Sotorasib in KRAS G12C-mutated non-small cell lung cancer: A multicenter real-world experience from the compassionate use program in Germany

Sotorasib is a first-in-class KRAS p.G12C-inhibitor that has entered clinical trials in pretreated patients with non-small cell lung cancer (NSCLC) in 2018. First response rates were promising in the CodeBreaK trials. It remains unclear whether response to sotorasib and outcomes differ in a real-wor...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of cancer (1990) 2024-04, Vol.201, p.113911-113911, Article 113911
Hauptverfasser: Stratmann, Jan A., Althoff, Friederike C., Doebel, Paula, Rauh, Jacqueline, Trummer, Arne, Hünerlitürkoglu, Ali Nuri, Frost, Nikolaj, Yildirim, Hüsameddin, Christopoulos, Petros, Burkhard, Oswald, Büschenfelde, Christian Meyer zum, Becker von Rose, Aaron, Alt, Jürgen, Aries, Sven P., Webendörfer, Maximilian, Kaldune, Stefan, Uhlenbruch, Mark, Tritchkova, Guergana, Waller, Cornelius F., Rittmeyer, Achim, Hoffknecht, Petra, Braess, Jan, Kopp, Hans-Georg, Grohé, Christian, Schäfer, Monica, Schumann, Christian, Griesinger, Frank, Kuon, Jonas, Sebastian, Martin, Reinmuth, Niels
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 113911
container_issue
container_start_page 113911
container_title European journal of cancer (1990)
container_volume 201
creator Stratmann, Jan A.
Althoff, Friederike C.
Doebel, Paula
Rauh, Jacqueline
Trummer, Arne
Hünerlitürkoglu, Ali Nuri
Frost, Nikolaj
Yildirim, Hüsameddin
Christopoulos, Petros
Burkhard, Oswald
Büschenfelde, Christian Meyer zum
Becker von Rose, Aaron
Alt, Jürgen
Aries, Sven P.
Webendörfer, Maximilian
Kaldune, Stefan
Uhlenbruch, Mark
Tritchkova, Guergana
Waller, Cornelius F.
Rittmeyer, Achim
Hoffknecht, Petra
Braess, Jan
Kopp, Hans-Georg
Grohé, Christian
Schäfer, Monica
Schumann, Christian
Griesinger, Frank
Kuon, Jonas
Sebastian, Martin
Reinmuth, Niels
description Sotorasib is a first-in-class KRAS p.G12C-inhibitor that has entered clinical trials in pretreated patients with non-small cell lung cancer (NSCLC) in 2018. First response rates were promising in the CodeBreaK trials. It remains unclear whether response to sotorasib and outcomes differ in a real-world setting when including patients underrepresented in clinical trials. Patients with KRAS p.G12C-mutated advanced or metastatic NSCLC received sotorasib within the German multicenter sotorasib compassionate use program between 2020 to 2022. Data on efficacy, tolerability, and survival were analyzed in the full cohort and in subgroups of special interest such as co-occurring mutations and across PD-L1 expression levels. We analyzed 163 patients who received sotorasib after a median of two treatment lines (range, 0 to 7). Every fourth patient had a poor performance status and 38% had brain metastases (BM). The objective response rate was 38.7%. The median overall survival was 9.8 months (95% CI, 6.5 to not reached). Median real-world (rw) progression-free survival was 4.8 months (9% CI, 3.9 to 5.9). Dose reductions and permanent discontinuation were necessary in 35 (21.5%) and 7 (4.3%) patients, respectively. Efficacy seems to be influenced by PD-L1 expression and a co-occurring KEAP1 mutation. KEAP1 was associated with an inferior survival. Other factors such as BM, STK11, and TP53 mutations had no impact on response and survival. First results from a real-world population confirm promising efficacy of sotorasib for the treatment of advanced KRAS p.G12C-mutated NSCLC. Patients with co-occurring KEAP1 mutations seem to derive less benefit. •Sotorasib showed promising efficacy in heavily pretreated real-world patients.•ECOG, brain metastases, STK11- and TP53-mutations had no impact on the ORR.•Patients with a co-occurring KEAP1-mutation derive less benefit.•Sotorasib may have initial intracranial activity, albeit only for a short time.
doi_str_mv 10.1016/j.ejca.2024.113911
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2929541566</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S095980492400087X</els_id><sourcerecordid>2929541566</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-d9749722d811bf6970c33661cc336b48ed836eaa91967560cc92c60e54baa7e83</originalsourceid><addsrcrecordid>eNp9kc9u1DAQxi1ERZfCC3BAPnLJYjuOYyMuqxUsiEqVWjhbjjNbvIrtxXYofQceGoctHDuHmctvvvnzIfSKkjUlVLw9rOFgzZoRxteUtorSJ2hFZa8aIjv2FK2I6lQjCVfn6HnOB0JILzl5hs5b2fY1-Ar9voklJpPdgF3AX643N3hH2bbxczEFRhxiaLI304Qt1DTN4RZbEyykd3iD_TwVZyEUSDiBmZq7mKYRw68jJAeVwvsUPS7fAdvojyZnF0PVxXMGfEzxNhm_zN1B8ibcv0BnezNlePlQL9C3jx--bj81l1e7z9vNZWM5IaUZVc9Vz9goKR32QvXEtq0Q1C5l4BJG2QowRlEl-k4QaxWzgkDHB2N6kO0FenPSrSv8mCEX7V1e7jMB4pw1U0x1nHZCVJSdUJtizgn2-picN-leU6IXF_RBLy7oxQV9cqE2vX7QnwcP4_-Wf2-vwPsTAPXKnw6Szvbvv0aXwBY9RveY_h8vs5kO</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2929541566</pqid></control><display><type>article</type><title>Sotorasib in KRAS G12C-mutated non-small cell lung cancer: A multicenter real-world experience from the compassionate use program in Germany</title><source>Elsevier ScienceDirect Journals</source><creator>Stratmann, Jan A. ; Althoff, Friederike C. ; Doebel, Paula ; Rauh, Jacqueline ; Trummer, Arne ; Hünerlitürkoglu, Ali Nuri ; Frost, Nikolaj ; Yildirim, Hüsameddin ; Christopoulos, Petros ; Burkhard, Oswald ; Büschenfelde, Christian Meyer zum ; Becker von Rose, Aaron ; Alt, Jürgen ; Aries, Sven P. ; Webendörfer, Maximilian ; Kaldune, Stefan ; Uhlenbruch, Mark ; Tritchkova, Guergana ; Waller, Cornelius F. ; Rittmeyer, Achim ; Hoffknecht, Petra ; Braess, Jan ; Kopp, Hans-Georg ; Grohé, Christian ; Schäfer, Monica ; Schumann, Christian ; Griesinger, Frank ; Kuon, Jonas ; Sebastian, Martin ; Reinmuth, Niels</creator><creatorcontrib>Stratmann, Jan A. ; Althoff, Friederike C. ; Doebel, Paula ; Rauh, Jacqueline ; Trummer, Arne ; Hünerlitürkoglu, Ali Nuri ; Frost, Nikolaj ; Yildirim, Hüsameddin ; Christopoulos, Petros ; Burkhard, Oswald ; Büschenfelde, Christian Meyer zum ; Becker von Rose, Aaron ; Alt, Jürgen ; Aries, Sven P. ; Webendörfer, Maximilian ; Kaldune, Stefan ; Uhlenbruch, Mark ; Tritchkova, Guergana ; Waller, Cornelius F. ; Rittmeyer, Achim ; Hoffknecht, Petra ; Braess, Jan ; Kopp, Hans-Georg ; Grohé, Christian ; Schäfer, Monica ; Schumann, Christian ; Griesinger, Frank ; Kuon, Jonas ; Sebastian, Martin ; Reinmuth, Niels</creatorcontrib><description>Sotorasib is a first-in-class KRAS p.G12C-inhibitor that has entered clinical trials in pretreated patients with non-small cell lung cancer (NSCLC) in 2018. First response rates were promising in the CodeBreaK trials. It remains unclear whether response to sotorasib and outcomes differ in a real-world setting when including patients underrepresented in clinical trials. Patients with KRAS p.G12C-mutated advanced or metastatic NSCLC received sotorasib within the German multicenter sotorasib compassionate use program between 2020 to 2022. Data on efficacy, tolerability, and survival were analyzed in the full cohort and in subgroups of special interest such as co-occurring mutations and across PD-L1 expression levels. We analyzed 163 patients who received sotorasib after a median of two treatment lines (range, 0 to 7). Every fourth patient had a poor performance status and 38% had brain metastases (BM). The objective response rate was 38.7%. The median overall survival was 9.8 months (95% CI, 6.5 to not reached). Median real-world (rw) progression-free survival was 4.8 months (9% CI, 3.9 to 5.9). Dose reductions and permanent discontinuation were necessary in 35 (21.5%) and 7 (4.3%) patients, respectively. Efficacy seems to be influenced by PD-L1 expression and a co-occurring KEAP1 mutation. KEAP1 was associated with an inferior survival. Other factors such as BM, STK11, and TP53 mutations had no impact on response and survival. First results from a real-world population confirm promising efficacy of sotorasib for the treatment of advanced KRAS p.G12C-mutated NSCLC. Patients with co-occurring KEAP1 mutations seem to derive less benefit. •Sotorasib showed promising efficacy in heavily pretreated real-world patients.•ECOG, brain metastases, STK11- and TP53-mutations had no impact on the ORR.•Patients with a co-occurring KEAP1-mutation derive less benefit.•Sotorasib may have initial intracranial activity, albeit only for a short time.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2024.113911</identifier><identifier>PMID: 38377774</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Further-line treatment ; KRAS G12C ; NSCLC ; Sotorasib ; Targeted therapy</subject><ispartof>European journal of cancer (1990), 2024-04, Vol.201, p.113911-113911, Article 113911</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-d9749722d811bf6970c33661cc336b48ed836eaa91967560cc92c60e54baa7e83</citedby><cites>FETCH-LOGICAL-c400t-d9749722d811bf6970c33661cc336b48ed836eaa91967560cc92c60e54baa7e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S095980492400087X$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38377774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stratmann, Jan A.</creatorcontrib><creatorcontrib>Althoff, Friederike C.</creatorcontrib><creatorcontrib>Doebel, Paula</creatorcontrib><creatorcontrib>Rauh, Jacqueline</creatorcontrib><creatorcontrib>Trummer, Arne</creatorcontrib><creatorcontrib>Hünerlitürkoglu, Ali Nuri</creatorcontrib><creatorcontrib>Frost, Nikolaj</creatorcontrib><creatorcontrib>Yildirim, Hüsameddin</creatorcontrib><creatorcontrib>Christopoulos, Petros</creatorcontrib><creatorcontrib>Burkhard, Oswald</creatorcontrib><creatorcontrib>Büschenfelde, Christian Meyer zum</creatorcontrib><creatorcontrib>Becker von Rose, Aaron</creatorcontrib><creatorcontrib>Alt, Jürgen</creatorcontrib><creatorcontrib>Aries, Sven P.</creatorcontrib><creatorcontrib>Webendörfer, Maximilian</creatorcontrib><creatorcontrib>Kaldune, Stefan</creatorcontrib><creatorcontrib>Uhlenbruch, Mark</creatorcontrib><creatorcontrib>Tritchkova, Guergana</creatorcontrib><creatorcontrib>Waller, Cornelius F.</creatorcontrib><creatorcontrib>Rittmeyer, Achim</creatorcontrib><creatorcontrib>Hoffknecht, Petra</creatorcontrib><creatorcontrib>Braess, Jan</creatorcontrib><creatorcontrib>Kopp, Hans-Georg</creatorcontrib><creatorcontrib>Grohé, Christian</creatorcontrib><creatorcontrib>Schäfer, Monica</creatorcontrib><creatorcontrib>Schumann, Christian</creatorcontrib><creatorcontrib>Griesinger, Frank</creatorcontrib><creatorcontrib>Kuon, Jonas</creatorcontrib><creatorcontrib>Sebastian, Martin</creatorcontrib><creatorcontrib>Reinmuth, Niels</creatorcontrib><title>Sotorasib in KRAS G12C-mutated non-small cell lung cancer: A multicenter real-world experience from the compassionate use program in Germany</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>Sotorasib is a first-in-class KRAS p.G12C-inhibitor that has entered clinical trials in pretreated patients with non-small cell lung cancer (NSCLC) in 2018. First response rates were promising in the CodeBreaK trials. It remains unclear whether response to sotorasib and outcomes differ in a real-world setting when including patients underrepresented in clinical trials. Patients with KRAS p.G12C-mutated advanced or metastatic NSCLC received sotorasib within the German multicenter sotorasib compassionate use program between 2020 to 2022. Data on efficacy, tolerability, and survival were analyzed in the full cohort and in subgroups of special interest such as co-occurring mutations and across PD-L1 expression levels. We analyzed 163 patients who received sotorasib after a median of two treatment lines (range, 0 to 7). Every fourth patient had a poor performance status and 38% had brain metastases (BM). The objective response rate was 38.7%. The median overall survival was 9.8 months (95% CI, 6.5 to not reached). Median real-world (rw) progression-free survival was 4.8 months (9% CI, 3.9 to 5.9). Dose reductions and permanent discontinuation were necessary in 35 (21.5%) and 7 (4.3%) patients, respectively. Efficacy seems to be influenced by PD-L1 expression and a co-occurring KEAP1 mutation. KEAP1 was associated with an inferior survival. Other factors such as BM, STK11, and TP53 mutations had no impact on response and survival. First results from a real-world population confirm promising efficacy of sotorasib for the treatment of advanced KRAS p.G12C-mutated NSCLC. Patients with co-occurring KEAP1 mutations seem to derive less benefit. •Sotorasib showed promising efficacy in heavily pretreated real-world patients.•ECOG, brain metastases, STK11- and TP53-mutations had no impact on the ORR.•Patients with a co-occurring KEAP1-mutation derive less benefit.•Sotorasib may have initial intracranial activity, albeit only for a short time.</description><subject>Further-line treatment</subject><subject>KRAS G12C</subject><subject>NSCLC</subject><subject>Sotorasib</subject><subject>Targeted therapy</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kc9u1DAQxi1ERZfCC3BAPnLJYjuOYyMuqxUsiEqVWjhbjjNbvIrtxXYofQceGoctHDuHmctvvvnzIfSKkjUlVLw9rOFgzZoRxteUtorSJ2hFZa8aIjv2FK2I6lQjCVfn6HnOB0JILzl5hs5b2fY1-Ar9voklJpPdgF3AX643N3hH2bbxczEFRhxiaLI304Qt1DTN4RZbEyykd3iD_TwVZyEUSDiBmZq7mKYRw68jJAeVwvsUPS7fAdvojyZnF0PVxXMGfEzxNhm_zN1B8ibcv0BnezNlePlQL9C3jx--bj81l1e7z9vNZWM5IaUZVc9Vz9goKR32QvXEtq0Q1C5l4BJG2QowRlEl-k4QaxWzgkDHB2N6kO0FenPSrSv8mCEX7V1e7jMB4pw1U0x1nHZCVJSdUJtizgn2-picN-leU6IXF_RBLy7oxQV9cqE2vX7QnwcP4_-Wf2-vwPsTAPXKnw6Szvbvv0aXwBY9RveY_h8vs5kO</recordid><startdate>202404</startdate><enddate>202404</enddate><creator>Stratmann, Jan A.</creator><creator>Althoff, Friederike C.</creator><creator>Doebel, Paula</creator><creator>Rauh, Jacqueline</creator><creator>Trummer, Arne</creator><creator>Hünerlitürkoglu, Ali Nuri</creator><creator>Frost, Nikolaj</creator><creator>Yildirim, Hüsameddin</creator><creator>Christopoulos, Petros</creator><creator>Burkhard, Oswald</creator><creator>Büschenfelde, Christian Meyer zum</creator><creator>Becker von Rose, Aaron</creator><creator>Alt, Jürgen</creator><creator>Aries, Sven P.</creator><creator>Webendörfer, Maximilian</creator><creator>Kaldune, Stefan</creator><creator>Uhlenbruch, Mark</creator><creator>Tritchkova, Guergana</creator><creator>Waller, Cornelius F.</creator><creator>Rittmeyer, Achim</creator><creator>Hoffknecht, Petra</creator><creator>Braess, Jan</creator><creator>Kopp, Hans-Georg</creator><creator>Grohé, Christian</creator><creator>Schäfer, Monica</creator><creator>Schumann, Christian</creator><creator>Griesinger, Frank</creator><creator>Kuon, Jonas</creator><creator>Sebastian, Martin</creator><creator>Reinmuth, Niels</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202404</creationdate><title>Sotorasib in KRAS G12C-mutated non-small cell lung cancer: A multicenter real-world experience from the compassionate use program in Germany</title><author>Stratmann, Jan A. ; Althoff, Friederike C. ; Doebel, Paula ; Rauh, Jacqueline ; Trummer, Arne ; Hünerlitürkoglu, Ali Nuri ; Frost, Nikolaj ; Yildirim, Hüsameddin ; Christopoulos, Petros ; Burkhard, Oswald ; Büschenfelde, Christian Meyer zum ; Becker von Rose, Aaron ; Alt, Jürgen ; Aries, Sven P. ; Webendörfer, Maximilian ; Kaldune, Stefan ; Uhlenbruch, Mark ; Tritchkova, Guergana ; Waller, Cornelius F. ; Rittmeyer, Achim ; Hoffknecht, Petra ; Braess, Jan ; Kopp, Hans-Georg ; Grohé, Christian ; Schäfer, Monica ; Schumann, Christian ; Griesinger, Frank ; Kuon, Jonas ; Sebastian, Martin ; Reinmuth, Niels</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-d9749722d811bf6970c33661cc336b48ed836eaa91967560cc92c60e54baa7e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Further-line treatment</topic><topic>KRAS G12C</topic><topic>NSCLC</topic><topic>Sotorasib</topic><topic>Targeted therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stratmann, Jan A.</creatorcontrib><creatorcontrib>Althoff, Friederike C.</creatorcontrib><creatorcontrib>Doebel, Paula</creatorcontrib><creatorcontrib>Rauh, Jacqueline</creatorcontrib><creatorcontrib>Trummer, Arne</creatorcontrib><creatorcontrib>Hünerlitürkoglu, Ali Nuri</creatorcontrib><creatorcontrib>Frost, Nikolaj</creatorcontrib><creatorcontrib>Yildirim, Hüsameddin</creatorcontrib><creatorcontrib>Christopoulos, Petros</creatorcontrib><creatorcontrib>Burkhard, Oswald</creatorcontrib><creatorcontrib>Büschenfelde, Christian Meyer zum</creatorcontrib><creatorcontrib>Becker von Rose, Aaron</creatorcontrib><creatorcontrib>Alt, Jürgen</creatorcontrib><creatorcontrib>Aries, Sven P.</creatorcontrib><creatorcontrib>Webendörfer, Maximilian</creatorcontrib><creatorcontrib>Kaldune, Stefan</creatorcontrib><creatorcontrib>Uhlenbruch, Mark</creatorcontrib><creatorcontrib>Tritchkova, Guergana</creatorcontrib><creatorcontrib>Waller, Cornelius F.</creatorcontrib><creatorcontrib>Rittmeyer, Achim</creatorcontrib><creatorcontrib>Hoffknecht, Petra</creatorcontrib><creatorcontrib>Braess, Jan</creatorcontrib><creatorcontrib>Kopp, Hans-Georg</creatorcontrib><creatorcontrib>Grohé, Christian</creatorcontrib><creatorcontrib>Schäfer, Monica</creatorcontrib><creatorcontrib>Schumann, Christian</creatorcontrib><creatorcontrib>Griesinger, Frank</creatorcontrib><creatorcontrib>Kuon, Jonas</creatorcontrib><creatorcontrib>Sebastian, Martin</creatorcontrib><creatorcontrib>Reinmuth, Niels</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stratmann, Jan A.</au><au>Althoff, Friederike C.</au><au>Doebel, Paula</au><au>Rauh, Jacqueline</au><au>Trummer, Arne</au><au>Hünerlitürkoglu, Ali Nuri</au><au>Frost, Nikolaj</au><au>Yildirim, Hüsameddin</au><au>Christopoulos, Petros</au><au>Burkhard, Oswald</au><au>Büschenfelde, Christian Meyer zum</au><au>Becker von Rose, Aaron</au><au>Alt, Jürgen</au><au>Aries, Sven P.</au><au>Webendörfer, Maximilian</au><au>Kaldune, Stefan</au><au>Uhlenbruch, Mark</au><au>Tritchkova, Guergana</au><au>Waller, Cornelius F.</au><au>Rittmeyer, Achim</au><au>Hoffknecht, Petra</au><au>Braess, Jan</au><au>Kopp, Hans-Georg</au><au>Grohé, Christian</au><au>Schäfer, Monica</au><au>Schumann, Christian</au><au>Griesinger, Frank</au><au>Kuon, Jonas</au><au>Sebastian, Martin</au><au>Reinmuth, Niels</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sotorasib in KRAS G12C-mutated non-small cell lung cancer: A multicenter real-world experience from the compassionate use program in Germany</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2024-04</date><risdate>2024</risdate><volume>201</volume><spage>113911</spage><epage>113911</epage><pages>113911-113911</pages><artnum>113911</artnum><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>Sotorasib is a first-in-class KRAS p.G12C-inhibitor that has entered clinical trials in pretreated patients with non-small cell lung cancer (NSCLC) in 2018. First response rates were promising in the CodeBreaK trials. It remains unclear whether response to sotorasib and outcomes differ in a real-world setting when including patients underrepresented in clinical trials. Patients with KRAS p.G12C-mutated advanced or metastatic NSCLC received sotorasib within the German multicenter sotorasib compassionate use program between 2020 to 2022. Data on efficacy, tolerability, and survival were analyzed in the full cohort and in subgroups of special interest such as co-occurring mutations and across PD-L1 expression levels. We analyzed 163 patients who received sotorasib after a median of two treatment lines (range, 0 to 7). Every fourth patient had a poor performance status and 38% had brain metastases (BM). The objective response rate was 38.7%. The median overall survival was 9.8 months (95% CI, 6.5 to not reached). Median real-world (rw) progression-free survival was 4.8 months (9% CI, 3.9 to 5.9). Dose reductions and permanent discontinuation were necessary in 35 (21.5%) and 7 (4.3%) patients, respectively. Efficacy seems to be influenced by PD-L1 expression and a co-occurring KEAP1 mutation. KEAP1 was associated with an inferior survival. Other factors such as BM, STK11, and TP53 mutations had no impact on response and survival. First results from a real-world population confirm promising efficacy of sotorasib for the treatment of advanced KRAS p.G12C-mutated NSCLC. Patients with co-occurring KEAP1 mutations seem to derive less benefit. •Sotorasib showed promising efficacy in heavily pretreated real-world patients.•ECOG, brain metastases, STK11- and TP53-mutations had no impact on the ORR.•Patients with a co-occurring KEAP1-mutation derive less benefit.•Sotorasib may have initial intracranial activity, albeit only for a short time.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>38377774</pmid><doi>10.1016/j.ejca.2024.113911</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0959-8049
ispartof European journal of cancer (1990), 2024-04, Vol.201, p.113911-113911, Article 113911
issn 0959-8049
1879-0852
language eng
recordid cdi_proquest_miscellaneous_2929541566
source Elsevier ScienceDirect Journals
subjects Further-line treatment
KRAS G12C
NSCLC
Sotorasib
Targeted therapy
title Sotorasib in KRAS G12C-mutated non-small cell lung cancer: A multicenter real-world experience from the compassionate use program in Germany
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T06%3A34%3A40IST&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=Sotorasib%20in%20KRAS%20G12C-mutated%20non-small%20cell%20lung%20cancer:%20A%20multicenter%20real-world%20experience%20from%20the%20compassionate%20use%20program%20in%20Germany&rft.jtitle=European%20journal%20of%20cancer%20(1990)&rft.au=Stratmann,%20Jan%20A.&rft.date=2024-04&rft.volume=201&rft.spage=113911&rft.epage=113911&rft.pages=113911-113911&rft.artnum=113911&rft.issn=0959-8049&rft.eissn=1879-0852&rft_id=info:doi/10.1016/j.ejca.2024.113911&rft_dat=%3Cproquest_cross%3E2929541566%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2929541566&rft_id=info:pmid/38377774&rft_els_id=S095980492400087X&rfr_iscdi=true