临床儿科杂志 ›› 2023, Vol. 41 ›› Issue (12): 946-954.doi: 10.12372/jcp.2023.23e0303
何冠兰, 韦秋芬(
), 李娜, 陈少萍, 刘云媛, 廖莎莎, 唐秀能(
)
收稿日期:2023-04-11
出版日期:2023-12-15
发布日期:2023-12-04
通讯作者:
唐秀能,韦秋芬 电子信箱:基金资助:
HE Guanlan, WEI Qiufen(
), LI Na, CHEN Shaoping, LIU Yunyuan, LIAO Shasha, TANG Xiuneng(
)
Received:2023-04-11
Published:2023-12-15
Online:2023-12-04
摘要:
目的 采用meta分析方法评估诺西那生钠治疗儿童脊髓性肌萎缩症(SMA)患者的临床疗效。方法 通过检索Cochrane Library、Embase、PubMed、Web of Science、ClinicalTrial.gov、CBM、CNKI、万方和VIP数据库,检索时限为建库至2022年12月31日。由2名研究者独立筛选文献、提取资料并评价纳入研究的偏倚风险后,采用Stata 14.0进行meta分析。结果 共纳入14篇队列研究,1 274例年龄<18岁SMA患者。治疗期间,运动功能指标费城儿童医院神经肌肉障碍婴儿测试评分(CHOP-INTEND)、Hammersmith婴儿神经病学检查第2部分(HINE-2)评分、Hammersmith运动功能(HFMSE)评分、上肢运动功能(RULM)评分均有显著改善,合并均数差分别为9.08(95%CI:7.17~10.99)、2.08(95%CI:1.26~2.90)、3.83(95%CI:2.15~5.50)、2.42(95%CI:1.33~3.52);临床改善率分别为0.77(95%CI:0.71~0.82)、0.39(95%CI:0.31~0.48)、0.53(95%CI:0.33~0.72)、0.56(95%CI:0.49~0.63)。结论 诺西那生钠对SMA 1、2、3型患儿的运动功能有较大改善,受纳入研究质量和样本量的限制,上述结论尚待更多高质量研究予以验证。
何冠兰, 韦秋芬, 李娜, 陈少萍, 刘云媛, 廖莎莎, 唐秀能. 诺西那生钠治疗脊髓性肌萎缩症患儿临床疗效的meta分析[J]. 临床儿科杂志, 2023, 41(12): 946-954.
HE Guanlan, WEI Qiufen, LI Na, CHEN Shaoping, LIU Yunyuan, LIAO Shasha, TANG Xiuneng. Meta-analysis of clinical efficacy of nusinersen in the treatment of children with spinal muscular atrophy[J]. Journal of Clinical Pediatrics, 2023, 41(12): 946-954.
表1
PubMed检索策略示例"
| 步骤 | 检索式 |
|---|---|
| #1 | "Muscular Atrophy, Spinal"[Mesh] |
| #2 | "Spinal Muscular atrophy"[Text Word] |
| #3 | SMA[Text Word] |
| #4 | #1 OR #2 OR #3 |
| #5 | "Oligonucleotides, Antisense"[Mesh] |
| #6 | nusinersen[Text Word] |
| #7 | spinraza[Text Word] |
| #8 | #5 OR #6 OR #7 |
| #9 | "treatment,outcome"[Mesh] |
| #10 | "treatment outcome*[Text Word]" |
| #11 | efficacy[Text Word] |
| #12 | #9 OR #10 OR #11 |
| #13 | #4 AND #8 AND #12 |
表2
纳入文献的基本信息"
| 作 者 | 年份 | 患者例数 | 人群来源 | SMA分型 | 随访时间/月 | 结局指标 |
|---|---|---|---|---|---|---|
| Tscherter[ | 2022 | 11 | 瑞士 | 1 | >6 | ① |
| Pechmann[ | 2022 | 256 | 德国 | 2、3 | 14 | ②③ |
| Pane[ | 2022 | 73 | 意大利 | 2、3 | 24 | ②③ |
| Kotulska[ | 2022 | 298 | 波兰 | 1、2、3 | 12 | ①② |
| Pera[ | 2021 | 77 | 美国、英国、意大利 | 3 | >6 | ②③ |
| Pane[ | 2021 | 122 | 意大利 | 1 | 12 | ①④ |
| Modrzejewska[ | 2021 | 26 | 波兰 | 1 | 18-26 | ① |
| Mendonca[ | 2021 | 21 | 巴西 | 1 | >6 | ①④ |
| Konersman[ | 2021 | 19 | 美国 | 1、2、3 | 22 | ①② |
| Coratti[ | 2021 | 77 | 美国、英国、意大利 | 2 | 12 | ②③ |
| Szabo[ | 2020 | 57 | 匈牙利 | 1、2、3 | 10 | ①②③ |
| Audic[ | 2020 | 123 | 法国 | 1、2 | 12 | ①④ |
| Aragon-Gawinska[ | 2020 | 53 | 法国、比利时 | 1 | 14 | ①④ |
| Pechmann[ | 2018 | 61 | 德国 | 1 | >6 | ①④ |
表3
纳入队列研究的质量评价结果"
| 作 者 | 年份 | 研究人群选择(0~4分) | 组间可比性(0~2分) | 结果测量(0~3分) | 总分 |
|---|---|---|---|---|---|
| Tscherter[ | 2022 | 3 | 2 | 3 | 8 |
| Pechmann[ | 2022 | 3 | 2 | 2 | 7 |
| Pane[ | 2022 | 3 | 2 | 3 | 8 |
| Kotulska[ | 2022 | 3 | 2 | 3 | 8 |
| Pera[ | 2021 | 3 | 2 | 3 | 8 |
| Pane[ | 2021 | 3 | 2 | 3 | 8 |
| Modrzejewska[ | 2021 | 3 | 2 | 3 | 8 |
| Mendonca[ | 2021 | 3 | 2 | 3 | 8 |
| Konersman[ | 2021 | 3 | 2 | 3 | 8 |
| Coratti[ | 2021 | 3 | 2 | 3 | 8 |
| Szabo[ | 2020 | 3 | 2 | 3 | 8 |
| Audic[ | 2020 | 3 | 2 | 3 | 8 |
| Aragon-Gawinska[ | 2020 | 3 | 2 | 3 | 8 |
| Pechmann[ | 2018 | 3 | 2 | 3 | 8 |
| 总分 | 42/56 | 28/28 | 41/42 |
表4
临床改善率"
| 结局指标 | 作 者 | 年份 | 事件数(X) | 总例数(N) | N×P1 | N×(1-P1) |
|---|---|---|---|---|---|---|
| CHOP INTEND 临床改善率 | Tscherter[ | 2022 | 10 | 11 | 10 | 1 |
| Kotulska[ | 2022 | 129 | 170 | 129 | 41 | |
| Pechmann[ | 2018 | 47 | 61 | 47 | 14 | |
| HINE-2 临床改善率 | Mendonca[ | 2021 | 6 | 21 | 6 | 15 |
| Konersman[ | 2021 | 1 | 5 | 1 | 4 | |
| Aragon-Gawinska[ | 2020 | 24 | 44 | 24 | 20 | |
| Pechmann[ | 2018 | 19 | 61 | 19 | 42 | |
| HINE-2临床改善率(亚组分析) | Mendonca[ | 2021 | 6 | 21 | 6 | 15 |
| Konersman[ | 2021 | 1 | 5 | 1 | 4 | |
| Pechmann[ | 2018 | 19 | 61 | 19 | 42 | |
| HFMSE临床改善率 | Kotulska[ | 2022 | 88 | 121 | 81 | 33 |
| Pechmann[ | 2022 | 63 | 147 | 63 | 84 | |
| Konersman[ | 2021 | 6 | 9 | 6 | 3 | |
| Coratti[ | 2021 | 26 | 77 | 26 | 51 | |
| RULM 临床改善率 | Pechmann[ | 2022 | 83 | 124 | 83 | 41 |
| Konersman[ | 2021 | 5 | 8 | 5 | 3 | |
| Coratti[ | 2021 | 27 | 73 | 27 | 46 | |
| RULM 临床改善率(亚组分析) | Pechmann[ | 2022 | 83 | 124 | 83 | 41 |
| Konersman[ | 2021 | 5 | 8 | 5 | 3 |
表5
GRADE系统分级结果"
| 结局指标 | 纳入 研究数 | 质量升级因素 | 结果汇总 | ||||
|---|---|---|---|---|---|---|---|
| 效应值 是否很大 | 存在剂量- 效应关系 | 存在降低疗效 的混杂因素 | 研究对象 /例 | MD/改善率 (95%CI) | 证据质量 | ||
| CHOP INTEND评分 | 8 | 效应值较大 | 否 | 否 | 369 | 9.08(7.17~10.99) | 中 |
| CHOP INTEND临床改善率 | 3 | 效应值较大 | 否 | 否 | 242 | 0.77(0.71~0.82) | 中 |
| HINE-2评分 | 6 | 否 | 否 | 否 | 219 | 2.08(1.26~2.90) | 低 |
| HINE-2临床改善率 | 4 | 否 | 否 | 否 | 131 | 0.39(0.31~0.48) | 低 |
| HFMSE评分 | 7 | 否 | 否 | 否 | 508 | 3.83(2.15~5.50) | 低 |
| HFMSE临床改善率 | 4 | 否 | 否 | 否 | 354 | 0.53(0.33~0.72) | 低 |
| RULM评分 | 6 | 否 | 否 | 否 | 306 | 2.42(1.33~3.52) | 低 |
| RULM临床改善率 | 3 | 否 | 否 | 否 | 205 | 0.56(0.49~0.63) | 低 |
| [1] |
Lunn MR, Wang CH. Spinal muscular atrophy[J]. The Lancet, 2008, 371: 2120-2133.
doi: 10.1016/S0140-6736(08)60921-6 |
| [2] |
Schorling DC, Pechmann A, Kirschner J. Advances in treatment of spinal muscular atrophy-new phenotypes, new challenges, new implications for care[J]. J Neuromuscul Dis, 2020, 7: 1-13.
doi: 10.3233/JND-190424 pmid: 31707373 |
| [3] |
Ramdas S, Servais L. New treatments in spinal muscular atrophy: an overview of currently available data[J]. Expert Opin Pharmacother, 2020, 21: 307-315.
doi: 10.1080/14656566.2019.1704732 pmid: 31973611 |
| [4] | 陈瑜毅, 韩蕴丽, 李杏, 等. 31例儿童脊髓性肌萎缩症临床与基因分析[J]. 临床儿科杂志, 2021, 39(10): 745-749. |
| [5] | Finkel RS, Chiriboga CA, Vajsar J, et al. Treatment of infantile-onset spinal muscular atrophy with nusinersen: a phase 2, open-label, dose-escalation study[J]. Lancet, 2016, 17, 388 (10063): 3017-3026. |
| [6] |
Finkel RS, Mercuri E, Darras BT, et al. Nusinersen versus sham control in infantile-onset spinal muscular atrophy[J]. N Engl J Med, 2017, 377(18): 1723-1732.
doi: 10.1056/NEJMoa1702752 |
| [7] | 脊髓性肌萎缩症临床实践指南工作组. 脊髓性肌萎缩症临床实践指南[J]. 中国循证儿科杂志, 2023, 18(1): 1-12. |
| [8] |
Mazzone ES, Mayhew A, Montes J, et al. Revised upper limb module for spinal muscular atrophy: development of a new module[J]. Muscle Nerve, 2017, 55: 869-874.
doi: 10.1002/mus.25430 pmid: 27701745 |
| [9] | 曾宪涛, 刘慧, 陈曦, 等. Meta分析系列之四: 观察性研究的质量评价工具[J]. 中国循证心血管医学杂志, 2012, 4(4): 297-299. |
| [10] | Wells G, Shea B, O'Connell D, et al. NewCastle-Ottawa Quality Assessment Scale--Cohort Studies[EB/OL]. [2012-06-15]. http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp. |
| [11] |
Yao H, Chen X, Tan X. Efficacy and safety of apatinib in the treatment of osteosarcoma: a single-arm meta-analysis among Chinese patients[J]. BMC Cancer, 2021, 21(1): 449.
doi: 10.1186/s12885-021-08154-3 pmid: 33892656 |
| [12] | 陈月红, 杜亮, 耿兴远, 等. 无对照二分类数据的meta分析在RevMan软件中的实现[J]. 中国循证医学杂志, 2014, 14(7): 889-896. |
| [13] |
Tscherter A, Rüsch CT, Baumann D, et al. Evaluation of real-life outcome data of patients with spinal muscular atrophy treated with nusinersen in Switzerland[J]. Neuromuscul Disord, 2022, 32(5): 399-409.
doi: 10.1016/j.nmd.2022.02.001 |
| [14] | Pechmann A, Behrens M, Dörnbrack K, et al. Improved upper limb function in non-ambulant children with SMA type 2 and 3 during nusinersen treatment: a prospective 3-years SMArtCARE registry study[J]. Orphanet J Rare Dis, 2022, 23, 17(1): 384. |
| [15] |
Pane M, Coratti G, Pera MC, et al. Nusinersen efficacy data for 24-month in type 2 and 3 spinal muscular atrophy[J]. Ann Clin Transl Neurol, 2022, 9(3): 404-409.
doi: 10.1002/acn3.v9.3 |
| [16] |
Kotulska K, Chmielewski D, Mazurkiewicz-Bełdzińska M, et al. Safety, tolerability, and efficacy of a widely available nusinersen program for polish children with spinal muscular atrophy[J]. Eur J Paediatr Neurol, 2022, 39: 103-109.
doi: 10.1016/j.ejpn.2022.06.001 |
| [17] |
Pera MC, Coratti G, Bovis F, et al. Nusinersen in pediatric and adult patients with type III spinal muscular atrophy[J]. Ann Clin Transl Neurol, 2021, 8(8): 1622-1634.
doi: 10.1002/acn3.v8.8 |
| [18] |
Pane M, Coratti G, Sansone VA, et al. Type I SMA "new natural history": long-term data in nusinersen-treated patients[J]. Ann Clin Transl Neurol, 2021, 8(3): 548-557.
doi: 10.1002/acn3.v8.3 |
| [19] |
Modrzejewska S, Kotulska K, Kopyta I, et al. Nusinersen treatment of spinal muscular atrophy type 1 - results of expanded access programme in Poland[J]. Neurol Neurochir Pol, 2021, 55(3): 289-294.
doi: 10.5603/PJNNS.a2021.0020 pmid: 33565602 |
| [20] |
de Holanda Mendonça R, Jorge Polido G, Ciro M, et al. Clinical outcomes in patients with spinal muscular atrophy type 1 treated with nusinersen[J]. J Neuromuscul Dis, 2021, 8(2): 217-224.
doi: 10.3233/JND-200533 pmid: 33459657 |
| [21] |
Konersman CG, Ewing E, Yaszay B, et al. Nusinersen treatment of older children and adults with spinal muscular atrophy[J]. Neuromuscul Disord, 2021, 31(3): 183-193.
doi: 10.1016/j.nmd.2020.12.006 |
| [22] |
Coratti G, Pane M, Lucibello S, et al. Age related treatment effect in type II spinal muscular atrophy pediatric patients treated with nusinersen[J]. Neuromuscul Disord, 2021, 31(7): 596-602.
doi: 10.1016/j.nmd.2021.03.012 |
| [23] |
Szabó L, Gergely A, Jakus R, et al. Efficacy of nusinersen in type 1, 2 and 3 spinal muscular atrophy: Real world data from Hungarian patients[J]. Eur J Paediatr Neurol, 2020, 27: 37-42.
doi: 10.1016/j.ejpn.2020.05.002 |
| [24] |
Audic F, de la Banda MGG, Bernoux D, et al. Effects of nusinersen after one year of treatment in 123 children with SMA type 1 or 2: a French real-life observational study[J]. Orphanet J Rare Dis, 2020, 15(1): 148.
doi: 10.1186/s13023-020-01414-8 pmid: 32532349 |
| [25] |
Aragon-Gawinska K, Daron A, Ulinici A, Vet al. Sitting in patients with spinal muscular atrophy type 1 treated with nusinersen[J]. Dev Med Child Neurol, 2020, 62(3): 310-314.
doi: 10.1111/dmcn.14412 pmid: 31799720 |
| [26] |
Pechmann A, Langer T, Schorling D, et al. Evaluation of children with SMA type 1 under treatment with nusinersen within the expanded access program in Germany[J]. J Neuromuscul Dis, 2018, 5(2): 135-143.
doi: 10.3233/JND-180315 pmid: 29689734 |
| [27] | 毛姗姗, 冯艺杰, 徐璐, 等. 诺西那生钠修正治疗儿童脊髓性肌萎缩症随访分析[J]. 中华儿科杂志, 2022, 60(7): 688-693. |
| [28] | 陈峥, Yoram Nevo, Tanya Moss. 诺西那生钠治疗脊髓性肌萎缩[J]. 中国临床研究, 2019, 32(6): 721-725. |
| [29] |
Nance JR. Spinal muscular atrophy[J]. Continuum (Minneap Minn), 2020, 26: 1348-1368.
doi: 10.1212/CON.0000000000000918 pmid: 33003005 |
| [30] |
Faravelli I, Nizzardo M, Comi GP, et al. Spinal muscular atrophy--recent therapeutic advances for an old challenge[J]. Nat Rev Neurol, 2015, 11: 351-359.
doi: 10.1038/nrneurol.2015.77 pmid: 25986506 |
| [31] |
Darras BT, Chiriboga CA, Iannaccone ST, et al. Nusinersen in later-onset spinal muscular atrophy: Long-term results from the phase 1/2 studies[J]. Neurology, 2019, 92(21): e2492- e2506.
doi: 10.1212/WNL.0000000000007527 |
| [32] |
Haataja L, Mercuri E, Regev R, et al. Optimality score for the neurologic examination of the infant at 12 and 18 months of age[J]. J Pediatr, 1999, 135: 153-161.
doi: 10.1016/S0022-3476(99)70016-8 |
| [33] |
Al-Zaidy SA, Kolb SJ, Lowes L, et al. AVXS-101 (Onasemnogene Abeparvovec) for SMA1: comparative study with a prospective natural history cohort[J]. J Neuromuscul Dis, 2019, 6(3): 307-317.
doi: 10.3233/JND-190403 pmid: 31381526 |
| [34] |
De Sanctis R, Pane M, Coratti G, et al. Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy[J]. Neuromuscul Disord, 2018, 28(1): 24-28.
doi: 10.1016/j.nmd.2017.09.015 |
| [35] | 胡超平, 李文辉, 朱小妹, 等. 脊髓性肌萎缩症自然病史的系统评价/meta分析[J]. 中国循证儿科杂志, 2022, 17(6): 420-425. |
| [36] |
Chabanon A, Seferian AM, Daron A, et al. Prospective and longitudinal natural history study of patients with type 2 and 3 spinal muscular atrophy: baseline data NatHisSMA study[J]. PLoS One, 2018, 13(7): e0201004.
doi: 10.1371/journal.pone.0201004 |
| [37] |
Coratti G, Messina S, Lucibello S, et al. Clinical variability in spinal muscular atrophy type III[J]. Ann Neurol, 2020, 88(6): 1109-1117.
doi: 10.1002/ana.v88.6 |
| [38] |
Coratti G, Pera MC, Montes J, et al. Different trajectories in upper limb and gross motor function in spinal muscular atrophy[J]. Muscle Nerve, 2021, 64(5): 552-559.
doi: 10.1002/mus.27384 pmid: 34327716 |
| [39] |
Gavriilaki M, Moschou M, Papaliagkas V, et al. Nusinersen in adults with 5q spinal muscular atrophy: a systematic review and meta-analysis[J]. Neurotherapeutics, 2022, 19(2): 464-475.
doi: 10.1007/s13311-022-01200-3 pmid: 35178673 |
| [40] | Wijngaarde CA, Stam M, Otto LAM, et al. Muscle strength and motor function in adolescents and adults with spinal muscular atrophy[J]. Neurology, 2020, 95(14): e1988-e1998. |
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