Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas

被引:19
作者
Khamaysa, Mohammed [1 ]
Pradat, Pierre-Francois [1 ,2 ,3 ]
机构
[1] Sorbonne Univ, Lab Imagerie Biomed, INSERM, CNRS, F-75006 Paris, France
[2] Hop La Pitie Salpetriere, AP HP, Ctr Referent SLA, Dept Neurol, F-75013 Paris, France
[3] Ulster Univ, Altnagelvin Hosp, Biomed Sci Res Inst, Northern Ireland Ctr Stratified Med,C TRIC, Derry Londonderry BT47 6SB, North Ireland
关键词
riluzole; preclinical models; protein homeostasis inductors; gene targeted strategies; ALS trials platforms; AMYOTROPHIC-LATERAL-SCLEROSIS; MESENCHYMAL STROMAL CELLS; MOTOR-NEURON DEGENERATION; RESONANCE-IMAGING FINDINGS; TRANSGENIC MOUSE MODEL; STEM-CELLS; DISEASE PROGRESSION; REPEAT EXPANSION; NUCLEOCYTOPLASMIC TRANSPORT; CYCLOOXYGENASE-2; INHIBITORS;
D O I
10.3390/jpm12101601
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Amyotrophic lateral sclerosis (ALS) is an extremely heterogeneous disease of motor neurons that eventually leads to death. Despite impressive advances in understanding the genetic, molecular, and pathological mechanisms of the disease, the only drug approved to date by both the FDA and EMA is riluzole, with a modest effect on survival. In this opinion view paper, we will discuss how to address some challenges for drug development in ALS at the conceptual, technological, and methodological levels. In addition, socioeconomic and ethical issues related to the legitimate need of patients to benefit quickly from new treatments will also be addressed. In conclusion, this brief review takes a more optimistic view, given the recent approval of two new drugs in some countries and the development of targeted gene therapies.
引用
收藏
页数:15
相关论文
共 134 条
[1]   Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial [J].
Abe, Koji ;
Aoki, Masashi ;
Tsuji, Shoji ;
Itoyama, Yasuto ;
Sobue, Gen ;
Togo, Masanori ;
Hamada, Chikuma ;
Tanaka, Masahiko ;
Akimoto, Makoto ;
Nakamura, Kazue ;
Takahashi, Fumihiro ;
Kondo, Kazuoki ;
Yoshino, Hiide .
LANCET NEUROLOGY, 2017, 16 (07) :505-512
[2]   ALS drug development guidances and trial guidelines Consensus and opportunities for alignment [J].
Andrews, Jinsy A. ;
Bruijn, Lucie I. ;
Shefner, Jeremy M. .
NEUROLOGY, 2019, 93 (02) :66-71
[3]  
[Anonymous], BIOGEN ANNOUNCES TOP
[4]  
[Anonymous], CLINICALTRIALSGOV
[5]  
[Anonymous], ASTRAZENECA UPDATE C
[6]   Emerging Oligonucleotide Therapeutics for Rare Neuromuscular Diseases [J].
Aoki, Yoshitsugu ;
Wood, Matthew J. A. .
JOURNAL OF NEUROMUSCULAR DISEASES, 2021, 8 (06) :869-884
[7]   Amyotrophic lateral sclerosis is a systemic disease: peripheral contributions to inflammation-mediated neurodegeneration [J].
Appel, Stanley H. ;
Beers, David R. ;
Zhao, Weihua .
CURRENT OPINION IN NEUROLOGY, 2021, 34 (05) :765-772
[8]   Ibudilast (MN-166) in amyotrophic lateral sclerosis- an open label, safety and pharmacodynamic trial [J].
Babu, Suma ;
Hightower, Baileigh G. ;
Chan, James ;
Zurcher, Nicole R. ;
Kivisakk, Pia ;
Tseng, Chieh-En J. ;
Sanders, Danica L. ;
Robichaud, Ashley ;
Banno, Haruhiko ;
Evora, Armineuza ;
Ashokkumar, Akshata ;
Pothier, Lindsay ;
Paganoni, Sabrina ;
Chew, Sheena ;
Dojillo, Joanna ;
Matsuda, Kazuko ;
Gudesblatt, Mark ;
Berry, James D. ;
Cudkowicz, Merit E. ;
Hooker, Jacob M. ;
Atassi, Nazem .
NEUROIMAGE-CLINICAL, 2021, 30
[9]   Safety of intrathecal injection of Wharton's jelly-derived mesenchymal stem cells in amyotrophic lateral sclerosis therapy [J].
Barczewska, Monika ;
Grudniak, Mariusz ;
Maksymowicz, Stanislaw ;
Siwek, Tomasz ;
Oldak, Tomasz ;
Jezierska-Wozniak, Katarzyna ;
Gladysz, Dominika ;
Maksymowicz, Wojciech .
NEURAL REGENERATION RESEARCH, 2019, 14 (02) :313-318
[10]   MRI in multiple sclerosis: correlation with expanded disability status scale (EDSS) [J].
Barkhof, F .
MULTIPLE SCLEROSIS JOURNAL, 1999, 5 (04) :283-286