Correlations Between Radiation Dose in Bone Marrow and Hematological Toxicity in Patients With Cervical Cancer: A Comparison of 3DCRT, IMRT, and RapidARC

OBJECTIVETo comparatively evaluate the hematological toxicity (HT) associated with 3 concurrent chemoradiotherapies that are routinely used to treat cervical cancer, including 3-dimensional conformal radiotherapy (3DCRT), intensity-modulated radiation therapy (IMRT), and RapidARC and to establish a...

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Veröffentlicht in:International journal of gynecological cancer 2016-05, Vol.26 (4), p.770-776
Hauptverfasser: Chang, Yu, Yang, Zhi-Yong, Li, Gui-Ling, Li, Qin, Yang, Qin, Fan, Ji-Quan, Zhao, Ying-Chao, Song, Ying-Qiu, Wu, Gang
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container_end_page 776
container_issue 4
container_start_page 770
container_title International journal of gynecological cancer
container_volume 26
creator Chang, Yu
Yang, Zhi-Yong
Li, Gui-Ling
Li, Qin
Yang, Qin
Fan, Ji-Quan
Zhao, Ying-Chao
Song, Ying-Qiu
Wu, Gang
description OBJECTIVETo comparatively evaluate the hematological toxicity (HT) associated with 3 concurrent chemoradiotherapies that are routinely used to treat cervical cancer, including 3-dimensional conformal radiotherapy (3DCRT), intensity-modulated radiation therapy (IMRT), and RapidARC and to establish a new normal tissue complication probability model of bone marrow (BM) to predict HT in cervical cancer patients undergoing concurrent chemoradiotherapy. METHODSPatients with cervical cancer (N = 100) who received concurrent cisplatin and whole-pelvic radiotherapy were enrolled in this study. Dosimetric parameters (including V10, V20, V30, and V40 and mean doses to the pelvic bone) and HT were analyzed. RESULTSThe V20, V30, and V40 and mean doses to the BM were lower in the IMRT and RapidARC groups than in the 3DCRT group, and the RapidARC group had higher V10 and V40 and mean values than the IMRT group. The V20, V30, and V40 and the mean dose to the pelvic bone were positively correlated with HT. Generalized linear normal tissue complication probability models of white blood cell (WBC) and absolute neutrophil cell (ANC) nadirs and BM V20 were established as followsWBC nadir = 3.382 – 4.056 • V20 + 0.295 • baseline of WBC (adjusted R = 0.246, F = 15.847) and ANC nadir = 2.438 – 2.780 • V20 + 0.233 • baseline of ANC (adjusted R = 0.236, F = 16.282). CONCLUSIONSThis study suggests that IMRT results in milder hematological toxicity than either 3DCRT or RapidARC. Dosimetric parameters were associated with the incidence of HT in cervical cancer patients who received concurrent chemoradiotherapies.
doi_str_mv 10.1097/IGC.0000000000000660
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METHODSPatients with cervical cancer (N = 100) who received concurrent cisplatin and whole-pelvic radiotherapy were enrolled in this study. Dosimetric parameters (including V10, V20, V30, and V40 and mean doses to the pelvic bone) and HT were analyzed. RESULTSThe V20, V30, and V40 and mean doses to the BM were lower in the IMRT and RapidARC groups than in the 3DCRT group, and the RapidARC group had higher V10 and V40 and mean values than the IMRT group. The V20, V30, and V40 and the mean dose to the pelvic bone were positively correlated with HT. Generalized linear normal tissue complication probability models of white blood cell (WBC) and absolute neutrophil cell (ANC) nadirs and BM V20 were established as followsWBC nadir = 3.382 – 4.056 • V20 + 0.295 • baseline of WBC (adjusted R = 0.246, F = 15.847) and ANC nadir = 2.438 – 2.780 • V20 + 0.233 • baseline of ANC (adjusted R = 0.236, F = 16.282). CONCLUSIONSThis study suggests that IMRT results in milder hematological toxicity than either 3DCRT or RapidARC. Dosimetric parameters were associated with the incidence of HT in cervical cancer patients who received concurrent chemoradiotherapies.</description><identifier>ISSN: 1048-891X</identifier><identifier>EISSN: 1525-1438</identifier><identifier>DOI: 10.1097/IGC.0000000000000660</identifier><identifier>PMID: 26844613</identifier><language>eng</language><publisher>England: by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology</publisher><subject>Adult ; Aged ; Antineoplastic Agents - therapeutic use ; Bone marrow ; Bone Marrow - radiation effects ; Cervical cancer ; Chemoradiotherapy - adverse effects ; Cisplatin - therapeutic use ; Dosimetry ; Female ; Follow-Up Studies ; Hematologic Diseases - diagnosis ; Hematologic Diseases - etiology ; Hematology ; Humans ; Middle Aged ; Neoplasm Staging ; Pelvis ; Prognosis ; Radiation therapy ; Radiotherapy Dosage ; Radiotherapy Planning, Computer-Assisted ; Radiotherapy, Conformal - adverse effects ; Radiotherapy, Intensity-Modulated - adverse effects ; Uterine Cervical Neoplasms - pathology ; Uterine Cervical Neoplasms - radiotherapy</subject><ispartof>International journal of gynecological cancer, 2016-05, Vol.26 (4), p.770-776</ispartof><rights>2016 by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology.</rights><rights>2016 2016 by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3390-86fc5c567eebe76067526cf8ce6323f91f8c655aeede0a54acbec32df43804b23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26844613$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, Yu</creatorcontrib><creatorcontrib>Yang, Zhi-Yong</creatorcontrib><creatorcontrib>Li, Gui-Ling</creatorcontrib><creatorcontrib>Li, Qin</creatorcontrib><creatorcontrib>Yang, Qin</creatorcontrib><creatorcontrib>Fan, Ji-Quan</creatorcontrib><creatorcontrib>Zhao, Ying-Chao</creatorcontrib><creatorcontrib>Song, Ying-Qiu</creatorcontrib><creatorcontrib>Wu, Gang</creatorcontrib><title>Correlations Between Radiation Dose in Bone Marrow and Hematological Toxicity in Patients With Cervical Cancer: A Comparison of 3DCRT, IMRT, and RapidARC</title><title>International journal of gynecological cancer</title><addtitle>Int J Gynecol Cancer</addtitle><description>OBJECTIVETo comparatively evaluate the hematological toxicity (HT) associated with 3 concurrent chemoradiotherapies that are routinely used to treat cervical cancer, including 3-dimensional conformal radiotherapy (3DCRT), intensity-modulated radiation therapy (IMRT), and RapidARC and to establish a new normal tissue complication probability model of bone marrow (BM) to predict HT in cervical cancer patients undergoing concurrent chemoradiotherapy. METHODSPatients with cervical cancer (N = 100) who received concurrent cisplatin and whole-pelvic radiotherapy were enrolled in this study. Dosimetric parameters (including V10, V20, V30, and V40 and mean doses to the pelvic bone) and HT were analyzed. RESULTSThe V20, V30, and V40 and mean doses to the BM were lower in the IMRT and RapidARC groups than in the 3DCRT group, and the RapidARC group had higher V10 and V40 and mean values than the IMRT group. The V20, V30, and V40 and the mean dose to the pelvic bone were positively correlated with HT. Generalized linear normal tissue complication probability models of white blood cell (WBC) and absolute neutrophil cell (ANC) nadirs and BM V20 were established as followsWBC nadir = 3.382 – 4.056 • V20 + 0.295 • baseline of WBC (adjusted R = 0.246, F = 15.847) and ANC nadir = 2.438 – 2.780 • V20 + 0.233 • baseline of ANC (adjusted R = 0.236, F = 16.282). CONCLUSIONSThis study suggests that IMRT results in milder hematological toxicity than either 3DCRT or RapidARC. Dosimetric parameters were associated with the incidence of HT in cervical cancer patients who received concurrent chemoradiotherapies.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Bone marrow</subject><subject>Bone Marrow - radiation effects</subject><subject>Cervical cancer</subject><subject>Chemoradiotherapy - adverse effects</subject><subject>Cisplatin - therapeutic use</subject><subject>Dosimetry</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hematologic Diseases - diagnosis</subject><subject>Hematologic Diseases - etiology</subject><subject>Hematology</subject><subject>Humans</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Pelvis</subject><subject>Prognosis</subject><subject>Radiation therapy</subject><subject>Radiotherapy Dosage</subject><subject>Radiotherapy Planning, Computer-Assisted</subject><subject>Radiotherapy, Conformal - adverse effects</subject><subject>Radiotherapy, Intensity-Modulated - adverse effects</subject><subject>Uterine Cervical Neoplasms - pathology</subject><subject>Uterine Cervical Neoplasms - radiotherapy</subject><issn>1048-891X</issn><issn>1525-1438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkdtO4zAQhq3VouW0b4CQJW434Nixk3DXmlMlEKgqYu8s15lQQxp3bZfCo_C2uBwktHMxMxp98480P0J7OTnMSV0ejc7lIfkeQpAfaCvnlGd5waqfqSdFlVV1_ncTbYfwkJiakvoX2qSiKgqRsy30Kp330OloXR_wEOIKoMdj3dj3ET5xAbDt8dD1gK-0926Fdd_gC5jr6Dp3b43u8MQ9W2Pjy5q8SYvQx4DvbJxhCf7pHZG6N-CP8QBLN19ob0NSdy1mJ3I8-YNHV-u8Vh7rhW0GY7mLNlrdBfj9WXfQ7dnpRF5kl9fnIzm4zAxjNckq0RpuuCgBplAKIkpOhWkrA4JR1tZ5agXnGqABonmhzRQMo02bXkSKKWU76OBDd-HdvyWEqB7c0vfppKK8rElVc8oStf9JLadzaNTC27n2L-rrkwmoPoCV6yL48NgtV-DVDHQXZyonam2aSqap_01jb2tLhzQ</recordid><startdate>201605</startdate><enddate>201605</enddate><creator>Chang, Yu</creator><creator>Yang, Zhi-Yong</creator><creator>Li, Gui-Ling</creator><creator>Li, Qin</creator><creator>Yang, Qin</creator><creator>Fan, Ji-Quan</creator><creator>Zhao, Ying-Chao</creator><creator>Song, Ying-Qiu</creator><creator>Wu, Gang</creator><general>by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</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></search><sort><creationdate>201605</creationdate><title>Correlations Between Radiation Dose in Bone Marrow and Hematological Toxicity in Patients With Cervical Cancer: A Comparison of 3DCRT, IMRT, and RapidARC</title><author>Chang, Yu ; 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METHODSPatients with cervical cancer (N = 100) who received concurrent cisplatin and whole-pelvic radiotherapy were enrolled in this study. Dosimetric parameters (including V10, V20, V30, and V40 and mean doses to the pelvic bone) and HT were analyzed. RESULTSThe V20, V30, and V40 and mean doses to the BM were lower in the IMRT and RapidARC groups than in the 3DCRT group, and the RapidARC group had higher V10 and V40 and mean values than the IMRT group. The V20, V30, and V40 and the mean dose to the pelvic bone were positively correlated with HT. Generalized linear normal tissue complication probability models of white blood cell (WBC) and absolute neutrophil cell (ANC) nadirs and BM V20 were established as followsWBC nadir = 3.382 – 4.056 • V20 + 0.295 • baseline of WBC (adjusted R = 0.246, F = 15.847) and ANC nadir = 2.438 – 2.780 • V20 + 0.233 • baseline of ANC (adjusted R = 0.236, F = 16.282). CONCLUSIONSThis study suggests that IMRT results in milder hematological toxicity than either 3DCRT or RapidARC. Dosimetric parameters were associated with the incidence of HT in cervical cancer patients who received concurrent chemoradiotherapies.</abstract><cop>England</cop><pub>by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology</pub><pmid>26844613</pmid><doi>10.1097/IGC.0000000000000660</doi><tpages>7</tpages></addata></record>
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subjects Adult
Aged
Antineoplastic Agents - therapeutic use
Bone marrow
Bone Marrow - radiation effects
Cervical cancer
Chemoradiotherapy - adverse effects
Cisplatin - therapeutic use
Dosimetry
Female
Follow-Up Studies
Hematologic Diseases - diagnosis
Hematologic Diseases - etiology
Hematology
Humans
Middle Aged
Neoplasm Staging
Pelvis
Prognosis
Radiation therapy
Radiotherapy Dosage
Radiotherapy Planning, Computer-Assisted
Radiotherapy, Conformal - adverse effects
Radiotherapy, Intensity-Modulated - adverse effects
Uterine Cervical Neoplasms - pathology
Uterine Cervical Neoplasms - radiotherapy
title Correlations Between Radiation Dose in Bone Marrow and Hematological Toxicity in Patients With Cervical Cancer: A Comparison of 3DCRT, IMRT, and RapidARC
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