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- Publisher Website: 10.1007/s00520-019-05111-6
- Scopus: eid_2-s2.0-85076527276
- PMID: 31832822
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Article: Febrile neutropenia and its associated hospitalization in breast cancer patients on docetaxel-containing regimen: A retrospective cohort study on duration of prophylactic GCSF administration
Title | Febrile neutropenia and its associated hospitalization in breast cancer patients on docetaxel-containing regimen: A retrospective cohort study on duration of prophylactic GCSF administration |
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Authors | |
Keywords | Hospitalization Docetaxel Prophylaxis Febrile neutropenia Breast cancer GCSF |
Issue Date | 2020 |
Citation | Supportive Care in Cancer, 2020, v. 28, n. 8, p. 3801-3812 How to Cite? |
Abstract | Purpose: To compare febrile neutropenia (FN) incidence and hospitalization among breast cancer patients on docetaxel with no granulocyte colony-stimulating factors (GCSF) primary prophylaxis (PP), 4/5-day PP, or 7-day PP. Methods: We identified 3916 breast cancer patients using docetaxel-cyclophosphamide (TC), doxorubicin-cyclophosphamide then docetaxel (AC-T), fluorouracil-epirubicin-cyclophosphamide then docetaxel (FEC-T), docetaxel-carboplatin-trastuzumab (TJH), or docetaxel-doxorubicin-cyclophosphamide (TAC) from a hospital pharmacy dispensing database in Hong Kong between 2014 and 2016. Patients were offered GCSF within 5 days since administering docetaxel. Outcomes included FN incidence, time to first hospitalization, hospitalization rate, and duration. Results: In TC regimen, FN incidence (with odds ratio, OR) of patients with no PP, 4/5-day PP, and 7-day PP was 21.69%, 7.95% (OR 0.31, p < 0.001), and 5.33% (OR 0.20, p < 0.001), respectively. In TJH regimen, FN incidence of patients with no PP, 4/5-day PP, and 7-day PP was 38.26%, 8.33% (OR 0.15, p < 0.001), and 8.57% (OR 0.15, p < 0.001), respectively. FN incidence of patients on AC-T regimen with no PP and 4/5-day PP was 20.93% and 6.84%, respectively (OR 0.28, p = 0.005); with FEC-T regimen, the incidence was 9.91% and 4.77%, respectively (OR 0.46, p = 0.035). Only 3.27% FN cases were not hospitalized. Mean (±standard deviation, SD) time to first hospitalization was 8.21 ± 2.44 days. Mean (±SD) duration of hospitalization for patients with no PP, 4/5-day PP, and 7-day PP was 4.66 ± 2.60, 4.37 ± 2.85, and 5.12 ± 2.97 days, respectively. Conclusion: GCSF prophylaxis in breast cancer patients on docetaxel could reduce FN incidence and hospitalization. 4/5-day PP demonstrated similar efficacy to 7-day PP with superior saving benefits on healthcare expenditure. |
Persistent Identifier | http://hdl.handle.net/10722/303636 |
ISSN | 2023 Impact Factor: 2.8 2023 SCImago Journal Rankings: 1.007 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lee, C. F. | - |
dc.contributor.author | Zhou, K. | - |
dc.contributor.author | Young, W. M. | - |
dc.contributor.author | Wong, C. S. | - |
dc.contributor.author | Ng, T. Y. | - |
dc.contributor.author | Lee, S. F. | - |
dc.contributor.author | Leung, K. | - |
dc.contributor.author | Wong, L. K.M. | - |
dc.contributor.author | So, K. H. | - |
dc.contributor.author | Tang, W. | - |
dc.contributor.author | Chong, G. | - |
dc.contributor.author | Chan, S. K. | - |
dc.contributor.author | Yip, Y. T.E. | - |
dc.contributor.author | Ma, V. Y.M. | - |
dc.contributor.author | Yeung, A. | - |
dc.contributor.author | Chin, C. H.Y. | - |
dc.contributor.author | Kwan, M. W. | - |
dc.contributor.author | Tsang, H. T. | - |
dc.date.accessioned | 2021-09-15T08:25:43Z | - |
dc.date.available | 2021-09-15T08:25:43Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Supportive Care in Cancer, 2020, v. 28, n. 8, p. 3801-3812 | - |
dc.identifier.issn | 0941-4355 | - |
dc.identifier.uri | http://hdl.handle.net/10722/303636 | - |
dc.description.abstract | Purpose: To compare febrile neutropenia (FN) incidence and hospitalization among breast cancer patients on docetaxel with no granulocyte colony-stimulating factors (GCSF) primary prophylaxis (PP), 4/5-day PP, or 7-day PP. Methods: We identified 3916 breast cancer patients using docetaxel-cyclophosphamide (TC), doxorubicin-cyclophosphamide then docetaxel (AC-T), fluorouracil-epirubicin-cyclophosphamide then docetaxel (FEC-T), docetaxel-carboplatin-trastuzumab (TJH), or docetaxel-doxorubicin-cyclophosphamide (TAC) from a hospital pharmacy dispensing database in Hong Kong between 2014 and 2016. Patients were offered GCSF within 5 days since administering docetaxel. Outcomes included FN incidence, time to first hospitalization, hospitalization rate, and duration. Results: In TC regimen, FN incidence (with odds ratio, OR) of patients with no PP, 4/5-day PP, and 7-day PP was 21.69%, 7.95% (OR 0.31, p < 0.001), and 5.33% (OR 0.20, p < 0.001), respectively. In TJH regimen, FN incidence of patients with no PP, 4/5-day PP, and 7-day PP was 38.26%, 8.33% (OR 0.15, p < 0.001), and 8.57% (OR 0.15, p < 0.001), respectively. FN incidence of patients on AC-T regimen with no PP and 4/5-day PP was 20.93% and 6.84%, respectively (OR 0.28, p = 0.005); with FEC-T regimen, the incidence was 9.91% and 4.77%, respectively (OR 0.46, p = 0.035). Only 3.27% FN cases were not hospitalized. Mean (±standard deviation, SD) time to first hospitalization was 8.21 ± 2.44 days. Mean (±SD) duration of hospitalization for patients with no PP, 4/5-day PP, and 7-day PP was 4.66 ± 2.60, 4.37 ± 2.85, and 5.12 ± 2.97 days, respectively. Conclusion: GCSF prophylaxis in breast cancer patients on docetaxel could reduce FN incidence and hospitalization. 4/5-day PP demonstrated similar efficacy to 7-day PP with superior saving benefits on healthcare expenditure. | - |
dc.language | eng | - |
dc.relation.ispartof | Supportive Care in Cancer | - |
dc.subject | Hospitalization | - |
dc.subject | Docetaxel | - |
dc.subject | Prophylaxis | - |
dc.subject | Febrile neutropenia | - |
dc.subject | Breast cancer | - |
dc.subject | GCSF | - |
dc.title | Febrile neutropenia and its associated hospitalization in breast cancer patients on docetaxel-containing regimen: A retrospective cohort study on duration of prophylactic GCSF administration | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1007/s00520-019-05111-6 | - |
dc.identifier.pmid | 31832822 | - |
dc.identifier.scopus | eid_2-s2.0-85076527276 | - |
dc.identifier.volume | 28 | - |
dc.identifier.issue | 8 | - |
dc.identifier.spage | 3801 | - |
dc.identifier.epage | 3812 | - |
dc.identifier.eissn | 1433-7339 | - |
dc.identifier.isi | WOS:000543089300035 | - |