Seidel Jazlyn A, Alder Laura, Salama April K S, Anders Carey K, Komisarow Jordan, Fecci Peter E, Sperduto Paul, Mullikin Trey, Kirkpatrick John P, Floyd Scott R, Reitman Zachary J, Vaios Eugene J
School of Medicine, Duke University, Durham, NC, 27710, USA.
Department of Medicine, Division of Medical Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
J Neurooncol. 2025 Jun 16. doi: 10.1007/s11060-025-05120-y.
Immunotherapy and stereotactic radiosurgery (SRS) are frequently combined in the management of brain metastases from non-small cell lung cancer (NSCLC) and melanoma. However, concurrent SRS and dual immune-checkpoint inhibition (ICPI) elevate the risk for symptomatic radionecrosis. As optimal radionecrosis management in the setting of immunotherapy is unknown, we aimed to characterize our institutional approaches and outcomes in patients with biopsy-proven radionecrosis.
Patients with NSCLC and melanoma brain metastases treated with SRS from 2014 to 2022 were identified from a prospective database. Only cases with biopsy-confirmed radionecrosis were included. The primary outcome was radiographic stabilization following treatment. Secondary outcomes included symptomatic resolution, overall survival, and cause of death.
Twenty-five patients [14 women (56%); median age, 58 years; 15 NSCLC (60%), 10 melanoma (40%); median follow-up: 66 months] with 30 cases of necrosis met inclusion criteria. 84% of patients received immunotherapy and twenty-one (84%) were symptomatic. Twenty-three cases (77%) received prophylactic steroids during SRS. Median time from SRS to biopsy-confirmed radionecrosis was 9.3 (95%CI: 6.8-17.9) months. Thirty-two interventions were performed: 21 laser interstitial thermal therapy, seven resection, and four medical management. Estimated 6-month radiographic stabilization was 80% (95%CI: 59-90%). Median time to stabilization with dual, single, and no ICPI was 2.7 (95%CI: 1.4-NR), 1.2 (95%CI: 0.8-NR), and 0 (95%CI: 0-NR) months, respectively. Three (14%) and two (29%) CTCAE grade ≥ 3 adverse events occurred following LITT and resection, respectively, with no grade 5 events.
Existing radionecrosis management strategies appear effective in patients receiving immunotherapy, though prospective trials are needed for validation.
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免疫疗法和立体定向放射外科(SRS)在非小细胞肺癌(NSCLC)和黑色素瘤脑转移瘤的治疗中经常联合使用。然而,同步进行SRS和双重免疫检查点抑制(ICPI)会增加出现症状性放射性坏死的风险。由于免疫疗法背景下最佳的放射性坏死管理方法尚不清楚,我们旨在描述我院对经活检证实为放射性坏死患者的治疗方法和结果。
从一个前瞻性数据库中识别出2014年至2022年接受SRS治疗的NSCLC和黑色素瘤脑转移瘤患者。仅纳入经活检确诊为放射性坏死的病例。主要结局是治疗后的影像学稳定。次要结局包括症状缓解、总生存期和死亡原因。
25例患者[14例女性(56%);中位年龄58岁;15例NSCLC(60%),10例黑色素瘤(40%);中位随访时间:66个月]共30例坏死符合纳入标准。84%的患者接受了免疫疗法,21例(84%)有症状。23例(77%)在SRS期间接受了预防性类固醇治疗。从SRS到活检证实为放射性坏死的中位时间为9.3(95%CI:6.8 - 17.9)个月。共进行了32次干预:21次激光间质热疗、7次切除术和4次药物治疗。估计6个月时的影像学稳定率为80%(95%CI:59 - 90%)。接受双重、单一和未接受ICPI治疗后达到稳定的中位时间分别为2.7(95%CI:1.4 - NR)、1.2(95%CI:0.8 - NR)和0(95%CI:0 - NR)个月。激光间质热疗(LITT)和切除术后分别发生3例(14%)和2例(29%)CTCAE≥3级不良事件,无5级事件。
现有的放射性坏死管理策略在接受免疫疗法的患者中似乎有效,不过仍需前瞻性试验进行验证。
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