r! E@ @3E2:? 4@G6C65 D6CG:46D 7C@> DA64:2=:DED]k^Am kAmw@H6G6C[ D@>6 |65:42C6 p5G2?E286 w|~D 2==@H E96 :?DFC65 E@ @3E2:? 962=E9 42C6 D6CG:46D 7C@> @FE\@7\?6EH@C< AC@G:56CD 3J A2J:?8 2 9:896C 4@DE E92? 7@C :?\?6EH@C< AC@G:565 D6CG:46D] %96D6 A=2?D 2C6 42==65 w|~ H:E9 A@:?E @7 D6CG:46 W!~$X @AE:@?D @C w|~!~$ A=2?D]k^Am kAmkDEC@?8ma]k^DEC@?8m !C676CC65 !C@G:56C W!!~X |65:42C6 p5G2?E286 !=2?Dk^Am kAmp?@E96C EJA6 @7 |65:42C6 p5G2?E286 !=2? :D E96 !C676CC65 !C@G:56C ~C82?:K2E:@? W!!~X A=2? AC@G:565 3J 2 AC:G2E6 :?DFC2?46 4@>A2?J] x? 2 !!~ E96 :?DFC65 A2JD =6DD :7 2 ?6EH@C< AC@G:56C :D FD65] r@?G6CD6=J[ E96 :?DFC65 A2JD >@C6 :7 E96 AC@G:56C :D ?@E :? E96 ?6EH@C<] %96 :?DFC65 :D ?@E C6DEC:4E65 7C@> @3E2:?:?8 D6CG:46D @FE @7 ?6EH@C< 2D 96 @C D96 4@F=5 36 :? E96 w|~ E92E :D ?@E 2 w|~!~$ A=2?] qFE E96 :?DFC65 A2JD E96 A6?2=EJ @7 2 9:896C 4@DE E@ 5@ D@]k^Am kAmkDEC@?8mb]k^DEC@?8m !C:G2E6 u66 7@C $6CG:46 W!uu$X |65:42C6 p5G2?E286 !=2?Dk^Am kAm%96 !C:G2E6 u66 7@C $6CG:46D W!uu$X |65:42C6 p5G2?E286 !=2? 5@6D ?@E A2J 244@C5:?8 E@ @C:8:?2= |65:42C6 8F:56=:?6D] |65:42C6 5@6D ?@E A2J 7@C D6CG:46D F?56C E96D6 A=2?D] x?DE625[ E96 A=2? :ED6=7 56E6C>:?6D 9@H >F49 :E H:== A2J 5@4E@CD[ @E96C AC@G:56CD 2?5 9@DA:E2=D] xE 2=D@ 6DE23=:D96D 9@H >F49 E96 :?DFC65 >FDE A2J H96? C646:G:?8 42C6] $@>6 !uu$ A=2?D 92G6 2 ?6EH@C< @7 AC@G:56CD H9@ 92G6 28C665 E@ EC62E A=2? >6>36CD] }@E 2== AC@G:56CD 2C6 H:==:?8 E@ 2446AE E96 A2J>6?E E6C>D @7 E96 !uu$ A=2?D]k^Am kAm$@>6 !uu$ A=2?D 4@?EC24E H:E9 AC@G:56CD H9@ 28C66 E@ EC62E :?DFC65D F?56C E96D6 A=2?D 6G6? :7 E96J 92G6 ?@E EC62E65 E96 A2E:6?E 367@C6] w@H6G6C[ @FE\@7\?6EH@C< AC@G:56CD 2?5 9@DA:E2=D >2J @AE ?@E E@ AC@G:56 EC62E>6?E F?56C 2 !uu$ 6G6? :7 E96J 92G6 AC6G:@FD=J EC62E65 E96 A2E:6?E] %96C67@C6[ :E 364@>6D :>A@CE2?E E@ >2<6 46CE2:? @?6’D EC62E:?8 A9JD:4:2?D H:== EC62E 2?5 2446AE E96 E6C>D @7 A2J>6?E F?56C !uu$ AC:@C E@ D:8?:?8 FA H:E9 2 !uu$ :7 @?6 H2?ED E@ 4@?E:?F6 EC62E>6?E 7C@> E92E 5@4E@C]k^Am kAmkDEC@?8mc]k^DEC@?8m $A64:2= }665D W$}!X |65:42C6 p5G2?E286 !=2?Dk^Am kAm%96 $A64:2= }665D |65:42C6 p5G2?E286 !=2?D AC@G:56 D6CG:46D 7@C :?5:G:5F2=D H:E9 DA64:7:4 ?665D @C 492C24E6C:DE:4D] %96J E2:=@C 36?67:ED[ AC@G:56C 49@:46D 2?5 5CF8 7@C>F=2C:6D E@ 36DE DF:E E96D6 A2CE:4F=2C ?665D] (:E9 E96 6I46AE:@?D @7 6>6C86?4J[ FC86?E 42C6[ 2 DF556? :==?6DD @C :?;FCJ @C 5:2=JD:D ?66565 H:E9 t?5\$E286\#6?2= s:D62D6 Wt$#sX[ 42C6 :D =:>:E65 E@ AC@G:56CD 2?5 9@DA:E2=D H:E9:? E96 A=2? ?6EH@C<]k^Am kAm~?=J E96D6 8C@FAD BF2=:7J 7@C $}! A=2?Di W`X A6CD@?D =:G:?8 :? 46CE2:? :?DE:EFE:@?D[ DF49 2D ?FCD:?8 9@>6Dj WaX A6CD@?D H9@ C6BF:C6 ?FCD:?8 42C6 2E 9@>6j WbX A6CD@?D 6=:8:3=6 7@C 3@E9 |65:42C6 2?5 |65:42:5j 2?5 WcX A6CD@?D H9@ 92G6 DA64:7:4 49C@?:4 @C 5:D23=:?8 4@?5:E:@?D[ =:<6 5:236E6D[ t$#s[ wx'^pxs$[ 49C@?:4 962CE 72:=FC6 @C 56>6?E:2]k^Am kAm|@DE $}!D C6BF:C6 E96 :?DFC65 E@ 92G6 2 AC:>2CJ 42C6 5@4E@C @C 2 42C6 4@@C5:?2E@C] |@DE D6CG:46D AC@G:565 3J 2 DA64:2=:DE H:== C6BF:C6 2 C676CC2= 7C@> E9:D AC:>2CJ 42C6 5@4E@C @C 42C6 4@@C5:?2E@C] p=D@[ E9@D6 @? |65:42:5 D9@F=5 56E6C>:?6 H96E96C E96 5@4E@C @C @E96C 962=E9 42C6 AC@G:56CD H:== 2446AE |65:42:5 367@C6 @3E2:?:?8 EC62E>6?E]k^Am kAmp=E9@F89 D@>6 $}!D =:>:E E96:C 6?C@==>6?E ?F>36C[ @?6 42? 6?C@== 2?J E:>6] %96C6 :D ?@ A2CE:4F=2C 6?C@==>6?E A6C:@5 2D H:E9 @C:8:?2= |65:42C6]k^Am kAmkDEC@?8md]k^DEC@?8m |65:42C6 |65:42= $2G:?8D p44@F?E W|$pXk^Am kAm%96 |65:42C6 |65:42= $2G:?8D p44@F?E A=2?D 2C6 4@?DF>6C\5:C64E65 |65:42C6 p5G2?E286 !=2?D] %96J 2C6 D:>:=2C E@ w62=E9 $2G:?8D p44@F?E A=2?D @776C65 @FED:56 @7 |65:42C6] %96 A=2?D 4@?E2:? EH@ A2CED] ~?6 A2CE AC@G:56D 2? :?DFC2?46 A=2? H:E9 2 9:89 565F4E:3=6] %96 :?DFC2?46 H:== ?@E A2J 2?J @7 E96 6IA6?D6D :?4FCC65 F?E:= E96 9:89 565F4E:3=6 :D >6E] %96 @E96C A2CE AC@G:56D 2 D2G:?8D A=2? E@ A2J 7@C 962=E9 42C6 4@DED] %96 |65:42C6 |$p 56A@D:ED >@?6J :?E@ J@FC >65:42= D2G:?8D 244@F?E 7C@> H9:49 E96 :?DFC65 42? FD6 7F?5D[ F?E:= 6I92FDE65[ E@ A2J 7@C 962=E9 42C6 AC:@C E@ >66E:?8 E96 565F4E:3=6]k^Am kAm|$pD AC@G:56 E96 25G2?E286 @7 7=6I:3:=:EJ :? 49@@D:?8 AC@G:56CD 7@C 962=E9 42C6] x? 255:E:@? E@ 4@G6C:?8 E96 962=E9 42C6 D6CG:46D E92E |65:42C6 AC@G:56D[ D@>6 |$p A=2?D[ 7@C 2? 6IEC2 4@DE[ 4@G6C 255:E:@?2= :E6>D H9:49 @C:8:?2= |65:42C6 5@6D ?@E 4@G6C[ DF49 2D 56?E2=[ G:D:@? 2?5 =@?8\E6C> 42C6]k^Am kAm}6IE H66< E96 7:?2= 4@=F>? @7 E9:D D6C:6D[ 255C6DD6D |65:42C6 !2CE s[ AC6D4C:AE:@? 5CF8 4@G6C286]k^Am kAmk6>m$2?5C2 (] #665 :D 2? 2EE@C?6J H:E9 z2EE6? U2>Aj q6?D@?[ 2? t=56C {2H 7:C> :? u@CE (@CE9[ %6I2D] $96 =:G6D :? 362FE:7F= $@>6CG6== r@F?EJ[ ?62C r92=< |@F?E2:?] x7 J@F 92G6 BF6DE:@?D 23@FE E9:D 4@=F>? @C H:D9 E@ DF886DE 2 E@A:4 @7 :?E6C6DE[ |D #665 >2J 36 4@?E24E65 3J A9@?6 2E adc\fhf\_a`` @C 3J 6>2:= 2E k2 9C67lQ>2:=E@iDHC665aoJ29@@]4@>QmDHC665aoJ29@@]4@>k^2m]k^6>mk^Am

Thank you for reading 6 free articles on our site. You can come back at the end of your 30-day period for another 6 free articles, or you can purchase a subscription at this time and continue to enjoy valuable local news and information. If you need help, please contact our office at 254-897-2282. You need an online service to view this article in its entirety.

Have an online subscription?

Login Now

Need an online subscription?

Subscribe

Login

Or, use your linked account:

Choose an online service.

Current print subscribers

...

 
Dementia Risk Lower in Peritoneal Dialysis Initiators - Renal and Urology News
March 26, 2015 Dementia Risk Lower in Peritoneal Dialysis Initiators - Renal and Urology News
Starting on peritoneal dialysis was associated with a 25% lower dementia risk versus starting on hemodialysis, a study showed.

Patients with end-stage renal disease (ESRD)who initiate renal replacement therapy on peritoneal dialysis (PD) are at lower risk of dementia than those who start on hemodialysis (HD), researchers concluded.

In a retrospective study of 121,623 patients initiating dialysis, Dawn F. Wolfgram, MD, of the Medical College of Wisconsin in Milwaukee, and colleagues found that those who started on PD had a 25% decreased risk of dementia compared with those who started on HD, after adjusting for age, gender, and other potential confounders. They obtained similar results when patients were matched by propensity score.

“This is the largest study to date in support of the hypothesis that the HD process itself, rather than simply the presence of ESRD, may contribute to the well-known higher prevalence of dementia among persons with ESRD,” the authors wrote in Peritoneal Dialysis International.

Dr. Wolfgram's team noted that their study “emphasizes the need for clinicians to regularly assess cognitive function among persons undergoing dialysis.” By helping clinicians tailor management to patients' cognitive abilities, early recognition of dementia may improve patient outcomes, they stated.

PD was the initial dialysis modality for 8,663 of the 121,623 study subjects. The mean age of the total cohort was 69.2 years.

The researchers used U.S. Renal Data System data for incident ESRD patients during calendar years 2006–2008. For all patients, they obtained Medicare claims data for 2004 through 2009, which includes ICD-9 comorbid disease diagnosis codes.

“Our use of Medicare data allowed us to exclude people who carried a dementia diagnosis at baseline, or who were recognized as having dementia during the 90 days after they initiated dialysis,” they wrote. “Thus we were not simply documenting that persons with dementia are unlikely to be able to initiate PD, a therapy which requires greater involvement of patients in care.”

The investigators also acknowledged study limitations. For example, they pointed out that non-medical factors impact the choice between PD and HD. “Physicians are more likely to encourage patients with subtle evidence of cognitive impairment to choose HD as their initial modality, biasing our results toward higher dementia risk in those initiated on HD. Although we excluded patients with pre-existing dementia from our analysis, it is possible that significant differences in baseline cognitive function between the PD and HD groups affected our results.”

Another limitation was that the researchers required 2 years of Medicare eligibility prior to the diagnosis of ESRD. As a result, their cohort was substantially older than the overall ESRD population and may have been healthier due to a survival effect, they noted. “Thus we cannot extrapolate our findings to younger persons with ESRD.”

...

 
Adjusting Starting Dose of Lenalidomide for Renal Function May Not ... - Cancer Therapy Advisor
March 26, 2015 Adjusting Starting Dose of Lenalidomide for Renal Function May Not ... - Cancer Therapy Advisor
Adjusting the starting dose of lenalidomide according to renal function did not compromise the efficacy or safety of lenalidomide.

According to a recent study published online early in the International Journal of Hematology, researchers have found that adjusting the starting dose of lenalidomide according to renal function did not compromise the efficacy or safety of lenalidomide plus low-dose dexamethasone in Chinese patients with advanced relapsed and/or refractory multiple myeloma and renal impairment.

For the study, researchers conducted a subgroup analysis of the MM-021 trial to assess the efficacy and safety of lenalidomide plus low-dose dexamethasone in Chinese patients with advanced relapsed or refractory multiple myeloma and renal impairment.

Researchers classified patients as having either no/mild renal impairment (CrCl ?60mL/min), moderate impairment (CrCl ?30 to <60 mL/min), or severe renal impairment (CrCl <30 mL/min).

RELATED: Carfilzomib Superior to Bortezomib for Relapsed Multiple Myeloma

Patients received lenalidomide at a starting dose of 25 mg/day on days 1-21, which was adjusted for baseline renal function. Patients received the regimen until disease progression or discontinuation.

Results showed response rates for mild, moderate, and severe impairment were 50%, 42%, and 42%, respectively. Patients with no/mild renal impairment experience a longer median progression-free survival and overall survival compared with those with moderate or severe renal impairment.

In regard to safety, grade 3-4 anemia, neutropenia, and thrombocytopenia were more common in patients with severe renal impairment.

Reference

  1. Zhou B-b, Yu L, Du X, et al. Lenalidomide plus low-dose dexamethasone in Chinese patients with relpased or refractory multiple myeloma and renal impairment. Int J Hematol. 2015. [Epub ahead of print]. doi: 10.1007/s12185-015-1771-7.

...

 
<< Start < Prev 181 182 183 184 185 186 187 188 189 190 Next > End >>

Page 185 of 2630
Share |
Copyright © 2024 Global Dialysis. All Rights Reserved.