A Study of Tucatinib With Trastuzumab and mFOLFOX6 Versus Standard of Care Treatment in First-line HER2+ Metastatic Colorectal Cancer

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorSeagen, a wholly owned subsidiary of Pfizer

About this trial

This study is being done to find out if tucatinib with other cancer drugs works better than standard of care to treat participants with HER2 positive colorectal cancer. This study will also determine what side effects happen when participants take this combination of drugs. A side effect is anything a drug does to the body besides treating your disease.

Participants in this study have colorectal cancer that has spread through the body (metastatic) and/or cannot be removed with surgery (unresectable).

Participants will be assigned randomly to the tucatinib group or standard of care group. The tucatinib group will get tucatinib, trastuzumab, and mFOLFOX6. The standard of care group will get either:

* mFOLFOX6 alone, * mFOLFOX6 with bevacizumab, or * mFOLFOX6 with cetuximab mFOLFOX6 is a combination of multiple drugs. All of the drugs given in this study are used to treat this type of cancer.

Eligibility criteria

Qualifiers

Histologically and/or cytologically confirmed adenocarcinoma of the colon or rectum which is locally advanced unresectable or metastatic

Able to provide the most recently available formalin-fixed paraffin-embedded (FFPE) tumor tissue blocks (or freshly sectioned slides) obtained prior to treatment initiation to a central laboratory

If archival tissue is not available, a newly-obtained baseline biopsy of an accessible tumor lesion is required within 35 days prior to start of study treatment

HER2+ disease as determined by a tissue based assay performed at a central laboratory.

Disqualifiers

Prior systemic anticancer therapy for colorectal cancer (CRC) in the locally advanced unresectable or metastatic setting; note that participants may have received a maximum of 2 doses of mFOLFOX6 in the locally advanced/unresectable or metastatic setting prior to randomization.

Note: May have received chemotherapy for CRC in the adjuvant setting if it was completed >6 months prior to enrollment

Radiation therapy within 14 days prior to enrollment (or within 7 days in the setting of stereotactic radiosurgery)

Previous treatment with anti-HER2 therapy

Trial design

Treatments tested in this trial

  • tucatinib
  • trastuzumab
  • bevacizumab
  • cetuximab
  • oxaliplatin
  • leucovorin
  • levoleucovorin
  • fluorouracil

Treatment groups

400 Participants
are divided into 2 treatment groups

Locations

381
Argentina
Centro de Investigacion Pergamino SA2700, PergaminoBuenos Aires, Argentina
Instituto Medico de la Fundacion Estudios ClinicosS2000DEJ, RosarioSanta Fe Province, Argentina
Instituto Medico Especializado Alexander Fleming1426, Buenos Aires Argentina
Hospital Britanico de Buenos Aires1280, CABA Argentina

Sponsors and collaborators

Seagen, a wholly owned subsidiary of Pfizer

Lead sponsor