查看“RRMM”的源代码

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            <strong>[[复发或难治性多发性骨髓瘤]]</strong>（<strong>[[RRMM]]</strong>）是指在接受过初始治疗并获得缓解后，病情再次进展或对当前治疗无反应的 <strong>[[多发性骨髓瘤]]</strong>（<strong>[[MM]]</strong>）阶段。随着蛋白酶体抑制剂、免疫调节剂及 <strong>[[CD38]]</strong> 单抗的广泛应用，临床上出现了大量针对上述三类药物均耐药的 <strong>[[三重耐药]]</strong>（Triple-class refractory）患者。进入 2026 年，<strong>[[RRMM]]</strong> 的治疗格局发生了剧变，以 <strong>[[BCMA]]</strong> 为靶点的 <strong>[[CAR-T]]</strong> 细胞疗法（如 <strong>[[伊基奥仑赛]]</strong>、<strong>[[西达基奥仑赛]]</strong>）和 <strong>[[双特异性抗体]]</strong>（如 <strong>[[泰立奇]]</strong>、<strong>[[艾瑞珂]]</strong>）已成为后线挽救治疗的标准方案，显著延长了末线患者的生存期。
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            <div style="font-size: 1.2em; font-weight: bold; letter-spacing: 1.2px;">复发或难治性多发性骨髓瘤</div>
            <div style="font-size: 0.7em; opacity: 0.85; margin-top: 4px; white-space: nowrap;">RRMM · Triple-class Refractory MM</div>
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                <div style="font-size: 0.8em; color: #64748b; margin-top: 12px;">核心靶标：<strong>[[BCMA]]</strong> / <strong>[[GPRC5D]]</strong></div>
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                    <th style="text-align: left; padding: 6px 12px; background-color: #f1f5f9; color: #475569; border-bottom: 1px solid #e2e8f0; width: 40%; font-weight: normal;"><strong>[[ICD-10]]</strong></th>
                    <td style="padding: 6px 12px; border-bottom: 1px solid #e2e8f0; color: #0f172a;">C90.00</td>
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                    <th style="text-align: left; padding: 6px 12px; background-color: #f1f5f9; color: #475569; border-bottom: 1px solid #e2e8f0; font-weight: normal;"><strong>[[ICD-11]]</strong></th>
                    <td style="padding: 6px 12px; border-bottom: 1px solid #e2e8f0; color: #0f172a;">2A80.0</td>
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                    <th style="text-align: left; padding: 6px 12px; background-color: #f1f5f9; color: #475569; border-bottom: 1px solid #e2e8f0; font-weight: normal;">常用标志物</th>
                    <td style="padding: 6px 12px; border-bottom: 1px solid #e2e8f0; color: #0f172a;">M蛋白、轻链、<strong>[[BCMA]]</strong></td>
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                    <th style="text-align: left; padding: 6px 12px; background-color: #f1f5f9; color: #475569; border-bottom: 1px solid #e2e8f0; font-weight: normal;">高危遗传学</th>
                    <td style="padding: 6px 12px; border-bottom: 1px solid #e2e8f0; color: #0f172a;">del(17p)、t(4;14)、1q21+</td>
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                    <th style="text-align: left; padding: 6px 12px; background-color: #f1f5f9; color: #475569; border-bottom: 1px solid #e2e8f0; font-weight: normal;">主要疗法</th>
                    <td style="padding: 6px 12px; border-bottom: 1px solid #e2e8f0; color: #1e40af;"><strong>[[CAR-T]]</strong>、<strong>[[双特异性抗体]]</strong></td>
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                    <th style="text-align: left; padding: 6px 12px; background-color: #f1f5f9; color: #475569; font-weight: normal;">相关实体</th>
                    <td style="padding: 12px; color: #0f172a;"><strong>[[IMWG]]</strong> / <strong>[[NCCN]]</strong></td>
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    <h2 style="background: #f1f5f9; color: #0f172a; padding: 10px 18px; border-radius: 0 6px 6px 0; font-size: 1.25em; margin-top: 40px; border-left: 6px solid #0f172a; font-weight: bold;">发病机制：克隆演变与免疫逃逸</h2>
    
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        <strong>[[RRMM]]</strong> 的发生是恶性浆细胞在治疗压力下不断进化的结果，其核心特征包括：
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        <li style="margin-bottom: 12px;">克隆异质性：随着病程进展，对化疗敏感的克隆被清除，具有 <strong>[[TP53]]</strong> 突变或高危细胞遗传学改变的耐药克隆逐渐占据主导地位。</li>
        <li style="margin-bottom: 12px;">靶点丢失：在接受针对 <strong>[[BCMA]]</strong> 的 <strong>[[CAR-T]]</strong> 或双抗治疗后，部分肿瘤细胞会通过基因缺失或下调抗原表达实现免疫逃逸。</li>
        <li style="margin-bottom: 12px;"><strong>[[髓外病变]]</strong>（EMD）：恶性细胞脱离骨髓微环境，在皮肤、肝脏或浆膜腔形成浸润，这是 <strong>[[RRMM]]</strong> 患者预后极差的标志。</li>
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                <th style="padding: 12px; border: 1px solid #cbd5e1; color: #0f172a; width: 25%; font-weight: bold;">耐药分类</th>
                <th style="padding: 12px; border: 1px solid #cbd5e1; color: #475569; font-weight: bold;">定义标准</th>
                <th style="padding: 12px; border: 1px solid #cbd5e1; color: #1e40af; font-weight: bold;">临床干预方向</th>
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                <td style="padding: 10px; border: 1px solid #cbd5e1;">双重耐药</td>
                <td style="padding: 10px; border: 1px solid #cbd5e1;">对一种 <strong>[[PI]]</strong>（如硼替佐米）和一种 <strong>[[IMiD]]</strong>（如来那度胺）均耐药。</td>
                <td style="padding: 10px; border: 1px solid #cbd5e1;">引入 <strong>[[CD38]]</strong> 单抗联合方案。</td>
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                <td style="padding: 10px; border: 1px solid #cbd5e1;"><strong>[[三重耐药]]</strong></td>
                <td style="padding: 10px; border: 1px solid #cbd5e1;">对 <strong>[[PI]]</strong>、<strong>[[IMiD]]</strong> 及 <strong>[[CD38]]</strong> 单抗均产生耐药。</td>
                <td style="padding: 10px; border: 1px solid #cbd5e1;">优先考虑 <strong>[[BCMA]]</strong> 靶向免疫治疗。</td>
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                <td style="padding: 10px; border: 1px solid #cbd5e1;">五重耐药</td>
                <td style="padding: 10px; border: 1px solid #cbd5e1;">对两种 <strong>[[PI]]</strong>、两种 <strong>[[IMiD]]</strong> 及 <strong>[[CD38]]</strong> 单抗均耐药。</td>
                <td style="padding: 10px; border: 1px solid #cbd5e1;">尝试 <strong>[[GPRC5D]]</strong> 靶点或 <strong>[[XPO1]]</strong> 抑制剂。</td>
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    <h2 style="background: #f1f5f9; color: #0f172a; padding: 10px 18px; border-radius: 0 6px 6px 0; font-size: 1.25em; margin-top: 40px; border-left: 6px solid #0f172a; font-weight: bold;">治疗策略：后线挽救与靶点轮替</h2>
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        针对 <strong>[[RRMM]]</strong> 的现代诊疗强调“深度缓解”与“生存质量”的平衡：
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        <li style="margin-bottom: 12px;">自体 <strong>[[CAR-T]]</strong> 疗法：通过回输修饰后的 T 细胞，<strong>[[伊基奥仑赛]]</strong> 和 <strong>[[西达基奥仑赛]]</strong> 在末线患者中实现了极高的 <strong>[[MRD]]</strong> 转阴率。</li>
        <li style="margin-bottom: 12px;">双特异性抗体（BsAb）：<strong>[[泰立奇]]</strong>（靶向 BCMA/CD3）和 <strong>[[泰立唯]]</strong>（靶向 GPRC5D/CD3）提供了现货型治疗选择，适用于无法等待 <strong>[[CAR-T]]</strong> 制备的急症进展患者。</li>
        <li style="margin-bottom: 12px;">靶点轮替逻辑：当 <strong>[[BCMA]]</strong> 疗法进展后，临床推荐转向针对 <strong>[[GPRC5D]]</strong> 或 <strong>[[FcRH5]]</strong> 等新靶点的药物。</li>
        <li style="margin-bottom: 12px;">支持治疗：包括针对 <strong>[[骨相关事件]]</strong> 的双膦酸盐治疗和针对免疫抑制的 <strong>[[IVIG]]</strong> 补充。</li>
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            <li style="margin-bottom: 8px;"><strong>[[三重耐药]]</strong>：当前 <strong>[[RRMM]]</strong> 定义的核心，决定了后续治疗强度的选择。</li>
            <li style="margin-bottom: 8px;"><strong>[[MRD]]</strong>：微小残留病，其持续阴性是评估 <strong>[[RRMM]]</strong> 长期预后的金标准。</li>
            <li style="margin-bottom: 8px;"><strong>[[BCMA]]</strong>：目前 <strong>[[RRMM]]</strong> 免疫治疗最重要的导航靶点。</li>
            <li style="margin-bottom: 8px;"><strong>[[自交异体干细胞移植]]</strong>：对于部分多次复发患者，<strong>[[造血干细胞移植]]</strong> 仍是桥接治疗的一种考虑。</li>
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        <span style="color: #0f172a; font-weight: bold; font-size: 1.05em; display: inline-block; margin-bottom: 15px;">学术参考文献与权威点评</span>
        
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            [1] Kumar SK, et al. (2024/2025). Managing relapsed or refractory multiple myeloma: current strategies and future directions. <strong>[[The Lancet Haematology]]</strong>.
            <br><span style="color: #475569;">[权威点评]：该综述强调了 <strong>[[CAR-T]]</strong> 疗法前置至早期复发阶段对于改善长期生存的决定性意义。</span>
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            [2] <strong>[[IMWG]]</strong> Consensus Criteria (2025 Update). Definition and response assessment in <strong>[[RRMM]]</strong> patients in the era of bispecifics. <strong>[[Blood]]</strong>.[Academic Review]
            <br><span style="color: #475569;">[学术点评]：更新了针对新型免疫疗法的疗效评估标准，特别增加了针对抗原丢失现象的监测指引。</span>
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            复发或难治性多发性骨髓瘤 (RRMM) 诊疗生态 · 知识图谱
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                <td style="width: 85px; background-color: #f8fafc; color: #334155; padding: 10px 12px; text-align: right; vertical-align: middle; white-space: nowrap;">关联靶点</td>
                <td style="padding: 10px 15px; color: #334155;"><strong>[[BCMA]]</strong>•<strong>[[CD38]]</strong>•<strong>[[GPRC5D]]</strong>•<strong>[[FcRH5]]</strong>•<strong>[[SLAMF7]]</strong></td>
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                <td style="width: 85px; background-color: #f8fafc; color: #334155; padding: 10px 12px; text-align: right; vertical-align: middle; white-space: nowrap;">核心药物</td>
                <td style="padding: 10px 15px; color: #334155;"><strong>[[伊基奥仑赛]]</strong>•<strong>[[西达基奥仑赛]]</strong>•<strong>[[泰立奇]]</strong>•<strong>[[泰立唯]]</strong>•<strong>[[泊马度胺]]</strong></td>
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                <td style="width: 85px; background-color: #f8fafc; color: #334155; padding: 10px 12px; text-align: right; vertical-align: middle; white-space: nowrap;">并发症管理</td>
                <td style="padding: 10px 15px; color: #334155;"><strong>[[CRS]]</strong>•<strong>[[ICANS]]</strong>•<strong>[[低丙种球蛋白血症]]</strong>•<strong>[[高钙血症]]</strong></td>
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                <td style="width: 85px; background-color: #f8fafc; color: #334155; padding: 10px 12px; text-align: right; vertical-align: middle; white-space: nowrap;">研究趋势</td>
                <td style="padding: 10px 15px; color: #334155;"><strong>[[双靶点CAR-T]]</strong>•<strong>[[异体通用型CAR-T]]</strong>•<strong>[[免疫检查点抑制剂联合方案]]</strong>•<strong>[[CELMoDs]]</strong></td>
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