article Open AccessTop 1% cited
Talimogene Laherparepvec Improves Durable Response Rate in Patients With Advanced Melanoma
Journal of Clinical Oncology · 2015 · Vol. 33(25) · pp. 2780–2788
Robert H.I. Andtbacka✉Howard L. KaufmanFrances A. CollichioThomas AmatrudaNeil SenzerJason ChesneyKeith A. DelmanLynn E. S̄pitlerIgor PuzanovSanjiv S. AgarwalaMohammed MilhemLee D. CranmerBrendan D. CurtiKarl D. LewisMerrick I. RossTroy H. GuthrieGerald P. LinetteGregory A. DanielsKevin J. HarringtonMark R. MiddletonWilson H. MillerJonathan S. ZagerYining YeBin YaoLi Ai(Amgen (United States))Susan Doleman(Amgen (United States))Ari M. Vanderwalde(Amgen (United States))Jennifer Gansert(Amgen (United States))Robert S. Coffin(Amgen (United States))
Abstract
T-VEC is the first oncolytic immunotherapy to demonstrate therapeutic benefit against melanoma in a phase III clinical trial. T-VEC was well tolerated and resulted in a higher DRR (P < .001) and longer median OS (P = .051), particularly in untreated patients or those with stage IIIB, IIIC, or IVM1a disease. T-VEC represents a novel potential therapy for patients with metastatic melanoma.
CAR-T cell therapy researchVirus-based gene therapy researchImmunotherapy and Immune ResponsesMedicineOncolytic virusInternal medicineMelanomaClinical endpointHazard ratioImmunotherapyGastroenterologyOdds ratioSurgery
MeSH terms
Adjuvants, ImmunologicAdultAgedAged, 80 and overAntineoplastic AgentsFatigueFemaleFeverHumansImmunotherapyMaleMelanomaMiddle AgedNeoplasm StagingSkin Neoplasms
Funding
- Amgen
Citations
2,541
FWCI
108.05
field-weighted impact
References
71
Percentile
100%
vs. same field & year
Citations per year
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