Buonomo Alessandro, Nucera Eleonora, Criscuolo Marianna
Allergy Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Department of Radiological and Hematological Sciences Fondazione, Policlinico Universitario A. Gemelli, IRCCS Università Cattolica del Sacro Cuore, Largo A. Gemelli, 100168, Rome, Italy.
Mediterr J Hematol Infect Dis. 2022 May 1;14(1):e2022040. doi: 10.4084/MJHID.2022.040. eCollection 2022.
Management of Indolent and Smoldering SM is focused on preventing anaphylactic reactions and identifying and avoiding symptom triggers. Skin and gastrointestinal symptoms are managed with H1- and H2-antihistamines. When skin symptoms are not adequately controlled, leukotriene antagonists and oral psoralen combined with ultraviolet therapy may be added. Proton pump inhibitors, sodium cromolyn, and oral corticosteroids may be added for gastrointestinal symptoms. Patients should be prescribed self-injectable epinephrine and trained to treat recurrent cardiovascular symptoms or anaphylaxis. Depression and cognitive impairment require a psychiatric evaluation for tailored treatment. Bone involvement is managed with bisphosphonates and eventually interferon. Omalizumab is effective on all vasomotor symptoms, including anaphylaxis, but not on respiratory, musculoskeletal, and neuropsychiatric symptoms. A cytoreductive treatment is not recommended unless anti-mediator therapy has failed. Venom immunotherapy is mandatory for patients with Hymenoptera venom allergy. There is no curative option for patients with advanced SM. The available therapeutic options include tyrosine-kinase inhibitors and cladribine, with variable duration and extent of response. Imatinib mesylate was the first drug approved for SM lacking the cKIT D816V mutation; dasatinib and nilotinib are ineffective. Midostaurin is active on both wild-type and mutant cKIT D816V, while Avapritinib is a selective cKIT D816V inhibitor: they are approved for the treatment of advanced SM. Cladribine is a purine analog with significant activity against monocytes that were thought to have a common progenitor with mast cells. Allogeneic stem cell transplantation is usually performed in younger selected patients.
惰性和冒烟型系统性肥大细胞增多症(SM)的管理重点在于预防过敏反应以及识别和避免症状触发因素。皮肤和胃肠道症状采用H1和H2抗组胺药进行治疗。当皮肤症状控制不佳时,可加用白三烯拮抗剂以及口服补骨脂素联合紫外线疗法。针对胃肠道症状可加用质子泵抑制剂、色甘酸钠和口服糖皮质激素。应为患者开具自动注射肾上腺素,并培训其治疗复发性心血管症状或过敏反应。抑郁和认知障碍需要进行精神科评估以制定个性化治疗方案。骨受累采用双膦酸盐治疗,最终可能使用干扰素。奥马珠单抗对包括过敏反应在内的所有血管运动症状均有效,但对呼吸、肌肉骨骼和神经精神症状无效。除非抗介质治疗失败,否则不建议进行减瘤治疗。对于膜翅目毒液过敏的患者,毒液免疫疗法是必需的。晚期SM患者没有治愈的选择。现有的治疗选择包括酪氨酸激酶抑制剂和克拉屈滨,反应持续时间和程度各不相同。甲磺酸伊马替尼是首个被批准用于治疗缺乏cKIT D816V突变的SM的药物;达沙替尼和尼洛替尼无效。米哚妥林对野生型和突变型cKIT D816V均有活性,而阿伐替尼是一种选择性cKIT D816V抑制剂:它们均被批准用于治疗晚期SM。克拉屈滨是一种嘌呤类似物,对被认为与肥大细胞有共同祖细胞的单核细胞具有显著活性。异基因干细胞移植通常在选定的年轻患者中进行。