Coexistence of a secondary STRN–ALK, EML4–ALK double-fusion variant in a lung adenocarcinoma patient with EGFR mutation: a case report. Issue 8 (4th July 2021)
- Record Type:
- Journal Article
- Title:
- Coexistence of a secondary STRN–ALK, EML4–ALK double-fusion variant in a lung adenocarcinoma patient with EGFR mutation: a case report. Issue 8 (4th July 2021)
- Main Title:
- Coexistence of a secondary STRN–ALK, EML4–ALK double-fusion variant in a lung adenocarcinoma patient with EGFR mutation: a case report
- Authors:
- Zeng, Qian
Gao, Han
Zhang, Longdan
Qin, Shouming
Gu, Yongyao
Chen, Quanfang - Abstract:
- Abstract : ALK -positive disease is characterized by the presence of ALK gene rearrangements that encode driver fusion oncoproteins. EML4 – ALK fusion is regarded as the most common type in advanced nonsmall cell lung cancers. STRN–ALK is a novel ALK fusion partner in NSCLC and is considered sensitive to targeted therapy. However, there was no study regarding effective therapy for EML4–ALK and STRN – ALK double fusion variants in EGFR -resistant mutant lung cancer. TP53, RB1, and EGFR exon 21 L858R were found in tumor tissues and plasma from patients with capture-based NGS. After 3 months of gefitinib treatment, an NGS of plasma circulating tumor DNA showed that all variants disappeared significantly, and the tumor mass regressed on CT. However, after 10 months, the patient developed drug resistance and the disease progressed with the appearance of new metastatic lesions in the liver and bones. A repeated NGS test revealed EGFR exon20 T790M and the appearance of a novel double-fusion EML4–ALK and STRN–ALK . A combined therapeutic regimen of crizotinib plus osimertinib showed a promising prognosis confirmed with lung CT scans showing stable lesions without any new metastasis. Moreover, a subsequent genotype by NGS also showed the disappearance of STRN–ALK and EGFR exon20 T790M . The therapeutic efficacy of crizotinib plus osimertinib on EML4–ALK and STRN–ALK double-fusion variant in patients with EGFR -resistant mutant lung cancer may provide a supportive reference for theAbstract : ALK -positive disease is characterized by the presence of ALK gene rearrangements that encode driver fusion oncoproteins. EML4 – ALK fusion is regarded as the most common type in advanced nonsmall cell lung cancers. STRN–ALK is a novel ALK fusion partner in NSCLC and is considered sensitive to targeted therapy. However, there was no study regarding effective therapy for EML4–ALK and STRN – ALK double fusion variants in EGFR -resistant mutant lung cancer. TP53, RB1, and EGFR exon 21 L858R were found in tumor tissues and plasma from patients with capture-based NGS. After 3 months of gefitinib treatment, an NGS of plasma circulating tumor DNA showed that all variants disappeared significantly, and the tumor mass regressed on CT. However, after 10 months, the patient developed drug resistance and the disease progressed with the appearance of new metastatic lesions in the liver and bones. A repeated NGS test revealed EGFR exon20 T790M and the appearance of a novel double-fusion EML4–ALK and STRN–ALK . A combined therapeutic regimen of crizotinib plus osimertinib showed a promising prognosis confirmed with lung CT scans showing stable lesions without any new metastasis. Moreover, a subsequent genotype by NGS also showed the disappearance of STRN–ALK and EGFR exon20 T790M . The therapeutic efficacy of crizotinib plus osimertinib on EML4–ALK and STRN–ALK double-fusion variant in patients with EGFR -resistant mutant lung cancer may provide a supportive reference for the patients with such genetic alteration. … (more)
- Is Part Of:
- Anti-cancer drugs. Volume 32:Issue 8(2021)
- Journal:
- Anti-cancer drugs
- Issue:
- Volume 32:Issue 8(2021)
- Issue Display:
- Volume 32, Issue 8 (2021)
- Year:
- 2021
- Volume:
- 32
- Issue:
- 8
- Issue Sort Value:
- 2021-0032-0008-0000
- Page Start:
- 890
- Page End:
- 893
- Publication Date:
- 2021-07-04
- Subjects:
- crizotinib -- double-fusion -- EML4–ALK -- gefitinib -- osimertinib -- STRN–ALK
Antineoplastic agents -- Periodicals
Cancer -- Chemotherapy -- Periodicals
Antineoplastic Agents -- therapeutic use -- Periodicals
Drug Therapy -- Periodicals
616.994061 - Journal URLs:
- http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=yrovft&AN=00001813-000000000-00000 ↗
http://ovidsp.tx.ovid.com/spb/ovidweb.cgi ↗
http://www.anti-cancerdrugs.com/ ↗
http://journals.lww.com/pages/default.aspx ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1097/CAD.0000000000001094 ↗
- Languages:
- English
- ISSNs:
- 0959-4973
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1547.287300
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