ATEMPT 2.0: Adjuvant T-DM1 vs TH

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorDana-Farber Cancer Institute

About this trial

This research study is studying how well newly diagnosed breast cancer that has tested positive for a protein called HER2 responds using one of two different combination of HER2-directed therapies as a treatment after surgery.

The name of the study drugs involved are:

* Trastuzumab-emtansine (T-DM1, Kadcyla) * Trastuzumab SC (Herceptin Hylecta) * Paclitaxel

Eligibility criteria

Qualifiers

Patients must have HER2-positive Stage I histologically confirmed invasive carcinoma of the breast. Patients must have node-negative (N0) or micrometastases (N1mic) breast cancer according to the AJCC 8th edition anatomic staging table.

If the patient has had a negative sentinel node biopsy, then no further axillary dissection is required, and the patient is determined to be node-negative. If an axillary dissection without sentinel lymph node biopsy is performed to determine nodal status, at least six axillary lymph nodes must be removed and analyzed, and determined to be negative, for the patient to be considered node-negative. Axillary nodes with single cells or tumor clusters ≤ 0.2 mm by either H&E or immunohistochemistry (IHC) will be considered node-negative.

Any axillary lymph node with tumor clusters between 0.02 and 0.2 cm is considered a micrometastasis. Patients with a micrometastasis are eligible. An axillary dissection is not required to be performed in patients with a micrometastasis found by sentinel node evaluation. In cases where the specific pathologic size of lymph node involvement is subject to interpretation, the principal investigator will make the final determination as to eligibility. The investigator must document approval in the patient medical record.

Patients who have an area of a T1aN0, ER+ (defined as >10%), HER2-negative cancer in addition to their primary HER2-positive tumor are eligible.

Disqualifiers

Pregnant women

Nursing women

Women of childbearing potential who are unwilling to employ adequate contraception (condoms, diaphragms, IUDs, surgical sterilization, abstinence, etc.).

Men who are unwilling to employ adequate contraception (condoms, surgical sterilization, abstinence, etc.).

Trial design

Treatments tested in this trial

  • trastuzumab-emtansine
  • Trastuzumab SC
  • Paclitaxel

Treatment groups

500 Participants
are divided into 2 treatment groups

Locations

53
California
UCSF Helen Diller Family Comprehensive Cancer Center94158, San Francisco United States
Connecticut
Smilow Cancer Hospital Care center at Derby06418, Derby United States
Smilow Cancer Hospital Care center at Fairfield06824, Fairfield United States
Smilow Cancer Hospital Care center at Glastonbury06033, Glastonbury United States

Sponsors and collaborators

Dana-Farber Cancer Institute

Lead sponsor

Genentech, Inc.

Collaborator