Impact of granulocyte-colony stimulating factor on docetaxel-induced febrile neutropenia in patients with breast cancer

Background Febrile neutropenia (FN) is a life-threatening complication of Docetaxel-based chemotherapy regimens (DBRs). Prophylactic granulocyte-colony stimulating factor (G-CSF) can reduce the risk of FN. This study investigated the effect of G-CSF on FN in patients receiving DBRs for breast cancer...

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Veröffentlicht in:Journal of oncology pharmacy practice 2022-12, Vol.28 (8), p.1681-1686
Hauptverfasser: Zekri, Jamal, Nawaz, Azhar, Rasool, Haleem, Ahmad, Imran, Abdel Rahman, Hossam, Dada, Reyad, Abdelghany, Ehab Mosaad, Farag, Kamel, Ibrahim, Refaei Belal, Deibas, Mohamed Youssef, Kamel, Mohamed Kamal, Allithy, Ahmed
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container_end_page 1686
container_issue 8
container_start_page 1681
container_title Journal of oncology pharmacy practice
container_volume 28
creator Zekri, Jamal
Nawaz, Azhar
Rasool, Haleem
Ahmad, Imran
Abdel Rahman, Hossam
Dada, Reyad
Abdelghany, Ehab Mosaad
Farag, Kamel
Ibrahim, Refaei Belal
Deibas, Mohamed Youssef
Kamel, Mohamed Kamal
Allithy, Ahmed
description Background Febrile neutropenia (FN) is a life-threatening complication of Docetaxel-based chemotherapy regimens (DBRs). Prophylactic granulocyte-colony stimulating factor (G-CSF) can reduce the risk of FN. This study investigated the effect of G-CSF on FN in patients receiving DBRs for breast cancer. Methods Patients treated between 2015 and 2017 were identified from the hospital’s pharmacy database and their medical records were examined retrospectively. Data from patients’ first four cycles of DBR were collected. FN rate, FN associated length of hospital stay (FN-LOS), and chemotherapy dose modification/delay due to FN were compared between patients who did (G-CSF group) or did not (non-GCSF group) receive prophylactic G-CSF. Results Of the 276 included patients, 83.3% received a DBR as adjuvant or neoadjuvant therapy, and 50% received docetaxel as combination therapy. Prophylactic G-CSF was administered with the first cycle of a DBR in 69.9% of patients who were significantly less likely to experience FN compared to the non-G-CSF group (6.2% vs. 15.7%; odds ratio: 0.36 [95% CI: 0.16–0.82]; p = 0.020). Collectively and after the 4 DBR treatment cycles, FN rate (4.8 vs. 8.5; odds ratio: 0.54 [95% CI: 0.30–0.97]; p = 0.043) and the mean FN-LOS (3.55 vs. 5.28 days; t = –2.22; p = 0.037) were reduced in the G-CSF group. There was no difference in DBR dose delay/reduction between both groups in cycles 2–4. Conclusion In patients receiving DBRs for breast cancer, prophylactic G-CSF significantly reduced both the rate of FN and duration of hospitalization for FN.
doi_str_mv 10.1177/10781552211030974
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Prophylactic granulocyte-colony stimulating factor (G-CSF) can reduce the risk of FN. This study investigated the effect of G-CSF on FN in patients receiving DBRs for breast cancer. Methods Patients treated between 2015 and 2017 were identified from the hospital’s pharmacy database and their medical records were examined retrospectively. Data from patients’ first four cycles of DBR were collected. FN rate, FN associated length of hospital stay (FN-LOS), and chemotherapy dose modification/delay due to FN were compared between patients who did (G-CSF group) or did not (non-GCSF group) receive prophylactic G-CSF. Results Of the 276 included patients, 83.3% received a DBR as adjuvant or neoadjuvant therapy, and 50% received docetaxel as combination therapy. Prophylactic G-CSF was administered with the first cycle of a DBR in 69.9% of patients who were significantly less likely to experience FN compared to the non-G-CSF group (6.2% vs. 15.7%; odds ratio: 0.36 [95% CI: 0.16–0.82]; p = 0.020). Collectively and after the 4 DBR treatment cycles, FN rate (4.8 vs. 8.5; odds ratio: 0.54 [95% CI: 0.30–0.97]; p = 0.043) and the mean FN-LOS (3.55 vs. 5.28 days; t = –2.22; p = 0.037) were reduced in the G-CSF group. There was no difference in DBR dose delay/reduction between both groups in cycles 2–4. Conclusion In patients receiving DBRs for breast cancer, prophylactic G-CSF significantly reduced both the rate of FN and duration of hospitalization for FN.</description><identifier>ISSN: 1078-1552</identifier><identifier>EISSN: 1477-092X</identifier><identifier>DOI: 10.1177/10781552211030974</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Breast cancer ; Cancer therapies ; Chemotherapy ; Colonies ; Colony-stimulating factor ; Granulocyte colony-stimulating factor ; Granulocytes ; Leukocytes (granulocytic) ; Medical records ; Neutropenia ; Patients</subject><ispartof>Journal of oncology pharmacy practice, 2022-12, Vol.28 (8), p.1681-1686</ispartof><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-b39e5943eab4dda1cc531cf4e2d8ff8fc257a2a747d031f6d7d5132502ef83e93</citedby><cites>FETCH-LOGICAL-c345t-b39e5943eab4dda1cc531cf4e2d8ff8fc257a2a747d031f6d7d5132502ef83e93</cites><orcidid>0000-0002-8221-9342 ; 0000-0002-1329-5106 ; 0000-0003-2542-0207</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/10781552211030974$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/10781552211030974$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>315,782,786,21826,27931,27932,43628,43629</link.rule.ids></links><search><creatorcontrib>Zekri, Jamal</creatorcontrib><creatorcontrib>Nawaz, Azhar</creatorcontrib><creatorcontrib>Rasool, Haleem</creatorcontrib><creatorcontrib>Ahmad, Imran</creatorcontrib><creatorcontrib>Abdel Rahman, Hossam</creatorcontrib><creatorcontrib>Dada, Reyad</creatorcontrib><creatorcontrib>Abdelghany, Ehab Mosaad</creatorcontrib><creatorcontrib>Farag, Kamel</creatorcontrib><creatorcontrib>Ibrahim, Refaei Belal</creatorcontrib><creatorcontrib>Deibas, Mohamed Youssef</creatorcontrib><creatorcontrib>Kamel, Mohamed Kamal</creatorcontrib><creatorcontrib>Allithy, Ahmed</creatorcontrib><title>Impact of granulocyte-colony stimulating factor on docetaxel-induced febrile neutropenia in patients with breast cancer</title><title>Journal of oncology pharmacy practice</title><description>Background Febrile neutropenia (FN) is a life-threatening complication of Docetaxel-based chemotherapy regimens (DBRs). Prophylactic granulocyte-colony stimulating factor (G-CSF) can reduce the risk of FN. This study investigated the effect of G-CSF on FN in patients receiving DBRs for breast cancer. Methods Patients treated between 2015 and 2017 were identified from the hospital’s pharmacy database and their medical records were examined retrospectively. Data from patients’ first four cycles of DBR were collected. FN rate, FN associated length of hospital stay (FN-LOS), and chemotherapy dose modification/delay due to FN were compared between patients who did (G-CSF group) or did not (non-GCSF group) receive prophylactic G-CSF. Results Of the 276 included patients, 83.3% received a DBR as adjuvant or neoadjuvant therapy, and 50% received docetaxel as combination therapy. Prophylactic G-CSF was administered with the first cycle of a DBR in 69.9% of patients who were significantly less likely to experience FN compared to the non-G-CSF group (6.2% vs. 15.7%; odds ratio: 0.36 [95% CI: 0.16–0.82]; p = 0.020). Collectively and after the 4 DBR treatment cycles, FN rate (4.8 vs. 8.5; odds ratio: 0.54 [95% CI: 0.30–0.97]; p = 0.043) and the mean FN-LOS (3.55 vs. 5.28 days; t = –2.22; p = 0.037) were reduced in the G-CSF group. There was no difference in DBR dose delay/reduction between both groups in cycles 2–4. Conclusion In patients receiving DBRs for breast cancer, prophylactic G-CSF significantly reduced both the rate of FN and duration of hospitalization for FN.</description><subject>Breast cancer</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Colonies</subject><subject>Colony-stimulating factor</subject><subject>Granulocyte colony-stimulating factor</subject><subject>Granulocytes</subject><subject>Leukocytes (granulocytic)</subject><subject>Medical records</subject><subject>Neutropenia</subject><subject>Patients</subject><issn>1078-1552</issn><issn>1477-092X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kctKBDEQRYMoqKMf4C7gxk1rnpPupYgvENwouGsySWXM0JO0SRqdvzcygqC4qoI691ZRF6ETSs4pVeqCEtVSKRmjlHDSKbGDDqhQqiEde9mtfZ03X8A-Osx5RQhpFWsP0Pv9etSm4OjwMukwDdFsCjQmDjFscC5-PQ26-LDErmIx4RiwjQaK_oCh8cFOBix2sEh-ABxgKimOELzGPuCxKiGUjN99ecWLBDoXbHQwkI7QntNDhuPvOkPPN9dPV3fNw-Pt_dXlQ2O4kKVZ8A5kJzjohbBWU2Mkp8YJYLZ1rnWGSaWZVkJZwqmbW2Ul5UwSBq7l0PEZOtv6jim-TZBLv_bZwDDoAHHKPZNSSS64FBU9_YWu4pRCva5nipO6aV5_O0N0S5kUc07g-jH5tU6bnpL-K4r-TxRVc77VZL2EH9f_BZ8Yl4r-</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Zekri, Jamal</creator><creator>Nawaz, Azhar</creator><creator>Rasool, Haleem</creator><creator>Ahmad, Imran</creator><creator>Abdel Rahman, Hossam</creator><creator>Dada, Reyad</creator><creator>Abdelghany, Ehab Mosaad</creator><creator>Farag, Kamel</creator><creator>Ibrahim, Refaei Belal</creator><creator>Deibas, Mohamed Youssef</creator><creator>Kamel, Mohamed Kamal</creator><creator>Allithy, Ahmed</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8221-9342</orcidid><orcidid>https://orcid.org/0000-0002-1329-5106</orcidid><orcidid>https://orcid.org/0000-0003-2542-0207</orcidid></search><sort><creationdate>20221201</creationdate><title>Impact of granulocyte-colony stimulating factor on docetaxel-induced febrile neutropenia in patients with breast cancer</title><author>Zekri, Jamal ; Nawaz, Azhar ; Rasool, Haleem ; Ahmad, Imran ; Abdel Rahman, Hossam ; Dada, Reyad ; Abdelghany, Ehab Mosaad ; Farag, Kamel ; Ibrahim, Refaei Belal ; Deibas, Mohamed Youssef ; Kamel, Mohamed Kamal ; Allithy, Ahmed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-b39e5943eab4dda1cc531cf4e2d8ff8fc257a2a747d031f6d7d5132502ef83e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Breast cancer</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Colonies</topic><topic>Colony-stimulating factor</topic><topic>Granulocyte colony-stimulating factor</topic><topic>Granulocytes</topic><topic>Leukocytes (granulocytic)</topic><topic>Medical records</topic><topic>Neutropenia</topic><topic>Patients</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zekri, Jamal</creatorcontrib><creatorcontrib>Nawaz, Azhar</creatorcontrib><creatorcontrib>Rasool, Haleem</creatorcontrib><creatorcontrib>Ahmad, Imran</creatorcontrib><creatorcontrib>Abdel Rahman, Hossam</creatorcontrib><creatorcontrib>Dada, Reyad</creatorcontrib><creatorcontrib>Abdelghany, Ehab Mosaad</creatorcontrib><creatorcontrib>Farag, Kamel</creatorcontrib><creatorcontrib>Ibrahim, Refaei Belal</creatorcontrib><creatorcontrib>Deibas, Mohamed Youssef</creatorcontrib><creatorcontrib>Kamel, Mohamed Kamal</creatorcontrib><creatorcontrib>Allithy, Ahmed</creatorcontrib><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of oncology pharmacy practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zekri, Jamal</au><au>Nawaz, Azhar</au><au>Rasool, Haleem</au><au>Ahmad, Imran</au><au>Abdel Rahman, Hossam</au><au>Dada, Reyad</au><au>Abdelghany, Ehab Mosaad</au><au>Farag, Kamel</au><au>Ibrahim, Refaei Belal</au><au>Deibas, Mohamed Youssef</au><au>Kamel, Mohamed Kamal</au><au>Allithy, Ahmed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of granulocyte-colony stimulating factor on docetaxel-induced febrile neutropenia in patients with breast cancer</atitle><jtitle>Journal of oncology pharmacy practice</jtitle><date>2022-12-01</date><risdate>2022</risdate><volume>28</volume><issue>8</issue><spage>1681</spage><epage>1686</epage><pages>1681-1686</pages><issn>1078-1552</issn><eissn>1477-092X</eissn><abstract>Background Febrile neutropenia (FN) is a life-threatening complication of Docetaxel-based chemotherapy regimens (DBRs). Prophylactic granulocyte-colony stimulating factor (G-CSF) can reduce the risk of FN. This study investigated the effect of G-CSF on FN in patients receiving DBRs for breast cancer. Methods Patients treated between 2015 and 2017 were identified from the hospital’s pharmacy database and their medical records were examined retrospectively. Data from patients’ first four cycles of DBR were collected. FN rate, FN associated length of hospital stay (FN-LOS), and chemotherapy dose modification/delay due to FN were compared between patients who did (G-CSF group) or did not (non-GCSF group) receive prophylactic G-CSF. Results Of the 276 included patients, 83.3% received a DBR as adjuvant or neoadjuvant therapy, and 50% received docetaxel as combination therapy. Prophylactic G-CSF was administered with the first cycle of a DBR in 69.9% of patients who were significantly less likely to experience FN compared to the non-G-CSF group (6.2% vs. 15.7%; odds ratio: 0.36 [95% CI: 0.16–0.82]; p = 0.020). Collectively and after the 4 DBR treatment cycles, FN rate (4.8 vs. 8.5; odds ratio: 0.54 [95% CI: 0.30–0.97]; p = 0.043) and the mean FN-LOS (3.55 vs. 5.28 days; t = –2.22; p = 0.037) were reduced in the G-CSF group. There was no difference in DBR dose delay/reduction between both groups in cycles 2–4. Conclusion In patients receiving DBRs for breast cancer, prophylactic G-CSF significantly reduced both the rate of FN and duration of hospitalization for FN.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><doi>10.1177/10781552211030974</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-8221-9342</orcidid><orcidid>https://orcid.org/0000-0002-1329-5106</orcidid><orcidid>https://orcid.org/0000-0003-2542-0207</orcidid></addata></record>
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1477-092X
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subjects Breast cancer
Cancer therapies
Chemotherapy
Colonies
Colony-stimulating factor
Granulocyte colony-stimulating factor
Granulocytes
Leukocytes (granulocytic)
Medical records
Neutropenia
Patients
title Impact of granulocyte-colony stimulating factor on docetaxel-induced febrile neutropenia in patients with breast cancer
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