Difference between revisions of "Melanoma, KIT-mutated"

From HemOnc.org - A Hematology Oncology Wiki
Jump to navigation Jump to search
m (Text replacement - "{| class="wikitable sortable" style="width: 75%; text-align:center;"" to "{| class="wikitable sortable" style="width: 60%; text-align:center;"")
Line 20: Line 20:
 
|}
 
|}
 
===Regimen variant #1, pre-planned escalation {{#subobject:662612|Variant=1}}===
 
===Regimen variant #1, pre-planned escalation {{#subobject:662612|Variant=1}}===
{| class="wikitable sortable" style="width: 75%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
!style="width: 33%"|Study
 
!style="width: 33%"|Study
 
!style="width: 33%"|Years of enrollment
 
!style="width: 33%"|Years of enrollment
Line 45: Line 45:
  
 
===Regimen variant #2 {{#subobject:d1f61b|Variant=1}}===
 
===Regimen variant #2 {{#subobject:d1f61b|Variant=1}}===
{| class="wikitable sortable" style="width: 75%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
!style="width: 33%"|Study
 
!style="width: 33%"|Study
 
!style="width: 33%"|Years of enrollment
 
!style="width: 33%"|Years of enrollment

Revision as of 01:10, 1 July 2021

Section editor
Bethbuchbinder.jpg
Elizabeth Buchbinder, MD
Dana-Farber Cancer Institute
Boston, MA

LinkedIn

Note: these are regimens tested in biomarker-specific populations, please see the main melanoma page for other regimens.

1 regimens on this page
2 variants on this page


Advanced or metastatic disease, TKI-naive

Imatinib monotherapy

back to top

Regimen variant #1, pre-planned escalation

Study Years of enrollment Evidence
Hodi et al. 2013 (BUS255) 2006-2011 Phase II

Biomarker eligibility criteria

  • Gene: KIT
  • Alteration: amplification and mutation
  • Acceptable methods of measurement: PCR or HPLC

Targeted therapy

  • Imatinib (Gleevec) as follows:
    • Starting dose: 400 mg PO once per day
    • Upon progression: 400 mg PO twice per day

Continued indefinitely

Regimen variant #2

Study Years of enrollment Evidence
Carvajal et al. 2011 (MSKCC 07-014) 2007-2010 Phase II

Patients had melanomas arising from mucosal, acral, and chronically sun-damaged skin with KIT mutations or amplifications.

Biomarker eligibility criteria

  • Gene: KIT
  • Alteration: amplification or mutation

Targeted therapy

Continued indefinitely

References

  1. MSKCC 07-014: Carvajal RD, Antonescu CR, Wolchok JD, Chapman PB, Roman RA, Teitcher J, Panageas KS, Busam KJ, Chmielowski B, Lutzky J, Pavlick AC, Fusco A, Cane L, Takebe N, Vemula S, Bouvier N, Bastian BC, Schwartz GK. KIT as a therapeutic target in metastatic melanoma. JAMA. 2011 Jun 8;305(22):2327-34. link to original article contains protocol link to PMC article PubMed NCT00470470
  2. BUS255: Hodi FS, Corless CL, Giobbie-Hurder A, Fletcher JA, Zhu M, Marino-Enriquez A, Friedlander P, Gonzalez R, Weber JS, Gajewski TF, O'Day SJ, Kim KB, Lawrence D, Flaherty KT, Luke JJ, Collichio FA, Ernstoff MS, Heinrich MC, Beadling C, Zukotynski KA, Yap JT, Van den Abbeele AD, Demetri GD, Fisher DE. Imatinib for Melanomas Harboring Mutationally Activated or Amplified KIT Arising on Mucosal, Acral, and Chronically Sun-Damaged Skin. J Clin Oncol. 2013 Sep 10;31(26):3182-90. Epub 2013 Jun 17. link to original article contains verified protocol link to PMC article PubMed NCT00424515