Successful treatment of Anti-melanoma differentiation-associated gene 5 (MDA-5) antibody-positive dermatomyositis with rapidly progressive interstitial lung disease complicated by bilateral breast cancer following the additional tofacitinib: A case report.

IF 0.9 Q4 RHEUMATOLOGY Modern rheumatology case reports Pub Date : 2024-09-27 DOI:10.1093/mrcr/rxae060
Takashi Yamane, Midori Kitayama
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Abstract

Anti-melanoma differentiation-associated gene 5 (MDA-5) antibody-positive dermatomyositis (MDA5-DM) is known to cause rapidly progressive interstitial lung disease (RP-ILD). Cancer complications in MDA5-DM are less frequently reported compared to other forms of DM, though they do occur. The treatment strategy for DM with aspects of paraneoplastic syndrome is usually to treat the cancer first, if possible. However, surgery is difficult in the setting of respiratory failure and carries the risk of acute exacerbation of interstitial lung disease, as does chemotherapy and radiotherapy. The prognosis of MDA5-DM with RP-ILD has improved with initial immunosuppressive combination therapy, but certain cases remain refractory to treatment. Recently, the efficacy of janus kinase (JAK) inhibitors in refractory MDA5-DM cases has been reported. However, immunosuppressive therapies, including JAK inhibitors, may have negative effect on cancer progression. Here, we report a 48-year-old woman suffering from MDA5-DM with RP-ILD complicated by bilateral breast cancer. Due to respiratory failure, radical breast cancer surgery and chemotherapy could not be performed, so endocrine therapy and combined immunosuppressive therapy were first administered. However, the patient's condition was refractory to this initial treatment. Therefore, tofacitinib in combination with plasma exchange therapy was initiated, leading to an improvement in ILD, and bilateral mastectomy could be performed. One year later, MDA-5 antibody titers became negative, and glucocorticoid was successfully discontinued after two years. To date, three years have passed without recurrence of either MDA5-DM or breast cancer. To our knowledge, this is the first report of MDA5-DM complicated by breast cancer, as well as the first case of JAK inhibitor use for MDA5-DM with cancer. For curative treatment of MD5-DM with RP-ILD, if comorbid cancers are found, collaboration with oncologists to balance the efficacy and adverse events of MDA5-DM with RP-ILD therapy is essential in determining the appropriate type and timing of treatment, which could lead to a favorable outcome.

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成功治疗抗黑色素瘤分化相关基因 5 (MDA-5) 抗体阳性皮肌炎伴快速进展性间质性肺病并发双侧乳腺癌的病例报告:病例报告。
抗黑色素瘤分化相关基因 5(MDA-5)抗体阳性皮肌炎(MDA5-DM)可导致快速进展性间质性肺病(RP-ILD)。与其他形式的皮肌炎相比,MDA5-DM 癌症并发症的报道较少,但确实存在。对于伴有副肿瘤综合征的 DM,治疗策略通常是尽可能先治疗癌症。然而,手术在呼吸衰竭的情况下很难进行,而且有间质性肺病急性加重的风险,化疗和放疗也是如此。MDA5-DM合并RP-ILD的预后在最初的免疫抑制联合治疗后有所改善,但某些病例仍然难治。最近,有报道称破伤风激酶(JAK)抑制剂对难治性 MDA5-DM 病例有疗效。然而,包括JAK抑制剂在内的免疫抑制疗法可能会对癌症进展产生负面影响。在此,我们报告了一名患有MDA5-DM的48岁女性,她患有RP-ILD,同时并发双侧乳腺癌。由于呼吸衰竭,无法进行乳腺癌根治术和化疗,因此首先进行了内分泌治疗和联合免疫抑制治疗。然而,患者的病情对最初的治疗产生了耐药性。因此,患者开始接受托法替尼联合血浆置换治疗,结果 ILD 有所改善,并得以实施双侧乳房切除术。一年后,MDA-5 抗体滴度转阴,两年后成功停用糖皮质激素。迄今为止,三年过去了,MDA5-DM 和乳腺癌均未复发。据我们所知,这是第一例MDA5-DM并发乳腺癌的报告,也是第一例使用JAK抑制剂治疗MDA5-DM合并癌症的病例。对于MDA5-DM合并RP-ILD的根治性治疗,如果发现合并癌症,则必须与肿瘤专家合作,平衡MDA5-DM合并RP-ILD治疗的疗效和不良反应,以确定适当的治疗类型和时机,从而获得良好的预后。
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