Study of the TheraBionic P1 Device in Patients With Metastatic Triple Negative Breast Cancer After Progression
A Pilot Study of the Efficacy of the TheraBionic P1 Device in Patients With Metastatic Triple Negative Breast Cancer in the Third-line Setting
The goal of this clinical trial is to learn if adding the TheraBionic P1 device to standard of care third line treatment for adult women with metastatic triple negative breast cancer (mTNBC) who have failed, not tolerated, or progressed on standard first- and second-line treatment options can work better than the standard of care alone. The main questions it aims to answer is:
- will the addition of the TheraBionic P1 device to standard of care third line treatment affect progression free and overall survival in these participants
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Jailan Elayoubi, M.D.
- 電話番号:1-800-527-6266
- メール:elayoubij@karmanos.org
研究場所
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Michigan
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Detroit、Michigan、アメリカ、48201
- Karmanos Cancer Institute
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コンタクト:
- Jailan Elayoubi, M.D.
- 電話番号:1-800-527-6266
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-
参加基準
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
説明
Inclusion Criteria:
- Participant must have histologically confirmed invasive breast cancer that is hormone receptor (HR) negative and Human Epidermal Growth Factor Receptor 2 (HER2) negative according to the American Society of Clinical Oncology (ASCO) College of American Pathologists (CAP) guidelines (Estrogen Receptor (ER) and progesterone receptor (PR) < 1% and HER2 negative by immuno-histochemistry (IHC) and/or fluorescent in situ hybridization [FISH]
- Participant must have evaluable disease as defined by the investigator using CT, MRI, or positron emission tomography (PET) scan
Participant must have refractory disease and failed, not tolerated, or progressed on at least two lines of prior standard therapeutic regimens for mTNBC.
• Participant must have a washout period of at least 14 days between the last line of treatment and the start of study treatment.
- Participant must be a woman of 22 years of age or older.
- Participant must have a life expectancy of at least three months
- Participant must have an Eastern Cooperative Oncology Group (ECOG) performance score of 0-2
It is unknown what effects this treatment has on human pregnancy or development of the embryo or fetus. Therefore, women of child-bearing potential must agree to avoid becoming pregnant and male participants should avoid impregnating a female partner and donating sperm starting at initiation of treatment up until at least 12 weeks after treatment discontinuation
- Surgically sterile (hysterectomy, bilateral oophorectomy, or bilateral salpingectomy)
- Post-menopausal, defined as no menses for at least 12 months prior to the screening visit without alternative medical causation.
- Agree to practice true abstinence from sexual intercourse when this is in line with the preferred and usual lifestyle of the participant. Periodic abstinence methods such as calendar, ovulation, symptothermal, or post ovulation tracking are not acceptable.
- Not in a sexual relationship in which they may become pregnant (i.e. same-sex relationship)
- If they are of child-bearing potential, agree to use at least one highly effective AND at least one additional method of contraception. Withdrawal is not an acceptable contraceptive method.
Exclusion Criteria:
- Participants with known active secondary malignancy, unless, in the opinion of the investigator, it is unlikely to interfere with the safety and efficacy of the endpoints.
- Participants with known untreated brain metastases will be excluded from this clinical trial. Stable brain metastases will be allowed, and it will be confirmed by stable brain magnetic resonance imaging (MRI) with and without contrast within 8 weeks of signing consent.
- Participants who are taking any other investigational drugs
- Participants who are pregnant or breastfeeding. If a breastfeeding participant would like to be part of this study, breastfeeding must be discontinued
- Participants with active oral mucosal inflammation, ulceration, or other pathology that could interfere with the use of TheraBionic P1 device (for example: mucositis, thrush, bleeding mucosal lesions, oral herpes, aphthous stomatitis, mouth ulcers, chancre sores, gingivostomatitis, herpangina, aphthae).
- Participants who plan to receive calcium channel blockers and any agent blocking L-type of T-type voltage gated calcium channels (for example: amlodipine, nifedipine, ethosuximide, supplemental vitamin C/ascorbic acid, etc.) unless their medical treatment is discontinued prior to treatment. Participant must agree to abstain from using calcium channel blockers for the duration of treatment on study
- Participants who plan to receive anticancer therapy that blocks L-type or T-type voltage gated calcium channels (i.e., eribulin, rucaparib, or niraparib) as part of their third line treatment. Participants who have received eribulin, rucaparib, or niraparib as part of a previous line of therapy are eligible, provided there has been at least 14 days between the last date of treatment and the start of study treatment.
- Participants that do not agree to be followed according to the study protocol or have cognitive or physical inability to follow the treatment plan
- Participants with a known severe (e.g., anaphylactic) allergy to nickel
研究計画
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:なし
- 介入モデル:単一グループの割り当て
- 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 |
|---|---|
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実験的:Amplitude-modulated radiofrequency electromagnetic fields device plus third line treatment
TheraBionic P1 amplitude-modulated radiofrequency electromagnetic fields device 3 times daily (continuous) plus standard of care third line treatment
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TheraBionic P1 is amplitude-modulated radiofrequency electromagnetic fields (AM RF EMF) device added to any third line treatment for triple negative breast cancer
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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 |
|---|---|---|
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6 month Progression Free Survival (PFS6)
時間枠:6 months after start of treatment
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PFS is defined as the interval from treatment initiation to the date of disease progression of death from any cause, whichever occurs first.
The treating investigator will determine disease progression.
PFS6 will be calculated as the proportion of participants who are alive without progression at six months post-treatment initiation.
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6 months after start of treatment
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Changes in Quality of Life Scores (QOL)
時間枠:From baseline to up to 1 year after treatment initiation
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QOL scores are evaluated using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ - C30).
It is 30-item questionnaire assessing cancer patients' health-related quality of life, covering functional scales (physical, role, emotional, cognitive, social), symptom scales (fatigue, pain, nausea, dyspnoea, etc.), and a global health/QoL scale.
We will record the time to deterioration of QOL, physical functioning, and role functioning, as reported by the participant, with deterioration defined as a decrease from baseline of 10 points or more on the EORTC QLQ - C30 maintained for two consecutive assessments or a decrease of 10 points or more in one assessment followed by death from any cause within three weeks.
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From baseline to up to 1 year after treatment initiation
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Overall Survival (OS)
時間枠:From baseline to up to 5 years after treatment initiation
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Participants will be followed for survival status every six months for five years after treatment is initiated.
OS is defined as the interval from treatment initiation to the date of death from any cause.
The distribution of time-to-event data (OS) will be graphically summarized using a Kaplan-Meier (KM) curve, with corresponding median and two-sided 95% Confidence Level (CI) computed using KM estimates.
OS rates every six months post-treatment will be estimated using KM estimates with two-sided 95% CIs provided for each time point.
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From baseline to up to 5 years after treatment initiation
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Progression Free Survival
時間枠:From baseline to up to 5 years after treatment initiation
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Participants will be followed for progression status every six months for five years after treatment is initiated.
Participants will not be followed for progression if they start another anti-cancer therapy during this time.
PFS is defined as the interval from treatment initiation to the date of disease progression of death from any cause, whichever occurs first.
The treating investigator will determine disease progression.
The distribution of time-to-event data (PFS) will be graphically summarized using a Kaplan-Meier (KM) curve, with corresponding median and two-sided 95% CI computed using KM estimates.
PFS rates every six months post-treatment will be estimated using KM estimates with two-sided 95% CIs provided for each time point.
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From baseline to up to 5 years after treatment initiation
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協力者と研究者
捜査官
- 主任研究者:Jailan Elayoubi, M.D.、Barbara Ann Karmanos Cancer Institute
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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