Respiratory outcomes of onasemnogene abeparvovec treatment for spinal muscular atrophy: national real-world cohort study

被引:2
作者
Lavie, Moran [1 ,2 ]
Rochman, Mika [1 ,2 ]
Domany, Keren Armoni [2 ,3 ]
Tripto, Inbal Golan [4 ]
Be'er, Moria [1 ,2 ]
Besor, Omri [1 ,5 ]
Sagi, Liora [2 ,6 ]
Aharoni, Sharon [2 ,7 ]
Ginsberg, Mira [2 ,8 ]
Noyman, Iris [9 ]
Levine, Hagit [2 ,10 ]
机构
[1] Tel Aviv Sourasky Med Ctr, Dana Dwek Childrens Hosp, Pediat Pulmonol Unit, Tel Aviv, Israel
[2] Tel Aviv Univ, Fac Med & Hlth Sci, Tel Aviv, Israel
[3] E Wolfson Med Ctr, Sylvan Adams Childrens Hosp, Pediat Pulmonol Unit, Holon, Israel
[4] Ben Gurion Univ Negev, Soroka Univ Med Ctr, Pediat Pulm Unit, Beer Sheva, Israel
[5] Maccabi Healthcare Serv, Dept Family Med, Tel Aviv, Israel
[6] Tel Aviv Sourasky Med Ctr, Dana Dwek Childrens Hosp, Pediat Neurol Unit, Tel Aviv, Israel
[7] Schneider Childrens Med Ctr, Neurol Inst, Petah Tiqwa, Israel
[8] Wolfson Med Ctr, Dept Pediat Neurol, Holon, Israel
[9] Ben Gurion Univ Negev, Soroka Univ Med Ctr, Pediat Neurol Unit, Beer Sheva, Israel
[10] Schneider Childrens Med Ctr, Pulm Inst, Petah Tiqwa, Israel
关键词
Spinal muscular atrophy; Respiratory; Onasemnogene abeparvovec; Nusinersen; Restrictive lung disease; OPEN-LABEL; THERAPY;
D O I
10.1007/s00431-024-05886-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Onasemnogene abeparvovec (OA) is a novel gene replacement therapy for patients with spinal muscular atrophy (SMA). This study provides real-world respiratory data for pediatric SMA patients receiving OA who were assessed before and one year after treatment in a multicenter cohort study conducted from 2019 to 2021. Twenty-five OA-treated SMA patients (23 with type 1 and 2 with type 2; median age at treatment 6.1 months, with a range of 0.36-23 months) were included. Sixteen were treatment-na & iuml;ve, and nine had received various prior treatments. Two patients died due to respiratory failure during the study period. Of the remaining 23 patients, four were put on non-invasive ventilation (NIV), bringing ventilated patients to a total of ten during the post-treatment year. Three patients required permanent NIV support, while 13 did not require any respiratory support. Ventilation time decreased from 14.3 to 11.1 hours per day, and respiratory hospitalizations decreased by 26% (from 0.76 to 0.57 per life year). Fifteen of the 23 patients maintained full oral nutrition at study closure compared to 20 of the 25 at study initiation. This real-world data analysis demonstrates that OA may improve respiratory outcomes in SMA patients. Importantly, compounding factors, such as age at treatment initiation, treatment combinations, and natural history, may influence the respiratory course, thus highlighting the need for standardized long-term management. What is Known: center dot Respiratory failure is a leading cause of mortality in untreated spinal muscular atrophy type 1 patients. center dot Onasemnogene abeparvovec (OA) improves neurological outcomes, but real-world respiratory data are limited. What is New: center dot Our real-world analysis suggests OA may improve respiratory outcomes. center dot Age at treatment and treatment combinations may also influence respiratory trajectory.
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页数:7
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共 21 条
[1]   Health outcomes in spinal muscular atrophy type 1 following AVXS-101 gene replacement therapy [J].
Al-Zaidy, Samiah ;
Pickard, A. Simon ;
Kotha, Kavitha ;
Alfano, Lindsay N. ;
Lowes, Linda ;
Paul, Grace ;
Church, Kathleen ;
Lehman, Kelly ;
Sproule, Douglas M. ;
Dabbous, Omar ;
Maru, Benit ;
Berry, Katherine ;
Arnold, W. David ;
Kissel, John T. ;
Mendell, Jerry R. ;
Shell, Richard .
PEDIATRIC PULMONOLOGY, 2019, 54 (02) :179-185
[2]   A breakthrough effect of gene replacement therapy on respiratory outcomes in children with spinal muscular atrophy [J].
AlNaimi, Amal ;
Hamad, Sara. G. ;
Mohamed, Reem B. A. ;
Ben-Omran, Tawfeg ;
Ibrahim, Khalid ;
Osman, Mahmoud F. El-Said ;
Abu-Hasan, Mutasim .
PEDIATRIC PULMONOLOGY, 2023, 58 (04) :1004-1011
[3]   Sleep disordered breathing in infants identified through newborn screening with spinal muscular atrophy [J].
Chiang, Jackie ;
Xiao, Lena ;
Nigro, Elisa ;
St-Laurent, Aaron ;
Weinstock, Lauren ;
Law, Eugenia ;
Janevski, Joanna ;
Kuyntjes, Sarah ;
Cithiravel, Nisha ;
Tran, Tuyen ;
Wolter, Nikolaus E. ;
Gonorazky, Hernan ;
Amin, Reshma .
SLEEP MEDICINE, 2023, 111 :161-169
[4]   Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy in patients with two copies of SMN2 (STR1VE): an open-label, single-arm, multicentre, phase 3 trial [J].
Day, John W. ;
Finkel, Richard S. ;
Chiriboga, Claudia A. ;
Connolly, Anne M. ;
Crawford, Thomas O. ;
Darras, Basil T. ;
Iannaccone, Susan T. ;
Kuntz, Nancy L. ;
Pena, Loren D. M. ;
Shieh, Perry B. ;
Smith, Edward C. ;
Kwon, Jennifer M. ;
Zaidman, Craig M. ;
Schultz, Meredith ;
Feltner, Douglas E. ;
Tauscher-Wisniewski, Sitra ;
Ouyang, Haojun ;
Chand, Deepa H. ;
Sproule, Douglas M. ;
Macek, Thomas A. ;
Mendell, Jerry R. .
LANCET NEUROLOGY, 2021, 20 (04) :284-293
[5]   Developmental milestones in type I spinal muscular atrophy [J].
De Sanctis, Roberto ;
Coratti, Giorgia ;
Pasternak, Amy ;
Montes, Jacqueline ;
Pane, Marika ;
Mazzone, Elena S. ;
Young, Sally Dunaway ;
Salazar, Rachel ;
Quigley, Janet ;
Pera, Maria C. ;
Antonaci, Laura ;
Lapenta, Leonardo ;
Glanzman, Allan M. ;
Tiziano, Danilo ;
Muntoni, Francesco ;
Darras, Basil T. ;
De Vivo, Darryl C. ;
Finkel, Richard ;
Mercuri, Eugenio .
NEUROMUSCULAR DISORDERS, 2016, 26 (11) :754-759
[6]   Emerging Therapies and Challenges in Spinal Muscular Atrophy [J].
Farrar, Michelle A. ;
Park, Susanna B. ;
Vucic, Steve ;
Carey, Kate A. ;
Turner, Bradley J. ;
Gillingwater, Thomas H. ;
Swoboda, Kathryn J. ;
Kiernan, Matthew C. .
ANNALS OF NEUROLOGY, 2017, 81 (03) :355-368
[7]  
fda, Package Insert-ZOLGENSMA-ZOLGENSMA (onasemnogene abeparvovec-xioi) suspension, for intravenous infusion
[8]   Treatment of infantile-onset spinal muscular atrophy with nusinersen: a phase 2, open-label, dose-escalation study [J].
Finkel, Richard S. ;
Chiriboga, Claudia A. ;
Vajsar, Jiri ;
Day, John W. ;
Montes, Jacqueline ;
De Vivo, Darryl C. ;
Yamashita, Mason ;
Rigo, Frank ;
Hung, Gene ;
Schneider, Eugene ;
Norris, Daniel A. ;
Xia, Shuting ;
Bennett, C. Frank ;
Bishop, Kathie M. .
LANCET, 2016, 388 (10063) :3017-3026
[9]   An updated systematic review on spinal muscular atrophy patients treated with nusinersen, onasemnogene abeparvovec (at least 24 months), risdiplam (at least 12 months) or combination therapies [J].
Giess, Doris ;
Erdos, Judit ;
Wild, Claudia .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2024, 51 :84-92
[10]   Natural history of infantile-onset spinal muscular atrophy [J].
Kolb, Stephen J. ;
Coffey, Christopher S. ;
Yankey, Jon W. ;
Krosschell, Kristin ;
Arnold, W. David ;
Rutkove, Seward B. ;
Swoboda, Kathryn J. ;
Reyna, Sandra P. ;
Sakonju, Ai ;
Darras, Basil T. ;
Shell, Richard ;
Kuntz, Nancy ;
Castro, Diana ;
Parsons, Julie ;
Connolly, Anne M. ;
Chiriboga, Claudia A. ;
McDonald, Craig ;
Burnette, W. Bryan ;
Werner, Klaus ;
Thangarajh, Mathula ;
Shieh, Perry B. ;
Finanger, Erika ;
Cudkowicz, Merit E. ;
McGovern, Michelle M. ;
McNeil, D. Elizabeth ;
Finkel, Richard ;
Iannaccone, Susan T. ;
Kaye, Edward ;
Kingsley, Allison ;
Renusch, Samantha R. ;
McGovern, Vicki L. ;
Wang, Xueqian ;
Zaworski, Phillip G. ;
Prior, Thomas W. ;
Burghes, Arthur H. M. ;
Bartlett, Amy ;
Kissel, John T. .
ANNALS OF NEUROLOGY, 2017, 82 (06) :883-891