Abstract 504P
Background
It is proved that anaplastic lymphoma kinase-rearranged non–small-cell lung cancer (ALK-rearranged NSCLC) is sensitive to ALK inhibitors while the chemotherapy resistance is unavoidable. In this study, safety and antitumor activity of the novel ALK inhibitor (ALKi) CT-707 is evaluated in Chinese patients with advanced ALK-rearranged NSCLC.
Methods
This Multi-center, open-label phase I study (NCT02695550) recruited adult patients with ALK-rearrangement (confirmed by fluorescence in situ hybridization and/or immunohistochemistry) of locally advanced/metastatic malignancies including non–small-cell lung cancer. This study consisted of a dose escalation study and a dose expansion study. CT-707 was administered orally once a day for 21 days. The Lung Cancer Center of Peking Union Medical College Hospital of Chinese Academy of Medical Sciences summarized the safety and effectiveness of the cases enrolled in this center.
Results
Thirteen patients who were treated with CT-707 from 450 to 600mg (in the dose increasing phase) were enrolled in this trial (two patients were previously treated with crizotinib). Twelve patients were diagnosed with lung adenocarcinoma and one patient was malignant pleural mesothelioma. After treatment, grade 3 diarrhea (600 mg QD) was found as dose-limiting toxicity (DLT). The most common adverse events included diarrhea (92%), elevated aspartate aminotransferase (61%), elevated alanine aminotransferase (54%), hair loss (38%), and vomiting (31%).ORR and disease control rate among patients were 10 of 13 (77%) and 11 of 13 (85%). The median progression-free survival was 13 months (95% CI:9.98-16.00).The overall survival rate of 12 months was 85%, which has not yet reached the median overall survival. Among all patients, ten patients observed partial response (PR). One patient reached a complete response (CR). However, no response of the disease was observed in patients with malignant pleural mesothelioma.
Conclusions
CT-707 is effective in Chinese patients with tumors harboring ALK rearrangements. It has reliable safety and tremendous clinical application value.
Clinical trial identification
NCT02695550; March 2016.
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
457P - The prevalence of vitamin D deficiency in Thai cancer patients, its dynamics and association with cancer survival
Presenter: Chavapon Ngokngarm
Session: Poster display session
Resources:
Abstract
458P - Mutation tracking in circulating tumour DNA predicts relapse in completely resected EGFR-mutated NSCLC
Presenter: Martin Filipits
Session: Poster display session
Resources:
Abstract
460P - Mendelian randomization study showed no causality between metformin use and lung cancer risk
Presenter: Jiayi Shen
Session: Poster display session
Resources:
Abstract
461P - Blood trace minerals and lung cancer: A Mendelian randomization study
Presenter: Wei Xian
Session: Poster display session
Resources:
Abstract
463P - Prediction of invasiveness in lung adenocarcinoma using machine learning algorithm based on 3D-CT imaging
Presenter: Yusuke Saeki
Session: Poster display session
Resources:
Abstract
459P - Fish intake, dietary polyunsaturated fatty acids, and lung cancer: systematic review and dose-response meta-analysis of 1.7 million men and women
Presenter: Chao Cao
Session: Poster display session
Resources:
Abstract
462P - Usefulness for prevention of postoperative cerebrovascular complications in patients with lung cancer using carotid ultrasonography
Presenter: Sadanori Takeo
Session: Poster display session
Resources:
Abstract
468P - Histological type analysis of 10-year follow-up of WJTOG0105: A phase III study comparing second- and third-generation regimens with concurrent thoracic radiotherapy in unresectable stage III non-small cell lung cancer
Presenter: Masahiro Tsuboi
Session: Poster display session
Resources:
Abstract
469P - Comparison of combined chemoradiotherapy regimens; Paclitaxel plus carboplatin and cisplatin plus etoposide for locally advanced non-small cell lung cancer: A randomised phase III trial
Presenter: Alper Ata
Session: Poster display session
Resources:
Abstract
472P - Integration of expression rate and absolute cell counts of PD-1+ stromal tumour-infiltrating lymphocytes: Prognostic significance in esophageal squamous cell carcinoma
Presenter: Qingkun Song
Session: Poster display session
Resources:
Abstract