Hematopoietic Stem Cell Transplantation in People With Active Secondary Progressive Multiple Sclerosis

被引:21
作者
Boffa, Giacomo [1 ]
Signori, Alessio [2 ]
Massacesi, Luca [3 ,4 ]
Mariottini, Alice [3 ,4 ]
Sbragia, Elvira [1 ]
Cottone, Salvatore [5 ]
Amato, Maria Pia [2 ,6 ,7 ]
Gasperini, Claudio [8 ]
Moiola, Lucia [9 ]
Meletti, Stefano [10 ,11 ,12 ]
Repice, Anna Maria [4 ]
Brescia Morra, Vincenzo [13 ]
Salemi, Giuseppe [14 ]
Patti, Francesco [15 ]
Filippi, Massimo [9 ]
De Luca, Giovanna [16 ]
Lus, Giacomo [17 ]
Zaffaroni, Mauro [18 ]
Sola, Patrizia [10 ,12 ]
Conte, Antonella [19 ,20 ]
Nistri, Riccardo [20 ,22 ]
Aguglia, Umberto [24 ]
Granella, Franco [25 ]
Galgani, Simonetta [26 ]
Caniatti, Luisa Maria [27 ]
Lugaresi, Alessandra [28 ,29 ]
Romano, Silvia [21 ,23 ]
Iaffaldano, Pietro [30 ]
Cocco, Eleonora [31 ]
Saccardi, Riccardo [32 ,33 ]
Angelucci, Emanuele [34 ]
Trojano, Maria [30 ]
Mancardi, Giovanni Luigi [1 ,36 ]
Sormani, Maria Pia [35 ]
Inglese, Matilde [1 ,37 ]
机构
[1] Univ Genoa, Dept Neurol Rehabil Ophthalmol Genet Maternal & Ch, Genoa, Italy
[2] Univ Genoa, Dept Hlth Sci, Biostat Unit AS, Genoa, Italy
[3] Univ Florence, Dept Neurosci Drugs & Child Hlth, Florence, Italy
[4] Careggi Univ Hosp, Dept Neurol 2, Florence, Italy
[5] Dept Neurol, Palermo, Italy
[6] Univ Florence, Dept NEUROFARBA, Sect Neurol Sci, Florence, Italy
[7] IRCCS Fdn Don Carlo Gnocchi, Florence, Italy
[8] Osped San Camillo Forlanini, Dept Neurol, Rome, Italy
[9] IRCCS San Raffaele Sci Inst, Neurol Unit, Milan, Italy
[10] IRCCS San Raffaele Sci Inst, Div Neurosci, Neuroimaging Res Unit, Milan, Italy
[11] Univ Modena & Reggio Emilia, Dept Biomed Metab & Neural Sci, Modena, Italy
[12] Azienda Osped Univ, Dept Neurosci, Neurol Unit, Modena, Italy
[13] Univ Federico II, Neurosci & Reprod & Odontostomatol Sci, Naples, Italy
[14] Univ Palermo, Dept Biomed Neurosci & Adv Diagnost, Palermo, Italy
[15] Univ Catania, Dept Med & Surg Sci & Adv Technol, AOU Policlin San Marco, Catania, Italy
[16] SS Annunziata Univ Hosp, MS Ctr, Neurol Unit, Chieti, Italy
[17] Univ Campania Luigi Vanvitelli, Dept Adv Med & Surg Sci, Div Neurol 2, Naples, Italy
[18] Osped Gallarate, Ctr Sclerosi Mltipla, ASST Valle Olona, Gallarate, Italy
[19] IRCCS Neuromed, Pozzilli, IS, Italy
[20] Sapienza Univ, Dept Human Neurosci, Rome, Italy
[21] Sapienza Univ, Dipartimento Neurosci Slute Mentale & Organi Senso, Rome, Italy
[22] Sapienza Univ, S Andrea Multiple Sclerosis Ctr, Rome, Italy
[23] S Andrea Hosp, Rome, Italy
[24] Magna Greacia Univ Catanzaro, Dept Med & Surg Sci, Catanzaro, Italy
[25] Univ Parma, Dept Med & Surg, Unit Neurosci, Parma, Italy
[26] San Camillo Forlanini Hosp, Dept Neurosci, Rome, Italy
[27] Azienda Osped Univ Ferrara, Dept Neurosci & Rehabil, Ferrara, Italy
[28] IRCCS Ist Sci Neurol Bologna, Bologna, Italy
[29] Univ Bologna, Dipartimento Sci Biomed e Neuromotorie, Bologna, Italy
[30] Univ Bari Aldo Moro, Dept Basic Med Sci Neurosci & Sense Organs, Bari, Italy
[31] Univ Cagliari, Dept Med Sci & Publ Hlth, Cagliari, Italy
[32] Binaghi Hosp, Multiple Sclerosis Ctr, ASL Cagliari, Cagliari, Italy
[33] Careggi Univ Hosp, Dept Cellular Therapies & Transfus Med RS, Florence, Italy
[34] Eatol & Terapie Cellulari, Genoa, Italy
[35] Osped Policlin IRCCS San Martino, Genoa, Italy
[36] Istituti Clin Sci Maugeri, Pavia, Italy
[37] Osped Policlin IRCCS San Mrtino, Genoa, Italy
关键词
LONG-TERM EVOLUTION; DISEASE PROGRESSION; INFLAMMATION; DISABILITY; PATHOLOGY; OUTCOMES; THERAPY; PLACEBO; MEMORY;
D O I
10.1212/WNL.0000000000206750
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and ObjectivesUncontrolled evidence suggests that autologous hematopoietic stem cell transplantation (AHSCT) can be effective in people with active secondary progressive multiple sclerosis (SPMS). In this study, we compared the effect of AHSCT with that of other anti-inflammatory disease-modifying therapies (DMTs) on long-term disability worsening in active SPMS.MethodsWe collected data from the Italian Bone Marrow Transplantation Study Group and the Italian Multiple Sclerosis Register. Patients were considered eligible if treatment had been started after the diagnosis of SPMS. Disability worsening was assessed by the cumulative proportion of patients with a 6-month confirmed disability progression (CDP) according to the Expanded Disability Status Scale (EDSS) score. Key secondary endpoints were the EDSS time trend after treatment start and the prevalence of disability improvement over time. Time to first CDP was assessed by means of proportional hazard Cox regression models. A linear mixed model with a time x treatment group interaction was used to assess the longitudinal EDSS time trends. Prevalence of improvement was estimated using a modified Kaplan-Meier estimator and compared between groups by bootstrapping the area under the curve.ResultsSeventy-nine AHSCT-treated patients and 1975 patients treated with other DMTs (beta interferons, azathioprine, glatiramer-acetate, mitoxantrone, fingolimod, natalizumab, methotrexate, teriflunomide, cyclophosphamide, dimethyl fumarate, and alemtuzumab) were matched to reduce treatment selection bias using propensity score and overlap weighting approaches. Time to first CDP was significantly longer in transplanted patients (hazard ratio [HR] = 0.50; 95% CI = 0.31-0.81; p = 0.005), with 61.7% of transplanted patients free from CPD at 5 years. Accordingly, EDSS time trend over 10 years was higher in patients treated with other DMTs than in AHSCT-treated patients (+0.157 EDSS points per year compared with -0.013 EDSS points per year; interaction p < 0.001). Patients who underwent AHSCT were more likely to experience a sustained disability improvement: 34.7% of patients maintained an improvement (a lower EDSS than baseline) 3 years after transplant vs 4.6% of patients treated by other DMTs (p < 0.001).DiscussionThe use of AHSCT in people with active SPMS is associated with a slowing of disability progression and a higher likelihood of disability improvement compared with standard immunotherapy.Classification of EvidenceThis study provides Class III evidence that autologous hematopoietic stem cell transplants prolonged the time to CDP compared with other DMTs.
引用
收藏
页码:E1109 / E1122
页数:14
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