Miura Hiroyuki, Miura Jun, Goto Shinichi, Yamamoto Tomoko
Department of Thoracic Surgery Akiru Municipal Medical Centre Tokyo Japan.
Department of Surgery Kyorin University School of Medicine Tokyo Japan.
Respirol Case Rep. 2024 Aug 13;12(8):e70003. doi: 10.1002/rcr2.70003. eCollection 2024 Aug.
One of the resistant mechanisms of EGFR-TKIs is BRAF V600E mutation. Herein, we present the case of a 54-year-old Japanese female who underwent a right middle lobectomy for pathological stage IIB lung adenocarcinoma. One year and nine months after the surgery, she developed multiple intrapulmonary metastases. Osimertinib was administered due to EGFR exon 19 deletion. Although all intrapulmonary metastases had shrunk, the nodule at the superior segment of left lung enlarged after postoperative 4 years. The tumour was resected and BRAF V600E mutation and exon 19 deletion were detected. Three months after treatment with dabrafenib and trametinib instead of osimertinib, the remaining intrapulmonary metastases increased again. The continued growth of the metastatic foci even after EGFR-TKI may indicate an acquired resistance. Thus, a repeat biopsy will aid in confirming the new gene expression. It should have been necessary to administer an additional dose of dabrafenib and trametinib without discontinuing osimertinib.
EGFR-TKIs的耐药机制之一是BRAF V600E突变。在此,我们报告一例54岁日本女性病例,她因病理IIB期肺腺癌接受了右肺中叶切除术。术后一年零九个月,她出现了多发肺内转移。因EGFR外显子19缺失给予奥希替尼治疗。尽管所有肺内转移灶均缩小,但术后4年左肺上叶结节增大。该肿瘤被切除,检测到BRAF V600E突变和外显子19缺失。在用达拉非尼和曲美替尼替代奥希替尼治疗三个月后,剩余的肺内转移灶再次增大。即使在使用EGFR-TKI后转移灶仍持续生长,这可能表明出现了获得性耐药。因此,再次活检将有助于确认新的基因表达情况。本应在不停用奥希替尼的情况下加用一剂达拉非尼和曲美替尼。