Systematic review and meta-analysis of febrile neutropenia risk with TCH(P) in HER2-positive breast cancer

被引:4
|
作者
Van Belle, Hannah [1 ]
Hurvitz, Sara A. [2 ]
Gilbar, Peter J. [3 ,4 ]
Wildiers, Hans [5 ,6 ,7 ]
机构
[1] Katholieke Univ Leuven, Fac Med, Leuven, Belgium
[2] Univ Calif Los Angeles, David Geffen Sch Med, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
[3] Toowoomba Hosp, Canc Care Serv, Toowoomba, Qld, Australia
[4] Univ Queensland, Rural Clin Sch, Fac Med, Toowoomba, Qld, Australia
[5] Univ Hosp Leuven, Leuven Canc Inst, Dept Gen Med Oncol, Herestr 49, B-3000 Leuven, Belgium
[6] Univ Hosp Leuven, Leuven Canc Inst, Multidisciplinary Breast Ctr, Herestr 49, B-3000 Leuven, Belgium
[7] Katholieke Univ Leuven, Dept Oncol, Lab Expt Oncol LEO, Leuven, Belgium
关键词
Febrile neutropenia; Granulocyte colony-stimulating factor; Neoadjuvant therapy; Breast neoplasms; Docetaxel; Carboplatin; COLONY-STIMULATING FACTOR; CHEMOTHERAPY DOSE INTENSITY; PERTUZUMAB PLUS TRASTUZUMAB; CLINICAL-PRACTICE GUIDELINE; PRIMARY PROPHYLAXIS; NEOADJUVANT DOCETAXEL; GROWTH-FACTORS; 2010; UPDATE; SAFETY; CARBOPLATIN;
D O I
10.1007/s10549-021-06387-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Docetaxel, carboplatin and trastuzumab, with or without pertuzumab (TCH(P)), has become the preferred (neo)adjuvant regimen for HER2-positive breast cancer. However, its associated febrile neutropenia (FN) risk is unclear: pivotal studies reported FN risks < 10%, but in clinical practice, a high FN rate (> 20%) was observed. This systematic review and meta-analysis determine the FN risk associated with TCH(P) and the indication for primary prophylactic granulocyte colony-stimulating factor (PP G-CSF). Methods The MEDLINE, Embase, Web of Science and Cochrane databases were searched for full-text English articles reporting the FN incidence in early breast cancer patients receiving (neo)adjuvant TCH(P). The primary endpoint was the pooled crude FN incidence in patients treated without PP G-CSF using the random effects method. Secondary endpoints were the FN risk with PP G-CSF support, age-related differences in FN and differences in risk with TCH versus TCHP. Results Seventeen studies were included in the systematic review. The pooled estimates of FN incidences were 27.6% (95% CI 18.6 to 37.1) in patients who did not receive PP G-CSF (primary meta-analysis, 9 studies, n = 889) versus 5.0% (95% CI 2.6 to 8.0) in patients administered PP G-CSF (secondary meta-analysis, 7 studies, n = 445). Two studies reported non-significant age-related differences in FN. The risk comparison between TCH and TCHP was inconclusive. Conclusions The crude FN risk associated with (neo)adjuvant TCH(P) is over 20%, the upper limit above which the international guidelines unanimously advise PP G-CSF administration. G-CSF prophylaxis effectively reduces FN risk and should become the standard of care with (neo)adjuvant TCH(P).
引用
收藏
页码:357 / 372
页数:16
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