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OpenTrials
Completed

NCT Number: NCT03200015

Rituximab, Cyclophosphamide, Vincristine and Prednisone (R-CHOP) Plus Metformin in Diffuse Large-B-cell Lymphoma

Evaluation of the safety and effectiveness of metformin as an adjunct to RCHOP chemotherapy for patients with newly diagnosed diffuse large-B cell lymphoma

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hospital Universitario Dr. José Eleuterio González

Monterrey, Nuevo León, 64610, Mexico

About this study

Patients with newly diagnosed diffuse large-B cell non Hodgkin lymphoma, irrespective of cell of origin status will receive metformin in combination to Rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone (RCHOP) chemotherapy for 6 cycles, until response evaluation as reported elsewhere:

1.- Rituximab 375 mg/m2 IV, day 1. 2.- Cyclophosphamide 750 mg/m2 IV, day 1. 3.- Doxorubicin 50 mg/m2 IV day 1. 4.- Vincristine 1.4 mg/m2 IV (2 mg maximum dose). 5.- Prednisone 60 mg/m2 PO days 1-5. Six cycles every 21 days.

Metformin will be added and administered in an outpatient basis, starting with 425 mg twice a day for 1 week, followed by 850 mg twice a day for 1 week, and lastly 850 mg every 8 hours maximum dose until re-staging. Laboratory tests will be performed serially.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with newly diagnosed nodal diffuse large-B cell non Hodgkin lymphoma according to the 2008 World Health Organization classification for lymphoid malignancies
  • No previous treatment other than prednisone or equivalent glucocorticoid up to 60 mg/m2 for 14 days
  • Good performance status (Eastern Cooperative Oncology Group scale 0-2)
  • Life expectancy >6 months
  • Independently of the diagnosis of diabetes mellitus (any type)

Exclusion criteria

  • History of intolerance or hypersensitivity reactions to metformin
  • Primary central nervous system lymphoma
  • History of other previous malignant neoplastic diseases <5 years prior to enrollment
  • Evidence of systemic infection at the time of study
  • HIV, hepatitis C or B virus infection
  • Aspartate transaminase or alanine transaminase >2x upper limit of normal, bilirubin >2.5 times upper limit of normal
  • Serum creatinine >1.5 mg/dL or chronic renal disease
  • Cardiac insufficiency (New York Heart Association scale >1 or ejection fraction <50%)
  • History of transformation from an indolent lymphoma
  • Pregnancy
  • History of lactic acidosis or alcoholism

Treatment and study plan

metformin

Drug

Potentially increasing the efficacy and safety of standard chemotherapy through several mechanisms

Primary outcomes

  1. Incidence of treatment-emergent adverse events

    Time frame: 6 months

    Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

  2. Response rates

    Time frame: 6 months

    Overall, partial and complete responses to chemoimmunotherapy

Secondary outcomes

  1. Progression-free survival

    Time frame: 2-5 years

    Survival with freedom from progression

  2. Overall survival

    Time frame: 2-5 years

    Survival from diagnosis until death or last follow-up

  3. Event-free survival

    Time frame: 2-5 years

    Survival from diagnosis until death or progression

  4. Time to progression or relapse

    Time frame: 2-5 years

    Time from diagnosis until disease progression or relapse

Sponsors and collaborators

Lead sponsor

Hospital Universitario Dr. Jose E. Gonzalez

Other

Registry information

Official study title

Effect of Metformin in Combination With R-CHOP for the First Line Treatment of Patients With Diffuse Large B-cell Lymphoma

Important dates

Study start
2017
Primary completion
2018
Study completion
2019
First posted
Jun 27, 2017
Registry last updated
Nov 7, 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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