2014
DOI: 10.1200/jco.2014.32.15_suppl.5610
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ADXS11-001 immunotherapy targeting HPV-E7: Final results from a phase 2 study in Indian women with recurrent cervical cancer.

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Cited by 24 publications
(12 citation statements)
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“…The overall 12-and 18-month survival rates were 36 and 28% with overall response rate of 11% (six complete and six partial). Of note, vaccination was well tolerated with only 2% of grade 3 adverse events [133]. On this basis a randomized Phase III study is planned.…”
Section: Immunotherapeutic Agents For CCmentioning
confidence: 98%
“…The overall 12-and 18-month survival rates were 36 and 28% with overall response rate of 11% (six complete and six partial). Of note, vaccination was well tolerated with only 2% of grade 3 adverse events [133]. On this basis a randomized Phase III study is planned.…”
Section: Immunotherapeutic Agents For CCmentioning
confidence: 98%
“…71 A Listeria-based vaccine, ADXS11-001, demonstrated an 11% response rate in a phase 2 investigation among patients with recurrent or refractory cervical cancer. 72 OPC Treatment for OPC is the same regardless of HPV status or p16 positivity, despite improved outcomes in HPVpositive OPC. Patients with early stage OPC can be treated with either primary surgery and/or definitive RT.…”
Section: Cervical Cancermentioning
confidence: 99%
“…Specifically, a live attenuated Listeria monocytogenes (Lm) vaccine containing an HPV-16-E7 fusion protein was initially used in a phase II study by a group in India [34]. In this study, 110 patients with recurrent squamous cell carcinoma (SCC) of the cervix were randomized to three doses of the vaccine alone versus four doses of the vaccine with concurrent cisplatin chemotherapy.…”
Section: Cervixmentioning
confidence: 99%