Department of Thoracic Oncology, National Cancer Center Hospital, Chuo-ku, Tokyo, Japan; Cancer Medicine, Cooperative Graduate School, The Jikei University Graduate School of Medicine, Minato-ku, Tokyo, Japan.
Department of Thoracic Oncology, National Cancer Center Hospital, Chuo-ku, Tokyo, Japan.
Clin Lung Cancer. 2024 Nov;25(7):e369-e378.e3. doi: 10.1016/j.cllc.2024.06.009. Epub 2024 Jul 2.
It is unclear how the duration and tapering pattern of corticosteroid therapy for pneumonitis changed after the introduction of durvalumab consolidation therapy.
We retrospectively evaluated the medical records of patients diagnosed with nonsmall cell lung cancer who received chemoradiotherapy between January 2014 and December 2020.
Data for 135 patients treated before durvalumab approval and 100 patients treated with durvalumab after its approval were analyzed. In both groups, more than 70% were male, with a median age of 66 y. Approximately 85% were smokers, and the most common tumor histology was adenocarcinoma. Most patients were treated with doses of 60 and 66 Gy (n = 127 [94%] vs. n = 95 [95%]). Among the patients treated with durvalumab, 57%, 38%, and 5% had grade 1, grade 2, and grade 3 pneumonitis; none had grade 4 or 5 pneumonitis. Patients treated with durvalumab exhibited a longer duration of corticosteroid therapy for pneumonitis (17 wk; range: 2-88 wk) than patients not treated with durvalumab (7 wk; range: 0.4-21 wk; P < 0.001). Pneumonitis relapse was more frequent in patients treated with durvalumab (n = 8; 23%) than in patients not treated with durvalumab (n = 2; 7%). Among the 8 patients treated with durvalumab, 2 had recurrent pneumonitis, 1 could not terminate corticosteroids.
Our data show that durvalumab prolongs the duration of corticosteroid therapy and increases the complexity of corticosteroid tapering patterns. This study can help manage pneumonitis caused by immune checkpoint inhibitors and other drugs used after chemoradiotherapy in routine practice and clinical trials.
尚不清楚在接受度伐利尤单抗巩固治疗后,间质性肺炎皮质类固醇治疗的持续时间和逐渐减量模式如何变化。
我们回顾性评估了 2014 年 1 月至 2020 年 12 月期间接受放化疗的非小细胞肺癌患者的病历。
分析了在度伐利尤单抗批准前治疗的 135 例患者和批准后治疗的 100 例患者的数据。在这两组中,超过 70%为男性,中位年龄为 66 岁。约 85%为吸烟者,最常见的肿瘤组织学类型为腺癌。大多数患者接受了 60 和 66 Gy 的剂量(n = 127 [94%] vs. n = 95 [95%])。在接受度伐利尤单抗治疗的患者中,57%、38%和 5%的患者出现 1 级、2 级和 3 级间质性肺炎;无一例患者出现 4 级或 5 级间质性肺炎。接受度伐利尤单抗治疗的患者间质性肺炎皮质类固醇治疗的持续时间(17 周;范围:2-88 周)长于未接受度伐利尤单抗治疗的患者(7 周;范围:0.4-21 周;P < 0.001)。接受度伐利尤单抗治疗的患者间质性肺炎复发更为频繁(n = 8;23%),而未接受度伐利尤单抗治疗的患者(n = 2;7%)。在接受度伐利尤单抗治疗的 8 例患者中,有 2 例出现复发性间质性肺炎,1 例无法终止皮质类固醇治疗。
我们的数据表明,度伐利尤单抗延长了皮质类固醇治疗的持续时间,并增加了皮质类固醇逐渐减量模式的复杂性。本研究有助于在常规实践和临床试验中管理免疫检查点抑制剂和其他化疗后药物引起的间质性肺炎。