Understanding Drug Classes

/Understanding Drug Classes

Understanding Drug Classes

By | 2014-09-14T11:32:11+00:00 December 5th, 2012|GIST Education, Research|

Understanding drug classes is important. Many new cancer drugs are entering clinical practice and clinical trials. Many GIST patients are no longer responding to Gleevec or Sutent and thus are looking for clinical trials. Understanding strategies and grouping these new drugs into classes with other similar drugs may help patients understand some of their choices. For additional information see the article by Dr. Jonathan Fletcher in the January 2007 edition of The Life Raft Group newsletter.

The classes of drugs we are talking about are related to one or more strategies to treat GIST. Other strategies may emerge over time, but for now these strategies include:

  • Inhibit KIT (and/or PDGFRA) signaling
  • Antiangiogenesis (impede tumor vascularization)
  • Destroy KIT
  • Inhibit the production of KIT (or PDGFRA)
  • Downstream signaling – Inhibit, destroy or prevent production of intermediate signaling proteins downstream of KIT (or PDGFRA)
  • Inhibit the cell cycle
  • Induce apoptosis
  • Inhibit IGF-1R signaling
  • Inhibit specific Gleevec/Sutent resistance mutations, especially the D842V mutation in PDGFRA

Strategy: Inhibit KIT signaling

Drug Class: KIT/PDGFRA
This class of drugs includes Gleevec, the drug that is approved for first-line treatment of metastatic GIST. Even in Gleevec-resistant GIST, Gleevec is sometimes used in combination with other drugs and in the absence of another therapy. This is because many tumors may still be sensitive to Gleevec resulting in a slowing of tumor progression.Gleevec binding to mutant KIT receptor blocks KIT signaling which inhibits proliferation and , is some cases, causes cell death.

One of the primary ways that drugs in this class hope to overcome Gleevec resistance is by inhibiting the secondary mutations that are the primary cause of resistance. Secondary KIT (or PDGFRA) mutations, especially in exons 13, 14 and 17, prevent Gleevec from being able to bind to the mutant receptor. Drugs that can bind to the KIT receptor, in spite of the secondary mutations, may overcome Gleevec-resistance.

Drugs in this class include Gleevec for first-line therapy, Tasigna (nilotinib) and Sprycel (dasatinib). There are also many other KIT/PDGFRA inhibitors in various stages of development. Masitinib is in phase III trials to see how it compares to Gleevec for first-line use. Most multi-targeted tyrosine kinase inhibitors also inhibit KIT and PDGFRA signaling, but they also add VEGF inhibition (see next section).

Search the LRG Clinical Trials Database for trials of KIT/PDGFRA inhibitors including multi-targeted kinase inhibitors:

Gleevec/Sutent resistant | First Line | Adjuvant | Advanced Search


Strategy: Inhibit KIT signaling; antiangiogenesis

Drug Class: KIT/PDGFRA/VEGF inhibitors a.k.a. Multi-targeted Tyrosine Kinase Inhibitors
This class of drug is similar to the KIT/PDGFRA inhibitors, except that they also inhibit one or more of the vascular endothelial growth factor receptors (VEGFR). They may also inhibit additional targets whose role in GIST is undetermined (such as RET). VEGFRs play an important role in the growth of new blood vessels in the body (angiogenesis). Without the growth of new blood vessels, tumors cannot grow beyond a few millimeters in size.

In addition to inhibiting PDGFRA, almost all of the drugs in this class also inhibit PDGFRB. PDGFRB may also be important in angiogenesis, so these drugs inhibit angiogenesis via at least two pathways (VEGFRs and PDGFRB). It should be noted that the drugs currently listed in the first class also inhibit PDGFRB.

In addition to their antiangiogenic effects, drugs in this class may also fit into the binding pocket of KIT (or PDGFRA) differently than Gleevec. To be effective against Gleevec-resistant GIST, it is widely believed that, in addition to their antiangiogenic effects, these drugs must also be effective at inhibiting the secondary mutations that cause Gleevec-resistance. The effects of multi-drug resistance proteins on drugs in this class have generally not been well characterized in the literature.

Approved drugs in this class include:

  • Sutent (approved for Gleevec-resistant GIST)
  • Stivara (regorafenib) – Has been submitted to the FDA for approval as 3rd-line therapy in GIST (August, 2012)
  • Nexavar (not approved for GIST). NOTE: Inhibition of PDGFRA by Nexavar has not been reported.
  • Votrient (pazopanib) – Not approved for GIST, in phase II trials for GIST

Drugs in this class that are not approved, but are in clinical trials include:

  • Vatalanib (PTK787)
  • Amuvatinib (MP470)
  • Motesanib (AMG706)
  • Tivozanib (AV-951)
  • Dovitinib (TKI-258)
  • Search the LRG Clinical Trials Database for trials of KIT/PDGFRA inhibitors including multi-targeted kinase inhibitors:Gleevec/Sutent resistant | First Line | Adjuvant | Advanced Search

Strategy: Antiangiogenesis

Drug Class: VEGF monoclonal antibody inhibitor
In addition to being able to be inhibited by tyrosine kinase inhibitors (like Sutent), VEGF signaling can be inhibited in other ways as well. One method is to use a drug that binds to the exterior portion of the VEGF receptor(s) and prevents the binding of the VEGF growth factor(s) to the VEGF receptor. Avastin is a drug in this class that is approved for colon cancer. A phase III trial that combines Avastin and Gleevec compared to Gleevec alone was terminated due to low enrollment.


Strategy: Destroy KIT

Drug Class: HSP90 inhibitors
Heat Shock Protein 90 (Hsp90) is a protein that has several functions in cells. It is an emerging therapeutic target of interest for the treatment of cancer. Proteins are the mainstay of structural and signaling elements of all cells. Hsp90 is a molecule that maintains the conformation and activity of specific proteins in the cell, also called “client proteins” of Hsp90. KIT is one of the client proteins of Hsp90. Hsp90 enables cancer cell survival by maintaining the function of their mutated client proteins including the KIT and PDGFRA proteins in GIST. Inhibition of Hsp90 therefore has the potential to destroy the activated KIT/PDGFRA proteins resulting in a therapeutic effect in GIST. Since the target of these drugs is Hsp90 and not KIT or PDGFRA, they should be unaffected by the secondary mutations that commonly cause resistance to Gleevec. In fact, preliminary work has suggested that the stronger KIT is activated, the better they work.

Drugs in this class include both oral and intravenous drugs. Some of the intravenous drugs, such as IPI-504, are also being developed as an oral version.

Drugs in this class include:

STA-9090 – In phase II trials for GIST
AT13387
– In a combination phase I/II trial for GIST
IPI-504 – Phase III trial in GIST terminated due to unaccepable toxicity (mostly in patients with prior liver surgery)
AUY-922 – In several phase II trials for GIST

17-DMAG
17AAG-In phase I and phase II trials for a variety of cancers. This drug has poor solubility.
KOS-1022 – An oral or I. V. drug in phase I trials for solid tumors.

Search for HSP90 inhibitors in the LRG drug database


Strategy: Inhibit the production of KIT (and possibly other important proteins)

Class: Transcription inhibitors
While flavopiridol is widely known as an inhibitor of cyclin-dependent kinase (CDK2 and CDK1), its effects may be mediated more by inhibition of transcription than anything else (Cell Cycle review, December 2004).

Work done at Memorial Sloan-Kettering found that in a GIST cell line, total KIT protein was significantly diminished in flavopiridol-treated cells after 24 hours. This resulted in an indirect reduction in KIT autophosphorylation (activation), comparable to Gleevec. They confirmed that transcriptional downregulation was the reason for reduced total KIT protein. They also found that flavopiridol, at clinically achievable doses, induces a high level of apoptosis (cell death) in GIST cells. They believe their findings justify a clinical evaluation of flavopiridol in treating patients with Gleevec-resistant GIST.

The way flavopiridol works against KIT is different than Gleevec. Flavopiridol reduces the total amount of KIT protein, where Gleevec inhibits the activation (phosyphorylation) of the KIT protein present without lowering the amount of KIT protein. One of the mechanisms of Gleevec-resistance is overexpression of KIT or PDGFRA (too much KIT or PDGFRA protein).

A combination of flavopiridol and doxorubicin is in phase I trials for Sarcoma. This trial also allows GIST patients. The study is ongoing, but not recruiting participants (2012).


Strategy: Target KIT downstream signaling

Classes: The drugs using this strategy come from several different classes.
Targeting signals downstream from KIT and PDGFRA is one strategy being investigated for Gleevec-resistant GIST and for many cancers in general. Some of the most promising targets appear to be:
PI3K – However, because of its widespread use in the human body, it may be a difficult protein to target. PI3K inhibitors in trials that GIST patients are eligible for
PKC theta – Remains a desirable target, but we are unaware of any drugs that currently target PKC theta.
AKT – A protein involved in the prevention of apoptosis (it may have other functions as well).
mTOR – Inhibiting mTOR may have multiple effects in cancer cells. mTOR is involved in cell growth, angiogenesis and cellular survival. A phase I/II trial for the mTOR inhibitor RAD001 + Gleevec is ongoing in GIST. It is unclear if this trial will proceed to more advanced stages. There are at least 3 other mTOR inhibitors either approved (Rapamune) or in clinical trials. In one study of 108 samples of tissue from patients, mTOR was activated more often in PDGFRA mutations and in wild-type GIST than in KIT mutate GISTs.2
BCL-2 – This protein is an important anti-apoptosis protein. A phase II GIST trial combining Gleevec with an antisense inhibitor of bcl-2 was unsuccessful.


Strategy: Induce apoptosis, inhibit cell cycle, destroy KIT

Class: HDAC inhibitors
Work presented at the Life Fest meeting in Dallas, showed that a histone deacetylase (HDAC) inhibitor was able to cause significant regression in a Gleevec-resistant xenografts model (mouse model). HDAC inhibitors are a new class of drugs that have shown anti-cancer activity in three major ways:

  • Inducing apoptosis
  • Arresting the cell cycle
  • Destabilizing certain cancer-causing proteins such as bcr-abl (and possibly KIT). This may occur because HDAC inhibitors cause hsp90 to become inactive, possibly resulting in the destruction of the KIT protein.

Another way that HDAC inhibitors might accomplish their effects is by “turning on” some tumor suppressor genes that have been silenced.

HDAC inhibitors are in various stages of development. LBH589 (panobinostat) in combination with Glivec is in a phase I trial for GIST in Germany.

  • Istodax (romidepsin)- FDA approved for cutaneous T cell lymphoma (CTCL)
  • Zolinza (vorinostat) – FDA-approved for cutaneous T-cell lymphoma (CTCL)
  • LBH589 – In phase II trials for solid tumors and a phase I trial in combination Glivec (see this trial)
  • Others

In summary, a number of different strategies are being tried to overcome Gleevec resistance. Different classes of drugs use different strategies to accomplish this. Some classes of drugs use multiple strategies. Understanding the classes and strategies may help patients evaluate their treatment options.

Find all GIST-eligible trials of HDAC inhibitors that the LRG is tracking


Strategy: Inhibit alternate pathway (IGF-1R)

Class: IGF-1R inhibitors

IGF-1R is a tyrosine kinase that, much like KIT, protrudes through the cell surface and begins to signal when an extracellular Insulin Growth Factor (IGF1) attaches to the outside portion of the receptor. Unlike KIT, IGF-1R has not been found to be mutated in GIST. However, IGF-1R has been found to be over-expressed in wildtype GIST tumor tissue. Up to now, KIT inhibitors have had limited impact in wild type GIST. IGF-1R is now viewed as a component of a potential “side channel” providing an alternative signaling path to KIT and potentially a target in GIST.IGF1-R overexpression might be limited to the pediatric-like GIST version of wildtype GIST (SDH-deficient GIST).

Search for recruiting IGF-1R trials in the LRG database


1. Ronald P. Dematteo, MD, Michael C. Heinrich, MD, Wa’El M. El-Rifai, MD and George Demetri, MD. Clinical Management of Gastrointestinal Stromal Tumors: Before and After STI-571

2. The activated targets of mTOR signaling pathway are characteristic for PDGFRA mutant and wild-type rather than KIT mutant GISTs.
Sápi ZFüle THajdu MMatolcsy AMoskovszky LMárk ASebestyén ABodoky G.

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