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NCT Number: NCT05521204

Olverembatinib for FGFR1-rearranged Neoplasms

FGFR1-rearranged myeloid/lymphoid neoplasms are a rare hematologic malignancy with very poor outcome despite intensive chemotherapy. The only curative option is thought to be allogeneic hematopoietic stem cell transplantation (HSCT) in remission.

This phase II study is aimed to evaluate the efficacy of Olverembatinib, consolidated with HSCT in the treatment of FGFR1-rearranged myeloid/lymphoid neoplasm.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, 215000, China

Location status: Recruiting

Location contact

Suning Chen, PhD

CONTACT

[email protected]

+8613814881746

About this study

FGFR1-rearranged myeloid/lymphoid neoplasms are a rare and highly heterogeneous hematological malignancy, mainly manifested as myeloproliferative neoplasms (MPNs) or acute leukemia, including T cells or B cells Cell lymphoblastic leukemia/lymphoma (T-cell or B-cell-ALL/LBL), acute myeloid leukemia (AML) and mixed cell leukemia (MPAL).

To date, there is no standard treatment. Conventional chemotherapy is frequently ineffective. The only curative option is thought to be allogeneic HSCT at present, TKIs may offer a therapeutic alternative in patients not eligible for allogeneic HSCT or to bridge the time between diagnosis and allogeneic HSCT.

Third-generation TKIs Olverembatinib is a pan- FGFR1 kinase inhibitor, and is supposed to be effective to achieve bone marrow remission in FGFR1-rearranged myeloid/lymphoid neoplasms.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with newly diagnosed, progressed or relapsed myeloid/lymphoid neoplasms with FGFR1 rearrangement according to the WHO-2016 diagnostic criteria. Patients who have received allogeneic hematopoietic stem cell transplantation or ponatinib should be excluded.
  • ECOG score: MPNs patients, 0-3 points; AL patients, 0-2 points.
  • Expected survival period ≥12 weeks.
  • Willingness and ability to comply with study procedures and follow-up examination.

Exclusion criteria

  • Patients who have received allogeneic hematopoietic stem cell or ponatinib.
  • Human immunodeficiency virus (HIV) infection, or chronic infection with hepatitis B virus (HBsAg positive) or hepatitis C virus (anti-HCV positive).
  • Patients who are pregnant, planning to become pregnant or breastfeeding.
  • Patients who may not be able to complete all study visits or procedures required by the study protocol, including follow-up visits, and/or fail to comply with all required study procedures.
  • Patients who suffer from any condition or illness that, in the opinion of the investigator, would compromise patient safety or interfere with the evaluation of the safety of the research drug.

Treatment and study plan

Olverembatinib

Drug

Given PO

Primary outcomes

  1. Overall Response Rate

    Time frame: Assessed at protocol-defined timepoints through end of study, up to approximately 48 months.

    The proportion of participants who achieve Overall Response (ORR) based on response criteria for myeloid/lymphoid neoplasms with FGFR1 rearrangement

Secondary outcomes

  1. Event-free survival (PFS)

    Time frame: From the first day of treatment until any failure (resistant disease, relapse, or death), assessed up to 2 to 4 years.

    The Kaplan-Meier method will be used to assess EFS probabilities.

  2. Overall survival (OS)

    Time frame: From the first day of treatment to time of death from any cause, assessed up 2 to 4 years.

    The Kaplan-Meier method will be used to assess OS probabilities.

  3. Incidence of adverse events (AEs)

    Time frame: Up to approximately 2 to 4 years.

    Will be graded according to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v) 5.0. The proportion of patients with AEs will be estimated, along with the Bayesian 95% credible interval.

Study contacts

Contact information is provided by the study sponsor or research team.

Suning Chen

CONTACT

[email protected]

+86-13814881746

Sponsors and collaborators

Lead sponsor

The First Affiliated Hospital of Soochow University

Other

Registry information

Official study title

A Study of Olverembatinib in the Treatment of Myeloid/Lymphoid Tumors With FGFR1 Rearrangement

Important dates

Study start
2022
Primary completion
2024
Study completion
2027
First posted
Aug 30, 2022
Registry last updated
Aug 30, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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