Durvalumab with chemoradiotherapy for limited-stage small-cell lung cancer

被引:15
|
作者
Park, Sehhoon [1 ]
Noh, Jae Myoung [2 ]
Choi, Yoon-La [3 ]
Chi, Sang Ah [4 ]
Kim, Kyunga [5 ]
Jung, Hyun Ae [1 ]
Lee, Se-Hoon [1 ]
Ahn, Jin Seok [1 ]
Ahn, Myung-Ju [1 ]
Sun, Jong-Mu [1 ,6 ]
机构
[1] Sungkyunkwan Univ, Samsung Med Ctr, Dept Med, Div Hematol Oncol,Sch Med, Seoul, South Korea
[2] Sungkyunkwan Univ, Samsung Med Ctr, Dept Radiat Oncol, Sch Med, Seoul, South Korea
[3] Sungkyunkwan Univ, Samsung Med Ctr, Dept Pathol & Translat Genom, Sch Med, Seoul, South Korea
[4] Sungkyunkwan Univ, Samsung Adv Inst Hlth Sci & Technol, Dept Hlth Sci & Technol, Seoul, South Korea
[5] Samsung Med Ctr, Res Inst Future Med, Biomed Stat Ctr, Seoul, South Korea
[6] Sungkyunkwan Univ, Samsung Med Ctr, Dept Med, Div Hematol Oncol,Sch Med, 81 Irwon Ro, Seoul 06351, South Korea
关键词
Limited-stage; Small-cell lung cancer; Durvalumab; Prophylactic cranial; irradiation; PD-L1; PROPHYLACTIC CRANIAL IRRADIATION; PLUS PLATINUM-ETOPOSIDE; OPEN-LABEL; THORACIC RADIOTHERAPY; PEMBROLIZUMAB; THERAPY; ATEZOLIZUMAB; PROGRESSION; NIVOLUMAB; PATTERNS;
D O I
10.1016/j.ejca.2022.03.034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The current standard treatment for limited-stage small-cell lung cancer (LS-SCLC) is chemotherapy with concurrent chemoradiotherapy (CCRT).Methods: In this single-arm phase II study, patients with LS-SCLC received four cycles of etoposide, cisplatin, and durvalumab every 3 weeks. Thoracic radiotherapy of 52.5 Gy in 25 oncedaily fractions was started with the third cycle of chemoimmunotherapy. After CCRT plus durvalumab, patients received durvalumab consolidation therapy every 4 weeks for a maximum of 2 years after study enrolment. Prophylactic cranial irradiation (PCI) was recommended. Results: Fifty-one patients were enrolled, and 50 were included in the full analysis set. With the median follow-up duration of 26.6 months, the median PFS was 14.4 months (95% confidence interval: 10.3-NA), and the 24-month PFS rate was 42.0%. The median overall survival was not reached with a 24-month overall survival rate of 67.8%. The positive PD-L1 group (n Z 22) was not associated with longer PFS (hazard ratio, 0.70; 0.31-1.58) and overall survival (0.64; 0.22-1.84) compared with the negative PD-L1 group (n = 20). Among the 43 patients who were candidates for PCI treatment, the PCI group (n = 22) had significantly fewer events of brain metastasis as the first failure sites compared to the no PCI group (n = 21) (13.6% vs. 42.9%, P = 0.033). There were several grade 3 or 4 adverse events which were well managed with appropriate supportive care.Conclusions: Durvalumab with CCRT for LS-SCLC exhibited promising clinical efficacy with a tolerable safety profile, prompting its validation in a randomized study. Trial registration: NCT03585998. 2022 Elsevier Ltd. All rights reserved.
引用
收藏
页码:42 / 53
页数:12
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