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Lunch and Poster Display session

202P - Complete response rates, treatment patterns and survival outcomes in patients treated with first-line pertuzumab-based therapy in HER2-positive advanced breast cancer: A SONABRE study

Date

16 May 2024

Session

Lunch and Poster Display session

Presenters

Nan Ding

Citation

Annals of Oncology (2024) 9 (suppl_4): 1-47. 10.1016/esmoop/esmoop103200

Authors

N. Ding1, S.M.E. Geurts1, J. Tol2, B.E.P.J. Vriens3, K.N.A. Aaldering4, E. Boon5, M.W. Dercksen6, F. Van den Berkmortel7, M.J.A.E. Pepels8, N.A..J..B. Peters9, J.B. Heijns10, L.V.D. Winkel11, A.J.O. de Fallois1, V.C.G. Tjan-Heijnen1, M. De Boer1

Author affiliations

  • 1 Maastricht University Medical Center (MUMC), Maastricht/NL
  • 2 Jeroen Bosch Hospital, 's-Hertogenbosch/NL
  • 3 Catharina Hospital Eindhoven, Eindhoven/NL
  • 4 Laurentius Ziekenhuis, Roermond/NL
  • 5 VieCuri Medical Center, Venlo/NL
  • 6 Maxima Medisch Centrum -Veldhoven, Veldhoven/NL
  • 7 Zuyderland Medical Center, Heerlen/NL
  • 8 Elkerliekziekenhuis, Helmond/NL
  • 9 St Jans Gasthuis, Weert/NL
  • 10 Amphia Ziekenhuis-location Molengracht, Breda/NL
  • 11 St.Anna Hospital, Geldrop/NL

Resources

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Abstract 202P

Background

Complete response (CR) rates on first-line pertuzumab-trastuzumab-chemotherapy (PTC) in HER2-positive (HER2+) advanced breast cancer (ABC) are unknown. We aimed to describe real world CR rates, predictors of CR, treatment patterns and outcome in patients treated with first-line PTC for HER2+ ABC.

Methods

We included patients with HER2+ ABC who started first-line PTC in ten Dutch hospitals in 2013-2019 from the SONABRE registry (NCT-03577197). CR was defined as no disease evidence on imaging, or post-resection and/or radiotherapy. Multivariable logistic regression was used to identify predictors for CR. Treatment patterns in patients achieving CR were reported. Progression-free survival (PFS) and overall survival (OS) from start of first-line PTC were computed with the Kaplan-Meier method.

Results

We identified 159 patients treated with first-line PTC, of whom 84% were <65 years, 48% hormone receptor-positive disease, 51% de novo disease, 75% visceral metastases, and 11% CNS metastases. The chemotherapy backbone included taxanes (93%). The median follow-up duration of 62 months. Forty patients (25%) reached CR. Patients with de Novo ABC (Odds ratio (OR)=2.35, 95% confidence interval(CI):1.05-5.28, p=0.04) and single organ metastasis (OR=3.44, 95%CI:1.58-7.49, p=0.002) were more likely to reach CR. Among patients reaching CR, 21 (53%) stopped pertuzumab and trastuzumab, 11 (27%) stopped pertuzumab but continued trastuzumab and 8 (20%) continued both until progression or last follow-up. In patients who achieved CR, the 5-year PFS rate was 59% (95%CI:39%-74%), while in those who did not, it was 9% (95%CI:4%-17%). The 5-year OS rates were 83% (95%CI:63%-93%) and 30% (95%CI:21%-40%), respectively.

Conclusions

In this real world cohort, one in four patients treated with first-line PTC reached CR. In 80% of the patients achieving CR, pertuzumab was stopped early. Patients reaching CR have a better prognosis than those not reaching CR. Prospective studies on the safety of HER2-targeted therapy discontinuation in patients with CR in HER2+ ABC are warranted.

Legal entity responsible for the study

Maastricht University Medical Center.

Funding

Novartis BV, Roche, Pfizer, Eli Lilly, Daiichi Sankyo, Gilead and AstraZeneca.

Disclosure

S.M.E. Geurts: Financial Interests, Institutional, Funding: Novartis BV, Roche, Pfizer, Eli Lilly, Daiichi Sankyo, Gilead, AstraZeneca; Financial Interests, Personal, Funding: AstraZeneca. A.J.O. de Fallois: Financial Interests, Institutional, Funding: Novartis BV, Roche, Pfizer, Eli Lilly, Daiichi Sankyo, Gilead, AstraZeneca. V.C.G. Tjan-Heijnen: Financial Interests, Institutional, Funding: Roche, Novartis, Pfizer, Eli Lilly, AstraZeneca, Eisai, Daiichi Sankyo, Gilead; Financial Interests, Personal, Funding: Roche, Novartis, Pfizer, Eli Lilly, Accord Healthcare. M. De Boer: Financial Interests, Institutional, Funding: Novartis BV, Roche, Pfizer, Eli Lilly, Daiichi Sankyo, Gilead, AstraZeneca. All other authors have declared no conflicts of interest.

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