Does Pemetrexed Work in Targetable, Nonsquamous Non-Small-Cell Lung Cancer? A Narrative Review

被引:11
|
作者
Shih, Jin-Yuan [1 ,2 ]
Inoue, Akira [3 ]
Cheng, Rebecca [4 ]
Varea, Rocio [4 ]
Kim, Sang-We [5 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Internal Med, 7 Zhongshan South Rd, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Grad Inst Clin Med, 7 Chung Shan S Rd, Taipei 100, Taiwan
[3] Tohoku Univ, Dept Palliat Med, Sch Med, Aoba Ku, 2-1 Seiryo Machi, Sendai, Miyagi 9808575, Japan
[4] Eli Lilly & Co, Fuxing North Rd 365, Taipei 105, Taiwan
[5] Asan Med Ctr, Dept Oncol, 88 Olymp Ro 43 Gil, Seoul 05505, South Korea
关键词
non-small-cell lung cancer; gain of function mutation; chemotherapy; pemetrexed; progression-free survival; RANDOMIZED PHASE-II; 1ST-LINE TREATMENT; CLINICAL-OUTCOMES; EGFR MUTATION; OPEN-LABEL; ADENOCARCINOMA PATIENTS; ROS1; REARRANGEMENT; PLUS CISPLATIN; CHEMOTHERAPY; ALK;
D O I
10.3390/cancers12092658
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary The chemotherapy agent pemetrexed is currently considered in combination with other therapies for the treatment of advanced nonsquamous non-small-cell lung cancer (NSCLC) in patients negative for gene mutations/rearrangements. The aim of this review was to highlight data from clinical studies with pemetrexed in patients with advanced nonsquamous NSCLC positive for gene mutations/rearrangements. The results of the review suggest that pemetrexed could be a treatment option in patients with advanced nonsquamous NSCLC positive for certain gene mutations/rearrangements. Pemetrexed is currently mainly considered for the treatment of advanced nonsquamous non-small-cell lung cancer (NSCLC) negative for gene mutations/rearrangements (wild-type disease (WTD)). This narrative review aimed to highlight the role of pemetrexed in the treatment of onco-driven nonsquamous advanced NSCLC by reviewing published clinical studies. For epidermal growth factor receptor (EGFR) mutations, patient survival following first-line pemetrexed-platinum was longer than for WTD. Later-line pemetrexed-based treatment after tyrosine kinase inhibitor (TKI) failure provided greater benefits than non-pemetrexed regimens. First- and later-line pemetrexed-based therapy also provided survival benefits in patients with anaplastic lymphoma kinase (ALK) or ROS proto-oncogene 1 (ROS1) rearrangements. In patients with rearranged during transfection (RET) proto-oncogene rearrangements, survival with pemetrexed was similar to that in ALK- and ROS1-positive patients and longer than that in patients with Kirsten rat sarcoma (KRAS) virus proto-oncogene mutations or WTD, although the available studies were limited. For Erb-b2 receptor tyrosine kinase 2 (ERRB2) mutations, first-line pemetrexed showed outcomes similar to those for EGFR and KRAS alterations. Data on pemetrexed in patients with KRAS mutations or MNNG HOS-transforming (MET) expression were limited. Pemetrexed could be an option for first- and second-line treatment for TKI failure in nonsquamous advanced NSCLC with select targetable driver mutations.
引用
收藏
页码:1 / 18
页数:18
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