- |||||||||| Yondelis (trabectedin) / Otsuka, PharmaMar, Valeo Pharma, Votrient (pazopanib) / Novartis, Halaven (eribulin mesylate) / Eisai
Clinical, Journal: Does the Use of Peripheral Immune-Related Markers Indicate Whether to Administer Pazopanib, Trabectedin, or Eribulin to Advanced Soft Tissue Sarcoma Patients? (Pubmed Central) - Nov 17, 2021 In the low platelet-to-lymphocyte ratio (PLR) subgroup, the OS of the patients administered eribulin for the first choice was longer than that of the others (HR = 0.32, 95%CI = 0.10-0.98, p = 0.046). Therefore, NLR and PLR might be used as prognostic indicators to dictate whether STS patients receive pazopanib, trabectedin, or eribulin.
- |||||||||| Halaven (eribulin mesylate) / Eisai
Real world data on outcome for HER2-positive metastatic breast cancer from two UK centres ([VIRTUAL]) - Nov 16, 2021 - Abstract #NCRI2021NCRI_160; Dual anti-HER2 monoclonal antibodies (Trastuzumab and Pertuzumab) with taxane is the standard of care as first-line treatment and antibody-drug conjugate Trastuzumab Emtansine (TDM-1) as second-line therapy for HER2-positive metastatic breast cancer (MBC)...19/22 patients received 3rd-line treatment using a combination of chemotherapy ±Trastuzumab; Capecitabine (10 patients), Eribulin (4 patients)...Impact statement Our results highlight poor patient outcomes following progression on dual anti-HER2 treatment. It provides baseline real time data which can be used to compare efficacy of new therapeutic agents like Trastuzumab Deruxtecan approved in this setting.
- |||||||||| Halaven (eribulin mesylate) / Eisai
Trial completion, Trial primary completion date, Metastases: Eribulin Mesylate in Treating Patients With Advanced or Recurrent Cervical Cancer (clinicaltrials.gov) - Nov 15, 2021 P2, N=32, Completed, It provides baseline real time data which can be used to compare efficacy of new therapeutic agents like Trastuzumab Deruxtecan approved in this setting. Active, not recruiting --> Completed | Trial primary completion date: Aug 2020 --> Feb 2021
- |||||||||| Halaven (eribulin mesylate) / Eisai
Journal, IO biomarker: Eribulin activates the cGAS-STING pathway via the cytoplasmic accumulation of mtDNA. (Pubmed Central) - Nov 12, 2021 While all clinically approved MTAs share an antimitotic mechanism of action, their distinct effects on interphase microtubules can promote differential downstream signaling consequences. We show that the microtubule destabilizer eribulin, but not the microtubule stabilizer paclitaxel, activates the cGAS-STING innate immune signaling pathway through the accumulation of mitochondrial DNA in the cytoplasm.
- |||||||||| Keytruda (pembrolizumab) / Merck (MSD), Halaven (eribulin mesylate) / Eisai
Clinical, Journal: Pembrolizumab plus eribulin in hormone-receptor-positive, HER2-negative, locally recurrent or metastatic breast cancer (KELLY): An open-label, multicentre, single-arm, phase Ⅱ trial. (Pubmed Central) - Oct 27, 2021 P2 Pembrolizumab plus eribulin demonstrates encouraging antitumour activity in patients with heavily pre-treated, HR+, HER2-negative, locally recurrent or metastatic BC. The safety and tolerability of the combination is similar to eribulin or pembrolizumab monotherapy.
- |||||||||| Halaven (eribulin mesylate) / Eisai
Enrollment closed, Enrollment change, Trial completion date, Trial primary completion date: Study to Assess Safety and Preliminary Activity of Eribulin Mesylate in Pediatric Participants With Relapsed/Refractory Rhabdomyosarcoma (RMS), Non-rhabdomyosarcoma Soft Tissue Sarcoma (NRSTS) and Ewing Sarcoma (EWS) (clinicaltrials.gov) - Oct 22, 2021 P2, N=23, Active, not recruiting, ClinicalTrials.gov Registration: NCT03051659. Recruiting --> Active, not recruiting | N=45 --> 23 | Trial completion date: Jun 2021 --> Dec 2021 | Trial primary completion date: Jun 2021 --> Jan 2021
- |||||||||| Halaven (eribulin mesylate) / Eisai, VS-6766 / Verastem
Clinical, Journal, Combination therapy, PD(L)-1 Biomarker, IO biomarker: The novel RAF/MEK inhibitor CH5126766/VS-6766 has efficacy in combination with eribulin for the treatment of TNBC. (Pubmed Central) - Oct 15, 2021 We also showed the suppressed expression of PD-L1 in the combination therapy in vivo. We demonstrated that combination therapy with eribulin and CH5126766 for triple-negative breast cancer inhibited cell growth by apoptosis and raised a possibility that immune responses through suppression of PD-L1 might partially contribute to inhibition of tumor growth, indicating the potential of this combination as a novel strategy for triple-negative breast cancer.
- |||||||||| Halaven (eribulin mesylate) / Eisai
Biomarker, P2 data, Clinical Trial,Phase II, Journal: An Exploratory Phase II Study of Eribulin Re-challenge After Short Term Therapy of 5-Fluorouracil for HER2 Negative, Advanced or Recurrent Breast Cancer. (Pubmed Central) - Oct 14, 2021 We demonstrated that combination therapy with eribulin and CH5126766 for triple-negative breast cancer inhibited cell growth by apoptosis and raised a possibility that immune responses through suppression of PD-L1 might partially contribute to inhibition of tumor growth, indicating the potential of this combination as a novel strategy for triple-negative breast cancer. In the first-line setting, the total PFS of eribulin was extended by S-1 administration before disease progression, compared with that of our previous report.
- |||||||||| ifosfamide / Generic mfg.
Clinical, Journal: Long-Term Survival of a Patient with Recurrent Dedifferentiated High-Grade Liposarcoma of the Retroperitoneum Under Adjuvant Treatment with Viscum album L. Extract: A Case Report. (Pubmed Central) - Oct 13, 2021 Three months after this first surgery, a recurrence occurred, and was treated with neoadjuvant and adjuvant doxorubicin plus ifosfamide and surgery (resection)...Finally, a fifth recurrence-5 months after the fifth surgery-was treated with subcutaneous and intravenous VAE applications and eribulin...On the basis of the antitumoral and immunomodulating effects of VAE and on the reported prolonged survival of VAE-treated patients with other types of tumors, the adjunct VAE treatment is presumed to have contributed to the favorable outcome. Regarding the clinical relevance of VAE treatment, further investigations are needed.
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