Nishino Mizuki, Kusumoto Masahiko, Bankier Alexander A, Kurihara Yasuyuki, Zhang Lin, Rasheed Zeshaan, Meinhardt Gerold, Arunachalam Meena, Taitt Corina, Wang Qiang, Powell Charles A
Department of Radiology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, MA.
Department of Diagnostic Radiology, National Cancer Center Hospital, Tokyo, Japan.
JCO Precis Oncol. 2023 Sep;7:e2300391. doi: 10.1200/PO.23.00391.
Trastuzumab deruxtecan (T-DXd) is an antibody-drug conjugate approved for the treatment of several advanced cancers; however, severe or fatal interstitial lung disease/pneumonitis can occur. We characterized the computed tomography (CT) patterns of T-DXd‒related pneumonitis as a marker for its clinical severity.
Ninety patients with advanced cancers who developed T-DXd‒related pneumonitis in two completed single-arm clinical trials were included. Three radiologists independently characterized the CT patterns of pneumonitis at diagnosis, for analyses of those patterns' relationships with clinical severity and pneumonitis outcome.
T-DXd‒related pneumonitis most commonly presented with cryptogenic organizing pneumonia (COP) pattern, observed in 65 patients (72%), followed by a newly identified COP/hypersensitivity pneumonitis (HP) pattern (13%), acute interstitial pneumonia (AIP)/acute respiratory distress syndrome (ARDS) pattern (11%), and HP pattern (3%). A subset of cases with COP pattern demonstrated an atypical distribution with upper and peripheral lung involvement (6/65; 9%). CT patterns were associated with Common Terminology Criteria for Adverse Events severity grades of pneumonitis, with the AIP/ARDS pattern having higher grades compared with others ( < .0001). Fatal pneumonitis was more common in the AIP/ARDS pattern than in others ( = .005). The onset of pneumonitis was earlier in the AIP/ARDS pattern compared with others (median time to onset: at 17.9 32.7 weeks of therapy; = .019). Pneumonitis was treated by withholding T-DXd with or without corticosteroids in most patients (78/90; 87%).
TDXd‒related pneumonitis most commonly demonstrated a COP pattern, with a subset having an atypical distribution. The AIP/ARDS pattern was indicative of severe, potentially fatal pneumonitis, and requires immediate clinical attention to mitigate serious adverse events.
德曲妥珠单抗(T-DXd)是一种已被批准用于治疗多种晚期癌症的抗体药物偶联物;然而,可能会发生严重或致命的间质性肺疾病/肺炎。我们将T-DXd相关肺炎的计算机断层扫描(CT)模式作为其临床严重程度的标志物进行了特征描述。
纳入了在两项完成的单臂临床试验中发生T-DXd相关肺炎的90例晚期癌症患者。三名放射科医生独立对诊断时肺炎的CT模式进行特征描述,以分析这些模式与临床严重程度及肺炎结局的关系。
T-DXd相关肺炎最常见的表现为隐源性机化性肺炎(COP)模式,65例患者(72%)出现该模式,其次是新发现的COP/过敏性肺炎(HP)模式(13%)、急性间质性肺炎(AIP)/急性呼吸窘迫综合征(ARDS)模式(11%)以及HP模式(3%)。一部分COP模式的病例表现为非典型分布,累及上肺和肺外周(6/65;9%)。CT模式与不良事件通用术语标准中肺炎的严重程度分级相关,AIP/ARDS模式的分级高于其他模式(P <.0001)。致命性肺炎在AIP/ARDS模式中比其他模式更常见(P =.005)。与其他模式相比,AIP/ARDS模式的肺炎发病更早(发病的中位时间:治疗17.9±32.7周;P =.019)。大多数患者(78/90;87%)通过停用T-DXd并加用或不加用糖皮质激素来治疗肺炎。
T-DXd相关肺炎最常见的表现为COP模式,一部分具有非典型分布。AIP/ARDS模式提示严重的、可能致命的肺炎,需要临床立即关注以减轻严重不良事件。