A single center analysis of first-line treatment in advanced KRAS mutant non-small cell lung cancer: real-world practice

被引:5
|
作者
Liu, Yanxia [1 ,2 ]
Gao, Yuan [1 ]
Wang, Ying [1 ]
Zhao, Cong [1 ,2 ]
Zhang, Zhiyun [1 ,2 ]
Li, Baolan [1 ]
Zhang, Tongmei [1 ]
机构
[1] Capital Med Univ, Beijing Chest Hosp, Med Oncol TB & Thorac Tumor Res Inst, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Chest Hosp, TB & Thorac Tumor Res Inst, Canc Res Ctr, Beijing, Peoples R China
关键词
KRAS mutation; NSCLC; First-line treatment; Immunotherapy; Antiangiogenic therapy; COOCCURRING GENOMIC ALTERATIONS; PLATINUM-BASED CHEMOTHERAPY; MUTATION STATUS; PD-1; BLOCKADE; EXPRESSION; ADENOCARCINOMA; PEMBROLIZUMAB; DOCETAXEL; ONCOGENE; OUTCOMES;
D O I
10.1186/s12885-022-10236-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose For the first-line treatment of KRAS mutant non-small cell lung cancer (NSCLC) patients, immunotherapy or platinum-based chemotherapy are the main treatment method. Here, we investigated the clinical efficacy and prognosis those two regimens as first-line treatment in real-world practice. Methods KRAS mutant NSCLC patients received chemotherapy or immunotherapy as first-line treatment from September 2014 to March 2022 were enrolled. Clinical characteristics, treatment scheme, clinical curative effect and follow-up data of enrolled patients were collected for analysis. Results Fifty patients received immunotherapy and 115 patients received chemotherapy were enrolled. Patients who received immunotherapy (HR = 0.350, 95%CI 0.156-0.781, P = 0.010), or pemetrexed-based regimen (HR = 0.486, 95%CI 0.255-0.928, P = 0.029), or antiangiogenic therapy (HR = 0.355, 95%CI 0.159-0.790, P = 0.011) were at a low risk of disease progression. And patients received antiangiogenic therapy had lower risk of death than those not (HR = 0.333, 95%CI 0.120-0.926, P = 0.035). Subgroup analysis revealed the immunotherapy compared to chemotherapy alone had lower risk of disease progression (HR = 0.377, 95%CI 0.166-0.856, P = 0.020) in PD-L1 expression >= 1% subgroup. And in non-G12C KRAS subgroup, but not in G12C KRAS subgroup, patients who received antiangiogenic therapy had lower risk of disease progression (HR = 0.254, 95%CI 0.098-0.656, P = 0.005) and death than those not (HR = 0.197, 95%CI 0.056-0.692, P = 0.011). In terms of different chemotherapy regimen, platinum-paclitaxel combined with antiangiogenic therapy achieved the highest ORR and DCR (P < 0.05), while the platinum-pemetrexed combined with antiangiogenic therapy had the longest PFS and OS (P < 0.001). Conclusion For the first-line treatment of KRAS mutant NSCLC patients, immunotherapy, antiangiogenic therapy, and pemetrexed-based regimen could obtain more benefits. Subgroup analysis revealed the benefits of immunotherapy compared to chemotherapy were applicable in PD-L1 expression >= 1% subgroup, and antiangiogenic therapy could benefit non-G12C KRAS subgroup, but not G12C KRAS subgroup. In terms of different chemotherapy regimen, platinum-pemetrexed combined with antiangiogenic therapy may be the preferred chemotherapy regimen.
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页数:14
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