Serum CA19-9 Response Is an Early Predictive Marker of Efficacy of Regorafenib in Refractory Metastatic Colorectal Cancer

Purpose: Regorafenib improves survival in chemorefractory metastatic colorectal cancer (mCRC) patients. However, regorafenib induces various adverse events (AEs) that often impair patients' quality of life. Identification of early predictive markers of the efficacy is warranted. Methods: We ret...

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Veröffentlicht in:Oncology 2017-01, Vol.93 (5), p.329-335
Hauptverfasser: Komori, Azusa, Taniguchi, Hiroya, Hamauchi, Satoshi, Masuishi, Toshiki, Kito, Yosuke, Narita, Yukiya, Tsushima, Takahiro, Ishihara, Makoto, Todaka, Akiko, Tanaka, Tsutomu, Yokota, Tomoya, Kadowaki, Shigenori, Machida, Nozomu, Ura, Takashi, Fukutomi, Akira, Ando, Masashi, Onozawa, Yusuke, Tajika, Masahiro, Yasui, Hirofumi, Muro, Kei, Mori, Keita, Yamazaki, Kentaro
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container_end_page 335
container_issue 5
container_start_page 329
container_title Oncology
container_volume 93
creator Komori, Azusa
Taniguchi, Hiroya
Hamauchi, Satoshi
Masuishi, Toshiki
Kito, Yosuke
Narita, Yukiya
Tsushima, Takahiro
Ishihara, Makoto
Todaka, Akiko
Tanaka, Tsutomu
Yokota, Tomoya
Kadowaki, Shigenori
Machida, Nozomu
Ura, Takashi
Fukutomi, Akira
Ando, Masashi
Onozawa, Yusuke
Tajika, Masahiro
Yasui, Hirofumi
Muro, Kei
Mori, Keita
Yamazaki, Kentaro
description Purpose: Regorafenib improves survival in chemorefractory metastatic colorectal cancer (mCRC) patients. However, regorafenib induces various adverse events (AEs) that often impair patients' quality of life. Identification of early predictive markers of the efficacy is warranted. Methods: We retrospectively examined 146 consecutive mCRC patients who received regorafenib. Clinical parameters, including patient background, AEs, and changes in biochemical parameters until day 28, were evaluated to identify efficacy predictors. Results: Median progression-free survival (PFS) was 2.1 months, and median overall survival was 6.6 months. Major AEs in all cycles were hand-foot skin reaction, hypertension, and increased aspartate transaminase. We extracted 121 patients for prognostic analysis. In univariate analysis, decreased carcinoembryonic antigen (HR: 0.570, p = 0.012) and decreased carbohydrate antigen 19-9 (CA19-9) (HR: 0.422, p = 0.0012) were identified as prognostic markers of PFS. Patients in whom serum CA19-9 decreased after regorafenib exhibited significantly better PFS (median 3.7 vs. 2.0 months, p = 0.004) than those in whom serum CA19-9 did not decrease. Multivariate analysis revealed early CA19-9 decrease as an independent predictive factor (HR: 0.415, 95% CI: 0.210-0.818, p = 0.011). Conclusion: Early response of CA19-9 may predict the efficacy of regorafenib. Additional studies are needed for external validation.
doi_str_mv 10.1159/000479280
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However, regorafenib induces various adverse events (AEs) that often impair patients' quality of life. Identification of early predictive markers of the efficacy is warranted. Methods: We retrospectively examined 146 consecutive mCRC patients who received regorafenib. Clinical parameters, including patient background, AEs, and changes in biochemical parameters until day 28, were evaluated to identify efficacy predictors. Results: Median progression-free survival (PFS) was 2.1 months, and median overall survival was 6.6 months. Major AEs in all cycles were hand-foot skin reaction, hypertension, and increased aspartate transaminase. We extracted 121 patients for prognostic analysis. In univariate analysis, decreased carcinoembryonic antigen (HR: 0.570, p = 0.012) and decreased carbohydrate antigen 19-9 (CA19-9) (HR: 0.422, p = 0.0012) were identified as prognostic markers of PFS. Patients in whom serum CA19-9 decreased after regorafenib exhibited significantly better PFS (median 3.7 vs. 2.0 months, p = 0.004) than those in whom serum CA19-9 did not decrease. Multivariate analysis revealed early CA19-9 decrease as an independent predictive factor (HR: 0.415, 95% CI: 0.210-0.818, p = 0.011). Conclusion: Early response of CA19-9 may predict the efficacy of regorafenib. Additional studies are needed for external validation.</description><identifier>ISSN: 0030-2414</identifier><identifier>EISSN: 1423-0232</identifier><identifier>DOI: 10.1159/000479280</identifier><identifier>PMID: 28866662</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Cancer metastasis ; Clinical Study ; Colorectal cancer ; Complications and side effects ; Drug therapy ; Genetic aspects ; Health aspects ; Identification and classification ; Patient outcomes ; Regorafenib ; Tumor markers</subject><ispartof>Oncology, 2017-01, Vol.93 (5), p.329-335</ispartof><rights>2017 S. Karger AG, Basel</rights><rights>2017 S. Karger AG, Basel.</rights><rights>COPYRIGHT 2017 S. Karger AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c337t-f50e679c7171910660faf62b76ff01405a5a7e82a514b8fdba2628a5685174f73</citedby><orcidid>0000-0002-3761-6971</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2422,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28866662$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Komori, Azusa</creatorcontrib><creatorcontrib>Taniguchi, Hiroya</creatorcontrib><creatorcontrib>Hamauchi, Satoshi</creatorcontrib><creatorcontrib>Masuishi, Toshiki</creatorcontrib><creatorcontrib>Kito, Yosuke</creatorcontrib><creatorcontrib>Narita, Yukiya</creatorcontrib><creatorcontrib>Tsushima, Takahiro</creatorcontrib><creatorcontrib>Ishihara, Makoto</creatorcontrib><creatorcontrib>Todaka, Akiko</creatorcontrib><creatorcontrib>Tanaka, Tsutomu</creatorcontrib><creatorcontrib>Yokota, Tomoya</creatorcontrib><creatorcontrib>Kadowaki, Shigenori</creatorcontrib><creatorcontrib>Machida, Nozomu</creatorcontrib><creatorcontrib>Ura, Takashi</creatorcontrib><creatorcontrib>Fukutomi, Akira</creatorcontrib><creatorcontrib>Ando, Masashi</creatorcontrib><creatorcontrib>Onozawa, Yusuke</creatorcontrib><creatorcontrib>Tajika, Masahiro</creatorcontrib><creatorcontrib>Yasui, Hirofumi</creatorcontrib><creatorcontrib>Muro, Kei</creatorcontrib><creatorcontrib>Mori, Keita</creatorcontrib><creatorcontrib>Yamazaki, Kentaro</creatorcontrib><title>Serum CA19-9 Response Is an Early Predictive Marker of Efficacy of Regorafenib in Refractory Metastatic Colorectal Cancer</title><title>Oncology</title><addtitle>Oncology</addtitle><description>Purpose: Regorafenib improves survival in chemorefractory metastatic colorectal cancer (mCRC) patients. However, regorafenib induces various adverse events (AEs) that often impair patients' quality of life. Identification of early predictive markers of the efficacy is warranted. Methods: We retrospectively examined 146 consecutive mCRC patients who received regorafenib. Clinical parameters, including patient background, AEs, and changes in biochemical parameters until day 28, were evaluated to identify efficacy predictors. Results: Median progression-free survival (PFS) was 2.1 months, and median overall survival was 6.6 months. Major AEs in all cycles were hand-foot skin reaction, hypertension, and increased aspartate transaminase. We extracted 121 patients for prognostic analysis. In univariate analysis, decreased carcinoembryonic antigen (HR: 0.570, p = 0.012) and decreased carbohydrate antigen 19-9 (CA19-9) (HR: 0.422, p = 0.0012) were identified as prognostic markers of PFS. Patients in whom serum CA19-9 decreased after regorafenib exhibited significantly better PFS (median 3.7 vs. 2.0 months, p = 0.004) than those in whom serum CA19-9 did not decrease. Multivariate analysis revealed early CA19-9 decrease as an independent predictive factor (HR: 0.415, 95% CI: 0.210-0.818, p = 0.011). Conclusion: Early response of CA19-9 may predict the efficacy of regorafenib. Additional studies are needed for external validation.</description><subject>Cancer metastasis</subject><subject>Clinical Study</subject><subject>Colorectal cancer</subject><subject>Complications and side effects</subject><subject>Drug therapy</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Identification and classification</subject><subject>Patient outcomes</subject><subject>Regorafenib</subject><subject>Tumor markers</subject><issn>0030-2414</issn><issn>1423-0232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNo90U1v1DAQBmALgei2cOCOkE-oHAL-iO3kuIoWqNQKVOAcTbzjrak3XmwHKf-eVLusL7alZ2akeQl5w9lHzlX7iTFWm1Y07BlZ8VrIigkpnpMVY5JVoub1BbnM-ffCjKr1S3IhmkYvR6zI_APTtKfdmrdVS-8xH-KYkd5kCiPdQAoz_Z5w623xf5HeQXrERKOjG-e8BTs_ve9xFxM4HP1A_bh8XQJbYprpHRbIBYq3tIshJrQFAu1gtJhekRcOQsbXp_uK_Pq8-dl9rW6_fbnp1reVldKUyimG2rTWcMNbzrRmDpwWg9HOMV4zBQoMNgIUr4fGbQcQWjSgdKO4qZ2RV-T62PeQ4p8Jc-n3PlsMAUaMU-55K1XNpDHNQt8f6Q4C9g8IoTzkGKbil6X0ay2NbNtGqAV-OEKbYs4JXX9Ifg9p7jnrnyLpz5Es9t1p_jTscXuW_zNYwNsjeIS0w3QGp_p_SCSM9A</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Komori, Azusa</creator><creator>Taniguchi, Hiroya</creator><creator>Hamauchi, Satoshi</creator><creator>Masuishi, Toshiki</creator><creator>Kito, Yosuke</creator><creator>Narita, Yukiya</creator><creator>Tsushima, Takahiro</creator><creator>Ishihara, Makoto</creator><creator>Todaka, Akiko</creator><creator>Tanaka, Tsutomu</creator><creator>Yokota, Tomoya</creator><creator>Kadowaki, Shigenori</creator><creator>Machida, Nozomu</creator><creator>Ura, Takashi</creator><creator>Fukutomi, Akira</creator><creator>Ando, Masashi</creator><creator>Onozawa, Yusuke</creator><creator>Tajika, Masahiro</creator><creator>Yasui, Hirofumi</creator><creator>Muro, Kei</creator><creator>Mori, Keita</creator><creator>Yamazaki, Kentaro</creator><general>S. 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However, regorafenib induces various adverse events (AEs) that often impair patients' quality of life. Identification of early predictive markers of the efficacy is warranted. Methods: We retrospectively examined 146 consecutive mCRC patients who received regorafenib. Clinical parameters, including patient background, AEs, and changes in biochemical parameters until day 28, were evaluated to identify efficacy predictors. Results: Median progression-free survival (PFS) was 2.1 months, and median overall survival was 6.6 months. Major AEs in all cycles were hand-foot skin reaction, hypertension, and increased aspartate transaminase. We extracted 121 patients for prognostic analysis. In univariate analysis, decreased carcinoembryonic antigen (HR: 0.570, p = 0.012) and decreased carbohydrate antigen 19-9 (CA19-9) (HR: 0.422, p = 0.0012) were identified as prognostic markers of PFS. Patients in whom serum CA19-9 decreased after regorafenib exhibited significantly better PFS (median 3.7 vs. 2.0 months, p = 0.004) than those in whom serum CA19-9 did not decrease. Multivariate analysis revealed early CA19-9 decrease as an independent predictive factor (HR: 0.415, 95% CI: 0.210-0.818, p = 0.011). Conclusion: Early response of CA19-9 may predict the efficacy of regorafenib. Additional studies are needed for external validation.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>28866662</pmid><doi>10.1159/000479280</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-3761-6971</orcidid></addata></record>
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source Karger Journals
subjects Cancer metastasis
Clinical Study
Colorectal cancer
Complications and side effects
Drug therapy
Genetic aspects
Health aspects
Identification and classification
Patient outcomes
Regorafenib
Tumor markers
title Serum CA19-9 Response Is an Early Predictive Marker of Efficacy of Regorafenib in Refractory Metastatic Colorectal Cancer
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