treatment of radioactive iodine-refractory metastatic differentiated thyroid carcinoma
TRANSCRIPT
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Treatment of radioactive iodine-refractory differentiated thyroid
carcinoma
Mauricio Lema Medina MD – Clínica de oncología Astorga, Clínica SOMA, Medellín
ACHO, Bogotá, 29.07.2016
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Page 2
@onconerd
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Mauricio Lema Medina
Conflicts of interest
Consulting and honoraria as a speaker: Pfizer, MSD, Novartis, ROCHE, Aztra-Zeneca, Boehringer-Ingelheim.
Harrisons’s, 19th Ed.
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>5.0cm2.1-5.0cm
Thyroid cancer in the United States
0-1.0cm1.1-2.0cm
Davies, JAMA 2006 295:2164
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Medullary Anaplastic
Papillary Follicular
Differentiated Thyroid Cancer (DTC)
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Thyroid Cancer: Treatment Strategy
• High Risk: (Age >45, male, metastasis, extrathyroidal extension, >4cm)– Total Thyroidectomy– RAI (131I) Ablation– TSH Suppression Therapy with Thyroid
Hormone– Follow Serial Thyroglobulin Levels (Tg)– XRT for recurrent local disease/positive margins– Surveillance: NeckUS, Tg, Neck MRI, Chest CT,
RAI Whole body scan, FDG-PET
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NCCN: Thyroid cancer – Papillary and Follicular
Page 9NCCN, 1.2016
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RAI-Refractory Disease• 25-50% of Metastatic Thyroid Cancers loose ability to
take up Iodine
• This is attributed to down regulation of the Na+/I- Symporter (NIS) and other genes of NaI metabolism
In other words, the cancer cells “forget” how to take up iodine and so
they are immune to the treatment.
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Fig. 1. Survival after the discovery of metastases according to the presence or absence of 131I uptake in the metastases.
Published in: C. Durante; N. et al; The Journal of Clinical Endocrinology & Metabolism 2006, 91, 2892-2899.DOI: 10.1210/jc.2005-2838Copyright © 2006
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Fig. 2. Survival after the discovery of distant metastases according to the age at discovery and to the extent of disease. 131I uptake was not taken into account, but was closely linked to the two other prognostic factors, and was invariably present in young patients with small metastases (group 1) and rarely present in older patients with large metastases (group 2). Group 1, Patients younger than 40 yr of age with metastases that were not visible on radiographs or that were micronodular (<1 cm in diameter). Group 2, Patients older than 40 yr with macronodular lung metastases or multiple bone metastases. Group 3, Patients older than 40 yr with normal x-rays or micronodular metastases and patients younger than 40 yr with macronodular lung metastases.
Published in: C. Durante; et al; The Journal of Clinical Endocrinology & Metabolism 2006, 91, 2892-2899.DOI: 10.1210/jc.2005-2838Copyright © 2006
Less than 40 yo with small
metastases
Older than 40 yo with macronodular lung metastases or bone metastases
RAI-Sensitive
RAI-Refractory
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Fig. 3. Survival after the discovery of distant metastases. Group 1, Patients with 131I uptake who attained negative imaging studies. Group 2, Patients with 131I uptake who did not attain negative imaging studies. Group 3, Patients with no 131I uptake.
Published in: C. Durante; et al; The Journal of Clinical Endocrinology & Metabolism 2006, 91, 2892-2899.DOI: 10.1210/jc.2005-2838Copyright © 2006
Attained negative imaging studies
Did not attain negative imaging studies
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Schlumberger M et al. N Engl J Med 2015;372:621-630.
Iodine-Refractory mDTC: diagnostic criteria
Evidence of radiologic progression within 13 months and at least one of the following criteria:
At least one measurable lesion without iodine uptake on any iodine-131 scan,
At least one measurable lesion that had progressed according to the Response Evaluation Criteria In Solid Tumors [RECIST], version 1.1, criteria within 12 months after iodine-131 therapy despite iodine-131 avidity at the time of treatment,
Or cumulative activity of iodine-131 that was >600 mCi
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RAI-refractory disease• Standard Chemotherapy has minimal efficacy.
1974 Doxorubicin became the only FDA approved drug for the treatment of advanced thyroid cancer.
•No longer used because recent data shows response is 5%
•High toxicity in patient with otherwise good QOL
Cooper DS, et al. Thyroid. 2009;9:1176-214.Hodak SP, Carty SE. Oncology. 2009;23:775-6.
Mehra R, Cohen RB. Hematol Oncol Clin North Am. 2008;22:1279-95,xi.
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Overcoming iodine resistance in DTC
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Selumetinib-Enhanced Radioiodine Uptake in Advanced Thyroid Cancer
RET NTRK1 RAS BRAF
70% of PTC have one of these mutually exclusive mutations
MAP Kinase pathway
DECREASE of theNa-I Symporter
Thyroid biosynthesis genesThyroid peroxidaseHo AL et al. N Engl J Med 2013;368:623-632.
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Selumetinib-Enhanced Radioiodine Uptake in Advanced Thyroid Cancer
Inhibition of BRAF RestoresNa-I Symporter
Ho AL et al. N Engl J Med 2013;368:623-632.
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Selumetinib-Enhanced Radioiodine Uptake in Advanced Thyroid Cancer
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Ho AL et al. N Engl J Med 2013;368:623-632.
Protocol Design and Changes in Iodine Uptake.
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Selumetinib-Enhanced Radioiodine Uptake in Advanced Thyroid Cancer
Ho AL et al. N Engl J Med 2013;368:623-632.
Patients screened 24Patients that could be evaluated 20BRAF mutations 9NRAS mutations 5Increased Iodine-24 uptake 12Increased Iodine-24 uptake enough for RAI therapy 8Increased Iodine-24 uptake in BRAF mutated patients 4/9Increased Ioding-24 uptake in NRAS mutated patients 5/5
Selumetinib produces clinically meaningful increases in iodine uptake and retention in a subgroup of patients with thyroid cancer that is refractory to radioiodine; the effectiveness may be greater in patients with RAS-mutant disease.
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Ho AL et al. N Engl J Med 2013;368:623-632.
Response to Iodine-131 Therapy with Selumetinib Treatment.
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Ho AL et al. N Engl J Med 2013;368:623-632.
Iodine-124 PET-CT Scans Obtained before and after Selumetinib Treatment in Selected Patients with Positive Responses.
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Ho AL et al. N Engl J Med 2013;368:623-632.
Quantification of Iodine-124 PET Uptake in a Lesion in a Patient with an NRAS Mutation Who Later Received Radioiodine.
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Targeted therapy in mDTC
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Thyroid Cancer is associated with aberrant cell signaling
Genetic Alteration PTC FTC BRAF V600E 44% 0% BRAF copy gain 3% 35% RET/PTC (1 and 3) 20% 0% RAS 8-10% 17-45% PI3KCA mutations 3% 6% PI3KCA copy gain 12% 28% PTEN 2% 7% Pax8/PPARγ 0% 35%Total >70% >65%
MA
P K
inas
ePI
3K/A
KT
Nikiforov, Mod Path, 2008, Xing Endocrine Rel Ca(2005), Wang et al, 2007
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Thyroid Cancer is associated with aberrant cell signaling
Genetic Alteration PTC FTC BRAF V600E 44% 0% BRAF copy gain 3% 35% RET/PTC (1 and 3) 20% 0% RAS 8-10% 17-45% PI3KCA mutations 3% 6% PI3KCA copy gain 12% 28% PTEN 2% 7% Pax8/PPARγ 0% 35%Total >70% >65%
MA
P K
inas
ePI
3K/A
KT
Nikiforov, Mod Path, 2008, Xing Endocrine Rel Ca(2005), Wang et al, 2007
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Cell signalling in differentiated thyroid cancer
Graphic adapted fromKeefe SM, et al. Clin Cancer Res. 2010;16:778-83.
RET/PTC
• HIF1a• Inhibition of apoptosis• Migration
EGFR
PI3K
VEGFR-2
Endothelial Cell
• Migration• Angiogenesis
Ras
B-Raf
MEK
ERK
PI3K
AKT
mTOR
S6K
Ras
Raf
MEK
ERK
AKT
mTOR
S6K
Tumor Cell
• Growth• Survival• Proliferation
• Growth• Survival• Proliferation
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Graphic adapted fromKeefe SM, et al. Clin Cancer Res. 2010;16:778-83.
MotesanibSorafenibSunitinibVandetanibXL-184
Axitinib MotesanibSorafenibSunitinibVandetanib
Vandetanib
Sorafenib Sorafenib
Targeting cell signaling in thyroid cancer
RET/PTC
• HIF1a• Inhibition of apoptosis• Migration
EGFR
PI3K
VEGFR-2
Endothelial Cell
• Migration• Angiogenesis
Ras
B-Raf
MEK
ERK
PI3K
AKT
mTOR
S6K
Ras
Raf
MEK
ERK
AKT
mTOR
S6K
Tumor Cell
• Growth• Survival• Proliferation
• Growth• Survival• Proliferation
EverolimusSirolimus
EverolimusSirolimus
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Targets of Kinase InhibitorsCompound Name VEGFR BRAF
PDGFR KIT RET Other
Sorafenib + + + + + FLT-3
Sunitinib + + + FLT-3Axitinib (AG-013736) + + + Motesanib (AMG-706) + + + +Pazopanib(GW786034) + + +
Vandetanib + + EGFRCabozantinib (XL184) + + C-METLenvatinib(E7080) + + + + FGFR
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UPCC 03305: Sorafenib in Advanced Thyroid Cancer February 2006-February 2011
Gupta-Abramson V, et al. J Clin Oncol 2008;26:4714–9
n=55
Eligibility criteria
• Metastatic, iodine refractory thyroid cancer
• Life expectancy >3 months
• Evidence of PD within 6 months of study entry
• ECOG 0–2
• Good organ and bone marrow function
Sorafenib400mg b.i.d.
Primary endpoints• RECIST• PFS• Response rate
b.i.d. = twice daily; RECIST = Response Evaluation Criteria In Solid Tumors; ULN = upper limit of normal
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UPCC 03305: Best Response in 46 Evaluable Patients
PapillaryFollicular/Hürthle CellMedullaryPoorly Differentiated/Anaplastic
302010
0–10–20–30–40–50–60–70–80–90–10 C
hang
e in
sum
of t
arge
t les
ion
by R
ECIS
Tco
mpa
red
to b
asel
ine
(%)
PD SD PR
Best response of advanced thyroid cancer patients to sorafenib
Brose M, et al. J Clin Oncol 2009;27(May 20 Suppl.):301s (Abstract 6002)
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Eligibility criteria• Locally advanced
or metastatic DTC• Progression
within 14 months • RAI refractory • No prior targeted
therapy, chemotherapy or thalidomide
Phase III Study of Sorafenib in Locally Advanced or Metastatic Patients with Radioactive Iodine Refractory Thyroid Cancer (DECISION) trial
• An International, multicentre, randomised, double-blind, phase III study of sorafenib versus placebo in locally advanced/metastatic RAI-refractory DTC
www.clinicaltrials.gov. NCT00984282
Offstudy
Disease progression
Crossover or continue
sorafenib 400mg orally b.i.d.
Ran
dom
isat
ion
(1:1
)(n
=380
)Progression
Sorafenib400mg orally
b.i.d.
Placebo
Investigator’s decisionn=190
n=190
Primary Endpoint:PFS (RECIST)Independent reviewMet primary endpointJanuary 2013
Secondary Endpoints:OS, TTP, RR, DCR, PRO, PKSafetyExploratory Biomarkers
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Brose M, DECISION trial, ASCO, 2013Brose M, DECISION trial, Lancet, 2014
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Brose M, DECISION trial, ASCO, 2013Brose M, DECISION trial, Lancet, 2014
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Brose M, DECISION trial, ASCO, 2013Brose M, DECISION trial, Lancet, 2014
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Brose M, DECISION trial, ASCO, 2013Brose M, DECISION trial, Lancet, 2014
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LENVATINIB
Schlumberger M, et al. NEJM, 2015
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Schlumberger M et al. N Engl J Med 2015;372:621-630.
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Schlumberger M et al. N Engl J Med 2015;372:621-630.
Kaplan–Meier Estimate of Progression-free Survival in the Intention-to-Treat Population.
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Schlumberger M et al. N Engl J Med 2015;372:621-630.
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Schlumberger M et al. N Engl J Med 2015;372:621-630.
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Copyright © 2016 Elsevier Ltd Terms and Conditions
BRAFm - RAI-Refractory PTC 51
No prior multikinase therapy (Cohort 1) 26
Prior multikinase therapy (Cohort 2) 25
Vemurafenib 960 mg PO twice a day
Endpoint: investigator-assessed ORR
Vemurafenib in patients with BRAFV600E-positive metastatic or unresectable papillary thyroid cancer refractory to radioactive iodine: a non-randomised,
multicentre, open-label, phase 2 trial
Brose MS, Lancet Oncol, 2016
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The Lancet Oncology DOI: (10.1016/S1470-2045(16)30166-8) Copyright © 2016 Elsevier Ltd Terms and Conditions
Vemurafenib in patients with BRAFV600E-positive metastatic or unresectable papillary thyroid cancer refractory to radioactive iodine: a non-randomised, multicentre, open-label, phase 2 trial
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The Lancet Oncology DOI: (10.1016/S1470-2045(16)30166-8) Copyright © 2016 Elsevier Ltd Terms and Conditions
No prior multikinase therapy Prior multikinase therapy
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Vemurafenib in patients with BRAFV600E-positive metastatic or unresectable papillary thyroid cancer refractory to radioactive iodine: a non-randomised,
multicentre, open-label, phase 2 trial
Copyright © 2016 Elsevier Ltd Terms and Conditions
BRAFm - RAI-Refractory PTC 51
No prior multikinase therapy (Cohort 1) 25
Prior multikinase therapy (Cohort 2) 26
PR in Cohort 1 10/26
DCR in Cohort 1 9/26
Median DOR Cohort 1 16 months
PR in Cohort 2 6/22
6-mo DCR in Cohort 2 6/22
Median DOR in Cohort 2 27 weeks
“Vemurafenib showed antitumour activity in patients with progressive, BRAFV600E-positive papillary thyroid cancer refractory to radioactive iodine who had never been treated with a multikinase inhibitor. As such, this agent represents a potential new treatment option for these patients”.
Brose MS, Lancet Oncol, 2016
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Progression after TKIs
Page 52
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De Souza JA, ASCO, 2016, Abstract 6013
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Proc ASCO, 2013, Abstract 6024
Overcoming Sorafenib Resistance
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De Souza JA, ASCO, 2016, Abstract 6013
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Ann Wild Gramza, ASCO, 2016
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Graphic adapted fromKeefe SM, et al. Clin Cancer Res. 2010;16:778-83.
MotesanibSorafenibSunitinibVandetanibXL-184
Axitinib MotesanibSorafenibSunitinibVandetanib
Vandetanib
Sorafenib Sorafenib
Targeting cell signaling in thyroid cancer
RET/PTC
• HIF1a• Inhibition of apoptosis• Migration
EGFR
PI3K
VEGFR-2
Endothelial Cell
• Migration• Angiogenesis
Ras
B-Raf
MEK
ERK
PI3K
AKT
mTOR
S6K
Ras
Raf
MEK
ERK
AKT
mTOR
S6K
Tumor Cell
• Growth• Survival• Proliferation
• Growth• Survival• Proliferation
EverolimusSirolimus
EverolimusSirolimus
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UPCC 19309: Everolimus + Sorafenib for DTC patients who progress on Sorafenib alone
n=35
Eligibility criteria
• Metastatic, iodine refractory thyroid cancer
• Life expectancy >3 months
• PD on sorafenib• ECOG 0–2
• Good organ and bone marrow function
Sorafenib + Everolimus
Intra-patientDose escalation
Primary endpoints• RECIST• PFS• Response rate
b.i.d. = twice daily; RECIST = Response Evaluation Criteria In Solid Tumors; ULN = upper limit of normal
22 patients accrued so far
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Min Lim S, Oncotarget, 2016
Somatic mutations that confer exceptional response to everolimus (NGS)
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Min Lim S, Oncotarget, 2016
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Min Lim S, Oncotarget, 2016
Somatic mutations that confer exceptional response to everolimus (NGS)
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NCCN: Thyroid cancer – Papillary and Follicular
Page 62NCCN, 1.2016
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Conclusions
RAI-Refractory mDTC
Sorafenib
Lenvatinib
Selumetinib + RAI in NRAS mutated
Vemurafenib in BRAF mutatedPreferred, unavailable
Not ready for prime-time
Needs more data
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