Pacritinib vs. Hydroxyurea in Advanced Proliferative Chronic Myelomonocytic Leukemia

Официальное название

A Randomized Phase 2 Study of Pacritinib vs. Hydroxyurea in Patients With Advanced Proliferative Chronic Myelomonocytic Leukemia

Обзор

The goal of this clinical trial is to learn if pacritinib works better than hydroxyurea to treat advanced proliferative chronic myelomonocytic leukemia in adults. The main questions it aims to answer are: * Does pacritinib improve disease control compared to hydroxyurea? * What medical problems do participants have when taking pacritinib or hydroxyurea? Researchers will compare pacritinib to hydroxyurea to see if pacritinib is more effective and better tolerated in people with advanced proliferative chronic myelomonocytic leukemia. Participants will be randomly assigned to receive either pacritinib twice a day or hydroxyurea for up to 48 weeks. After treatment ends, participants will be followed for up to one year.

Подробное описание

This is a randomized, multicenter, open-label Phase 2 clinical trial evaluating the efficacy and safety of pacritinib compared to hydroxyurea in adult participants with advanced proliferative chronic myelomonocytic leukemia (CMML). Approximately 66 participants will be randomized in a 2:1 ratio to receive either pacritinib 200 mg twice daily (n=44) or hydroxyurea (n=22) for up to 48 weeks. Randomization will be stratified based on prior therapy (i.e., prior use of hydroxyurea or hypomethylating agents vs. no prior therapy).

The study includes:

* A 28-day screening period * A 48-week treatment period * A 30-day post-treatment follow-up * A survival follow-up phase lasting approximately one year after randomization Participants receiving pacritinib who are not deriving benefit by Week 24, as assessed by the treating physician, will discontinue treatment. Participants in the hydroxyurea arm who are not deriving benefit by Week 24-or who experience non-leukemic disease progression-may switch to pacritinib for the remainder of the treatment period, provided they meet predefined "Safe to Switch" criteria.

Participants who discontinue study therapy due to toxicity, disease progression, or other protocol-defined criteria will enter survival follow-up to monitor overall survival, event-free survival, leukemic-free survival, and receipt of allogeneic hematopoietic stem cell transplant. Data will be collected at least every three months until death, hematopoietic stem cell transplant, or leukemic transformation.

An independent data monitoring committee will oversee safety, with the first review after enrollment of \~18 participants and subsequent reviews approximately every 6 months.

Вмешательства

• Препарат Pacritinib
  100-mg capsules
• Препарат Hydroxyurea
  capsules or tablets

Первичные конечные точки

• Clinical benefit at Week 24, defined as achieving erythroid response in the absence of leukemic transformation. [Срок оценки: Measured from Week 24 through the end of treatment, up to 48 weeks.]
• Clinical benefit at Week 24, defined as achieving platelet response in the absence of leukemic transformation. [Срок оценки: Measured from Week 24 through the end of treatment, up to 48 weeks.]
• Clinical benefit at Week 24, defined as achieving neutrophil response in the absence of leukemic transformation. [Срок оценки: Measured from Week 24 through the end of treatment, up to 48 weeks.]
• Clinical benefit at Week 24, defined as achieving spleen response in the absence of leukemic transformation. [Срок оценки: Measured from Week 24 through the end of treatment, up to 48 weeks.]
• Clinical benefit at Week 24, defined as achieving symptom response in the absence of leukemic transformation. [Срок оценки: Measured from Week 24 through the end of treatment, up to 48 weeks.]

Вторичные конечные точки (12)

• Clinical benefit at any time, defined as achieving at least one of the primary endpoint clinical benefit response criteria at any time on study. [Срок оценки: Measured from the start of study treatment to the end of treatment, for up to 48 weeks.]
• Achieving response at Week 24 and 48 according to the IWG 2015 criteria), including the following subtypes: complete response, complete cytogenetic remission, partial remission, marrow response [Срок оценки: Measured from Week 24 through the end of treatment, up to 48 weeks.]
• Duration of response for primary endpoint (clinical benefit by Week 24) [Срок оценки: Measured from Week 24 through the end of treatment, up to 48 weeks.]
• Event-free survival [Срок оценки: Measured from the start of study treatment to the end of treatment, for up to 48 weeks.]
• Leukemia-free survival, where events include death from any cause or transformation to AML (including granulocytic sarcoma) [Срок оценки: Measured from the start of study treatment to the end of treatment, for up to 48 weeks.]
• Overall survival [Срок оценки: Measured from the date of initiating study treatment to the date of death from any cause, assessed up to 24 months.]
• Incidence of allogeneic hematopoietic stem cell transplant. [Срок оценки: Measured from the date of initiating study treatment to the date of allogeneic hematopoietic stem cell transplant., assessed for up to 24 months]
• Adverse events and laboratory abnormalities as graded by NCI CTCAE v5.0. [Срок оценки: From the start of the adverse event collection period through 30 days following the last dose of study treatment.]
• Change in arterial blood pressure measured in mmHg. [Срок оценки: From the start of the study treatment through 30 days following the last dose of study treatment.]
• Change in pulse rate measured in beats per minute. [Срок оценки: From the start of the study treatment through 30 days following the last dose of study treatment.]
• Change in respiratory rate measured in breaths per minute. [Срок оценки: From the start of the study treatment through 30 days following the last dose of study treatment.]
• Change in corrected QT interval measured in milliseconds using 12-lead electrocardiogram. [Срок оценки: From the start of the study treatment through 30 days following the last dose of study treatment.]

Критерии участия

Критерии включения

• Diagnosis of CMML-1 (5th WHO classification), with <10% bone marrow blasts on morphology and <5% peripheral blood blasts.
• Proliferative disease, defined as white blood cell count ≥13 × 10⁹/L.
• Advanced disease, defined as at least one of the following features during screening: spleen palpable ≥5cm below the lower costal margin in the midclavicular line; TSS ≥20; or platelet count <100 × 10⁹/L. For participants in whom spleen palpation is not feasible, an ultrasound exam may be performed for assessment of spleen craniocaudal length (length ≥12 cm by ultrasound is considered splenomegaly).
• ECOG performance status ≤2.
• Adequate organ function: AST and ALT ≤3 × ULN, total bilirubin ≤4 × ULN (≤8 × ULN in participants with Gilbert's syndrome), creatinine clearance >30 mL/min, absolute neutrophil count ≥0.5 × 10⁹/L, PT and PTT ≤1.5 × ULN.
• Women of child-bearing potential must have a negative serum pregnancy test within 7 days prior to enrollment and, along with male participants, must agree to use a highly effective method of contraception from the first dose through 90 days after the last dose.

Критерии исключения

• Active malignancy diagnosed within the past 2 years, except for curatively treated non-invasive cancers (e.g., basal/squamous cell skin cancer, low-risk prostate cancer on stable endocrine therapy with PSA stable ≥3 months).
• Allogeneic hematopoietic stem cell transplant within 12 months prior to enrollment, or requiring immunosuppressive therapy within 6 months before enrollment.
• Likely to undergo allogeneic hematopoietic stem cell transplant within 6 months, per investigator assessment.
• Prior systemic treatment with any JAK inhibitor.
• Treatment with hypomethylating agents or cytotoxic chemotherapy (excluding hydroxyurea) within 28 days prior to enrollment.
• Participation in another interventional study or use of experimental therapy within 28 days or 5 half-lives, whichever is longer.
• Use of hematologic support drugs within 28 days prior to enrollment. Supportive care permitted.
• Use of strong CYP3A4 inhibitors or inducers within 14 days or 5 half-lives before enrollment, whichever is shorter.
• Use of systemic anticoagulants or antiplatelets (except aspirin ≤100 mg/day) within 14 days prior. Therapeutic anticoagulation allowed if stable for ≥90 days without bleeding events.
• CTCAE Grade ≥2 bleeding within 3 months prior to enrollment, unless due to a reversible cause (e.g., trauma, surgery).
• QTcF >450 ms (men) or >470 ms (women); QTcF up to 480 ms allowed if QRS >100 ms. QTcF may be repeated if affected by reversible factors.
• CTCAE Grade ≥3 cardiac event within 3 months before enrollment.
• Symptomatic heart failure with limitations on ordinary activity.
• Uncontrolled infection at study entry.
• Moderate/severe hepatic impairment (Child-Pugh B or C), or active viral hepatitis:
• HBV: Exclude if HBsAg+ or HBV DNA detectable. HBV antiviral therapy allowed if HBV DNA undetectable.
• HCV: Allowed if HCV Ab+ but RNA negative.
• Uncontrolled HIV or detectable viral load while on antiretrovirals.
• Known hypersensitivity to pacritinib or its excipients (microcrystalline cellulose, polyethylene glycol, magnesium stearate).

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

США · 4 центра

• Moffitt Cancer Center — Tampa
• Winship Cancer Institute at Emory — Atlanta
• Mayo Clinic Rochester — Rochester
• MD Anderson Cancer Center — Houston

Идентификаторы

NCT: NCT07033598 · PROSPERA · ABNL-MARRO 002

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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