Back to Authors

Филиппова, Е. А.

https://orcid.org/0000-0001-7172-0433

Mayo Clinic

Center of Palliative Medicine De Vita, St Petersburg, Russia

Citations 1

Telisotuzumab Vedotin Monotherapy in Patients With Previously Treated c-Met Protein–Overexpressing Advanced Nonsquamous EGFR -Wildtype Non–Small Cell Lung Cancer in the Phase II LUMINOSITY Trial
Camidge, D. Ross , Bar, Jair , Goldman, Jonathan W. , Moiseenko, Fedor , Филиппова, Е. А. , Çiçin, İrfan , Daaboul, Nathalie , Liu, Chunling , Bradbury, Penelope A., Moskovitz, Mor, Katgı, Nuran , Cuppens, Kristof , Wu, Shang‐Yin , Baijal, Shobhit , Kuo, Chih‐Hsi S. , Planchard, David , Baik, Christina S. , Li, Martha, Ansell, Peter , Xia, Summer, Bolotin, Ellen, Looman, Jim, Ratajczak, Christine K. , Horinouchi, Hidehito , Goldman, Jonathan W , Moiseenko, Fedor , Cicin, Irfan , Zer Kuch, Alona , Girard, Nicolas , Cuppens, Kristof , Han, Ji-Youn , Wu, Shang-Yin , Mansfield, Aaron S , Kuo, Chih-Hsi , Nishino, Kazumi , Lee, Se-Hoon , Planchard, David , Lu, Shun , Filippova, Elena, Ciuleanu, Tudor–Eliade , Tomasini, Pascale , Girard, Nicolas , Mansfield, Aaron S.

Journal of Clinical Oncology | June 6, 2024 | Volume: 42 | Issue: 25 | Pages: 3000-3011

10.1200/jco.24.00720 Get It

PURPOSE Telisotuzumab vedotin (Teliso-V) is a c-Met–directed antibody-drug conjugate with a monomethyl auristatin E cytotoxic payload. The phase II LUMINOSITY trial (ClinicalTrials.gov identifier: NCT03539536 ) aimed to identify the optimal c-Met protein–overexpressing non–small cell lung cancer (NSCLC) population for treatment with Teliso-V (stage I) and expand the selected group for efficacy evaluation (stage II). Stage II enrolled patients with nonsquamous epidermal growth factor receptor ( EGFR )-wildtype NSCLC. METHODS Eligible patients had locally advanced/metastatic c-Met protein–overexpressing NSCLC and ≤2 previous lines of therapy (including ≤1 line of systemic chemotherapy). c-Met protein overexpression in nonsquamous EGFR -wildtype NSCLC was defined as ≥25% tumor cells with 3+ staining (high [≥50% 3+]; intermediate [≥25%–<50%]). Teliso-V was administered at 1.9 mg/kg once every 2 weeks. The primary end point was overall response rate (ORR) by independent central review. RESULTS In total, 172 patients with nonsquamous EGFR -wildtype NSCLC received Teliso-V in stages I and II. ORR was 28.6% (95% CI, 21.7 to 36.2; c-Met high, 34.6% [95% CI, 24.2 to 46.2]; c-Met intermediate, 22.9% [95% CI, 14.4 to 33.4]). The median duration of response was 8.3 months (95% CI, 5.6 to 11.3; c-Met high, 9.0 [95% CI, 4.2 to 13.0]; c-Met intermediate: 7.2 [95% CI, 5.3 to 11.5]). The median overall survival was 14.5 months (95% CI, 9.9 to 16.6; c-Met high, 14.6 [95% CI, 9.2 to 25.6]; c-Met intermediate, 14.2 [95% CI, 9.6 to 16.6]). The median progression-free survival was 5.7 months (95% CI, 4.6 to 6.9; c-Met high, 5.5 [95% CI, 4.1 to 8.3]; c-Met intermediate: 6.0 [95% CI, 4.5 to 8.1]). Most common any-grade treatment-related adverse events (AEs) were peripheral sensory neuropathy (30%), peripheral edema (16%), and fatigue (14%); the most common grade ≥3 AE was peripheral sensory neuropathy (7%). CONCLUSION Teliso-V was associated with durable responses in c-Met protein–overexpressing nonsquamous EGFR -wildtype NSCLC, especially in those with high c-Met. AEs were generally manageable.