Clincosm LogoSign in Get a demo

TAHP for Patients With HER2-positive Early Breast Cancer and Subsequent AHP Adjuvant tHerapy After Surgery

Sponsor
Samsung Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT03881878
Collaborator
(none)
67
Enrollment
1
Location
2
Arms
41.2
Anticipated Duration (Months)
1.6
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This study was phase IB-II clinical trial that designed to evaluate the efficacy and safety of docetaxel + atezolizumab + Herceptin sc plus pertuzumab(TAHP) plus adjuvant therapy of atezolizumab + trastuzumab + pertuzumab(AHP) after surgery in female patients with HER2-positive early breast cancer.

Adjuvant AHP (atezolizumab + Herceptin SC + pertuzumab) will be continued for remaining 1 year.

For non-p CR patients, they are going to treat with 4 cycles of AC rather than Taxane only before AHP adjuvant therapy.

Condition or Disease Intervention/Treatment Phase
  • Drug: TAHP and AHP
  • Drug: TAHP plus AC and AHP
 Phase 1/Phase 2

Detailed Description

A, Neoadjuvant setting); 6 cycles q3weeks, intravenous(IV) administration

  • Docetaxel (75mg/m2, intravenous(IV)) Day(D)1

  • Atezolizumab (1200mg, IV) D1

  • Herceptin sc (600mg subcutaneous(SC))D1

  • Pertuzumab (840mg loading dose at Cycle 1 followed by 420mg(IV))D1

B, Adjuvant setting : 11-12 cycles q3weeks [patients with pCR]

  • Atezolizumab (1200mg, IV)

  • Trastuzumab (600mg, SC)

  • Pertuzumab (420mg, IV) D1

[patients with non-pCR]

  • Doxorubicin(60mg/m2), cyclophosphamide (600mg/m2) D1 X 4cycles 3weeks

  • Atezolizumab (1200mg, IV)

  • Trastuzumab (600mg, SC)

  • Pertuzumab (420mg, IV) D1 X 11-12 cycles q3weeks

Study Design

Study Type:
Interventional
Anticipated Enrollment :
67 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
(A, Neoadjuvant setting): TAHP (Docetaxel, Atezolizumab, Trastuzumab sc and Pertuzumab) D1 X 6 cycles q3weeks, intravenous(IV) administration (B, Adjuvant setting) : patients with pCR: AHP(Atezolizumab, Trastuzumab sc and Pertuzumab) D1 X 11-12 cycles q3weeks patients with non-pCR: Doxorubicin plus cyclophosphamide: D1 X 4cycles q3weeks followed by AHP (Atezolizumab, Trastuzumab sc and Pertuzumab) D1 X 11-12 cycles q3weeks(A, Neoadjuvant setting): TAHP (Docetaxel, Atezolizumab, Trastuzumab sc and Pertuzumab) D1 X 6 cycles q3weeks, intravenous(IV) administration (B, Adjuvant setting) : patients with pCR: AHP(Atezolizumab, Trastuzumab sc and Pertuzumab) D1 X 11-12 cycles q3weeks patients with non-pCR: Doxorubicin plus cyclophosphamide: D1 X 4cycles q3weeks followed by AHP (Atezolizumab, Trastuzumab sc and Pertuzumab) D1 X 11-12 cycles q3weeks
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Docetaxel Plus Atezolizumab Plus Herceptin SC and Pertuzumab (TAHP) for Patients With HER2-positive Early Breast Cancer and Subsequent Atezolizumab Plus Herceptin SC and Pertuzumab (AHP) Adjuvant tHerapy After Surgery
Anticipated Study Start Date :
May 27, 2019
Anticipated Primary Completion Date :
Oct 31, 2022
Anticipated Study Completion Date :
Oct 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: pathologic Complete response

(A, Neoadjuvant setting): D1 X 6 cycles, q3weeks Docetaxel (75mg/m2, IV) Atezolizumab (1200mg, IV) Trastuzumab (600mg, SC) Pertuzumab (840mg loading dose at Cycle 1 followed by 420mg, IV) (B, Adjuvant setting) : D1 X 11-12 cycles, q3weeks Atezolizumab (1200mg, IV) Trastuzumab (600mg, SC) Pertuzumab (420mg, IV)

Drug: TAHP and AHP
(A, Neoadjuvant setting): D1 X 6 cycles, q3weeks Docetaxel (75mg/m2, IV) Atezolizumab (1200mg, IV) Tastuzumab (600mg, SC) Pertuzumab (840mg loading dose at Cycle 1 followed by 420mg, IV) (B, Adjuvant setting) : patients with pCR:D1 X 11-12 cycles, q3weeks Atezolizumab (1200mg, IV) Trastuzumab (600mg, SC) Pertuzumab (420mg, IV)
Experimental: non-pathologic Complete response

(A, Neoadjuvant setting): D1 X 6 cycles, q3weeks Docetaxel (75mg/m2, IV) Atezolizumab (1200mg, IV) Trastuzumab (600mg, SC) Pertuzumab (840mg loading dose at Cycle 1 followed by 420mg, IV) (B, Adjuvant setting) : Doxorubicin(60mg/m2) plus cyclophosphamide (600mg/m2) : D1 X 4cycles q3weeks followed by Atezolizumab (1200mg, IV), Trastuzumab (600mg, SC) and Pertuzumab (420mg, IV) D1 X 11-12 cycles q3weeks

Drug: TAHP plus AC and AHP
(A, Neoadjuvant setting): D1 X 6 cycles, q3weeks Docetaxel (75mg/m2, IV) Atezolizumab (1200mg, IV) Tastuzumab (600mg, SC) Pertuzumab (840mg loading dose at Cycle 1 followed by 420mg, IV) (B, Adjuvant setting) : patients with non-pCR Doxorubicin(60mg/m2) plus cyclophosphamide (600mg/m2) D1 X 4cycles q3weeks followed by Atezolizumab (1200mg, IV), Trastuzumab (600mg, SC) and Pertuzumab (420mg, IV) D1 X 11-12 cycles q3weeks

Outcome Measures

Primary Outcome Measures

  1. Pathologic CR(pCR) rate of neo-adjuvant chemotherapy [Pathologic Clinical response is perforemed after end of cycle 6 (each cycle is 21days).]

    pCR rate of neoadjuvant chemotherapy with the patients with HER2+ EBC

Secondary Outcome Measures

  1. Event free survival(EFS) [3 years]

    Event free survival of the patient with pCR vs. non-pCR

Other Outcome Measures

  1. Adverse events will be measured by the CTCAE scale, version 5.0 [1 year]

    safety and toxicity

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:

  1. Patient is an adult, female ≥ 18 years old at the time of informed consent

  2. Patient has histologically confirmed diagnosis of breast cancer

  3. Patients with locally advanced breast cancer (T2-3N0-3)

  4. Patients with early breast cancer with high-risk (T1cN1)

  5. Patients with locally advanced inflammatory breast cancer

  6. Patient has HER2-positive breast cancer as 3+ by IHC or in-situ hybridization (ISH) amplified BC patients

  7. ER+ or ER-

  8. Agree to informed consent and willing and able to comply with the protocol

  9. Available pre-chemotherapy and surgery tissue (except pCR)

  10. For women who are not postmenopausal (≥ 12 months of non-therapy-induced amenorrhea) or surgically sterile (absence of ovaries and/or uterus): agreement to remain abstinent or use single or combined contraceptive methods that result in a failure rate of < 1% per year during the treatment period and for at least 7 months after the last dose of study drugs. Abstinence is only acceptable if it is in line with the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of contraception.

Examples of contraceptive methods with a failure rate of < 1% per year include tubal ligation, male sterilization, hormonal implants, established, proper use of combined oral or injected hormonal contraceptives, and certain intrauterine devices. Alternatively, two methods (e.g., two barrier methods such as a condom and a cervical cap) may be combined to achieve a failure rate of < 1% per year. Barrier methods must always be supplemented with the use of a spermicide.

  1. Patient has adequate bone marrow and organ function

  2. LVEF ≥55% at baseline

Exclusion Criteria:

  1. HER2-negative in surgery sample

  2. Tumor size less than 2cm or and N0

  3. Patients who have metastatic disease (M1)

  4. Patients who are not available tumor tissue

  5. Pregnant or lactating or intending to become pregnant during or within 7 months after the last dose of study treatment

  6. Patients who have serious underlying co-morbidities which could cause end-organ dysfunction

  7. Any previous treatment against including chemo, hormonal therapy

  8. Administration of a live, attenuated vaccine within 4 weeks before Day 1 or anticipation that such a live attenuated vaccine will be required during the study

  9. History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins

  10. Known hypersensitivity or allergy to biopharmaceuticals produced in Chinese hamster ovary cells or any component of the atezolizumab formulation

  11. Patients with prior allogeneic stem cell or solid organ transplantation

  12. History of autoimmune disease including, but not limited to, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener's granulomatosis, Sjögren's syndrome, Bell's palsy, Guillain-Barré syndrome, multiple sclerosis, vasculitis, or glomerulonephritis

  13. History of idiopathic pulmonary fibrosis (including bronchiolitis obliterans with organizing pneumonia) or evidence of active pneumonitis on screening chest computed tomography scan

  14. Known clinically significant liver disease, including active viral, alcoholic, or other hepatitis, cirrhosis, fatty liver, and inherited liver disease

  15. History of HIV infection, active hepatitis B (chronic or acute), or hepatitis C infection. Patients with past or resolved hepatitis B infection (defined as having a negative HBsAg test and a positive hepatitis B core antigen [anti-HBc] test) are eligible.

  16. Patients positive for hepatitis C virus (HCV) antibody are eligible only if polymerase chain reaction assay (PCR) is negative for HCV RNA

  17. Active tuberculosis

  18. Severe infections within 4 weeks prior to Day 1, including, but not limited to, hospitalization for complications of infection, bacteremia, or severe pneumonia. Signs or symptoms of significant infection within 2 weeks prior to Day 1

  19. Received oral or IV antibiotics within 2 weeks prior to Cycle 1 Day 1

  20. Previous or concomitant malignancy of any other type that could affect compliance with the protocol or interpretation of results. Patients with curatively treated basal cell carcinoma of the skin or in situ cervix cancer are generally eligible

  21. Congestive heart failure or abnormal LVEF(LVEF is not ≥55% at baseline)

  22. Total bili >1.5 ULN (except for Gilbert's syndrome), AST/ALT > 1.5 ULN, ALP > 2.5 ULN

Contacts and Locations

Locations

Site City State Country Postal Code
1 Samsung Medical Center Seoul Korea, Republic of 135-710

Sponsors and Collaborators

  • Samsung Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yeon Hee Park, Clinical Professor, Samsung Medical Center
ClinicalTrials.gov Identifier:
NCT03881878
Other Study ID Numbers:
  • 2019-01-064
First Posted:
Mar 20, 2019
Last Update Posted:
Mar 21, 2019
Last Verified:
Mar 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Breast Neoplasms

Study Results

No Results Posted as of Mar 21, 2019