Metronomic Oral Paclitaxel Monotherapy for Advanced HER2-Negative Breast Cancer: A Two-Stage Dose-Finding and Expansion Study

NCT07602907 | Recruiting Phase 2

• 1 other identifier: METRO - P
• Study Type: interventional
• Target: 73
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this clinical trial is to evaluate the safety, tolerability, and preliminary anti-tumor activity of metronomic oral paclitaxel solution in patients with advanced HER2-negative breast cancer who have previously received systemic anti-cancer treatments. The main questions this study aims to answer are: What doses of metronomic oral paclitaxel solution can be safely administered to patients with advanced HER2-negative breast cancer? How well does metronomic oral paclitaxel solution control tumor growth? What side effects and treatment-related medical problems occur during treatment? This study will include two stages. In the first stage, researchers will evaluate different dosing schedules of oral paclitaxel solution to identify a dose（OTD） with an acceptable balance between safety and potential anti-tumor activity. In the second stage, additional participants will receive the selected dose（OTD） to further evaluate its effectiveness and safety. Participants will: Receive metronomic oral paclitaxel solution according to the assigned dose schedule. Visit the study clinic regularly for physical examinations, laboratory tests, tumor imaging assessments, and safety evaluations. Complete assessments of treatment response, side effects, and quality of life during the study. Continue follow-up after treatment to collect information about disease status and survival.

Conditions

Advanced Breast Cancer; HER2-negative Breast Cancer

Outcome Measures

Primary Outcomes (2)

• Optimal Tolerated Dose (OTD) of metronomic oral paclitaxel

  To evaluate the safety, tolerability, and Disease Control Rate (DCR) of different doses of metronomic oral paclitaxel solution in patients with advanced HER2-negative breast cancer, and select the Optimal Tolerated Dose (OTD) for subsequent combination therapy.

  TRAE assessment: Within 7 days after the first dose DCR assessment: At the first efficacy evaluation (planned at 6 weeks after the first dose)

• Disease Control Rate (DCR)

  Disease control rate (DCR) is defined as the proportion of participants who achieve a complete response (CR), partial response (PR), or stable disease (SD) according to RECIST version 1.1.

  Up to approximately 24 months from the first dose of combination therapy

Study Arms (5)

Metronomic Oral Paclitaxel 50 mg QD

EXPERIMENTAL

Drug: Paclitaxel Oral Solution (50mg/qd)

Metronomic Oral Paclitaxel 100 mg/d TIW

EXPERIMENTAL

Drug: Paclitaxel Oral Solution (100mg/TIW)

Metronomic Oral Paclitaxel （OTD）

EXPERIMENTAL

Drug: Paclitaxel Oral Solution (OTD)

Metronomic Oral Paclitaxel 150 mg/d TIW

EXPERIMENTAL

Drug: Paclitaxel Oral Solution (150mg/TIW)

Metronomic Oral Paclitaxel 200 mg/d TIW

EXPERIMENTAL

Drug: Paclitaxel Oral Solution (200mg/TIW)

Interventions

Paclitaxel Oral Solution (50mg/qd) DRUG

Paclitaxel oral solution, 50 mg orally once daily (QD), continuously administered. Each treatment cycle is 21 days.

Metronomic Oral Paclitaxel 50 mg QD

Paclitaxel Oral Solution (100mg/TIW) DRUG

Paclitaxel oral solution, 100 mg orally three times weekly (TIW). Each treatment cycle is 21 days.

Metronomic Oral Paclitaxel 100 mg/d TIW

Paclitaxel Oral Solution (OTD) DRUG

Optimal tolerated dose (OTD) of metronomic paclitaxel oral solution.Each treatment cycle is 21 days.

Metronomic Oral Paclitaxel （OTD）

Paclitaxel Oral Solution (150mg/TIW) DRUG

Paclitaxel oral solution, 150 mg orally three times weekly (TIW). Each treatment cycle is 21 days.

Metronomic Oral Paclitaxel 150 mg/d TIW

Paclitaxel Oral Solution (200mg/TIW) DRUG

Paclitaxel oral solution 200 mg orally three times weekly (TIW). Each treatment cycle is 21 days.

Metronomic Oral Paclitaxel 200 mg/d TIW

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age ≥ 18 years, male or female. 2.Histologically confirmed unresectable locally advanced, recurrent, or metastatic HER2-negative breast cancer, regardless of hormone receptor (HR) status. For patients with HR+/HER2-negative subtype: prior treatment with at least 1 line of CDK4/6 inhibitor plus endocrine therapy is required, and the patient is considered no longer suitable for further endocrine therapy by the investigator.
• Patients have received 1-4 prior lines of systemic anti-tumor therapy for recurrent or metastatic disease.
• Line of therapy is defined as a systemic treatment regimen for recurrent or metastatic disease. First-line therapy is the first regimen used in the recurrent/metastatic setting; any subsequent regimen that adds a new drug class (e.g., anti-angiogenic, immunotherapy) is considered a new line.
• Neoadjuvant or adjuvant therapy is not counted as a treatment line.
• Disease recurrence \>6 months after neoadjuvant therapy is counted as first-line; recurrence ≤6 months is considered continuation of prior therapy and not a new line.
• Disease recurrence \>12 months after adjuvant therapy is counted as first-line; recurrence ≤12 months is considered continuation of prior therapy, and subsequent regimens start at second-line.
• Prior treatment with taxane is allowed if both criteria are met:
• Interval from last dose of taxane to first study dose ≥ 4 weeks;
• No unresolved taxane-related Grade ≥3 toxicity in the past. 5.Body surface area (BSA): 1.38 m² ≤ BSA ≤ 1.87 m². 6.ECOG performance status 0-1. 7.At least one measurable lesion per RECIST 1.1. 8.Expected survival ≥ 12 weeks. 9.Adequate bone marrow function: ANC ≥ 1.5 × 10⁹/L Platelets ≥ 100 × 10⁹/L Hemoglobin ≥ 90 g/L 10.Adequate hepatic function: Total bilirubin ≤ 1.5 × ULN ALT/AST ≤ 2.5 × ULN (no liver metastasis) ALT/AST ≤ 5 × ULN (with liver metastasis) 11.Adequate renal function: Serum creatinine ≤ 1.5 mg/dL Or creatinine clearance (Ccr) ≥ 60 mL/min (calculated by Cockcroft-Gault formula) if serum creatinine \>1.5 mg/dL.
• Pre-existing peripheral neuropathy \< Grade 2 (CTCAE v6.0). 13.Known CNS metastases are allowed only if all of the following are met:
• CNS lesions stable for ≥4 weeks before enrollment, per RANO-BM criteria (no new lesions, target lesion volume change \<20%, no clear progression of non-target lesions on baseline and follow-up MRI).
• No corticosteroid use, or current dexamethasone ≤4 mg/day (or equivalent), with no dose increase within 7 days before enrollment.
• For patients with prior local CNS treatment: no imaging progression after treatment completion; neurologic symptoms stable for ≥2 weeks before first study dose; no steroid or ≤4 mg/day dexamethasone (or equivalent).
• No leptomeningeal disease.
• Whole-brain radiotherapy completed \>14 days before enrollment.

You may not qualify if:

• Patients with suspected major infectious diseases, neurological disorders, or intestinal obstruction.
• Patients with a diagnosis of other cancer types (except non-melanoma skin cancer, cervical carcinoma in situ, or other cancers with no recurrence or metastasis for ≥5 years and considered cured).
• Patients who have undergone major surgery, including organ resection within 4 weeks before enrollment, or radiotherapy within 2 weeks before enrollment.
• Disease progression during prior taxane salvage therapy (at least 2 cycles completed), or recurrence/metastasis within 12 months after neoadjuvant/adjuvant therapy.
• Patients requiring long-term concomitant use of P-glycoprotein (P-gp) inhibitors or immunosuppressive agents during the study.
• Patients receiving long-term treatment with steroids or other immunosuppressive agents (except oral, topical, or local injection).
• Patients with myocardial infarction, congestive heart failure, rapidly changing arrhythmia on ECG, severe or unstable angina pectoris, or other serious heart diseases.
• Patients with other severe medical diseases (uncontrolled diabetes mellitus and hypertension, chronic obstructive pulmonary disease (COPD), or dyspnea at rest due to any cause).
• Patients with a history of drug or alcohol abuse within the past 3 months.
• Pregnant or breastfeeding women, or patients who cannot or will not use effective contraceptive methods.
• Patients with or suspected of having bile acid excretion disorders.
• Active tendency of gastrointestinal bleeding or use of oral vitamin K antagonists (low-dose warfarin and acetylsalicylic acid are allowed as long as INR ≤2.0).
• Patients with severe hypersensitivity to the active ingredients or excipients of the study drugs.
• History of HIV seropositivity (HIV testing is not mandatory).
• Gastrointestinal dysfunction or diseases that may significantly alter the absorption of study drugs (e.g., ulcerative diseases, poorly controlled nausea, vomiting, diarrhea, malabsorption syndrome), except patients with prior gastrectomy.

Sponsors & Collaborators

• Zhejiang Cancer Hospital: lead

Study Sites (1)

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, 310022, China

RECRUITING

Related Publications (1)

• Mo H, Yu Y, Sun X, Ge H, Yu L, Guan X, Zhai J, Zhu A, Wei Y, Wang J, Yan X, Qian H, Xu B, Ma F. Metronomic chemotherapy plus anti-PD-1 in metastatic breast cancer: a Bayesian adaptive randomized phase 2 trial. Nat Med. 2024 Sep;30(9):2528-2539. doi: 10.1038/s41591-024-03088-2. Epub 2024 Jul 5.

  PMID: 38969879 RESULT

MeSH Terms

Interventions

Paclitaxel

Intervention Hierarchy (Ancestors)

Taxoids; Cyclodecanes; Cycloparaffins; Hydrocarbons, Alicyclic; Hydrocarbons, Cyclic; Hydrocarbons; Organic Chemicals; Diterpenes; Terpenes

Central Study Contacts

Lei Lei

CONTACT

+8613750802564; leilei@zjcc.org.cn

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: May 9, 2026
• First Posted: May 22, 2026
• Study Start: August 4, 2026
• Primary Completion (Estimated): August 20, 2029
• Study Completion (Estimated): August 20, 2029
• Last Updated: August 11, 2026

Record last verified: 2026-08

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)