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Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

4581 - Analysis of parameters to predict the effectiveness of scalp cooling to prevent chemotherapy-induced alopecia in breast cancer patients

Date

22 Oct 2018

Session

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

Topics

Management of Systemic Therapy Toxicities;  Supportive Care and Symptom Management

Tumour Site

Breast Cancer

Presenters

Christian Kurbacher

Citation

Annals of Oncology (2018) 29 (suppl_8): viii603-viii640. 10.1093/annonc/mdy300

Authors

C.M. Kurbacher1, S. Herz1, A.T. Kurbacher1, G. Kolberg1, N. Kettelhoit1, A. Schott1, J.A. Kurbacher2

Author affiliations

  • 1 Gynaecology I (gynaecological Oncology, Gynaecological Center Bonn-Friedensplatz, 53111 - Bonn/DE
  • 2 Gynaecology Ii (general Gynaecology And Obstetrics), Gynaecological Center Bonn-Friedensplatz, 53111 - Bonn/DE

Resources

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Abstract 4581

Background

Sensor-controlled scalp cooling (SCSC) has been found to be effective to prevent chemotherapy (Ctx)-induced alopecia (CIA). This retrospective study sought to obtain detailed information which clinical parameter is able to predict the success of SCSC in patients (pts) with primary (PBC) or recurrent/metastatic breast cancer (R/MBC) exposed to neoadjuvant (NACT), adjuvant (ACT), or palliative Ctx (PCT) using anthracyclines (A), taxanes (T), both given at different schedules (A+T/A→T, T→A) or none of them (non-A/non-T).

Methods

109 pts who underwent SCSC were included: NACT, 47 (54.6%); ACT, 40 (45.4%); PCT 22; dose-dense (dd) Ctx, 38 (44.2%); non-dd Ctx 48 (55.8%); premenopausal, 48 (55.8%); postmenopausal, 38 (44.2%). Ctx regimens were: A+T/A→T, 41 (37.6%), T→A, 23 (26.7%), T, 34 (31.2%), non-A/non-T, 11 (10.1%). 3 wks after the last Ctx cycle, CIA was quantified according to the Dean score (DS). Data were analyzed in regard to the SCSC completion rate, and the quality of hair preservation (success: DS 0-2, failure: DS 3-4). The following parameters were investigated in regard to the success of SCSC: menopausal status, pretreatment, setting of Ctx, Ctx schedule, Ctx regimen.

Results

Success rate was 67.9% with 47 pts (43.1%) experiencing complete (DS 0), and 27 (24.8%) showing partial response (DS 1-2). 30 pts (27.5%) stopped SCSC prematurely with CIA being the reason in 21 pts (19.3%). Effectiveness of SCSC did not differ for most analyzed subgroups. The relative risk (RR) to experience CIA was 1.18 (CI: 0.91-1.53, p=NS) for post- vs premenopausal pts, 1.27 (CI: 0.99-1.64, p=NS) for Ctx-naïve vs pretreated pts, 1.18 (CI: 0.89-1.56, p=NS) for dd Ctx vs non-dd Ctx, 1.42 (CI: 1.03-1.80, p = 0.05) for NACT/ACT vs PCT, and 1.42 (1.11-1.85, 0.012) for A-based Ctx vs non A-based Ctx. Success rates for A+T/A→T, T→A, T, and non-A/non-T were 48.8%, 73.9%, 79.4%, and 90.9% (p = 0.015).

Conclusions

SCSC could effectively prevent CIA in a real-world population of pts with PBC or R/MBC with all subgroups of pts benefiting. NACT/ACT and A-based Ctx are associated with lower success rates of SCSC. However, the effectiveness of SCSC associated with A-based Ctx can be as high providing that Ctx does not start with an anthracycline.

Clinical trial identification

Legal entity responsible for the study

Christian M. Kurbacher, Gynaecological Centre Bonn-Friedensplatz.

Funding

Has not received any funding,

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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