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Abemaciclib

(Redirected from LY2835219)

Abemaciclib, sold under the brand name Verzenio among others, is a medication for the treatment of advanced or metastatic breast cancers. It was developed by Eli Lilly and it acts as a CDK inhibitor selective for CDK4 and CDK6.[4]

Abemaciclib
Clinical data
Pronunciation/əˌbɛməˈsaɪklɪb/
ə-BEM-ə-SY-klib
Trade namesVerzenio, Verzenios, Ramiven, others
Other namesLY2835219
AHFS/Drugs.comMonograph
License data
Routes of
administration		By mouth
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability45%
Protein binding96.3%
Elimination half-life18.3 hrs
Excretion81% via feces, 3% via urine
Identifiers
  • N-[5-[(4-Ethyl-1-piperazinyl)methyl]-2-pyridinyl]-5-fluoro-4-[4-fluoro-2-methyl-1-(1-methylethyl)-1H-benzimidazol-6-yl]-2-pyrimidinamine
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
PDB ligand
CompTox Dashboard (EPA)
ECHA InfoCard100.233.787 Edit this at Wikidata
Chemical and physical data
FormulaC27H32F2N8
Molar mass506.606 g·mol−1
3D model (JSmol)
  • CCN1CCN(CC1)Cc2ccc(nc2)Nc3ncc(c(n3)c4cc5c(c(c4)F)nc(n5C(C)C)C)F
  • InChI=1S/C27H32F2N8/c1-5-35-8-10-36(11-9-35)16-19-6-7-24(30-14-19)33-27-31-15-22(29)25(34-27)20-12-21(28)26-23(13-20)37(17(2)3)18(4)32-26/h6-7,12-15,17H,5,8-11,16H2,1-4H3,(H,30,31,33,34)
  • Key:UZWDCWONPYILKI-UHFFFAOYSA-N

It was designated as a breakthrough therapy for breast cancer by the US Food and Drug Administration (FDA) in October 2015.[5]

In September 2017, it was approved for use in the United States by the FDA for the treatment of certain breast cancers.[6]

Medical uses

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Since September 2017, abemaciclib has been approved in the US for "adults who have hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer that has progressed after taking therapy that alters a patient's hormones".[6]

In studies that compared fulvestrant plus abemaciclib to fulvestrant plus placebo in breast cancer patients, progression-free survival under abemaciclib therapy was 16.4 months on average, as compared to 9.3 months under the placebo arm.

Side effects

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Side effects that occurred in 20% or more of patients in studies were diarrhea, nausea and vomiting, leukopenia (low white blood cell count) including neutropenia, anemia (low red blood cell count), thrombocytopenia (low platelet count), stomach pain, infections, fatigue, decreased appetite, and headache.[7][8]

Interactions

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As abemaciclib is mainly metabolized by the liver enzyme CYP3A4, inhibitors of this enzyme (such as ketoconazole) are expected to increase its blood plasma concentrations. Conversely, CYP3A4 inducers lower plasma concentrations of abemaciclib, as has been shown in a study with rifampicin.[8]

Pharmacology

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Mechanism of action

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Like the related drugs palbociclib and ribociclib, abemaciclib inhibits the enzymes cyclin-dependent kinase 4 (CDK4) and cyclin-dependent kinase 6 (CDK6).[8] These enzymes are responsible for phosphorylating and thus deactivating the retinoblastoma protein, which plays a role in cell cycle progression from the G1 (first gap) to the S (synthesis) phase.[9] Blocking this pathway prevents cells from progressing to the S phase, thereby inducing apoptosis (cell death).[8] In vitro analysis using cancer cell lines, it is reported that abemaciclib induces non-apoptotic cell death characterized by formation of cytoplasmic vacuoles derived from lysosomes. This result suggests that there may be a mechanism of action other than inhibition of a cyclin-dependent kinase.[10]

Pharmacokinetics

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N-desethylabemaciclib (M2), the main metabolite

After oral intake, absolute bioavailability is 45%. Highest blood plasma concentrations are reached after 8 hours on average (range: 4.1–24.0 hours). When in the circulation, 96.3% of abemaciclib is bound to plasma proteins. The substance is mainly metabolized by the liver enzyme CYP3A4 to N-desethylabemaciclib (M2), and to a lesser extent to hydroxy derivatives (M18, M20) and another oxidative metabolite (M1). These metabolites have high plasma protein binding rates similar to the parent substance.[8]

Abemaciclib is excreted mainly via the feces (81%) and to a small extent via the urine (3%). Its elimination half-life is 18.3 hours on average.[8]

Clinical trials

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Successful trials against pre-treated metastatic breast cancer were announced for Phase I in May 2014,[11] Phase II in December 2014,[12] and Phase III in February 2017.[13] Abemaciclib was approved by the FDA in September 2017 either in combination with fulvestrant or as a monotherapy for women with HR , HER2- advanced or metastatic breast cancer that had progressed while receiving endocrine therapy.[14] Abemaciclib was approved for the adjuvant treatment of HR , HER2-, node-positive adjuvant breast cancer at high risk of recurrence in March 2023.[15][16]

As of 2023, abemaciclib was involved in two Phase III clinical trials:

  • The SARC041 study compares abemaciclib versus placebo in patients with advanced dedifferentiated liposarcoma.[17]
  • The CYCLONE 3 study compares abemaciclib versus placebo in combination with abiraterone and prednisone in patients with high-risk, metastatic, hormone-sensitive prostate cancer.[18]

Abemaciclib is in Phase I and II clinical trials for head and neck squamous cell carcinoma,[19] biliary tract carcinoma,[20] brain tumors,[21][22][23] neurofibromatosis,[24] Kaposi sarcoma,[25] metastatic renal cell carcinoma,[26] and Mantle Cell lymphoma.[27]

Chemistry

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Abemaciclib may be synthesized in a four step manner using a Suzuki coupling, followed by a Buchwald–Hartwig amination with the final step being a reductive amination using the Leuckart reaction.[28]

References

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  1. ^ "Verzenio (Eli Lilly Australia Pty Ltd)". Therapeutic Goods Administration (TGA). 28 September 2022. Archived from the original on 18 March 2023. Retrieved 9 April 2023.
  2. ^ "Summary Basis of Decision (SBD) for Verzenio". Health Canada. 23 October 2014. Archived from the original on 31 May 2022. Retrieved 29 May 2022.
  3. ^ "Verzenios EPAR". European Medicines Agency. 27 September 2018. Retrieved 17 June 2024.
  4. ^ Lu J (August 2015). "Palbociclib: a first-in-class CDK4/CDK6 inhibitor for the treatment of hormone-receptor positive advanced breast cancer". Journal of Hematology & Oncology. 8 (1): 98. doi:10.1186/s13045-015-0194-5. PMC 4534142. PMID 26264704.
  5. ^ Digiulio S (8 October 2015). "FDA's Breakthrough Therapy Designation to Abemaciclib for Breast Cancer". Oncology Times. LWW Journals. Archived from the original on 4 June 2021. Retrieved 30 March 2016.
  6. ^ a b "FDA approves new treatment for certain advanced or metastatic breast cancers" (Press release). Food and Drug Administration. 28 September 2017. Archived from the original on 23 April 2019. Retrieved 29 September 2017.
  7. ^ Drugs.com: Abemaciclib Monograph. Accessed 22 November 2017.
  8. ^ a b c d e f "Highlights of Prescribing Information for Verzenio" (PDF). September 2017. Archived (PDF) from the original on 5 September 2021. Retrieved 22 November 2017.
  9. ^ Goodrich DW, Wang NP, Qian YW, Lee EY, Lee WH (October 1991). "The retinoblastoma gene product regulates progression through the G1 phase of the cell cycle". Cell. 67 (2): 293–302. doi:10.1016/0092-8674(91)90181-w. PMID 1655277. S2CID 12990398.
  10. ^ Hino H, Iriyama N, Kokuba H, et al. (June 2020). "Abemaciclib induces atypical cell death in cancer cells characterized by formation of cytoplasmic vacuoles derived from lysosomes". Cancer Sci. 111 (6): 2132–2145. doi:10.1111/cas.14419. PMC 7293084. PMID 32304130.
  11. ^ "LY2835219 Shows Strong Single-Agent Activity in Preliminary Study in Metastatic Breast Cancer". Archived from the original on 18 September 2015. Retrieved 8 January 2016.
  12. ^ Dickler MN, Tolaney SM, Rugo HS, Cortés J, Diéras V, Patt D, et al. (September 2017). "MONARCH 1, A Phase II Study of Abemaciclib, a CDK4 and CDK6 Inhibitor, as a Single Agent, in Patients with Refractory HR /HER2- Metastatic Breast Cancer". Clinical Cancer Research. 23 (17): 5218–5224. doi:10.1158/1078-0432.CCR-17-0754. PMC 5581697. PMID 28533223.{{cite journal}}: CS1 maint: overridden setting (link)
  13. ^ Sledge GW, Toi M, Neven P, Sohn J, Inoue K, Pivot X, et al. (September 2017). "MONARCH 2: Abemaciclib in Combination With Fulvestrant in Women With HR /HER2- Advanced Breast Cancer Who Had Progressed While Receiving Endocrine Therapy". Journal of Clinical Oncology. 35 (25): 2875–2884. doi:10.1200/JCO.2017.73.7585. PMID 28580882.{{cite journal}}: CS1 maint: overridden setting (link)
  14. ^ Center for Drug Evaluation and Research (9 February 2019). "FDA approves abemaciclib for HR-positive, HER2-negative breast cancer". FDA.
  15. ^ Royce M, Osgood C, Mulkey F, Bloomquist E, Pierce WF, Roy A, et al. (April 2022). "FDA Approval Summary: Abemaciclib With Endocrine Therapy for High-Risk Early Breast Cancer". Journal of Clinical Oncology. 40 (11): 1155–1162. doi:10.1200/JCO.21.02742. PMC 8987222. PMID 35084948.{{cite journal}}: CS1 maint: overridden setting (link)
  16. ^ Center for Drug Evaluation and Research (24 March 2023). "FDA D.I.S.C.O. Burst Edition: FDA approval of Verzenio (abemaciclib) with endocrine therapy for patients with HR-positive, HER2-negative, node-positive, early breast cancer". FDA.
  17. ^ "SARC041: Study of Abemaciclib Versus Placebo in Patients With Advanced Dedifferentiated Liposarcoma". www.clinicaltrials.gov. Retrieved 20 July 2023.
  18. ^ "A Study of Abemaciclib (LY2835219) With Abiraterone in Men With Prostate Cancer That Has Spread to Other Parts of the Body and is Expected to Respond to Hormonal Treatment (Metastatic Hormone-Sensitive Prostate Cancer) (CYCLONE 3)". www.clinicaltrials.gov. Retrieved 20 July 2023.
  19. ^ "Immune Modulation by Abemaciclib in HNSCC. (AIM Trial)". www.clinicaltrials.gov. Retrieved 20 July 2023.
  20. ^ "A Study to Evaluate Abemaciclib in Advanced Biliary Tract Carcinoma". www.clinicaltrials.gov. Retrieved 20 July 2023.
  21. ^ "Abemaciclib (LY2835219) in Patients With Recurrent Primary Brain Tumors". www.clinicaltrials.gov. Retrieved 20 July 2023.
  22. ^ "Abemaciclib in Children With DIPG or Recurrent/Refractory Solid Tumors (AflacST1501)". www.clinicaltrials.gov. Retrieved 20 July 2023.
  23. ^ "Abemaciclib w/Bevacizumab in Recurrent GBM Pts w/Loss of CDKN2A/B or Gain or Amplification of CDK4/6". www.clinicaltrials.gov. Retrieved 20 July 2023.
  24. ^ "Cyclin-Dependent Kinase (CDK)4/6 Inhibitor Abemaciclib for Neurofibromatosis Type I (NF1) Related Atypical Neurofibromas". www.clinicaltrials.gov. Retrieved 20 July 2023.
  25. ^ "Abemaciclib in Patients With HIV-associated and HIV-negative Kaposi Sarcoma". www.clinicaltrials.gov. Retrieved 20 July 2023.
  26. ^ "A Study of Abemaciclib in Combination With Sunitinib in Metastatic Renal Cell Carcinoma". www.clinicaltrials.gov. Retrieved 20 July 2023.
  27. ^ "Study of LY2835219 for Mantle Cell Lymphoma". www.clinicaltrials.gov. Retrieved 20 July 2023.
  28. ^ Frederick MO, Kjell DP (February 2015). "A synthesis of abemaciclib utilizing a Leuckart–Wallach reaction". Tetrahedron Letters. 56 (7): 949–951. doi:10.1016/j.tetlet.2014.12.082.
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