A phase II single-arm clinical trial known as innovaTV 204 (GCT1015-04 or innovaTV 204/GOG-3023/ENGOT-cx6; NCT03438396), evaluating tisotumab vedotin administered every three weeks (Q3W) for the treatment of patients who have relapsed or progressed on or after prior treatment for recurrent or metastatic cervical cancer shows positive topline results.
Preliminary data from the trial, which is sponsored by Genmab in collaboration with Seattle Genetics, the European Network of Gynaecological Oncological Trial Groups (ENGOT), the Belgian Gynaecological Oncology Group and the Gynecologic Oncology Group, showed a 24% confirmed objective response rate (ORR) by independent central review [95% Confidence Interval: 15.9%-33.3%] with a median duration of response (DOR) of 8.3 months. The most common treatment-related adverse events (greater than or equal to 20 percent) included alopecia, epistaxis (nose bleeds), nausea, conjunctivitis, fatigue and dry eye. The investigators confirmed that that the data will be submitted for presentation at an upcoming medical meeting.
Tisotumab vedotin is an investigational antibody-drug conjugate (ADC) directed to tissue factor, which is expressed on cervical cancer and can promote tumor growth, angiogenesis and metastases.
Antibody-drug Conjugates are highly targeted biopharmaceutical drugs that combine monoclonal antibodies specific to surface antigens present on particular tumor cells with highly potent anti-cancer agents linked via a chemical linker. Tisotumab vedotin is composed of Genmab’s fully human monoclonal antibody specific for tissue factor and Seattle Genetics’ ADC technology that utilizes a protease-cleavable linker that covalently attaches the microtubule-disrupting agent monomethyl auristatin E (MMAE) to the antibody and releases it upon internalization, inducing target cell death.
In cancer biology, tissue factor is a protein that can promote tumor growth, angiogenesis and metastases. Based on its high expression on many solid tumors and its rapid internalization, tissue factor was selected as a target for an ADC approach.
Standard therapies for previously treated recurrent and/or metastatic cervical cancer generally result in limited objective response rates of typically less than 15% with median overall survival ranging from 6.0 to 9.4 months, in an all-comers population.
Tisotumab vedotin is being developed by Genmab in collaboration with Seattle Genetics, under an agreement in which the companies share all costs and profits for the product on a 50:50 basis.
Meeting an unmet medical need
“Available therapies [followng] progression after first line chemotherapy in recurrent or metastatic cervical cancer are limited,” noted Roger Dansey, M.D., Chief Medical Officer at Seattle Genetics.
“[And as a result] … there is a high unmet need for new effective and tolerable treatment options for women with advanced cervical cancer, regardless of biomarkers and histology,” added Jan van de Winkel, Ph.D., Chief Executive Officer of Genmab.
“Tisotumab vedotin has demonstrated clinically meaningful and durable objective responses with a manageable safety profile,” Dansey observed.
“These promising topline data from innovaTV 204 will be the basis of further engagement with the U.S. Food and Drug Administration (FDA) as we continue to progress and expand our tisotumab vedotin development program in solid tumors with our partners at Seattle Genetics,” Van de Winkel concluded.
Cervical cancer originates in the cells lining the cervix. Over 13,500 women are expected to be diagnosed with cervical cancer in the U.S. in 2020, with approximately 4,200 deaths.  Cervical cancer remains one of the leading causes of cancer death in women globally, with over 311,000 women dying annually; the vast majority of these women being in the developing world. 
Routine medical examinations and the human papillomavirus (HPV) vaccine have lowered the incidence of cervical cancer in the developed world. Despite these advances, women are still diagnosed with cervical cancer, which often recurs or becomes metastatic.
Additional clinical trials of tisotumab vedotin are currently enrolling patients, including in combination with pembrolizumab, carboplatin or bevacizumab, and with a weekly dosing schedule in patients with locally advanced or metastatic cervical cancer. Tisotumab vedotin is also being evaluated in other tissue factor expressing tumor types, including ovarian and other solid tumors.
Tisotumab vedotin is, in addition to cervical cancer, being evaluated in ongoing clinical trials as monotherapy in a range of solid tumors, including recurrent and/or metastatic cervical cancer, ovarian cancer and in combination with other commonly used therapies in recurrent or metastatic cervical cancer. These trials are evaluating tisotumab vedotin on a weekly or every three weeks dosing schedule.
A Trial of Tisotumab Vedotin in Cervical Cancer – NCT03438396
A Trial of Tisotumab Vedotin in Japanese Subjects With Advanced Solid Malignancies (innovaTV 206) – NCT03913741
Tisotumab Vedotin Continued Treatment in Patients With Solid Tumors – NCT03245736
Efficacy and Safety Study of Tisotumab Vedotin for Patients With Solid Tumors (innovaTV 207) – NCT03485209
A Study of Weekly Tisotumab Vedotin for Patients With Platinum-Resistant Ovarian Cancer With Safety Run-in (innovaTV 208) – NCT03657043
Tisotumab Vedotin (HuMax®-TF-ADC) Safety Study in Patients With Solid Tumors – NCT02552121
Safety and Efficacy of Tisotumab Vedotin Monotherapy & in Combination With Other Cancer Agents in Subjects With Cervical Cancer – NCT03786081
Tisotumab Vedotin (HuMax®-TF-ADC) Safety Study in Patients With Solid Tumors – NCT02001623
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An edited version of this article was first published in ADC Review | Journal of Antibody-drug Conjugates.