Prognostic role of distant disease-free interval from completion of adjuvant trastuzumab in HER2-positive early breast cancer: analysis from the ALTTO (BIG 2-06) trial

被引:3
作者
Lambertini, Matteo [1 ,2 ]
Agbor-Tarh, Dominique [3 ]
Metzger-Filho, Otto [4 ]
Ponde, Noam F. [5 ]
Poggio, Francesca [6 ]
Hilbers, Florentine S. [7 ]
Korde, Larissa A. [8 ]
Chumsri, Saranya [9 ]
Werner, Olena [10 ]
Del Mastro, Lucia [1 ,6 ]
Caparica, Rafael [11 ,12 ]
Moebus, Volker [13 ]
Moreno-Aspitia, Alvaro [9 ]
Piccart, Martine J. [11 ,12 ]
de Azambuja, Evandro [11 ,12 ]
机构
[1] Univ Genoa, Sch Med, Dept Internal Med & Med Specialties DiMI, Genoa, Italy
[2] IRCCS Osped Policlin San Martino, Dept Med Oncol, UOC Clin Oncol Med, Genoa, Italy
[3] Frontier Sci Scotland, Kingussie, Scotland
[4] Harvard Med Sch, Dana Farber Canc Inst, Dept Med, Boston, MA 02115 USA
[5] AC Camargo Canc Ctr, Breast Canc Unit, Sao Paulo, Brazil
[6] IRCCS Osped Policlin San Martino, Breast Unit, Genoa, Italy
[7] Breast Int Grp, Brussels, Belgium
[8] NCI, Clin Invest Branch, Bethesda, MD 20892 USA
[9] Mayo Clin, Oncol Dept, Jacksonville, FL 32224 USA
[10] Novartis Int AG, Basel, Switzerland
[11] Inst Jules Bordet, Med Oncol Dept, Brussels, Belgium
[12] Univ Libre Bruxelles ULB, Brussels, Belgium
[13] Univ Hosp Frankfurt, Dept Hematol Oncol, Med Clin 2, Frankfurt, Germany
关键词
breast cancer; HER2-positive; adjuvant therapy; trastuzumab; prognosis; (NEO)ADJUVANT TRASTUZUMAB; CLINICAL-OUTCOMES; SURVIVAL; THERAPY; RETREATMENT; EMTANSINE; LAPATINIB; RELAPSE;
D O I
10.1136/esmoopen-2020-000979
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background In HER2-positive breast cancer, time elapsed between completion of (neo)adjuvant trastuzumab and diagnosis of metastatic disease ('trastuzumab-free interval', TFI) is crucial to choose the optimal first-line treatment. Nevertheless, there is no clear evidence to support its possible prognostic role. Methods In the Adjuvant Lapatinib and/or Trastuzumab Treatment Optimisation (ALTTO) trial, patients with HER2-positive early breast cancer were randomised to 1 year of either trastuzumab alone, lapatinib alone, their sequence or their combination. This exploratory analysis included only patients in the trastuzumab alone or trastuzumab plus lapatinib arms who developed a distant disease-free survival (DDFS) event. Overall survival (OS) was defined as time between date of DDFS event and death; age at diagnosis, tumour size and hormone receptor status were the variables included in the multivariate models. Results Out of 8381 patients included in ALTTO, 404 patients in the trastuzumab alone and trastuzumab plus lapatinib arms developed a DDFS event, of which 201 occurred 12 months (group A) and 203 >12 months (group B) after completion of adjuvant trastuzumab. No significant difference in location of first DDFS event was observed (p=0.073); a numerically higher number of patients in group A than in group B developed brain metastasis (26% vs 15%). Choice of first-line therapy differed between the two groups (p=0.022): in group A, more patients received lapatinib (25% vs 11%) and less pertuzumab (8% vs 17%). Median OS was 29.3 and 18.4 months in groups B and A, respectively (adjusted HR 0.69; 95% CI 0.54-0.89; p=0.004). The longer OS for patients in group B was observed across the analysed subgroups without interaction according to hormone receptor status (p=0.814) nor type of administered adjuvant anti-HER2 treatment (p=0.233). Conclusions TFI has prognostic value in patients with HER2-positive early breast cancer treated with adjuvant trastuzumab-based therapy. TFI is a valid tool to better individualise clinical recommendations and to design future first-line treatment trials for metastatic patients.
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页数:10
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