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논문 기본 정보

자료유형
학술저널
저자정보
Jihyoun Lee (Soonchunhyang University Seoul Hospital) Jong Eun Lee (Soonchunhyang University Cheonan Hospital) Zisun Kim (Soonchunhyang University Bucheon Hospital) Sun Wook Han (Soonchunhyang University Cheonan Hospital) Sung Mo Hur (Soonchunhyang University Bucheon Hospital) Sung Yong Kim (Soonchunhyang University Cheonan Hospital) Min Hyuk Lee (Soonchunhyang University Seoul Hospital) Cheol Wan Lim (Soonchunhyang University Bucheon Hospital)
저널정보
대한외과학회 Annals of Surgical Treatment and Research Annals of Surgical Treatment and Research Vol.94 No.5
발행연도
2018.5
수록면
223 - 228 (6page)

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Purpose: Primary prophylaxis with granulocyte colony-stimulating factor can effectively prevent febrile neutropenia (FN) during breast cancer treatment. The aims of this study were to evaluate the incidence of FN and the ANC profile in patients undergoing chemotherapy and pegfilgrastim primary prophylaxis.
Methods: Patients receiving 6 cycles of adjuvant docetaxel, doxorubicin, and cyclophosphamide (TAC) chemotherapy were included in this study. Pegfilgrastim was administered with analgesics 24 hours after treatment. Laboratory tests were performed on day 0 (before chemotherapy) and ANC was measured daily starting day 5 until it were restored to 1,000/㎣. Bone pain was checked via the numeral rating scale (NRS).
Results: A total of 61 patients and 366 cycles were evaluated. Mean age was 49.2 ± 7.1 years. FN was seen in 5 patients (16.4%) and 12 cycles (3.3%) with pegfilgrastim. Grades 3 and 4 neutropenia was seen in 91.5% of cycles with FN. The ANC nadir was most commonly seen at day 7 and the mean ANC nadir depth was 265.7/㎥. Age was negatively correlated with nadir depth (r = –0.137, P = 0.009). Severe pain higher than NRS 7 occurred in less than 20% of patients after the administration of pegfilgrastim.
Conclusion: Incidence of FN was low during the chemotherapy by primary prophylaxis with pegfilgrastim. The ANC nadir was seen on day 7 after chemotherapy. Bone pain with pegfilgrastim was well tolerated during TAC chemotherapy.

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INTRODUCTION
METHODS
RESULTS
DISCUSSION
REFERENCES

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