Bone & soft tissue sarcoma Central nervous sytem …...Elderly –poor performance and GBL •5...
Transcript of Bone & soft tissue sarcoma Central nervous sytem …...Elderly –poor performance and GBL •5...
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Bone & soft tissue sarcomaCentral nervous sytem tumors
Dr.Lövey József
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Bone tumors
• Very rare (0,8 / 100 000)
• Etiology– Metaphysis
– Radiation
– Chemicals?
– Rare genetic syndroms
• Histology– 60 different entitites
• Specialized centres
• International collaboration
• Osteogenic tumors– Benign: osteoma, malignant osteosarcoma
• Chondrogenic tumors– Chondroma, chondrosarcoma.
• Giant cell tumor, intermediatemalignancy
• Bone-marrow origin– Ewing-sarcoma
• Angiogenic tumors– haemangioma, haemangioendothelioma,
angiosarcoma
• Other tumors of connective tissue origin– desmoplastic fibroma, fibrosarcoma.
• Other tumors– Chordoma, Schwannoma
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Bone tumors staging
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Bone tumors - treatment• Benign
– Excochleation – spongioplastics
– Radical removal („agressive” benign tumors)
• Low grade malignant
– Radical surgery with good margin
• Osteosarcoma
– Function preservation (70%) (radiation resistant)
• Neoadjuvant chemo-surgery –adjuvant chemotherapy
– Extra-radical surgery (e.g. hemipelvectomy)
– Metastatectomy
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Bone tumors - treatment
• Ewing-sarcoma– Radio and chemotherapy sensitive– Neoadjuvant chemotherapy– Surgery (or radiotherayp if surgery not possible)– Consolidation chemotherapy
• Chordoma, chondorsarcoma– Surgery– Axial (e.g skull base): adjuvant radiotherapy– Radiotherapy alone (proton, heavy ion)
• Pharmaceuticals– MTX, doxorubicin, ciszplain, ifoszfamid– Vincristin, ifosfamid, MESNA, doxorubicin
cyclphosphamid, actinomycin D– ASCT
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Soft tissue sarcomas• Incidence: 2-5/ 100 000 • Mortality: 1-3 / 100 000• Etiology
– Genetic syndroms, radiotherapy, HSV, chemicals
• Heterogeneous: ~ 80 histology entity– fatty– fibroblast/ myofibroblastic– myogen– pericitaer– vascular– nerve sheath– chondro-ossealis differenciation– gastrointestinalis stromal tumor (GIST)– Sarcomas with unclear differenciation– undifferenciated/non classifiable (MFH),
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Soft tissue sarcoma staging
• Imaging
– CT, MR, PET-CT
– 65% extremity and torso
– 15% retroperitoneal
– 10% head and neck
• Staging
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Sof tissue sarcomas - treatment• Exclusively in high-volume centers (survival)
• Histology before treatment
• Complete resection if feasible with good margins
• Neoadjuvant chemo / radiotherapy
• Postoperative high risk (grade, centrality)– adjuvant chemotherapy
• Small margin, R1, R2, G3– Adjuvant radiotherapy
• Irresectable – locally advanced– Chemotherapy + radiotherapy
• Metastatic– chemo or targeted therapy, metastatectomy
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CNS tumors
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• Incidence: 3160 female, 3880 mae
• Mortality: 2765 female, 3340 male
• Etiology
– Inherited (<5%) v Hippel-Lindau, Li-Fraumeni, neurofibromatosis, sclerosis tuberosa
– Radiaton
– Lower in allergic / atopic people
– Mobile phone: not proven
Epidemiology, etiology
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Histology
• NEURO-EPITHELIAL• Glioma:
– Astrocytoma (A1-3)
– Ependymoma (E2-3)
– Oligodendrogliomas(O2-O3)
– Glioblastoma (GBL): GradeIV!!
• Embrional: PNET, Medulloblastoma....
• Pinealoma
• Neuronal orogon– Ganglioglioma
– Neurocytoma
• Periferial nerves– Schwannoma
– Neurofibroma
• NON-NEUROEPITHELIAL• Meningioma
• Choroid plexus
• Germinoma
• Primery CNS lymphoma
• Hyophysis tumors
• Mesenchymal tumours (eg. Sarcomas of the base of the skull)
• others
13
WHO 2016 (Acta neuropathologica. 2016;131:803-820)
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Molecular pathology-Haarlem consensus
• Molecular pathology is obligatory part of diagnostics
• Morphology and molecular pathology should be blended
• „Layers” should be used
• E.g. High-grade glioma (Gr III.) under microscopybut IDH wild type therefore glioblastoma bymolecular fenotype
Louis DN, Brain Pathol. 2014;24(5):429-35.
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Gliomas
• Cell type– Astrocyte
– Oligodendroglia
– Ependymoma
• Grade– I. Pl. pylocytic
– astrocytoma
– II. Diffuse glioma, low-grade glioma
– III. Anapalstic glioma
– IV. Glioblastomamultiforme
• Molecular markers
– IDH 1-2 mutation (prog)
– 1p19q kodel (prog/pred)
– MGMT promoter metilationstatus (pred, prog?)
– ATRX loss (diag/prog)
– H3-K27M mutátion (diag)
– TERT mutation (diag/prog)
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Low-grade glioma
• Slow growth
• Median survival 10-15 years
• Young age population
• Diffuse infiltration
• Complete resection is rare
• Treatment vs. Quality of life
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Low-grade glioma- treatment
• Active surveillance
– But surgery improved a lot
• Maximal safe resection
– Neuronavigation
– Awake surgery
– fMRI
– Diffusion tenzor imaging (DTI)
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20
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Low-grade glioma- adjuvant treatment
• Prognostic factors
– Resection
– Oligodendroglioma vs. astrocytoma szövettan
– Age under/over 40
– KPS under/over 70
– Neurology deficit
– 1p19q kodeletion
– IDH 1, 2 mutation.
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R9802 SCHEMA
Presented By Jan Buckner at 2014 ASCO Annual Meeting
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ASCO 2014: Overall Survival
Presented By Jan Buckner at 2014 ASCO Annual Meeting
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Overall Survival<br />ASCO 2014
Presented By Jan Buckner at 2014 ASCO Annual Meeting
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• 45-54 Gy / 1,8-2 Gy fractions
• Always based on image fusion
• FLAIR, T2, ususall non contrast enhancement
• 3D conformal / IMRT, /hyppocampus sparing
• GTV-CTV extension 1-1,5 cm
Grade II. radiotherapy
Fused MR image Treatment planning CT
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Anaplastic (Gr III.) gliomas
Grade III.
glioma
IDH wt
(GBL like)
1p19q non
kodel
MGMT
methylated
RT or
TMZ/PCV
MGMT non
methylated
RT + TMZ?
1p19q kodel
RT +6x PCV
(TMZ)
TMZ / PCV
IDH mutant
ATRX loss (astrocytoma)
RT
TMZ
1p19q kodel
(oligodenroglioma)
RT +6x PCV
(TMZ)
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EORTC 26951
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RTOG9402
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Anaplastic (Gr III.) gliomas
Grade III.
glioma
IDH wt
(GBL like)
1p19q non
kodel
MGMT
metilált
RT vagy
TMZ/PCV
MGMT nem
metilált
RT + TMZ?
1p19q kodel
RT +6x PCV
(TMZ)
TMZ / PCV
IDH mutant
ATRX vesztés (astrocytoma)
RT
TMZ
1p19q kodel
(oligodenroglioma)
RT +6x PCV
(TMZ)
CATNON
CATNON
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CATNON
OS PFS
Adjuvant TMZ median 5 -year (%) median
No (372) 41,1 month 44,1% 19 month
Yes (373) NR 55,9% 42,8 month
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Grade III. radiotherapy• 60 Gy (50-54 Gy to low grade part)
• Conformal, MR / PET-CT fusion
• GTV-CTV : 1,5- 2 cm
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Glioblastoma
• Most ferquent glioma
• Primary / secondary
• Very bad prognosis
• Surgery / biopsy only alone– Survival 4-7 months
• Adjuvant radiotherapy (from the 70s)– 8-10 months
• Adjuvant chemoradiation + maintenancechemotherapy (60 Gy + 75mg/m2 temozolomide+ 6x temozolomide (since 2005)– 14,6 months
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TMZ and RT in Newly Diagnosed GBM Overall Survival
(months)
0 6 12 18 24 30 36 420
10
20
30
40
50
60
70
80
90
100
O N Number of patients at risk :
261 286 240 144 59 23 2 0219 287 246 174 109 57 27 4
RT TMZ/RT
Median OS, mo: 12.1 14.6
2-yr survival: 10% 26%
HR [95% C.I.]: 0.63 [0.52-0.75]
p <0.0001
TMZ/RT
RTTMZ/RT
%
RT
R Stupp, et al. Proc ASCO 2004; abs #2.
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RPA (recursive partition analyzis)• RPA III: < 50 y, PS 0, MMSE >27, complete resection
• RPA IV: <50 év, PS 1-2, / > 50 y, MMSE >27, complete / partial resection
• RPA V: >50, MMSE <27, csak biopisza
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Further options is GBL
• Adding bevacizumab to standard treatment
– RTOG 08-25, AVAglio
• PFS and QoL better, OS same
– Other targeted therapy
• No benefit
• Immunotherapy
– Many type of immunotherapy – no results yet
• EF-14 trial : alternating electromagnetic fields
– 16,6 – 19,6 hónap
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EF-14: Stupp + TTF (JAMA 2015)
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Elderly – poor performance and GBL
• 5 randomized trial
– BSC worse than active treatment
– High- dose chemoradiation rarely useful
– 60 Gy / 2 Gy worse than accelerated RT (13x3)
– Accelerated RT + TMZ better than RT alone
– MGMT promoter methylated: temozolomide as goodas radiotherapy (NOA-08)
Malmström et al Lancet Oncol 2012, Wick W et al Lancet Oncol 2012, Roa W et al JCO 2015, Guedes de Castro et al IJROBP 20125, Perry JR et al NEJM 2017
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Recurrent GBL
• Reoperation
• Reirradiation
– After 2 years
• Bevacizumab (Avastin)
– Off label, median survival ~ 9 months
• Lomustin /CCNU
– median survival ~9 months
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Survival
Glioma type Treatment Median
survival
Grade II glioma good prognosis obszervation / RT/
TMZ
>15 y
Grade II. glioma poor prognosis RT 7,8 y
RT + PCV 13,3 y
Grade III. oligo 1p19q kodel RT 7-8 y
RT + PCV 14,7y
Grade III. glioma non 1p19q
kodel
RT / TMZ 2-3 y
RT + PCV/TMZ 2-3 y
Grade IV. glioblastoma RT-TMZ + TMZ 14-16
month
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Ependymoma• Rare tumor
• Surgery first
• Molecular pathology (RELA fusion gene)
• Low risk (Grade II, complete resection)– Observation
• Medium risk (grade III., one focus, resected)– Local radiotherapy
• High risk (multifocal disease, tumor in liquor)– CNS axis irradiation + boost to primary site(s)
• Recurrence: platinum based chemo, temozolomide
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Tomura et al. AJNR 2013
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Craniospinal irradiation
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Medulloblastoma / PNET
• Rare in adults, typically in posterior fossa
• Resection
• High risk (>1,5ccm residual tumor, anaplastic / largecell, supratentorial primary, tumor in liquor)– CNS axis irradiation + boost + chemotherapy (36 + 24)
– Chemo based on pediatric trials (VCR)
• Low risk– CNS axis irrad + boost +- chemotherapy
• Molecular subtyping already established in children– WNT-activated, SHH-activated, non-WNT/SHH-activated
groups: types 3 and 4
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Meningioma
• Treated by size and symptoms
• Small tumor without symptoms– Observation
– If grows: surgery +- RT (grade III, incomplete resectiongrade II)
– RT, if surgery is not feasible
• Large tumor no symptoms– Surgery +- RT (grade III, incomplete resection grade II)
– RT, if surgery is not feasible
– Observation
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Meningioma
• Small tumor with symptoms
–Surgery +- RT (grade III)
–RT, if surgery is not feasible
• Large tumor with symptoms
–Surgery +- RT (grade III, incompleteresection grade I-II)
–RT, if surgery is not feasible
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Meningioma
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Meningioma radiotherapy
• Grade I– 45-54 Gy fractionated
• Grade II– 54-60 Gy fractionated
• Grade III– 60 Gy frakcionated
• Grade I– Streotactic radiosurgery 1x12-16 Gy
• All grade– Fractionated stereotactic radiotherapy (e.g. 6x6 Gy)
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Recurrent meningioma
• Re-resection
• Reirradiation (stereotactic)
• Pharmaceutical therapy
– IF-alfa
– Somatostatin analogue / isotope therapy
– Sunitinib
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