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
