论文已发表
注册即可获取德孚的最新动态
IF 收录期刊
Authors Song P, Zhang J, Zhang L
Received 28 January 2019
Accepted for publication 12 March 2019
Published 17 April 2019 Volume 2019:12 Pages 2943—2948
DOI https://doi.org/10.2147/OTT.S203192
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Ms Aruna Narula
Peer reviewer comments 2
Editor who approved publication: Dr Tohru Yamada
Abstract: In this case report, we describe a
tortuous, yet rare, treatment process of the patient. The first biopsy of the
patient suggested inflammatory myofibroblastic tumor, ALK (D5F3) positive.
Considering the benign progression of the disease, and no indication for
surgical resection, oral prednisone was given first. However, the disease
rapidly progressed, and a second biopsy revealed a pulmonary sarcomatoid
cancer. Since the biopsy was ALK (D5F3) positive, the effect of crizotinib
treatment was significant, though crizotinib resistance unfortunately only
occurred after 4 months. The third biopsy pathology was performed and
confirmed lung adenocarcinoma. After switching to pembrolizumab treatment, the
lesions were significantly reduced after four courses of treatment. The current
condition of patient persisted in partial response.
Keywords: sequential
biopsies, EML4-ALK, immunotherapy, lung adenocarcinoma
摘要视频链接:Immunotherapy for ALK lung cancer