Metronomic chemotherapy regimens and targeted therapies in non-Hodgkin lymphoma: The best of two worlds

Novel drugs are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs). Notwithstanding, especially in aggressive subtypes, chemotherapy remains the pillar of treatment. Indeed, the combination of highly effective Maximum-Tolerated-Dose Chemotherapy (MTD-CHEMO) + “novel drugs”...

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Veröffentlicht in:Cancer letters 2022-01, Vol.524, p.144-150
Hauptverfasser: Cox, Maria Christina, Bocci, Guido
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container_title Cancer letters
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Bocci, Guido
description Novel drugs are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs). Notwithstanding, especially in aggressive subtypes, chemotherapy remains the pillar of treatment. Indeed, the combination of highly effective Maximum-Tolerated-Dose Chemotherapy (MTD-CHEMO) + “novel drugs”, has so far, fallen short from expectations, often because it caused excessive toxicity. Metronomic chemotherapy (mCHEMO), which is the frequent, long-term administration of low dose cytotoxic drugs, may allow more effective and tolerable combinations. mCHEMO pharmacodynamics, has been described as pleiotropic. In fact, it may have different cellular and molecular targets, when drugs or their schedules are modified. Although mCHEMO has been little explored in NHLs, pre-clinical studies - in lymphoma models - which addressed the activity of mCHEMO in combination with novel drugs, have shown very promising results. These included inhibitors of histone deacetylase, mTOR and PI3K/mTOR, as well as the immune checkpoint inhibitor anti-PD-L1. Moreover, a few impressive reports have recently shown all-oral mCHEMO schedules, with or without rituximab, can effectively shrink both B and T-cell aggressive NHLs. Indeed, these regimens allowed elderly-frail patients to achieve sustained remission, while toxicity proved manageable. In our opinion, all-oral mCHEMO, is an active, easy-to start, well-tolerated, and inexpensive therapeutic approach, which deserves further investigation. Most importantly, mCHEMO, holds promise to empower the activity of novel targeted therapies, without causing excessive toxicity. •Targeted therapies are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs).•All-oral metronomic chemotherapy (mCHEMO) schedules have shown good activity and tolerability in elderly-frail NHL patients.•In NHLs, the combination of targeted therapies with mCHEMO schedules have shown promising pre-clinical and clinical results.•mCHEMO may be an ideal platform for further improving the armamentarium of NHLs therapies.
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Notwithstanding, especially in aggressive subtypes, chemotherapy remains the pillar of treatment. Indeed, the combination of highly effective Maximum-Tolerated-Dose Chemotherapy (MTD-CHEMO) + “novel drugs”, has so far, fallen short from expectations, often because it caused excessive toxicity. Metronomic chemotherapy (mCHEMO), which is the frequent, long-term administration of low dose cytotoxic drugs, may allow more effective and tolerable combinations. mCHEMO pharmacodynamics, has been described as pleiotropic. In fact, it may have different cellular and molecular targets, when drugs or their schedules are modified. Although mCHEMO has been little explored in NHLs, pre-clinical studies - in lymphoma models - which addressed the activity of mCHEMO in combination with novel drugs, have shown very promising results. These included inhibitors of histone deacetylase, mTOR and PI3K/mTOR, as well as the immune checkpoint inhibitor anti-PD-L1. 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inhibitors</topic><topic>TOR Serine-Threonine Kinases - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cox, Maria Christina</creatorcontrib><creatorcontrib>Bocci, Guido</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cox, Maria Christina</au><au>Bocci, Guido</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metronomic chemotherapy regimens and targeted therapies in non-Hodgkin lymphoma: The best of two worlds</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2022-01-01</date><risdate>2022</risdate><volume>524</volume><spage>144</spage><epage>150</epage><pages>144-150</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>Novel drugs are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs). Notwithstanding, especially in aggressive subtypes, chemotherapy remains the pillar of treatment. Indeed, the combination of highly effective Maximum-Tolerated-Dose Chemotherapy (MTD-CHEMO) + “novel drugs”, has so far, fallen short from expectations, often because it caused excessive toxicity. Metronomic chemotherapy (mCHEMO), which is the frequent, long-term administration of low dose cytotoxic drugs, may allow more effective and tolerable combinations. mCHEMO pharmacodynamics, has been described as pleiotropic. In fact, it may have different cellular and molecular targets, when drugs or their schedules are modified. Although mCHEMO has been little explored in NHLs, pre-clinical studies - in lymphoma models - which addressed the activity of mCHEMO in combination with novel drugs, have shown very promising results. These included inhibitors of histone deacetylase, mTOR and PI3K/mTOR, as well as the immune checkpoint inhibitor anti-PD-L1. 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subjects 1-Phosphatidylinositol 3-kinase
Administration, Metronomic
Aged
Apoptosis
Cancer therapies
Cell cycle
Cell growth
Chemotherapy
Clinical studies
Cytotoxicity
Diffuse large B-Cell
Dose-Response Relationship, Drug
Drug dosages
Elderly
Frailty
Geriatric Assessment
Histone deacetylase
Histone Deacetylase Inhibitors - therapeutic use
Histone Deacetylases - genetics
Humans
Immune checkpoint inhibitors
Immune Checkpoint Inhibitors - therapeutic use
Immunosuppressive agents
Lymphocytes T
Lymphoma
Lymphoma, Non-Hodgkin - drug therapy
Lymphoma, Non-Hodgkin - genetics
Lymphoma, Non-Hodgkin - pathology
Lymphoma, T-Cell - drug therapy
Lymphoma, T-Cell - pathology
Metronomic chemotherapy
Non-Hodgkin's lymphoma
Non-Hodgkin-lymphoma
PD-L1 protein
Pharmaceutical industry
Pharmacodynamics
Phosphatidylinositol 3-Kinases - genetics
Preclinical studies
Remission
Rituximab
Rituximab - therapeutic use
Schedules
Signal Transduction - drug effects
T-cell lymphoma
TOR protein
TOR Serine-Threonine Kinases - antagonists & inhibitors
TOR Serine-Threonine Kinases - genetics
title Metronomic chemotherapy regimens and targeted therapies in non-Hodgkin lymphoma: The best of two worlds
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