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A randomized controlled trial comparing concurrent chemoradiation versus concurrent chemoradiation followed by adjuvant chemotherapy in locally advanced cervical cancer patients: ACTLACC trial

To compare response rate and survivals of locally advanced stage cervical cancer patients who had standard concurrent chemoradiation therapy (CCRT) alone to those who had adjuvant chemotherapy (ACT) after CCRT. Patients aged 18-70 years who had International Federation of Gynecology and Obstetrics s...

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Published in:Journal of gynecologic oncology 2019, 30(4), , pp.1-13
Main Authors: Tangjitgamol, Siriwan, Tharavichitkul, Ekkasit, Tovanabutra, Chokaew, Rongsriyam, Kanisa, Asakij, Tussawan, Paengchit, Kannika, Sukhaboon, Jirasak, Penpattanagul, Somkit, Kridakara, Apiradee, Hanprasertpong, Jitti, Chomprasert, Kittisak, Wanglikitkoon, Sirentra, Atjimakul, Thiti, Pariyawateekul, Piyawan, Katanyoo, Kanyarat, Tanprasert, Prapai, Janweerachai, Wanwipa, Sangthawan, Duangjai, Khunnarong, Jakkapan, Chottetanaprasith, Taywin, Supawattanabodee, Busaba, Lertsanguansinchai, Prasert, Srisomboon, Jatupol, Isaranuwatchai, Wanrudee, Lorvidhaya, Vichan
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container_title Journal of gynecologic oncology
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creator Tangjitgamol, Siriwan
Tharavichitkul, Ekkasit
Tovanabutra, Chokaew
Rongsriyam, Kanisa
Asakij, Tussawan
Paengchit, Kannika
Sukhaboon, Jirasak
Penpattanagul, Somkit
Kridakara, Apiradee
Hanprasertpong, Jitti
Chomprasert, Kittisak
Wanglikitkoon, Sirentra
Atjimakul, Thiti
Pariyawateekul, Piyawan
Katanyoo, Kanyarat
Tanprasert, Prapai
Janweerachai, Wanwipa
Sangthawan, Duangjai
Khunnarong, Jakkapan
Chottetanaprasith, Taywin
Supawattanabodee, Busaba
Lertsanguansinchai, Prasert
Srisomboon, Jatupol
Isaranuwatchai, Wanrudee
Lorvidhaya, Vichan
description To compare response rate and survivals of locally advanced stage cervical cancer patients who had standard concurrent chemoradiation therapy (CCRT) alone to those who had adjuvant chemotherapy (ACT) after CCRT. Patients aged 18-70 years who had International Federation of Gynecology and Obstetrics stage IIB-IVA without para-aortic lymph node enlargement, Eastern Cooperative Oncology Group scores 0-2, and non-aggressive histopathology were randomized to have CCRT with weekly cisplatin followed by observation (arm A) or by ACT with paclitaxel plus carboplatin every 4 weeks for 3 cycles (arm B). Data analysis of 259 patients showed no significant difference in complete responses at 4 months after treatment between arm A (n=129) and arm B (n=130): 94.1% vs. 87.0% (p=0.154) respectively. With the median follow-up of 27.4 months, 15.5% of patients in arm A and 10.8% in arm B experienced recurrences (p=0.123). There were no significant differences of overall or loco-regional failure. However, systemic recurrences were significantly lower in arm B than arm A: 5.4% vs. 10.1% (p=0.029). The 3-year progression-free survival (PFS) and 3-year overall survival (OS) of the patients in both arms were not significantly different. The hazard ratio of PFS and OS of arm B compared to arm A were 1.26 (95% CI=0.82-1.96; p=0.293) and 1.42 (95% CI=0.81-2.49; p=0.221) respectively. ACT with paclitaxel plus carboplatin after CCRT did not improve response rate and survival compared to CCRT alone. Only significant decrease of systemic recurrences with ACT was observed, but not overall or loco-regional failure. ClinicalTrials.gov Identifier: NCT02036164, Thai Clinical Trials Registry Identifier: TCTR 20140106001.
doi_str_mv 10.3802/jgo.2019.30.e82
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Patients aged 18-70 years who had International Federation of Gynecology and Obstetrics stage IIB-IVA without para-aortic lymph node enlargement, Eastern Cooperative Oncology Group scores 0-2, and non-aggressive histopathology were randomized to have CCRT with weekly cisplatin followed by observation (arm A) or by ACT with paclitaxel plus carboplatin every 4 weeks for 3 cycles (arm B). Data analysis of 259 patients showed no significant difference in complete responses at 4 months after treatment between arm A (n=129) and arm B (n=130): 94.1% vs. 87.0% (p=0.154) respectively. With the median follow-up of 27.4 months, 15.5% of patients in arm A and 10.8% in arm B experienced recurrences (p=0.123). There were no significant differences of overall or loco-regional failure. However, systemic recurrences were significantly lower in arm B than arm A: 5.4% vs. 10.1% (p=0.029). The 3-year progression-free survival (PFS) and 3-year overall survival (OS) of the patients in both arms were not significantly different. The hazard ratio of PFS and OS of arm B compared to arm A were 1.26 (95% CI=0.82-1.96; p=0.293) and 1.42 (95% CI=0.81-2.49; p=0.221) respectively. ACT with paclitaxel plus carboplatin after CCRT did not improve response rate and survival compared to CCRT alone. Only significant decrease of systemic recurrences with ACT was observed, but not overall or loco-regional failure. 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Asian Society of Gynecologic Oncology, Korean Society of Gynecologic Oncology.</rights><rights>Copyright © 2019. 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Patients aged 18-70 years who had International Federation of Gynecology and Obstetrics stage IIB-IVA without para-aortic lymph node enlargement, Eastern Cooperative Oncology Group scores 0-2, and non-aggressive histopathology were randomized to have CCRT with weekly cisplatin followed by observation (arm A) or by ACT with paclitaxel plus carboplatin every 4 weeks for 3 cycles (arm B). Data analysis of 259 patients showed no significant difference in complete responses at 4 months after treatment between arm A (n=129) and arm B (n=130): 94.1% vs. 87.0% (p=0.154) respectively. With the median follow-up of 27.4 months, 15.5% of patients in arm A and 10.8% in arm B experienced recurrences (p=0.123). There were no significant differences of overall or loco-regional failure. However, systemic recurrences were significantly lower in arm B than arm A: 5.4% vs. 10.1% (p=0.029). The 3-year progression-free survival (PFS) and 3-year overall survival (OS) of the patients in both arms were not significantly different. The hazard ratio of PFS and OS of arm B compared to arm A were 1.26 (95% CI=0.82-1.96; p=0.293) and 1.42 (95% CI=0.81-2.49; p=0.221) respectively. ACT with paclitaxel plus carboplatin after CCRT did not improve response rate and survival compared to CCRT alone. Only significant decrease of systemic recurrences with ACT was observed, but not overall or loco-regional failure. 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Tharavichitkul, Ekkasit ; Tovanabutra, Chokaew ; Rongsriyam, Kanisa ; Asakij, Tussawan ; Paengchit, Kannika ; Sukhaboon, Jirasak ; Penpattanagul, Somkit ; Kridakara, Apiradee ; Hanprasertpong, Jitti ; Chomprasert, Kittisak ; Wanglikitkoon, Sirentra ; Atjimakul, Thiti ; Pariyawateekul, Piyawan ; Katanyoo, Kanyarat ; Tanprasert, Prapai ; Janweerachai, Wanwipa ; Sangthawan, Duangjai ; Khunnarong, Jakkapan ; Chottetanaprasith, Taywin ; Supawattanabodee, Busaba ; Lertsanguansinchai, Prasert ; Srisomboon, Jatupol ; Isaranuwatchai, Wanrudee ; Lorvidhaya, Vichan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-9d69447cbb80b2f5d8aaf224dfdbea6edf063599f472f3613bb46d61f1f7dbbb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adenocarcinoma - mortality</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma - therapy</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Carboplatin - administration &amp; dosage</topic><topic>Carboplatin - adverse effects</topic><topic>Carcinoma, Squamous Cell - mortality</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - therapy</topic><topic>Chemoradiotherapy - adverse effects</topic><topic>Chemotherapy, Adjuvant - adverse effects</topic><topic>Female</topic><topic>Humans</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Paclitaxel - administration &amp; dosage</topic><topic>Paclitaxel - adverse effects</topic><topic>Treatment Outcome</topic><topic>Uterine Cervical Neoplasms - mortality</topic><topic>Uterine Cervical Neoplasms - pathology</topic><topic>Uterine Cervical Neoplasms - therapy</topic><topic>산부인과학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tangjitgamol, Siriwan</creatorcontrib><creatorcontrib>Tharavichitkul, Ekkasit</creatorcontrib><creatorcontrib>Tovanabutra, Chokaew</creatorcontrib><creatorcontrib>Rongsriyam, Kanisa</creatorcontrib><creatorcontrib>Asakij, Tussawan</creatorcontrib><creatorcontrib>Paengchit, Kannika</creatorcontrib><creatorcontrib>Sukhaboon, Jirasak</creatorcontrib><creatorcontrib>Penpattanagul, Somkit</creatorcontrib><creatorcontrib>Kridakara, Apiradee</creatorcontrib><creatorcontrib>Hanprasertpong, Jitti</creatorcontrib><creatorcontrib>Chomprasert, Kittisak</creatorcontrib><creatorcontrib>Wanglikitkoon, Sirentra</creatorcontrib><creatorcontrib>Atjimakul, Thiti</creatorcontrib><creatorcontrib>Pariyawateekul, Piyawan</creatorcontrib><creatorcontrib>Katanyoo, Kanyarat</creatorcontrib><creatorcontrib>Tanprasert, Prapai</creatorcontrib><creatorcontrib>Janweerachai, Wanwipa</creatorcontrib><creatorcontrib>Sangthawan, Duangjai</creatorcontrib><creatorcontrib>Khunnarong, Jakkapan</creatorcontrib><creatorcontrib>Chottetanaprasith, Taywin</creatorcontrib><creatorcontrib>Supawattanabodee, Busaba</creatorcontrib><creatorcontrib>Lertsanguansinchai, Prasert</creatorcontrib><creatorcontrib>Srisomboon, Jatupol</creatorcontrib><creatorcontrib>Isaranuwatchai, Wanrudee</creatorcontrib><creatorcontrib>Lorvidhaya, Vichan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Journal of gynecologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tangjitgamol, Siriwan</au><au>Tharavichitkul, Ekkasit</au><au>Tovanabutra, Chokaew</au><au>Rongsriyam, Kanisa</au><au>Asakij, Tussawan</au><au>Paengchit, Kannika</au><au>Sukhaboon, Jirasak</au><au>Penpattanagul, Somkit</au><au>Kridakara, Apiradee</au><au>Hanprasertpong, Jitti</au><au>Chomprasert, Kittisak</au><au>Wanglikitkoon, Sirentra</au><au>Atjimakul, Thiti</au><au>Pariyawateekul, Piyawan</au><au>Katanyoo, Kanyarat</au><au>Tanprasert, Prapai</au><au>Janweerachai, Wanwipa</au><au>Sangthawan, Duangjai</au><au>Khunnarong, Jakkapan</au><au>Chottetanaprasith, Taywin</au><au>Supawattanabodee, Busaba</au><au>Lertsanguansinchai, Prasert</au><au>Srisomboon, Jatupol</au><au>Isaranuwatchai, Wanrudee</au><au>Lorvidhaya, Vichan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A randomized controlled trial comparing concurrent chemoradiation versus concurrent chemoradiation followed by adjuvant chemotherapy in locally advanced cervical cancer patients: ACTLACC trial</atitle><jtitle>Journal of gynecologic oncology</jtitle><addtitle>J Gynecol Oncol</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>30</volume><issue>4</issue><spage>e82</spage><epage>e82</epage><pages>e82-e82</pages><issn>2005-0380</issn><eissn>2005-0399</eissn><abstract>To compare response rate and survivals of locally advanced stage cervical cancer patients who had standard concurrent chemoradiation therapy (CCRT) alone to those who had adjuvant chemotherapy (ACT) after CCRT. Patients aged 18-70 years who had International Federation of Gynecology and Obstetrics stage IIB-IVA without para-aortic lymph node enlargement, Eastern Cooperative Oncology Group scores 0-2, and non-aggressive histopathology were randomized to have CCRT with weekly cisplatin followed by observation (arm A) or by ACT with paclitaxel plus carboplatin every 4 weeks for 3 cycles (arm B). Data analysis of 259 patients showed no significant difference in complete responses at 4 months after treatment between arm A (n=129) and arm B (n=130): 94.1% vs. 87.0% (p=0.154) respectively. With the median follow-up of 27.4 months, 15.5% of patients in arm A and 10.8% in arm B experienced recurrences (p=0.123). There were no significant differences of overall or loco-regional failure. However, systemic recurrences were significantly lower in arm B than arm A: 5.4% vs. 10.1% (p=0.029). The 3-year progression-free survival (PFS) and 3-year overall survival (OS) of the patients in both arms were not significantly different. The hazard ratio of PFS and OS of arm B compared to arm A were 1.26 (95% CI=0.82-1.96; p=0.293) and 1.42 (95% CI=0.81-2.49; p=0.221) respectively. ACT with paclitaxel plus carboplatin after CCRT did not improve response rate and survival compared to CCRT alone. Only significant decrease of systemic recurrences with ACT was observed, but not overall or loco-regional failure. ClinicalTrials.gov Identifier: NCT02036164, Thai Clinical Trials Registry Identifier: TCTR 20140106001.</abstract><cop>Korea (South)</cop><pub>Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology</pub><pmid>31074236</pmid><doi>10.3802/jgo.2019.30.e82</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-2369-6106</orcidid><orcidid>https://orcid.org/0000-0002-9237-7539</orcidid><orcidid>https://orcid.org/0000-0003-3906-9980</orcidid><orcidid>https://orcid.org/0000-0001-5367-8884</orcidid><orcidid>https://orcid.org/0000-0001-5860-9554</orcidid><orcidid>https://orcid.org/0000-0003-1295-3514</orcidid><orcidid>https://orcid.org/0000-0002-0640-6824</orcidid><orcidid>https://orcid.org/0000-0003-1798-8871</orcidid><orcidid>https://orcid.org/0000-0002-8163-1626</orcidid><orcidid>https://orcid.org/0000-0002-5282-1500</orcidid><orcidid>https://orcid.org/0000-0003-3286-5052</orcidid><orcidid>https://orcid.org/0000-0003-3460-8236</orcidid><orcidid>https://orcid.org/0000-0003-3416-1710</orcidid><orcidid>https://orcid.org/0000-0002-6561-5589</orcidid><orcidid>https://orcid.org/0000-0002-5819-9580</orcidid><orcidid>https://orcid.org/0000-0002-9785-1201</orcidid><orcidid>https://orcid.org/0000-0002-4892-0645</orcidid><orcidid>https://orcid.org/0000-0002-6307-1346</orcidid><orcidid>https://orcid.org/0000-0001-7705-6537</orcidid><orcidid>https://orcid.org/0000-0003-4434-8917</orcidid><orcidid>https://orcid.org/0000-0003-2589-8470</orcidid><orcidid>https://orcid.org/0000-0002-5495-1421</orcidid><orcidid>https://orcid.org/0000-0001-8203-0761</orcidid><orcidid>https://orcid.org/0000-0002-8368-6065</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 2005-0380
ispartof Journal of Gynecologic Oncology, 2019, 30(4), , pp.1-13
issn 2005-0380
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language eng
recordid cdi_nrf_kci_oai_kci_go_kr_ARTI_5761637
source PubMed Central Free
subjects Adenocarcinoma - mortality
Adenocarcinoma - pathology
Adenocarcinoma - therapy
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Carboplatin - administration & dosage
Carboplatin - adverse effects
Carcinoma, Squamous Cell - mortality
Carcinoma, Squamous Cell - pathology
Carcinoma, Squamous Cell - therapy
Chemoradiotherapy - adverse effects
Chemotherapy, Adjuvant - adverse effects
Female
Humans
Middle Aged
Original
Paclitaxel - administration & dosage
Paclitaxel - adverse effects
Treatment Outcome
Uterine Cervical Neoplasms - mortality
Uterine Cervical Neoplasms - pathology
Uterine Cervical Neoplasms - therapy
산부인과학
title A randomized controlled trial comparing concurrent chemoradiation versus concurrent chemoradiation followed by adjuvant chemotherapy in locally advanced cervical cancer patients: ACTLACC trial
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