Loading…
Response to a Combination of Full-Dose Osimertinib and Ceritinib in a Non-Small Cell Lung Cancer Patient with EML4-ALK Rearrangement and Epidermal Growth Factor Receptor Co-Mutation
Lung cancer has been the leading cause of cancer-related deaths in both developed and developing countries, with most primary lung cancers being non-small cell lung carcinomas. Treatment for this condition is sometimes individualized. With developments in modern treatment and phase III clinical tria...
Saved in:
Published in: | Case reports in oncology 2021-07, Vol.14 (2), p.1085-1091 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c529t-290446b290483cc33dc6cb75039753f2ce52bc68f5b9f98dbe343a1a8d7817d13 |
---|---|
cites | |
container_end_page | 1091 |
container_issue | 2 |
container_start_page | 1085 |
container_title | Case reports in oncology |
container_volume | 14 |
creator | Nguyen, Thai Hoa Thi Pham, Xuan Dung Dao, Khanh Linh Vo, Thanh Toan |
description | Lung cancer has been the leading cause of cancer-related deaths in both developed and developing countries, with most primary lung cancers being non-small cell lung carcinomas. Treatment for this condition is sometimes individualized. With developments in modern treatment and phase III clinical trial results, epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) and ALK-TKI have proven thier superior effectivity in comparison with the standard platinum-based doublet and are commonly approved as first-line indications in previously untreated advanced non-small cell lung cancer (NSCLC) patients with EGFR or ALK mutations. In the majority of cases, the presence of the ALK rearrangement mutation does not overlap with other mutations in NSCLC. Here, we report a patient with concomitant ALK rearrangement and EGFR mutation treated with a combination of TKIs: osimertinib and ceritinib. |
doi_str_mv | 10.1159/000516404 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1159_000516404</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_3ae8c74b71404ba0a951a8d30497a924</doaj_id><sourcerecordid>2570105852</sourcerecordid><originalsourceid>FETCH-LOGICAL-c529t-290446b290483cc33dc6cb75039753f2ce52bc68f5b9f98dbe343a1a8d7817d13</originalsourceid><addsrcrecordid>eNptksFu1DAQhiMEoqVw4M7BUk8cAnYcO_EFqQq7pSJl0QJna-I4qZfETp2Eigfj_XCaakUlLvbY_-_PnvFE0WuC3xHCxHuMMSM8xemT6JRwnsScZezpP_FJ9GIcDxhzwTh7Hp3QlCY8S_lp9Gevx8HZUaPJIUCF6ytjYTLOIteg7dx18UcX1N1oeu0nY02FwNao0N6sK2PDuS_Oxt966LoghKGcbYsKsEp79DXQtJ3QnZlu0Oa6TOOL8jPaa_AebKv7RVuIm8HU2gcGuvTuLni3oCbng1PpYQkKF1_P0_3bXkbPGuhG_ephPot-bDffi09xubu8Ki7KWLFETHEicJryaplyqhSlteKqyhimImO0SZRmSaV43rBKNCKvKx0KAwTyOstJVhN6Fl2t3NrBQQ7e9OB_SwdG3m8430oIRVGdlhR0rrK0ykj4hwowCLaAKE5FBiJJA-vDyhrmqte1Cnl76B5BHyvW3MjW_ZJ5IgQVy2POHwDe3c56nOTBzd6G_GXCMkwwy1kSXG9Xl_JuHL1ujjcQLJdukcduCd43q_cn-Fb7o_Mon_9XLva71SGHuqF_AXK9xak</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2570105852</pqid></control><display><type>article</type><title>Response to a Combination of Full-Dose Osimertinib and Ceritinib in a Non-Small Cell Lung Cancer Patient with EML4-ALK Rearrangement and Epidermal Growth Factor Receptor Co-Mutation</title><source>PubMed Central</source><source>Karger Open Access</source><creator>Nguyen, Thai Hoa Thi ; Pham, Xuan Dung ; Dao, Khanh Linh ; Vo, Thanh Toan</creator><creatorcontrib>Nguyen, Thai Hoa Thi ; Pham, Xuan Dung ; Dao, Khanh Linh ; Vo, Thanh Toan</creatorcontrib><description>Lung cancer has been the leading cause of cancer-related deaths in both developed and developing countries, with most primary lung cancers being non-small cell lung carcinomas. Treatment for this condition is sometimes individualized. With developments in modern treatment and phase III clinical trial results, epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) and ALK-TKI have proven thier superior effectivity in comparison with the standard platinum-based doublet and are commonly approved as first-line indications in previously untreated advanced non-small cell lung cancer (NSCLC) patients with EGFR or ALK mutations. In the majority of cases, the presence of the ALK rearrangement mutation does not overlap with other mutations in NSCLC. Here, we report a patient with concomitant ALK rearrangement and EGFR mutation treated with a combination of TKIs: osimertinib and ceritinib.</description><identifier>ISSN: 1662-6575</identifier><identifier>EISSN: 1662-6575</identifier><identifier>DOI: 10.1159/000516404</identifier><identifier>PMID: 34326746</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Abdomen ; Case Report ; Case reports ; ceritinib ; Chemotherapy ; Clinical trials ; Drug dosages ; Edema ; Epidermal growth factor ; Lung cancer ; Lymphatic system ; Magnetic resonance imaging ; Medical imaging ; Medical prognosis ; Metastasis ; Mutation ; non-small cell lung cancer ; osimertinib ; Pain ; Patients ; Pleural effusion ; Targeted cancer therapy ; Tomography ; Tumors ; tyrosine kinase inhibitors</subject><ispartof>Case reports in oncology, 2021-07, Vol.14 (2), p.1085-1091</ispartof><rights>2021 The Author(s). Published by S. Karger AG, Basel</rights><rights>2021 The Author(s). Published by S. Karger AG, Basel . This work is licensed under the Creative Commons Attribution – Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2021 by S. Karger AG, Basel 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-290446b290483cc33dc6cb75039753f2ce52bc68f5b9f98dbe343a1a8d7817d13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299391/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299391/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27612,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Nguyen, Thai Hoa Thi</creatorcontrib><creatorcontrib>Pham, Xuan Dung</creatorcontrib><creatorcontrib>Dao, Khanh Linh</creatorcontrib><creatorcontrib>Vo, Thanh Toan</creatorcontrib><title>Response to a Combination of Full-Dose Osimertinib and Ceritinib in a Non-Small Cell Lung Cancer Patient with EML4-ALK Rearrangement and Epidermal Growth Factor Receptor Co-Mutation</title><title>Case reports in oncology</title><addtitle>Case Rep Oncol</addtitle><description>Lung cancer has been the leading cause of cancer-related deaths in both developed and developing countries, with most primary lung cancers being non-small cell lung carcinomas. Treatment for this condition is sometimes individualized. With developments in modern treatment and phase III clinical trial results, epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) and ALK-TKI have proven thier superior effectivity in comparison with the standard platinum-based doublet and are commonly approved as first-line indications in previously untreated advanced non-small cell lung cancer (NSCLC) patients with EGFR or ALK mutations. In the majority of cases, the presence of the ALK rearrangement mutation does not overlap with other mutations in NSCLC. Here, we report a patient with concomitant ALK rearrangement and EGFR mutation treated with a combination of TKIs: osimertinib and ceritinib.</description><subject>Abdomen</subject><subject>Case Report</subject><subject>Case reports</subject><subject>ceritinib</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Drug dosages</subject><subject>Edema</subject><subject>Epidermal growth factor</subject><subject>Lung cancer</subject><subject>Lymphatic system</subject><subject>Magnetic resonance imaging</subject><subject>Medical imaging</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Mutation</subject><subject>non-small cell lung cancer</subject><subject>osimertinib</subject><subject>Pain</subject><subject>Patients</subject><subject>Pleural effusion</subject><subject>Targeted cancer therapy</subject><subject>Tomography</subject><subject>Tumors</subject><subject>tyrosine kinase inhibitors</subject><issn>1662-6575</issn><issn>1662-6575</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>M--</sourceid><sourceid>DOA</sourceid><recordid>eNptksFu1DAQhiMEoqVw4M7BUk8cAnYcO_EFqQq7pSJl0QJna-I4qZfETp2Eigfj_XCaakUlLvbY_-_PnvFE0WuC3xHCxHuMMSM8xemT6JRwnsScZezpP_FJ9GIcDxhzwTh7Hp3QlCY8S_lp9Gevx8HZUaPJIUCF6ytjYTLOIteg7dx18UcX1N1oeu0nY02FwNao0N6sK2PDuS_Oxt966LoghKGcbYsKsEp79DXQtJ3QnZlu0Oa6TOOL8jPaa_AebKv7RVuIm8HU2gcGuvTuLni3oCbng1PpYQkKF1_P0_3bXkbPGuhG_ephPot-bDffi09xubu8Ki7KWLFETHEicJryaplyqhSlteKqyhimImO0SZRmSaV43rBKNCKvKx0KAwTyOstJVhN6Fl2t3NrBQQ7e9OB_SwdG3m8430oIRVGdlhR0rrK0ykj4hwowCLaAKE5FBiJJA-vDyhrmqte1Cnl76B5BHyvW3MjW_ZJ5IgQVy2POHwDe3c56nOTBzd6G_GXCMkwwy1kSXG9Xl_JuHL1ujjcQLJdukcduCd43q_cn-Fb7o_Mon_9XLva71SGHuqF_AXK9xak</recordid><startdate>20210708</startdate><enddate>20210708</enddate><creator>Nguyen, Thai Hoa Thi</creator><creator>Pham, Xuan Dung</creator><creator>Dao, Khanh Linh</creator><creator>Vo, Thanh Toan</creator><general>S. Karger AG</general><general>Karger Publishers</general><scope>M--</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20210708</creationdate><title>Response to a Combination of Full-Dose Osimertinib and Ceritinib in a Non-Small Cell Lung Cancer Patient with EML4-ALK Rearrangement and Epidermal Growth Factor Receptor Co-Mutation</title><author>Nguyen, Thai Hoa Thi ; Pham, Xuan Dung ; Dao, Khanh Linh ; Vo, Thanh Toan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-290446b290483cc33dc6cb75039753f2ce52bc68f5b9f98dbe343a1a8d7817d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Abdomen</topic><topic>Case Report</topic><topic>Case reports</topic><topic>ceritinib</topic><topic>Chemotherapy</topic><topic>Clinical trials</topic><topic>Drug dosages</topic><topic>Edema</topic><topic>Epidermal growth factor</topic><topic>Lung cancer</topic><topic>Lymphatic system</topic><topic>Magnetic resonance imaging</topic><topic>Medical imaging</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Mutation</topic><topic>non-small cell lung cancer</topic><topic>osimertinib</topic><topic>Pain</topic><topic>Patients</topic><topic>Pleural effusion</topic><topic>Targeted cancer therapy</topic><topic>Tomography</topic><topic>Tumors</topic><topic>tyrosine kinase inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nguyen, Thai Hoa Thi</creatorcontrib><creatorcontrib>Pham, Xuan Dung</creatorcontrib><creatorcontrib>Dao, Khanh Linh</creatorcontrib><creatorcontrib>Vo, Thanh Toan</creatorcontrib><collection>Karger Open Access</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Case reports in oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nguyen, Thai Hoa Thi</au><au>Pham, Xuan Dung</au><au>Dao, Khanh Linh</au><au>Vo, Thanh Toan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Response to a Combination of Full-Dose Osimertinib and Ceritinib in a Non-Small Cell Lung Cancer Patient with EML4-ALK Rearrangement and Epidermal Growth Factor Receptor Co-Mutation</atitle><jtitle>Case reports in oncology</jtitle><addtitle>Case Rep Oncol</addtitle><date>2021-07-08</date><risdate>2021</risdate><volume>14</volume><issue>2</issue><spage>1085</spage><epage>1091</epage><pages>1085-1091</pages><issn>1662-6575</issn><eissn>1662-6575</eissn><abstract>Lung cancer has been the leading cause of cancer-related deaths in both developed and developing countries, with most primary lung cancers being non-small cell lung carcinomas. Treatment for this condition is sometimes individualized. With developments in modern treatment and phase III clinical trial results, epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) and ALK-TKI have proven thier superior effectivity in comparison with the standard platinum-based doublet and are commonly approved as first-line indications in previously untreated advanced non-small cell lung cancer (NSCLC) patients with EGFR or ALK mutations. In the majority of cases, the presence of the ALK rearrangement mutation does not overlap with other mutations in NSCLC. Here, we report a patient with concomitant ALK rearrangement and EGFR mutation treated with a combination of TKIs: osimertinib and ceritinib.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>34326746</pmid><doi>10.1159/000516404</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1662-6575 |
ispartof | Case reports in oncology, 2021-07, Vol.14 (2), p.1085-1091 |
issn | 1662-6575 1662-6575 |
language | eng |
recordid | cdi_crossref_primary_10_1159_000516404 |
source | PubMed Central; Karger Open Access |
subjects | Abdomen Case Report Case reports ceritinib Chemotherapy Clinical trials Drug dosages Edema Epidermal growth factor Lung cancer Lymphatic system Magnetic resonance imaging Medical imaging Medical prognosis Metastasis Mutation non-small cell lung cancer osimertinib Pain Patients Pleural effusion Targeted cancer therapy Tomography Tumors tyrosine kinase inhibitors |
title | Response to a Combination of Full-Dose Osimertinib and Ceritinib in a Non-Small Cell Lung Cancer Patient with EML4-ALK Rearrangement and Epidermal Growth Factor Receptor Co-Mutation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T16%3A17%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Response%20to%20a%20Combination%20of%20Full-Dose%20Osimertinib%20and%20Ceritinib%20in%20a%20Non-Small%20Cell%20Lung%20Cancer%20Patient%20with%20EML4-ALK%20Rearrangement%20and%20Epidermal%20Growth%20Factor%20Receptor%20Co-Mutation&rft.jtitle=Case%20reports%20in%20oncology&rft.au=Nguyen,%20Thai%20Hoa%20Thi&rft.date=2021-07-08&rft.volume=14&rft.issue=2&rft.spage=1085&rft.epage=1091&rft.pages=1085-1091&rft.issn=1662-6575&rft.eissn=1662-6575&rft_id=info:doi/10.1159/000516404&rft_dat=%3Cproquest_cross%3E2570105852%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c529t-290446b290483cc33dc6cb75039753f2ce52bc68f5b9f98dbe343a1a8d7817d13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2570105852&rft_id=info:pmid/34326746&rfr_iscdi=true |