Survival Outcomes, Digital TILs, and On-treatment PET/CT During Neoadjuvant Therapy for HER2-positive Breast Cancer: Results from the Randomized PREDIX HER2 Trial

被引:24
作者
Matikas, Alexios [1 ,2 ,3 ]
Johansson, Hemming [3 ]
Gryback, Per [4 ]
Bjohle, Judith [1 ,2 ]
Acs, Balazs [3 ,5 ]
Boyaci, Ceren [3 ,5 ]
Lekberg, Tobias [1 ,2 ,3 ]
Fredholm, Hanna [1 ,2 ,4 ]
Elinder, Ellinor [6 ]
Margolin, Sara [6 ,7 ]
Isaksson-Friman, Erika [8 ]
Bosch, Ana [9 ]
Lindman, Henrik [10 ]
Adra, Jamila [11 ]
Andersson, Anne [12 ]
Agartz, Susanne [3 ]
Hellstrom, Mats [1 ,2 ]
Zerdes, Ioannis [1 ,2 ,3 ]
Hartman, Johan [3 ,5 ]
Bergh, Jonas [1 ,2 ,3 ]
Hatschek, Thomas [1 ,2 ,3 ]
Foukakis, Theodoros [1 ,2 ,3 ]
机构
[1] Karolinska Univ Hosp, Breast Ctr, Theme Canc, Stockholm, Sweden
[2] Karolinska Comprehens Canc Ctr, Stockholm, Sweden
[3] Karolinska Inst, Dept Oncol Pathol, Stockholm, Sweden
[4] Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
[5] Karolinska Univ Hosp, Dept Clin Pathol & Canc Diagnost, Stockholm, Sweden
[6] Soder Sjukhuset, Dept Oncol, Stockholm, Sweden
[7] Karolinska Inst, Sodersjukhuset, Dept Clin Sci & Educ, Stockholm, Sweden
[8] St Goran Hosp, Breast Ctr, Stockholm, Sweden
[9] Skane Univ Hosp, Dept Hematol Oncol & Radiat Phys, Lund, Sweden
[10] Uppsala Univ Hosp, Dept Oncol, S-17176 Uppsala, Sweden
[11] Sahlgrens Univ Hosp, Dept Oncol, S-17176 Gothenburg, Sweden
[12] Umea Univ Hosp, Dept Radiat Sci, Oncol Unit, Umea, Sweden
基金
瑞典研究理事会;
关键词
PATHOLOGICAL COMPLETE RESPONSE; DE-ESCALATION STRATEGIES; PHASE-II; TRASTUZUMAB EMTANSINE; PREDICTIVE MARKERS; FINAL ANALYSIS; OPEN-LABEL; PERTUZUMAB; SAFETY; CHEMOTHERAPY;
D O I
10.1158/1078-0432.CCR-22-2829
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: PREDIX HER2 is a randomized Phase II trial that compared neoadjuvant docetaxel, trastuzumab, and pertuzumab (THP) with trastuzumab emtansine (T-DM1) for HER2-positive breast cancer. Rates of pathologic complete response (pCR) did not differ between the two groups. Here, we present the survival out-comes from PREDIX HER2 and investigate metabolic response and tumor-infiltrating lymphocytes (TIL) as prognostic factors.Patients and Methods: In total, 202 patients with HER2-positive breast cancer were enrolled and 197 patients received six cycles of either THP or T-DM1. Secondary endpoints included event-free survival (EFS), recurrence-free survival (RFS), and overall survival (OS). Assessment with PET/CT was performed at baseline, after two and six treatment cycles. TILs were assessed manually at baseline biopsies, while image-based evaluation of TILs [digital TILs (DTIL)] was performed in digitized full-face sections.Results: After a median follow-up of 5.21 years, there was no difference between the two treatment groups in terms of EFS [HR = 1.26; 95% confidence interval (CI), 0.54-2.91], RFS (HR = 0.69; 95% CI, 0.24-1.93), or OS (HR = 0.52; 95% CI, 0.09-2.82). Higher SUVmax at cycle 2 (C2) predicted lower pCR (ORadj = 0.65; 95% CI, 0.48-0.87; P = 0.005) and worse EFS (HRadj = 1.27; 95% CI, 1.12-1.4 1; P < 0.001). Baseline TILs and DTILs provided additional prognostic information to clinical parameters and C2 SUVmax.Conclusions: Long-term outcomes following neoadjuvant T-DM1 were similar to neoadjuvant THP. SUVmax after two cycles of neoadjuvant therapy for HER2-positive breast cancer may be an independent predictor of both short-and long-term outcomes. Combined assessment with TILs may facilitate early selection of poor responders for alternative treatment strategies.
引用
收藏
页码:532 / 540
页数:9
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