A Study of Tucatinib and Trastuzumab in People With Rectal Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The study researchers believe that a combination of the drugs trastuzumab and tucatinib, given with standard chemotherapy (capecitabine and oxaliplatin/FOLFOX), may help participants with rectal cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Willing and able to provide written informed consent for the trial.

Be ≥18 years of age on the date of signing informed consent.

ECOG performance status of 0 or 1.

Histologically confirmed rectal adenocarcinoma.

Disqualifiers

Recurrent rectal cancer.

Prior pelvic radiation therapy, chemotherapy, or surgery for rectal cancer.

Tumor is causing symptomatic bowel obstruction (patients who have a temporary diverting ostomy are eligible).

Other invasive malignancy ≤ 5 years prior to registration. Exceptions are non-melanoma skin cancer that has undergone potentially curative therapy and in situ cervical carcinoma.

Trial design

Design model

Single group

Treatments tested in this trial

  • Trastuzumab

    Drug

    Patients will then be given tucatinib (300 mg BID orally) and trastuzumab (8 mg/kg on day 1, then 6 mg/kg starting cycle 2 and every three weeks) therapy for an initial 6 week lead-in period. All patients, regardless of findings on rectal MRI will then transition to standard of care induction chemotherapy with continuation of the trastuzumab and tucatinib for a total of five additional cycles (15 extra weeks).

  • Tucatinib

    Drug

    Patients will then be given tucatinib (300 mg BID orally) and trastuzumab (8 mg/kg on day 1, then 6 mg/kg starting cycle 2 and every three weeks) therapy for an initial 6 week lead-in period. All patients, regardless of findings on rectal MRI will then transition to standard of care induction chemotherapy with continuation of the trastuzumab and tucatinib for a total of five additional cycles (15 extra weeks).

Treatment groups

37 Participants
are divided into 1 treatment group
Group A: Participant with Rectal AdenocarcinomaExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Clinical complete response of study participants

The primary objective of this trial is to determine the clinical complete response rate after the completion of initial neoadjuvant tucatinib and trastuzumab followed by standard of care induction chemotherapy (assessed around week 21 ± 4 weeks) in subjects with HER2-positive, RAS wild-type locally advanced rectal adenocarcinoma

Time frame
21 +/- 4 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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