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Adding Capivasertib to Standard Treatment in HR Positive, HER2 Negative Metastatic Breast Cancer Based on ctDNA Testing (MONITOR)

2026年9月1日 更新者:SWOG Cancer Research Network

MONITOR (Molecular Assessment and Identification of ctDNA and Optimizing Treatment for HR-positive, Her2-negative Metastatic Breast Cancer)

The purpose of this research is to see if adding the investigational targeted drug capivasertib to standard endocrine therapy (hormone-blocking treatment) combined with a medicine that slows cancer cell growth can improve response to treatment for patients with metastatic breast cancer that's hormone receptor (HR)-positive and human epidermal growth factor receptor 2 (HER2)-negative.

調査の概要

詳細な説明

This study is being done to answer the following questions:

Can adding the medicine capivasertib to standard treatment options help keep the cancer from growing or spreading?

Standard treatment is the care that most people receive for metastatic breast cancer. This study looks at different treatment combinations for people with metastatic breast cancer that's HR-positive and HER2-negative. Researchers hope to learn:

How well the cancer responds to different treatment combinations? How long patients live after receiving different treatment combinations? How cancer-related markers in the blood (called circulating tumor DNA or ctDNA) change with treatment - and whether those changes are linked to certain results? What happens when patients switch treatments after the cancer gets worse?

研究の種類

介入

入学 (推定)

1084

段階

  • フェーズ 3

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:SWOG Clinical Trials Partnerships
  • 電話番号:210-614-8808
  • メール:CTP@swog.org

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Registration Step 1 Inclusion Criteria:

  • Participants must have histologically or cytologically confirmed adenocarcinoma of the breast with unresectable or metastatic disease.
  • Participants must have evidence of either 1) measurable disease with or without non-measurable disease, or 2) non-measurable disease only, but the non-measurable disease must include bone metastases. Participants must have a CT scan or MRI of the chest and abdomen AND a whole-body bone scan within 28 days prior to registration. X-rays, scans, or other tests for assessment of non-measurable disease must have been performed within 42 days prior to registration. All disease must be assessed and documented on the Baseline Tumor Assessment Form.

Note: Participants cannot have only non-measurable disease without bone involvement.

  • Participants must have HER2-negative breast cancer, defined as a negative in situ hybridization test or an IHC status of 0 or 1+. If IHC is 2+ (i.e. indeterminate), a negative in situ hybridization (FISH, CISH, or SISH) test is required by local laboratory testing (as per the ASCO-CAP guidelines).
  • Participants' most recent tumor biopsy or surgical resection specimen must be either ER-positive, PgR-positive, or both, as defined by immunohistochemistry (IHC) ≥1% (as per the ASCO-CAP guidelines).
  • Female participants must be at post-menopausal status or be receiving ovarian ablation with a GnRH agonist such as goserelin. Pre-menopausal (and peri-menopausal, i.e. those that do not meet the criteria defined for post-menopausal below) women are eligible if amenable to treatment with an GnRH agonist. Male participants should also receive GnRH agonist. These participants must begin concomitant treatment with GnRH agonist at least 14 days prior to Cycle 1, Day 1 and must be willing to continue concomitant treatment for the duration of the study. Post-menopausal status is defined by any one of the following criteria: Prior bilateral oophorectomy, Age ≥60 years, or Age <60 and amenorrhea for 12 months following cessation of all exogenous hormonal treatments/chemotherapy/ovarian suppression/tamoxifen or similar. Participants should also have serum estradiol and follicle stimulating hormone (FSH) levels confirmed as being within the standard laboratory reference range for post-menopausal females per local institution standards.
  • Participants must be ≥ 18 years old at the time of registration.
  • Participants must have Zubrod Performance Status of 0 or 1.
  • Participants must have a complete medical history and physical exam within 28 days prior to registration.
  • Participants must have adequate organ and marrow function within 28 days prior to registration.
  • Participants must have a calculated creatinine clearance ≥ 50 mL/min using the Cockcroft-Gault Formula. This specimen must have been drawn and processed within 28 days prior to registration. For creatinine clearance formula see the tools on the CRA Workbench https://txwb.crab.org/TXWB/Tools.aspx.
  • Participants must be given the opportunity to participate in the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) form.
  • Participants must agree to have blood specimens submitted for ctDNA molecular response assessment.
  • Participants must be offered the opportunity to participate in planned non-real time ctDNA analysis.

Registration Step 1 Exclusion Criteria:

  • Participants must not have active central nervous system (CNS) disease or evidence of active leptomeningeal disease.
  • Participants must not have had endocrine resistance as defined as breast cancer recurrence within 12 months of cessation of endocrine therapy in the adjuvant setting. Prior adjuvant CDK4/6 inhibitor use is allowed as long as participants did not have a recurrence within 12 months of completion of treatment with an adjuvant CDK4/6 inhibitor.
  • Participants must not have initiated, but must be planning to initiate, NSAI + palbociclib or ribociclib as the initial therapy for unresectable or metastatic disease.
  • Participants must not have received prior systemic therapy in the metastatic setting, including chemotherapy or hormone therapy. Prior exposure to any chemotherapy or anti-cancer agents including hormonal therapy in the (neo)adjuvant setting is allowed as long as appropriate washout period before randomization/enrollment is met.
  • Participants must not be concurrently using hormone replacement therapy.
  • Participants must not have received prior fulvestrant or PI3K/AKT inhibitor treatment.
  • Participants must not have received strong inhibitors or potent inducers or substrates of CYP3A4 or substrates of CYP2D6 within 14 days (21 days for St. John's Wort) prior to registration.
  • Participants must agree to not use herbal or natural products intended as treatment or prophylaxis for any type of cancer.
  • Participants must not have radiotherapy within 14 days prior to the Step 1 registration.
  • Participants must not have a major surgical procedure (excluding placement of vascular access) or significant traumatic injury within 28 days prior to Step 1 registration or an anticipated need for major surgery during the study.
  • Participants must not have any unresolved toxicities from prior therapy greater than Common Terminology Criteria for Adverse Events (CTCAE) grade 1 at the time of registration with the exception of alopecia, lymphocyte decrease, grade 2 lymphopenia and grade 2 prior chemotherapy-therapy related neuropathy.
  • Participants must not have uncontrolled diabetes mellitus or risk for hyperglycemia within 28 days prior to registration. Participants must plan to have serum glucose performed prior to beginning Step 1 treatment.
  • Participants with known human immunodeficiency virus (HIV) infection must be on effective anti-retroviral therapy at registration and have undetectable viral load on the most recent test results prior to registration. All of the following criteria are required to define an HIV infection that is well controlled: undetectable viral RNA load, CD4+ count of > 350, no history of AIDS-defining opportunistic infection within the past 12 months, and on anti HIV medications for at least 28 days.

Note: Lower CD4+ count values are acceptable if clinically indicated and the participant has a potentially curable malignancy or for interventions in a later stage of development that have demonstrated prior activity within a given cancer.

  • Participants with a history of hepatitis C virus (HCV) infection must have been treated and cured. Participants currently being treated for HCV infection must have undetectable HCV viral load test on the most recent test results, if indicated.
  • Participants must not have acute hepatitis B. Participants with a known history of chronic hepatitis B virus (HBV) infection must have both a negative HBsAg result and an HBV DNA viral load below the lower limit of quantification on the most recent test results prior to registration. Participants with a positive HBsAg due to recent vaccination are eligible if HBV DNA viral load is below the lower limit of quantification. Note: Participants receiving anti-viral therapies which are strong inhibitors or inducers of CYP3A4 will be excluded due to the potential for drug-drug interaction with capivasertib.
  • Participants must not have impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of the study drugs (e.g. ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection).
  • Participants with a history of CNS metastases or cord compression must have been clinically stable (i.e. non-active disease) for at least 28 days since completion of definitive treatment and must not be receiving systemic steroids. In the case of brain metastases, the participant must have stable or improved imaging at least 4 weeks after completion of definitive treatment.
  • Participants must not have or had a prior or concurrent malignancy whose natural history or treatment (in the opinion of the treating physician) has the potential to interfere with the safety or efficacy assessment of the study regimen.
  • Participants must not have clinically significant, uncontrolled heart disease and/or cardiac repolarization abnormality, as confirmed by triplicate ECG within 28 days prior to registration.
  • Participants must not have a major known bleeding disorder (e.g., bleeding diathesis) or be receiving anticoagulant therapy that would preclude intramuscular administration of fulvestrant or Luteinizing Hormone-Releasing Hormone (LHRH) agonists.
  • Participants must not have a history of (noninfectious) interstitial lung disease (ILD)/pneumonitis that required steroids or have current ILD/pneumonitis symptoms.
  • Participants must not be pregnant or nursing (nursing includes breast milk fed to an infant by any means, including from the breast, milk expressed by hand, or pumped). Individuals who are of reproductive potential must have agreed to use an effective contraceptive method with details provided as a part of the consent process. A person who has had menses at any time in the preceding 12 consecutive months or who has semen likely to contain sperm is considered to be of "reproductive potential." In addition to routine contraceptive methods, "effective contraception" also includes refraining from sexual activity that might result in pregnancy and surgery intended to prevent pregnancy (or with a side-effect of pregnancy prevention) including hysterectomy, bilateral oophorectomy, bilateral tubal ligation/occlusion, and vasectomy with testing showing no sperm in the semen. Participants must have a negative urine pregnancy test within 14 days prior to registration.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ:Cohort A, Arm 1
Continue NSAI + CDK4/6i
NSAI: Dosed per standard practice, Days 1-28 of every cycle; CDK4/6 Inhibitor (Palbociclib or Ribociclib): Dosed per standard practice, Days 1-21 of every cycle x 4 cycles
他の名前:
  • Cohort B, Arm 1
ctDNA Assay
実験的:Cohort A, Arm 2
NSAI + CDK4/6i + Capivasertib
ctDNA Assay
NSAI: Dosed per standard practice, Days 1-28 of every cycle; CDK4/6 Inhibitor (Palbociclib or Ribociclib): Dosed per standard practice, Days 1-21 of every cycle x 4 cycles; Capivasertib: Dosed 4 days on and 3 days off weekly, every cycle
他の名前:
  • Cohort A, Arm 2
実験的:Cohort A, Arm 3
Fulvestrant + CDK4/6i + Capivasertib
ctDNA Assay
NSAI: Dosed per standard practice, Days 1-28 of every cycle; CDK4/6 Inhibitor (Palbociclib or Ribociclib): Dosed per standard practice, Days 1-21 of every cycle x 4 cycles Capivasertib: Dosed 4 days on and 3 days off weekly, every cycle Fulvestrant: Dosed days 1 and 15 of Cycle 1 and Day 1 of Cycles 2+
他の名前:
  • Cohort A, Arm 3
アクティブコンパレータ:Cohort B, Arm 1
Continue NSAI + CDK4/6i
NSAI: Dosed per standard practice, Days 1-28 of every cycle; CDK4/6 Inhibitor (Palbociclib or Ribociclib): Dosed per standard practice, Days 1-21 of every cycle x 4 cycles
他の名前:
  • Cohort B, Arm 1
ctDNA Assay

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
PFS
時間枠:Up to 5 years after Step 1 Registration
To evaluate progression-free survival (PFS) in participants with HR-positive and HER2 negative unresectable or metastatic breast cancer with detectable circulating tumor DNA (ctDNA) at baseline who do not achieve molecular response but show no evidence of progression per RECIST 1.1 after three cycles of standard of care (SOC) treatment with non-steroidal aromatase inhibitor (NSAI) + CDK4/6 inhibitor in Arms 2 and 3. PFS will be evaluated separately in participants randomized to NSAI + CDK4/6 inhibitor + capivasertib (Arm 2) and fulvestrant + CDK4/6 inhibitor + capivasertib (Arm 3) and compared to historical control.
Up to 5 years after Step 1 Registration

二次結果の測定

結果測定
メジャーの説明
時間枠
Molecular Response
時間枠:Up to 15 weeks after Step 1 Registration
All Participants: To assess the percentage of participants who achieve molecular response after cycle 3 of SOC treatment and show stable disease or better per RECIST 1.1.
Up to 15 weeks after Step 1 Registration
Cohort A Overall Survival
時間枠:Up to 5 years after Step 1 Registration
To evaluate the overall survival (OS) for participants on Arms 1, 2, and 3 (separately).
Up to 5 years after Step 1 Registration
Cohort A Clinical Benefit Rate
時間枠:Up to 5 years after Step 1 Registration
To estimate the clinical benefit rate (CBR) (confirmed or unconfirmed complete or partial response or stable disease ≥ 6 months per RECIST 1.1) separately in Arms 1, 2 and 3 of this participant population from Step 2 Registration.
Up to 5 years after Step 1 Registration
Cohort A Overall Response Rate
時間枠:Up to 5 years after Step 1 Registration
To estimate the overall response rate (ORR) (confirmed complete and partial responses per RECIST 1.1) separately in Arms 1, 2 and 3 of this participant population, among those with measurable disease at Step 2 Registration.
Up to 5 years after Step 1 Registration
Cohort A Toxicities
時間枠:Up to 5 years after Step 1 Registration
To estimate the frequency and severity of toxicities in each arm of this participant population.
Up to 5 years after Step 1 Registration
Cohort A PFS Differences
時間枠:Up to 5 years after Step 1 Registration
To explore differences in the following clinical outcome for participants in Arms 1, 2, and 3: PFS.
Up to 5 years after Step 1 Registration
Cohort A ORR Differences
時間枠:Up to 5 years after Step 1 Registration
To explore differences in the following clinical outcome for participants in Arms 1, 2, and 3: ORR.
Up to 5 years after Step 1 Registration
Cohort A CBR Differences
時間枠:Up to 5 years after Step 1 Registration
To explore differences in the following clinical outcome for participants in Arms 1, 2, and 3: CBR.
Up to 5 years after Step 1 Registration
Cohort B PFS
時間枠:Up to 5 years after Step 1 Registration
To assess PFS in participants who achieve molecular response and show stable disease or better per RECIST 1.1 after three cycles of SOC treatment and then continue SOC treatment with non-steroidal aromatase inhibitor + CDK4/6 inhibitor.
Up to 5 years after Step 1 Registration
Cohort B Toxicities
時間枠:Up to 5 years after Step 1 Registration
To evaluate the frequency and severity of toxicities in this participant population.
Up to 5 years after Step 1 Registration
Cohort C PFS2
時間枠:Up to 5 years after Step 1 Registration
To evaluate PFS2 in participants from Cohort A, Arm 1 who subsequently switch to Fulvestrant + CDK4/6 inhibitor + Capivasertib after progression on SOC treatment.
Up to 5 years after Step 1 Registration
Cohort C Toxicities
時間枠:Up to 5 years after Step 1 Registration
To evaluate the frequency and severity of toxicities in this participant population.
Up to 5 years after Step 1 Registration
Specimen Banking
時間枠:Up to 2 years after Step 1 Registration
To bank specimens for future correlative studies.
Up to 2 years after Step 1 Registration
PRO-CTCAE
時間枠:Up to 5 years after Step 1 Registration
To compare the severity and frequency of participant-reported symptoms using selected PRO-CTCAE items (including nausea, vomiting, shortness of breath, rash, diarrhea, fatigue, abdominal pain among Cohort A, Arms 1, 2, and 3, Cohort B, Arm 1, and Cohort C, Arm 3.
Up to 5 years after Step 1 Registration

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Kevin Kalinsky, M.D.、SWOG Cancer Research Network

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年10月30日

一次修了 (推定)

2034年10月30日

研究の完了 (推定)

2035年10月30日

試験登録日

最初に提出

2026年8月28日

QC基準を満たした最初の提出物

2026年9月1日

最初の投稿 (実際)

2026年9月3日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月3日

QC基準を満たした最後の更新が送信されました

2026年9月1日

最終確認日

2026年9月1日

詳しくは

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個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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はい

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