PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
February 19, 2026Clinical Cancer Research0 citations

Abstract PS4-07-25: Real World Analysis of Efficacy, Toxicity, and Treatment Patterns of Pembrolizumab-Containing Regimens for Older Adults with Early-Stage Triple Negative Breast Cancer

View Full Paper
CSC. SmithARAvina RamiTLT. Li

Key Points

  • This analysis aims to evaluate the efficacy, toxicity, and treatment patterns of pembrolizumab-containing regimens in older adults with early-stage triple negative breast cancer.
  • Reviewed medical records of patients ≥ 65 years diagnosed with early-stage TNBC.
  • Included patients receiving neoadjuvant pembrolizumab-containing regimens.
  • Examined relative dose intensity, hospitalizations, immune related adverse events, and pathological complete response rates.
  • Used statistical tests like Kruskal-Wallis and chi-square for analysis.
  • Median age of patients was 70 years; 41% were hospitalized during treatment.
  • Overall pathological complete response rate was 43%.
  • 41% of patients discontinued treatment early due to adverse events, and 39% experienced an immune related adverse event.
  • Older patients (>70) had higher rates of immune related adverse events and lower relative dose intensity.

Abstract

Abstract Background: Older adults are underrepresented in clinical trials of neoadjuvant chemotherapy and pembrolizumab for early-stage triple negative breast cancer (TNBC), limiting evidence to guide treatment in this population. Given the potential toxicity of multi-agent regimens, we examined treatment patterns, efficacy, and safety outcomes for patients ≥ 65 years who received neoadjuvant pembrolizumab containing treatments for early-stage TNBC. Methods: Through medical review at a National Cancer Institute-designated comprehensive cancer center, we abstracted records for those aged ≥ 65 years at the time of a stage I-III TNBC diagnosis during 08/2021-05/2024. Patients were included if they received a pembrolizumab-containing regimen as neoadjuvant therapy. The primary endpoint was relative dose intensity (RDI), defined as the average percent of planned neoadjuvant treatment received across agents. We also ascertained records for hospitalizations, early treatment discontinuation, immune related adverse events (IRAE), and pathological complete response (pCR) status at surgery. We examined associations between age (65-70) vs (70) and occurrence of these events. In addition, we examined if treatment-related factors including RDI, duration of neoadjuvant therapy, anthracycline receipt, and age were associated with pCR. We used Kruskal-Wallis rank sum test for continuous variables and chi-square test for categorical variables. Results: Overall, 85 women were included in analyses; median age was 70. At the time of diagnosis, n=13 (15%) had heart disease, n=4 (5%) lung disease, n=6 (7%) chronic kidney disease, and n=1 (1%) cognitive impairment. For treatment regimens, 42% (n=36) received KEYNOTE 522 (carboplatin + paclitaxel + doxorubicin + cyclophosphamide + pembrolizumab), 41% (n=35) received carboplatin + paclitaxel + pembrolizumab, 4 (5%) doxorubicin + cyclophosphamide, + taxane + pembrolizuamb, and 4 (5%) docetaxel + carboplatin + pembrolizumab. Across regimens, median RDI was 90% (range 20-100%), and 55% (n=47) receieved ≥85% RDI. During neoadjuvant therapy, 41% (n=35) of patients were hospitalized at least once, 6% of all patients (n=5) required ICU admission, and 41% (n=35) discontinued treatment early due to adverse events. Overall, 39% (n=33) experienced an IRAE, of which 49% (n=16) required steroids. There were 3 deaths attributed to neoadjuvant treatment, specifically pneumonitis, pneumonia/septic shock, and multi-organ failure. Patients age 70, when compared to ages 65-70, were more likely to experience IRAE (OR 2.8, p=0.024) and receive lower RDI (OR 0.3, p=0.013). Rates of hospitalization, early treatment discontinuation, and path CR did not differ by age. The overall pCR rate was 43%. Factors including RDI, treatment duration, anthracycline, hospitalizations, immune related adverse events, and age were not associated with pCR. Conclusions: In this real-world cohort, half of older adults with early-stage TNBC received a non-anthracycline containing chemotherapy regimen with pembrolizumab, most commonly carboplatin and paclitaxel. Early discontinuation of neoadjuvant therapy was frequent with nearly 45% not receiving ≥85% RDI. Rates of hospitalization, immune related adverse events, and death were high, while pCR rates were lower than reported in clincal trials. Safer, more effective treatments are needed for older adults with early-stage TNBC. Citation Format: C. Smith, A. Rami, T. Li, P. Patel, M. Ling, R. Freedman. Real World Analysis of Efficacy, Toxicity, and Treatment Patterns of Pembrolizumab-Containing Regimens for Older Adults with Early-Stage Triple Negative Breast Cancer abstract. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS4-07-25.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Smith et al. (2026) studied this question.

synapsesocial.com/papers/6996a83eecb39a600b3eeb60https://doi.org/10.1158/1557-3265.sabcs25-ps4-07-25
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Abstract PS1-01-29: Real-world immune toxicity and survival outcomes by age in triple-negative breast cancer patients receiving pembrolizumab2026
  2. 2Abstract PS4-07-26: Safety and efficacy of neoadjuvant cyclophosphamide, methotrexate, fluorouracil (CMF) and pembrolizumab in older adults with early triple negative breast cancer (TNBC)2026
  3. 3Age-related immune toxicity and treatment outcomes in triple-negative breast cancer treated with pembrolizumab.2026
  4. 4Abstract PS2-06-20: Fr-popea: French real-world-data of peri-operative pembrolizumab KN522 regimen in extreme ages subgroups (<30 y.o and >70 y.o) with high-risk TNBC2026
  5. 5Real-world effectiveness and safety of first-line pembrolizumab plus chemotherapy in patients aged ≥65 years with metastatic triple-negative breast cancer.2026