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培非格司亭±环丙沙星用于TAC(多西他赛/阿霉素/环磷酰胺)化疗方案对乳腺癌进行一级预防。GEPARTRIO研究结果

Pegfilgrastim +/- ciprofloxacin for primary prophylaxis with TAC (docetaxel/doxorubicin/cyclophosphamide) chemotherapy for breast cancer. Results from the GEPARTRIO study.

作者信息

von Minckwitz G, Kümmel S, du Bois A, Eiermann W, Eidtmann H, Gerber B, Hilfrich J, Huober J, Costa S D, Jackisch C, Grasshoff S-T, Vescia S, Skacel T, Loibl S, Mehta K M, Kaufmann M

机构信息

German Breast Group, Neu-Isenburg, Germany.

出版信息

Ann Oncol. 2008 Feb;19(2):292-8. doi: 10.1093/annonc/mdm438. Epub 2007 Sep 9.

Abstract

BACKGROUND

TAC (docetaxel/doxorubicin/cyclophosphamide) is associated with high incidences of grade 4 neutropenia and febrile neutropenia (FN). This analysis compared the efficacies of four regimens for primary prophylaxis of FN and related toxic effects in breast cancer patients receiving neoadjuvant TAC.

PATIENTS AND METHODS

Patients with stage T2-T4 primary breast cancer were scheduled to receive 6-8 cycles of TAC. Primary prophylaxis was: ciprofloxacin 500 mg orally twice daily on days 5-14 (n = 253 patients; 1478 cycles), daily granulocyte colony-stimulating factor (G-CSF) (filgrastim 5 microg/kg/day or lenograstim 150 microg/m(2)/day) on days 5-10 (n = 377; 2400 cycles), pegfilgrastim 6 mg on day 2 (n = 305; 1930 cycles), or pegfilgrastim plus ciprofloxacin (n = 321; 1890 cycles).

RESULTS

Pegfilgrastim with/without ciprofloxacin was significantly more effective than daily G-CSF or ciprofloxacin in preventing FN (5% and 7% versus 18% and 22% of patients; all P < 0.001), grade 4 neutropenia, and leukopenia. Pegfilgrastim plus ciprofloxacin completely prevented first cycle FN (P < 0.01 versus pegfilgrastim alone) and fatal neutropenic events.

CONCLUSION

Ciprofloxacin alone, or daily G-CSF from day 5-10 (as in common practice), provided suboptimal protection against FN and related toxic effects in patients receiving TAC. Pegfilgrastim was significantly more effective in this setting, especially if given with ciprofloxacin.

摘要

背景

多西他赛/阿霉素/环磷酰胺(TAC)与4级中性粒细胞减少症和发热性中性粒细胞减少症(FN)的高发生率相关。本分析比较了四种方案对接受新辅助TAC治疗的乳腺癌患者进行FN一级预防及其相关毒性作用的疗效。

患者与方法

T2 - T4期原发性乳腺癌患者计划接受6 - 8个周期的TAC治疗。一级预防方案为:第5 - 14天口服环丙沙星500 mg,每日两次(n = 253例患者;1478个周期);第5 - 10天每日使用粒细胞集落刺激因子(G - CSF)(非格司亭5 μg/kg/天或来格司亭150 μg/m²/天)(n = 377例;2400个周期);第2天使用聚乙二醇化重组人粒细胞刺激因子6 mg(n = 305例;1930个周期);或聚乙二醇化重组人粒细胞刺激因子加环丙沙星(n = 321例;1890个周期)。

结果

聚乙二醇化重组人粒细胞刺激因子联合或不联合环丙沙星在预防FN(患者比例分别为5%和7%,而每日G - CSF组和环丙沙星组分别为18%和22%;所有P < 0.001)、4级中性粒细胞减少症和白细胞减少症方面显著优于每日使用G - CSF或环丙沙星。聚乙二醇化重组人粒细胞刺激因子加环丙沙星完全预防了首个周期的FN(与单用聚乙二醇化重组人粒细胞刺激因子相比,P < 0.01)以及致命的中性粒细胞减少事件。

结论

单独使用环丙沙星,或如常规做法在第5 - 10天每日使用G - CSF,对接受TAC治疗的患者预防FN及其相关毒性作用的效果欠佳。在这种情况下,聚乙二醇化重组人粒细胞刺激因子显著更有效,尤其是与环丙沙星联合使用时。

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