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Clinical management and outcomes associated with etoposide, doxorubicin, and cisplatin plus mitotane treatment in metastatic adrenocortical carcinoma: a single institute experience
Background Adrenocortical carcinoma (ACC) is a rare and aggressive disease that is often diagnosed at an advanced stage. There is no standard treatment for metastatic ACC; EDP-M (etoposide, doxorubicin, and cisplatin plus mitotane) is one treatment option. A randomized controlled trial (FIRM-ACT) ev...
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Published in: | International journal of clinical oncology 2021-12, Vol.26 (12), p.2275-2281 |
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container_title | International journal of clinical oncology |
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creator | Uchihara, Masaki Tanioka, Maki Kojima, Yuki Nishikawa, Tadaaki Sudo, Kazuki Shimoi, Tatsunori Noguchi, Emi Maeshima, Akiko Miyagi Yonemori, Kan |
description | Background
Adrenocortical carcinoma (ACC) is a rare and aggressive disease that is often diagnosed at an advanced stage. There is no standard treatment for metastatic ACC; EDP-M (etoposide, doxorubicin, and cisplatin plus mitotane) is one treatment option. A randomized controlled trial (FIRM-ACT) evaluating the efficacy of EDP-M showed progression-free survival (PFS) was 5.0 months, overall survival (OS) was 14.8 months, the response rate was 19%, and adrenal insufficiency occurred in 3.4% of patients. However, the efficacy and safety of this regimen in Asia are not fully reported.
Methods
We retrospectively analyzed 43 patients diagnosed with metastatic ACC at the National Cancer Center Hospital between 1997 and 2020. We evaluated PFS, OS, and response in 17 patients who received EDP-M as first-line therapy.
Results
The median age at treatment initiation was 45 years (range 18–74). Eight patients (47%) had autonomous hormone production, including six patients with hypercortisolism. The best response of partial response and stable disease was seen in two (12%) and ten (59%) patients, respectively. The median PFS was 6.2 months [95% confidence interval (CI): 4.3–10.0]. The median OS was 15.4 months (95% CI 11.6–not reached). Three patients received only one cycle due to adverse effects associated with hypercortisolism. Grade 3/4 adverse events associated with adrenal insufficiency occurred in three (17%) cases, resulting in EDP-M discontinuation.
Conclusions
The EDP-M regimen had similar PFS to that observed in FIRM-ACT. Adrenal insufficiency was more frequent in the current study, but this could be managed with supportive endocrinological care such as cortisol replacement. |
doi_str_mv | 10.1007/s10147-021-02021-8 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2595783961</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2595783961</sourcerecordid><originalsourceid>FETCH-LOGICAL-c399t-2d8befbe61d9931a85243580461390e0b7e2f620c21102aaac9e959c8e0fdda73</originalsourceid><addsrcrecordid>eNp9kc1u1TAQhS0EouXCC7BAltg24J8kttmhK_6kSt2062hiTy6uEjvYjijv1QfEvbfAjsV4RppzvrF0CHnN2TvOmHqfOeOtapjgtR5e_YSc81aqRiklntZZtrwxvejOyIucbxnjqu_Ec3Im27bXWnfn5H4_--AtzHSBAAdcMBQKwdG4FRsXzBRyjtZDQUd_-vKdYolrzN7hBXXxLqZt9NaHi6PJ-rzOUHyg67xluvgSCwSkJSGUI7quFiyQS1VZCi5hiDamcvyChVRRcYEPFGj24TBjNeTiy1aQ4t2KyWOw-JI8m2DO-Oqx78jN50_X-6_N5dWXb_uPl42VxpRGOD3iNGLPnTGSg-5EKzvN2p5Lw5CNCsXUC2YF50wAgDVoOmM1ssk5UHJH3p64a4o_NsxluI1bCvXkIDrTKS1NRe2IOKlsijknnIY1-QXSr4Gz4SGo4RTUUCMajkENuprePKK3cUH31_InmSqQJ0Guq3DA9O_2f7C_AWAKo3U</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2595783961</pqid></control><display><type>article</type><title>Clinical management and outcomes associated with etoposide, doxorubicin, and cisplatin plus mitotane treatment in metastatic adrenocortical carcinoma: a single institute experience</title><source>Springer Nature</source><creator>Uchihara, Masaki ; Tanioka, Maki ; Kojima, Yuki ; Nishikawa, Tadaaki ; Sudo, Kazuki ; Shimoi, Tatsunori ; Noguchi, Emi ; Maeshima, Akiko Miyagi ; Yonemori, Kan</creator><creatorcontrib>Uchihara, Masaki ; Tanioka, Maki ; Kojima, Yuki ; Nishikawa, Tadaaki ; Sudo, Kazuki ; Shimoi, Tatsunori ; Noguchi, Emi ; Maeshima, Akiko Miyagi ; Yonemori, Kan</creatorcontrib><description>Background
Adrenocortical carcinoma (ACC) is a rare and aggressive disease that is often diagnosed at an advanced stage. There is no standard treatment for metastatic ACC; EDP-M (etoposide, doxorubicin, and cisplatin plus mitotane) is one treatment option. A randomized controlled trial (FIRM-ACT) evaluating the efficacy of EDP-M showed progression-free survival (PFS) was 5.0 months, overall survival (OS) was 14.8 months, the response rate was 19%, and adrenal insufficiency occurred in 3.4% of patients. However, the efficacy and safety of this regimen in Asia are not fully reported.
Methods
We retrospectively analyzed 43 patients diagnosed with metastatic ACC at the National Cancer Center Hospital between 1997 and 2020. We evaluated PFS, OS, and response in 17 patients who received EDP-M as first-line therapy.
Results
The median age at treatment initiation was 45 years (range 18–74). Eight patients (47%) had autonomous hormone production, including six patients with hypercortisolism. The best response of partial response and stable disease was seen in two (12%) and ten (59%) patients, respectively. The median PFS was 6.2 months [95% confidence interval (CI): 4.3–10.0]. The median OS was 15.4 months (95% CI 11.6–not reached). Three patients received only one cycle due to adverse effects associated with hypercortisolism. Grade 3/4 adverse events associated with adrenal insufficiency occurred in three (17%) cases, resulting in EDP-M discontinuation.
Conclusions
The EDP-M regimen had similar PFS to that observed in FIRM-ACT. Adrenal insufficiency was more frequent in the current study, but this could be managed with supportive endocrinological care such as cortisol replacement.</description><identifier>ISSN: 1341-9625</identifier><identifier>EISSN: 1437-7772</identifier><identifier>DOI: 10.1007/s10147-021-02021-8</identifier><identifier>PMID: 34468885</identifier><language>eng</language><publisher>Singapore: Springer Singapore</publisher><subject>Adolescent ; Adrenal Cortex Neoplasms - drug therapy ; Adrenocortical Carcinoma - drug therapy ; Adult ; Adverse events ; Aged ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Cancer Research ; Chemotherapy ; Cisplatin ; Cisplatin - adverse effects ; Doxorubicin ; Doxorubicin - adverse effects ; Etoposide ; Etoposide - adverse effects ; Humans ; Medicine ; Medicine & Public Health ; Metastases ; Metastasis ; Middle Aged ; Mitotane - adverse effects ; Neuroendocrine tumors ; Oncology ; Original Article ; Patients ; Retrospective Studies ; Surgical Oncology ; Survival ; Treatment Outcome ; Young Adult</subject><ispartof>International journal of clinical oncology, 2021-12, Vol.26 (12), p.2275-2281</ispartof><rights>Japan Society of Clinical Oncology 2021</rights><rights>2021. Japan Society of Clinical Oncology.</rights><rights>Japan Society of Clinical Oncology 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-2d8befbe61d9931a85243580461390e0b7e2f620c21102aaac9e959c8e0fdda73</citedby><cites>FETCH-LOGICAL-c399t-2d8befbe61d9931a85243580461390e0b7e2f620c21102aaac9e959c8e0fdda73</cites><orcidid>0000-0002-6558-2246</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34468885$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uchihara, Masaki</creatorcontrib><creatorcontrib>Tanioka, Maki</creatorcontrib><creatorcontrib>Kojima, Yuki</creatorcontrib><creatorcontrib>Nishikawa, Tadaaki</creatorcontrib><creatorcontrib>Sudo, Kazuki</creatorcontrib><creatorcontrib>Shimoi, Tatsunori</creatorcontrib><creatorcontrib>Noguchi, Emi</creatorcontrib><creatorcontrib>Maeshima, Akiko Miyagi</creatorcontrib><creatorcontrib>Yonemori, Kan</creatorcontrib><title>Clinical management and outcomes associated with etoposide, doxorubicin, and cisplatin plus mitotane treatment in metastatic adrenocortical carcinoma: a single institute experience</title><title>International journal of clinical oncology</title><addtitle>Int J Clin Oncol</addtitle><addtitle>Int J Clin Oncol</addtitle><description>Background
Adrenocortical carcinoma (ACC) is a rare and aggressive disease that is often diagnosed at an advanced stage. There is no standard treatment for metastatic ACC; EDP-M (etoposide, doxorubicin, and cisplatin plus mitotane) is one treatment option. A randomized controlled trial (FIRM-ACT) evaluating the efficacy of EDP-M showed progression-free survival (PFS) was 5.0 months, overall survival (OS) was 14.8 months, the response rate was 19%, and adrenal insufficiency occurred in 3.4% of patients. However, the efficacy and safety of this regimen in Asia are not fully reported.
Methods
We retrospectively analyzed 43 patients diagnosed with metastatic ACC at the National Cancer Center Hospital between 1997 and 2020. We evaluated PFS, OS, and response in 17 patients who received EDP-M as first-line therapy.
Results
The median age at treatment initiation was 45 years (range 18–74). Eight patients (47%) had autonomous hormone production, including six patients with hypercortisolism. The best response of partial response and stable disease was seen in two (12%) and ten (59%) patients, respectively. The median PFS was 6.2 months [95% confidence interval (CI): 4.3–10.0]. The median OS was 15.4 months (95% CI 11.6–not reached). Three patients received only one cycle due to adverse effects associated with hypercortisolism. Grade 3/4 adverse events associated with adrenal insufficiency occurred in three (17%) cases, resulting in EDP-M discontinuation.
Conclusions
The EDP-M regimen had similar PFS to that observed in FIRM-ACT. Adrenal insufficiency was more frequent in the current study, but this could be managed with supportive endocrinological care such as cortisol replacement.</description><subject>Adolescent</subject><subject>Adrenal Cortex Neoplasms - drug therapy</subject><subject>Adrenocortical Carcinoma - drug therapy</subject><subject>Adult</subject><subject>Adverse events</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Cancer Research</subject><subject>Chemotherapy</subject><subject>Cisplatin</subject><subject>Cisplatin - adverse effects</subject><subject>Doxorubicin</subject><subject>Doxorubicin - adverse effects</subject><subject>Etoposide</subject><subject>Etoposide - adverse effects</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Mitotane - adverse effects</subject><subject>Neuroendocrine tumors</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Patients</subject><subject>Retrospective Studies</subject><subject>Surgical Oncology</subject><subject>Survival</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>1341-9625</issn><issn>1437-7772</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1TAQhS0EouXCC7BAltg24J8kttmhK_6kSt2062hiTy6uEjvYjijv1QfEvbfAjsV4RppzvrF0CHnN2TvOmHqfOeOtapjgtR5e_YSc81aqRiklntZZtrwxvejOyIucbxnjqu_Ec3Im27bXWnfn5H4_--AtzHSBAAdcMBQKwdG4FRsXzBRyjtZDQUd_-vKdYolrzN7hBXXxLqZt9NaHi6PJ-rzOUHyg67xluvgSCwSkJSGUI7quFiyQS1VZCi5hiDamcvyChVRRcYEPFGj24TBjNeTiy1aQ4t2KyWOw-JI8m2DO-Oqx78jN50_X-6_N5dWXb_uPl42VxpRGOD3iNGLPnTGSg-5EKzvN2p5Lw5CNCsXUC2YF50wAgDVoOmM1ssk5UHJH3p64a4o_NsxluI1bCvXkIDrTKS1NRe2IOKlsijknnIY1-QXSr4Gz4SGo4RTUUCMajkENuprePKK3cUH31_InmSqQJ0Guq3DA9O_2f7C_AWAKo3U</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Uchihara, Masaki</creator><creator>Tanioka, Maki</creator><creator>Kojima, Yuki</creator><creator>Nishikawa, Tadaaki</creator><creator>Sudo, Kazuki</creator><creator>Shimoi, Tatsunori</creator><creator>Noguchi, Emi</creator><creator>Maeshima, Akiko Miyagi</creator><creator>Yonemori, Kan</creator><general>Springer Singapore</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><orcidid>https://orcid.org/0000-0002-6558-2246</orcidid></search><sort><creationdate>20211201</creationdate><title>Clinical management and outcomes associated with etoposide, doxorubicin, and cisplatin plus mitotane treatment in metastatic adrenocortical carcinoma: a single institute experience</title><author>Uchihara, Masaki ; 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Adrenocortical carcinoma (ACC) is a rare and aggressive disease that is often diagnosed at an advanced stage. There is no standard treatment for metastatic ACC; EDP-M (etoposide, doxorubicin, and cisplatin plus mitotane) is one treatment option. A randomized controlled trial (FIRM-ACT) evaluating the efficacy of EDP-M showed progression-free survival (PFS) was 5.0 months, overall survival (OS) was 14.8 months, the response rate was 19%, and adrenal insufficiency occurred in 3.4% of patients. However, the efficacy and safety of this regimen in Asia are not fully reported.
Methods
We retrospectively analyzed 43 patients diagnosed with metastatic ACC at the National Cancer Center Hospital between 1997 and 2020. We evaluated PFS, OS, and response in 17 patients who received EDP-M as first-line therapy.
Results
The median age at treatment initiation was 45 years (range 18–74). Eight patients (47%) had autonomous hormone production, including six patients with hypercortisolism. The best response of partial response and stable disease was seen in two (12%) and ten (59%) patients, respectively. The median PFS was 6.2 months [95% confidence interval (CI): 4.3–10.0]. The median OS was 15.4 months (95% CI 11.6–not reached). Three patients received only one cycle due to adverse effects associated with hypercortisolism. Grade 3/4 adverse events associated with adrenal insufficiency occurred in three (17%) cases, resulting in EDP-M discontinuation.
Conclusions
The EDP-M regimen had similar PFS to that observed in FIRM-ACT. Adrenal insufficiency was more frequent in the current study, but this could be managed with supportive endocrinological care such as cortisol replacement.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>34468885</pmid><doi>10.1007/s10147-021-02021-8</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-6558-2246</orcidid></addata></record> |
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subjects | Adolescent Adrenal Cortex Neoplasms - drug therapy Adrenocortical Carcinoma - drug therapy Adult Adverse events Aged Antineoplastic Combined Chemotherapy Protocols - adverse effects Cancer Research Chemotherapy Cisplatin Cisplatin - adverse effects Doxorubicin Doxorubicin - adverse effects Etoposide Etoposide - adverse effects Humans Medicine Medicine & Public Health Metastases Metastasis Middle Aged Mitotane - adverse effects Neuroendocrine tumors Oncology Original Article Patients Retrospective Studies Surgical Oncology Survival Treatment Outcome Young Adult |
title | Clinical management and outcomes associated with etoposide, doxorubicin, and cisplatin plus mitotane treatment in metastatic adrenocortical carcinoma: a single institute experience |
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