Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display session

566P - Shorter duration of primary prophylaxis filgrastim for 4AC-4T dose dense in early breast cancer in resource-limited settings

Date

07 Dec 2024

Session

Poster Display session

Presenters

Giang Pham

Citation

Annals of Oncology (2024) 35 (suppl_4): S1595-S1615. 10.1016/annonc/annonc1695

Authors

G.H. Pham1, H.T. Phung Thi2, H.G. Yi3, L.T. Nguyen4

Author affiliations

  • 1 Department Of Oncology And Hematology, Vinmec Times City International Hospital, 100000 - Ha Noi/VN
  • 2 Medical Oncology Department, K Hospital - Vietnam National Cancer Hospital - BASE 3, 100000 - Hanoi/VN
  • 3 Oncology And Hematology, Vinmec International Hospital, 11622 - Hanoi/VN
  • 4 Medical Oncology No. 6, K Hospital - Vietnam National Cancer Hospital - BASE 3, 100000 - Hanoi/VN

Resources

This content is available to ESMO members and event participants.

Abstract 566P

Background

4AC-4T (Doxorubicin/cyclophosphamide (60/600 mg/m2) followed by paclitaxel (175 mg/m2)) dose dense chemotherapy is widely used in early-stage breast cancer. However, when giving this regimen in developing countries, there is a limited access to Peg-filgrastim, and the optimal and cost-effective duration of filgrastim for primary prophylaxis of febrile neutropenia (FN) is unknown.

Methods

This is a prospective cohort study on 93 breast cancer patients who were treated with (neo)adjuvant 4AC-4T dose dense regimen at Vietnam National Cancer Hospital from 06/2023 to 06/2024. The patients received filgrastim on day 3, 4, 5, 6, 7 after AC and day 3, 4 after T. Additional dose(s) of filgrastim was given if neutropenia of grade ≥2 was recorded on day 1 of the following cycle, and chemotherapy will be given ≥24 hours later. Rate of FN and neutropenia were assessed.

Results

The median age of patients was 48 (IQR 40-53) years old, 60.2% and 39.8% patients received 4AC-4T in adjuvant and neoadjuvant settings respectively. A total of 744 cycles of chemotherapy were given, in which FN occurred in 4 cycles (0.54%), all of which were during 4AC. Grade 1, 2, 3, 4 neutropenia were recorded after 58 (7.80%), 62 (8.33%), 26 (3.49%) and 6 (0.81%) cycles respectively, most of which occurred during 4AC (41, 48, 22, and 4 events respectively). One, two and three doses of filgrastim were added at the begining of the next cycle to correct the neutropenia after 91 (12.23%), 21 (2.82%) and 6 (0.81%) cycles, respectively. Among 4 patients who had FN, one case was treated in as outpatient and 3 cases required hospitalization.

Conclusions

This shorter duration of primary prophylaxis filgrastim allowed most patients to underwent 4AC-4T dose dense regimen without complications, which could reduce cost and side effects of G-CSF, but a closer monitoring should be given after AC. There should be larger randomized study to further evaluate the effectiveness of this schedule, especially in resource limited settings.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.