Abstract 265P
Background
In early stage triple negative breast cancer (TNBC), surgery following neoadjuvant chemotherapy is standard of treatment. Adjuvant capecitabine showed improved survival in patients with residual disease. However, the data on clinical benefits of adjuvant capecitabine according to residual cancer burden (RCB) are insufficient.
Methods
Among patients with early TNBC who received neoadjuvant chemotherapy followed by surgery at Asan Medical Center in Seoul, Republic of Korea, between February 2008 and December 2021, those with residual tumors were included. Recurrence-free survival (RFS) as per STEEP version 2.0 was compared according to adjuvant capecitabine and RCB class.
Results
The study included 922 patients, with a median age of 47 years (range: 24–78). Of these, 230 (24.9%) received adjuvant capecitabine (capecitabine group) while 692 (75.0%) did not receive any adjuvant chemotherapy (observation group). Most patients (87.8%) received anthracycline and cyclophosphamide, with or without taxane, as part of their neoadjuvant chemotherapy regimen. RCB class well discriminated patients into prognostic groups with 2-year RFS of 69%, 58%, and 31% for patients with RCB class 1 (n=126), 2 (n=577), and 3 (n=219), respectively. No significant differences in clinical characteristics, including RCB class, were observed between the two groups (p=0.23). RFS analysis showed a trend toward improved outcomes in the capecitabine group (log-rank p=0.06). Specifically, no significant differences were found in RFS between the groups for RCB class 1 (p > 0.99) and 2 (p=0.43). However, in RCB class 3 patients, capecitabine group showed significantly better RFS compared to the observation group (log-rank p=0.02) and this was consistent in the multivariable analysis, showing a hazard ratio of 0.45 (95% CI: 0.25–0.81, p=0.007), indicating a statistically significant benefit of adjuvant capecitabine in this subgroup.
Conclusions
Adjuvant capecitabine showed clinical benefit in patients with TNBC who had residual tumor after neoadjuvant chemotherapy, and the benefit was more significant in patients with higher tumor burden with RCB class 3.
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.
Resources from the same session
354P - Synergistic preclinical efficacy through combination of the CDK4 and CDK2 selective inhibitors, PF-07220060 and PF-07104091, respectively, in HR+ HER2- breast cancer
Presenter: Lars Anders
Session: Poster session 14
355P - EVERolimus effectiveness after proGREssion on CDK4/6 inhibitors for ENdocrine receptor-positive/HER2-negative, advanced breast cancer: EVERGREEN quasi-experimental study
Presenter: Soraia Lobo-Martins
Session: Poster session 14
356P - Real-world effectiveness in subgroups of palbociclib + endocrine therapy in HR+/HER2- ABC patients: Interim results of the PERFORM study
Presenter: Georg Pfeiler
Session: Poster session 14
358P - Everolimus or ribociclib in patients with HER2-negative, hormone-receptor positive metastatic breast cancer and circulating tumor cells: Results from DETECT IVa
Presenter: Tanja Fehm
Session: Poster session 14
359P - Overall survival of palbociclib (PAL) + endocrine therapy (ET) in Japanese patients with hormone receptor-positive (HR+)/ human epidermal growth factor receptor 2-negative (HER2-) advanced breast cancer (ABC) in the 1st line (1L) or 2nd line (2L) setting: A multicenter observational study
Presenter: Takahiro Nakayama
Session: Poster session 14
360P - Identification of circulating immune factors as predictive biomarkers of CDK4/6i treatment efficacy in advanced breast cancer
Presenter: Sara Cabrero-de las Heras
Session: Poster session 14
361P - PALVEN: A phase Ib study of palbociclib, letrozole and venetoclax in ER and BCL2-positive metastatic breast cancer
Presenter: Christine Muttiah
Session: Poster session 14
362P - Dose reductions due to treatment-related side effects and survival outcomes in breast cancer patients treated with CDK4/6 Inhibitors
Presenter: Pinar Kubilay Tolunay
Session: Poster session 14
363P - Palbociclib exposure in relation to response and toxicity in patients with advanced breast cancer
Presenter: Sanne Buijs
Session: Poster session 14