Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Department of Pathology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
BMC Pulm Med. 2023 Aug 8;23(1):289. doi: 10.1186/s12890-023-02569-3.
Olaparib, a poly (ADP-ribose) polymerase (PARP) inhibitor, has demonstrated effectiveness in treating ovarian, breast, and other cancers, particularly those with specific molecular subtypes including, but not limited to, BRCA1/2 mutations. Consequently, its utilization is expected to increase in the future. For this reason, it is important to acknowledge the potential for adverse events associated with olaparib, including the relatively rare but significant risk of drug-induced interstitial lung disease (DIILD). Since DIILD can lead to fatal outcomes, its early detection is crucial. The dissemination of knowledge regarding DIILD can be facilitated through case reports; however, specific reports of DIILD caused by olaparib have only been published in Japanese. To the best of our knowledge, this is the first report in English of our experience with three cases of DIILD caused by olaparib.
Cases 1, 2, and 3 involved Japanese women with ovarian cancer who had been receiving olaparib at a dose of 600 mg/day. Case 1, a 72-year-old woman who had been on olaparib for 4 months, and case 2, a 51-year-old woman who had been on olaparib for 8 months, reported fever and general malaise. Chest computed tomography (CT) revealed pale ground glass opacity (GGO) similar to hypersensitivity pneumonitis. The severity grade was 2 in both cases. Case 3, a 78-year-old woman who had been on olaparib for 3 weeks, presented with cough and reported dyspnea on exertion. Chest CT revealed non-specific interstitial pneumonia and organizing pneumonia-like shadows. The severity grade was 4. Olaparib was discontinued in all cases. Case 1 received 0.6 mg/kg of prednisolone due to mild hypoxia, while prednisolone was not administered in case 2 due to the absence of hypoxia. Case 3 received steroid pulse therapy due to severe hypoxia. Olaparib administration was not resumed in any patient.
DIILD caused by olaparib in Japan, including the present three cases, commonly presents with GGO, similar to hypersensitivity pneumonitis on chest CT. The prognosis for the majority of patients is favorable; however, there have been instances of severe cases. Early recognition of drug-induced lung injury and further accumulation of cases is important.
奥拉帕利是一种聚(ADP-核糖)聚合酶(PARP)抑制剂,已被证明在治疗卵巢癌、乳腺癌和其他癌症方面具有疗效,特别是在具有特定分子亚型的癌症中,包括但不限于 BRCA1/2 突变。因此,预计未来它的使用将会增加。鉴于此,了解与奥拉帕利相关的不良反应的可能性非常重要,包括相对罕见但具有重要意义的药物引起的间质性肺病(DIILD)风险。由于 DIILD 可导致致命后果,因此早期发现至关重要。通过病例报告可以促进对 DIILD 的了解,但仅在日本发表了关于奥拉帕利引起的 DIILD 的具体报告。据我们所知,这是第一份用英语报告的我们治疗三例由奥拉帕利引起的 DIILD 的经验。
病例 1、2 和 3 涉及 3 名日本卵巢癌女性患者,她们均接受了奥拉帕利 600mg/天的治疗。病例 1 为一名 72 岁女性,接受奥拉帕利治疗 4 个月,病例 2 为一名 51 岁女性,接受奥拉帕利治疗 8 个月,均出现发热和全身不适。胸部计算机断层扫描(CT)显示苍白的磨玻璃样混浊(GGO)类似于过敏性肺炎。在这两个病例中,严重程度均为 2 级。病例 3 为一名 78 岁女性,接受奥拉帕利治疗 3 周,出现咳嗽和活动时呼吸困难。胸部 CT 显示非特异性间质性肺炎和机化性肺炎样阴影。严重程度为 4 级。所有患者均停止使用奥拉帕利。病例 1 因轻度低氧血症接受 0.6mg/kg 泼尼松龙治疗,而病例 2 因无低氧血症而未给予泼尼松龙。病例 3 因严重低氧血症接受类固醇冲击治疗。未在任何患者中恢复使用奥拉帕利。
包括本研究中的 3 例病例在内,日本的奥拉帕利引起的 DIILD 通常表现为 GGO,与胸部 CT 上的过敏性肺炎相似。大多数患者的预后良好;然而,也有严重病例。早期识别药物引起的肺损伤并进一步积累病例非常重要。