Comprehensive molecular and clinical insights into non-small cell lung cancer transformation to small cell lung cancer with an illustrative case report

被引:2
|
作者
Tomic, Kresimir [1 ]
Krpina, Kristina [2 ]
Baticic, Lara [3 ]
Samarzija, Miroslav [2 ]
Vranic, Semir [4 ,5 ]
机构
[1] Univ Clin Hosp Mostar, Dept Oncol, Mostar, Bosnia & Herceg
[2] Univ Hosp Ctr Zagreb, Clin Resp Dis Jordanovac, Zagreb, Croatia
[3] Univ Rijeka, Fac Med, Dept Med Chem Biochem & Clin Chem, Rijeka, Croatia
[4] Qatar Univ, Coll Med, QU Hlth, Doha, Qatar
[5] Qatar Univ, Coll Med, Qu Hlth, Doha 2713, Qatar
关键词
Non-small cell lung cancer; epidermal growth factor receptor; tyrosine kinase inhibitors; immunotherapy; histologic transformation; small cell lung cancer; TYROSINE KINASE INHIBITORS; ACQUIRED-RESISTANCE; TKI THERAPY; ADENOCARCINOMA; OSIMERTINIB; CARCINOMA; IMMUNOTHERAPY; SUBTYPES; OUTCOMES;
D O I
10.1080/1061186X.2024.2332733
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Histologic transformation to small cell lung cancer (tSCLC) is a rare but increasingly recognised mechanism of acquired resistance to tyrosine kinase inhibitors (TKI) in patients with epidermal growth factor receptor (EGFR)-positive non-small cell lung cancer (NSCLC). Beyond its acknowledged role in TKI resistance, histologic transformation to SCLC might be an important, yet under-recognised, mechanism of resistance in NSCLC treated with immunotherapy. Our review identified 32 studies that investigated tSCLC development in patients with EGFR-mutated NSCLC treated with TKI therapy and 16 case reports of patients treated with immunotherapy. It revealed the rarity of tSCLC, with a predominance of EGFR exon 19 mutations and limited therapeutic options and outcomes. Across all analysed studies in EGFR-mutated NSCLC treated with TKI therapy, the median time to tSCLC development was similar to 17 months, with a median overall survival of 10 months. Histologic transformation of EGFR-mutated NSCLC to SCLC is a rare, but challenging clinical problem with a poor prognosis. A small number of documented cases of tSCLC after immunotherapy highlight the need for rebiopsies at progression to diagnose this potential resistance mechanism. Further research is needed to better understand the mechanisms underlying this phenomenon and to develop more effective treatment strategies for patients with tSCLC.
引用
收藏
页码:499 / 509
页数:11
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