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Durable Responses to Trastuzumab Deruxtecan in Patients with Leptomeningeal Metastases from Breast Cancer with Variable HER2 Expression

Overview
Journal J Neurooncol
Publisher Springer
Date 2024 Jul 29
PMID 39073687
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Abstract

Purpose: Emerging data suggest that trastuzumab deruxtecan (T-DXd) is an active treatment for brain metastases from HER2 + breast cancer. We aimed to characterize the activity of T-DXd in the treatment of leptomeningeal metastases (LM) from a range of HER2-altered cancers.

Methods: We reviewed neuro-oncology clinic records between July 2020 and December 2023 to identify patients who received T-DXd to treat LM.

Results: Of 18 patients identified, 6 had HER2 + breast cancer, 8 had HER2-low/negative breast cancer, 2 had HER2 + gastroesophageal cancer, and 2 had HER2-mutant non-small cell lung cancer (NSCLC). 10/18 (56%) patients had cytologically confirmed LM by CSF cytology or circulating tumor cell (CTC) capture. A partial response (PR) on MRI using the EORTC/RANO-LM Revised-Scorecard occurred in 4/6 (67%) patients with HER2 + breast LM, 2/8 (25%) patients with HER2-low/negative breast cancer, and 0/4 (0%) patients with HER2 + gastroesophageal cancer or HER2-mutant NSCLC. Median overall survival after initiating T-DXd was 5.8 months. Survival after initiating T-DXd was numerically longer for HER2 + breast cancer patients compared with HER2-low/negative breast and HER2-altered non-breast cancer patients (13.9 months vs. 5.2 months and 4.6 months, respectively). Landmark analysis showed that patients with radiologic LM response to T-DXd by 2.5 months had longer survival than non-responders (14.2 months vs. 2.6 months, HR 0.18, 95% CI 0.05-0.63, p < 0.05), and landmark analyses at 3.5 and 4.5 months after starting T-DXd showed a similar but nonsignificant trend.

Conclusion: T-DXd induces LM responses in a subset of patients, and such responses may be associated with prolongation of survival. Prospective trials are needed to clarify the role of T-DXd in treating LM and which patients are most likely to benefit.

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PMID: 39712454 PMC: 11661909. DOI: 10.1002/mco2.70020.

References
1.
Roy-OReilly M, Lanman T, Ruiz A, Rogawski D, Stocksdale B, Nagpal S . Diagnostic and Therapeutic Updates in Leptomeningeal Disease. Curr Oncol Rep. 2023; 25(8):937-950. PMC: 10326117. DOI: 10.1007/s11912-023-01432-2. View

2.
Ahn M, Chiu C, Cheng Y, Han J, Goldberg S, Greystoke A . Osimertinib for Patients With Leptomeningeal Metastases Associated With EGFR T790M-Positive Advanced NSCLC: The AURA Leptomeningeal Metastases Analysis. J Thorac Oncol. 2019; 15(4):637-648. DOI: 10.1016/j.jtho.2019.12.113. View

3.
Gainor J, Sherman C, Willoughby K, Logan J, Kennedy E, Brastianos P . Alectinib salvages CNS relapses in ALK-positive lung cancer patients previously treated with crizotinib and ceritinib. J Thorac Oncol. 2014; 10(2):232-6. PMC: 4304931. DOI: 10.1097/JTO.0000000000000455. View

4.
Gainor J, Chi A, Logan J, Hu R, Oh K, Brastianos P . Alectinib Dose Escalation Reinduces Central Nervous System Responses in Patients with Anaplastic Lymphoma Kinase-Positive Non-Small Cell Lung Cancer Relapsing on Standard Dose Alectinib. J Thorac Oncol. 2016; 11(2):256-60. PMC: 4743545. DOI: 10.1016/j.jtho.2015.10.010. View

5.
Li Z, Li P, Yan B, Gao Q, Jiang X, Zhan Z . Sequential ALK inhibitor treatment benefits patient with leptomeningeal metastasis harboring non-EML4-ALK rearrangements detected from cerebrospinal fluid: A case report. Thorac Cancer. 2019; 11(1):176-180. PMC: 6938764. DOI: 10.1111/1759-7714.13259. View