Di Marino Pietro, Chiapperino Cosima, Primavera Francesca Chiara, Martino Maria Teresa, Brocco Davide, Carella Consiglia, Grassadonia Antonino, Tinari Nicola, De Tursi Michele
Clinical Oncology Unit, SS Annunziata Hospital, Chieti, Italy.
Department of Pharmacy, University G. D'Annunzio, Chieti- Pescara, Italy.
Onco Targets Ther. 2022 Apr 11;15:407-410. doi: 10.2147/OTT.S315385. eCollection 2022.
Osimertinib is an irreversible tyrosine kinase inhibitor approved for the treatment of metastatic epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC). In clinical trials, osimertinib has exhibited excellent activity and less toxicity compared to gefitinib, erlotinib and standard chemotherapy.
Herein, we describe the case of a 69-year-old man who received first-line osimertinib for metastatic EGFR-mutated NSCLC. Suspected osimertinib-induced pancytopenia together with a partial treatment response was assessed after 10 days of therapy. Osimertinib was resumed at 40 mg daily a month later while the patient exhibited durable stable disease. No other adverse events occurred.
In the current case, first-line treatment with osimertinib at 80 mg daily in a patient with EGFR-mutated NSCLC resulted in severe pancytopenia and a rapid treatment response. Dose reduction to 40 mg daily resulted in excellent activity without any further adverse events. Osimertinib could be safely resumed at a reduced dose even after pancytopenia.
奥希替尼是一种不可逆的酪氨酸激酶抑制剂,被批准用于治疗转移性表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)。在临床试验中,与吉非替尼、厄洛替尼和标准化疗相比,奥希替尼表现出优异的活性和较低的毒性。
在此,我们描述了一名69岁男性的病例,他接受一线奥希替尼治疗转移性EGFR突变的NSCLC。治疗10天后评估了疑似奥希替尼引起的全血细胞减少以及部分治疗反应。一个月后,患者病情持续稳定,奥希替尼以每日40 mg的剂量恢复使用。未发生其他不良事件。
在当前病例中,EGFR突变的NSCLC患者每日80 mg一线使用奥希替尼导致严重全血细胞减少和快速治疗反应。剂量减至每日40 mg导致优异的活性且无任何进一步不良事件。即使在出现全血细胞减少后,奥希替尼也可以安全地以降低的剂量恢复使用。