- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07856303
SHR-A1811 Versus Trastuzumab Plus Pertuzumab in ctDNA-Positive HER2-Positive Early Breast Cancer After Pathologic Complete Response
A Randomized, Open-Label, Phase II Study of Intensified Adjuvant SHR-A1811 Versus Trastuzumab Plus Pertuzumab in Patients With Initially Stage IIB-IIIC HER2-Positive Early Breast Cancer Who Achieved Pathologic Complete Response After Neoadjuvant Therapy and Have Postoperative ctDNA Positivity
This investigator-initiated, single-center, randomized, open-label, phase II trial will evaluate the efficacy and safety of intensified adjuvant SHR-A1811 compared with trastuzumab plus pertuzumab in women with initially stage IIB-IIIC HER2-positive early breast cancer who achieved pathologic complete response after neoadjuvant systemic therapy and have detectable postoperative circulating tumor DNA (ctDNA). Eligible participants will be randomized 1:1 and stratified by hormone receptor status, HER2 test category, and initial clinical anatomic stage. The primary endpoint is invasive disease-free survival.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Patients who have completed neoadjuvant systemic therapy and curative breast and axillary surgery with ypT0/is ypN0 disease will undergo postoperative ctDNA testing 14 to 42 days after the last definitive surgery and before initiation of adjuvant systemic therapy. Participants with ctDNA positivity and no clinical or radiographic evidence of recurrent or metastatic disease will be randomized to SHR-A1811 or trastuzumab plus pertuzumab. Post-randomization ctDNA results will not be used for clinical management and will remain blinded to investigators and participants until the primary analysis database is locked, unless a future ethics-approved protocol amendment specifies otherwise.
Studietyp
Inskrivning (Beräknad)
Fas
- Fas 2
Kontakter och platser
Studiekontakt
- Namn: Zhimin Shao
- Telefonnummer: 8888 86-021-64175590
- E-post: zhimingshao@yahoo.com
Studieorter
-
-
-
Shanghai, Kina
- Department of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai
-
Kontakt:
- Zhimin Shao
- Telefonnummer: 86-021-641755901105
- E-post: zhimingshao@yahoo.com
-
Kontakt:
- Lei Fan
- Telefonnummer: 86-021-641755901105
- E-post: cmchen@medmail.com.cn
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Written informed consent before any study-specific procedure and willingness to comply with study visits and sample collection.
- Female, aged 18 years or older.
- Histologically confirmed invasive breast carcinoma at initial diagnosis, without distant metastasis.
- HER2-positive tumor at initial diagnosis, defined as IHC 3+ or IHC 2+ with ISH amplification; hormone receptor status must be known.
- Initial clinical anatomic stage IIB-IIIC according to the AJCC 8th edition.
- Completion of at least 6 cycles and at least 16 weeks of standard neoadjuvant systemic therapy.
- Definitive breast surgery and appropriate axillary staging or dissection, with pathologically complete resection.
- Pathologic complete response, defined as no residual invasive carcinoma in the breast or regional lymph nodes (ypT0/is ypN0); residual ductal carcinoma in situ is permitted.
- Postoperative ctDNA positivity confirmed by the designated central testing laboratory 14-42 days after the last definitive surgery and before initiation of any adjuvant systemic therapy.
- No clinical, pathologic, or radiographic evidence of locoregional recurrence or distant metastasis before randomization; baseline chest CT is required to assess interstitial lung disease/noninfectious pneumonitis.
- Randomization within 12 weeks after the last definitive surgery; extension to 14 weeks may be permitted for documented surgical complications, reoperation, or sequential radiotherapy with principal investigator approval.
- ECOG performance status 0 or 1.
- Left ventricular ejection fraction at least 50% within 28 days before randomization, without clinically significant cardiac dysfunction.
- Adequate bone marrow, hepatic, renal, and coagulation function.
- Negative pregnancy test for participants of childbearing potential and agreement to use highly effective contraception for the protocol-specified period.
Exclusion Criteria:
- Clinical, radiographic, or pathologic evidence of unresectable locally advanced, recurrent, or metastatic disease, or disease progression during neoadjuvant therapy.
- Failure to achieve ypT0/is ypN0 or any residual invasive carcinoma in the breast or regional lymph nodes.
- Prior ipsilateral or contralateral breast cancer, including ductal carcinoma in situ; lobular carcinoma in situ is permitted.
- Any postoperative systemic anticancer therapy before randomization, including trastuzumab, pertuzumab, another anti-HER2 agent, chemotherapy, antibody-drug conjugate, or endocrine therapy; bridging therapy is not permitted.
- Prior neoadjuvant treatment with T-DM1, trastuzumab deruxtecan, SHR-A1811, or another HER2-directed antibody-drug conjugate.
- Prior or current interstitial lung disease/noninfectious pneumonitis requiring corticosteroid treatment, active interstitial lung disease on screening imaging, clinically significant pulmonary fibrosis, severe chronic obstructive pulmonary disease, resting hypoxemia, or another pulmonary disorder that would interfere with pulmonary toxicity assessment.
- Clinically significant cardiovascular disease, including symptomatic heart failure or NYHA class II-IV heart failure, myocardial infarction or unstable angina within 6 months before screening, uncontrolled clinically significant arrhythmia, QTcF greater than 470 ms, or blood pressure above 150/90 mmHg despite appropriate treatment.
- Active or uncontrolled infection requiring systemic treatment, or active HBV/HCV or HIV not meeting protocol and institutional control criteria.
- Toxicities from prior therapy not recovered to grade 1 or lower, except alopecia, hyperpigmentation, and stable grade 2 peripheral neuropathy judged clinically insignificant by the investigator.
- Another malignancy within 5 years before screening, except adequately treated basal or squamous cell skin cancer, cervical carcinoma in situ, or another malignancy with a low risk of recurrence.
- Severe hypersensitivity to a study drug or any of its excipients.
- Pregnancy, breastfeeding, or plans for pregnancy during the protocol-specified period.
- Any serious medical or psychosocial condition that, in the investigator's judgment, would make study treatment, follow-up, or interpretation of results unsafe or unreliable.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: SHR-A1811
Participants will receive SHR-A1811 4.8 mg/kg by intravenous infusion once every 3 weeks for 14 cycles. Dose interruption and reduction will be managed according to the protocol and study drug management instructions. |
4.8 mg/kg by intravenous infusion once every 3 weeks for 14 cycles. |
|
Aktiv komparator: Trastuzumab Plus Pertuzumab
Participants will receive trastuzumab plus pertuzumab once every 3 weeks. Including treatment received during the neoadjuvant period, the total perioperative duration of dual HER2-targeted therapy will be approximately 1 year. |
Loading dose: 8 mg/kg IV. Maintenance dose: 6 mg/kg IV Q3W. Loading dose: 840 mg IV. Maintenance dose: 420 mg IV Q3W. |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Invasive Disease-Free Survival (IDFS)
Tidsram: At 3 years after randomization
|
IDFS is defined as the time from randomization to the first occurrence of ipsilateral invasive breast tumor recurrence, regional invasive recurrence, distant recurrence, contralateral invasive breast cancer, secondary invasive primary cancer (nonbreast), or death from any cause. |
At 3 years after randomization
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Distant Disease-Free Survival (DDFS)
Tidsram: Up to 5 years after randomization
|
DDFS is defined as the time from randomization to the first occurrence of distant recurrence, secondary invasive primary cancer (nonbreast), or death from any cause. |
Up to 5 years after randomization
|
|
Overall Survival (OS)
Tidsram: Up to 5 years after randomization
|
Time from randomization to death from any cause. |
Up to 5 years after randomization
|
|
Brain Metastasis-Free Interval (BMFI)
Tidsram: Up to 5 years after randomization
|
Time from randomization to brain metastasis |
Up to 5 years after randomization
|
|
Treatment-Emergent Adverse Events
Tidsram: From randomization through 40 days after the last dose of study treatment
|
Number and percentage of participants with treatment-emergent adverse events and serious adverse events, graded according to NCI CTCAE version 5.0. |
From randomization through 40 days after the last dose of study treatment
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
- Patologiska processer
- Neoplasmer efter plats
- Neoplasmer
- Sjukdomsegenskaper
- Neoplastiska processer
- Hudsjukdomar
- Bröstsjukdomar
- Sjukdomsprogression
- Patologiska tillstånd, tecken och symtom
- Hud- och bindvävssjukdomar
- Patologiskt komplett svar
- Neoplasma, rest
- Bröstneoplasmer
- Aminosyror, peptider och proteiner
- Proteiner
- Antikroppar, monoklonal, humaniserad
- Antikroppar, monoklonal
- Antikroppar
- Immunglobuliner
- Immunoproteiner
- Blodproteiner
- Serumglobuliner
- Globuliner
- Trastuzumab
- pertuzumab
Andra studie-ID-nummer
- SCHBCC-N0123
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
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