Title: CA Cancer J Clin 200454:94109
1- CA Cancer J Clin 20045494109
2STS Sites
- Extremity (59),
- Trunk (19),
- Retroperitoneum (15),
- Head and neck (9)
3(No Transcript)
4STS - Histologies
- Malignant fibrous histiocytoma (28)
- Leiomyosarcoma (12)
- Liposarcoma (15)
- Synovial sarcoma (10)
- Malignant peripheral nerve sheath tumors (6)
- Rhabdomyosarcoma (childhood)
5STS Risk Factors
- Radiation Therapy
- Herbicides
- Phenoxyacetic acid
- Wood preservatives
- Chlorophenols
- Chronic lymphedema
- Lymphangiosarcoma
- Stewart-Treves syndrome
6STS Work-up
- Chest X Rays
- All patients
- CT of the Chest (contrast enhanced)
- If primary tumor size gt 5 cm
- CT of the Abdomen / Pelvis
- If liposarcoma of the extremity
- MRI (contrast enhanced)
- Sarcomas of the extremity
- Differentiation between malignancy a benign
- T1 weighted contrast MRI can assess intratumoral
necrosis
7Biopsy techniques
- FNA aspiration
- Acceptable if experienced cytopathologist
available - Limited information about tumor grade
- Method of choice for recurrences
- Accuracy ranges from 60-96
8Biopsy techniques
- Core needle biopsy
- Safe, accurate and economical
- More tissue
- Cytogenetics
- Electron microscopy
- Flow cytometry
- Accuracy93
9Biopsy techniques
- Incisional biopsy
- If FNA or Core biopsies are non diagnostic
- Incision wound in longitudinal access
- Performed by the same surgeon that is going to
treat de patient - Excisional biopsy
- For small (lt 3 cm), superficial tumors
- No advantage over other biopsy techniques
10Grade
- Metastatic potential by grade
- Low-Grade 5-10
- Intermediate-Grade 25-30
- High-Grade 50-60
11Size
- T1 - lt 5 cm (5-survival 84)
- T2 - gt 5 cm
- 5-10 cm (5-year survival 70)
- 10-15 cm (5-year survival 50)
- gt 15 cm (5-year survival 33)
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13Treatment for T lt 5 cm
- Wide surgical resection
- 2 cm margin (free-of-disease)
- Include the biopsy site in the en-bloc resection
- Limb-sparing procedures if possible
14Radiation therapy
- Following limb-sparing procedures
- Local control 78-91
- High-Grade tumors
- Local control 70 (no RT) and 98 (RT)
- Local control 66 (no BT) and 89 (BT)
- No difference with RT in Low-Grade tumors
- No benefit of RT in High-Grade tumors lt5 cm
15Radiation therapy
- Margins
- 5-7 cm
- Dose
- Preoperative 5000 cGy en 25 fractions
- Wound complications 35
- Postoperative 6000-7000 cGy
- Wound complications 17
16Brachytherapy
- Advantages
- 5-6 days of therapy instead of weeks
- Less radiation scatter in critical anatomic sites
- Less expensive (in the US)
- Can be used in recurrences
- Disadvantages
- Hospitalization and bed rest
17Prognostic factors for poor long-term functional
outcome after radiation therapy
- Large tumors
- Large doses of RT (gt 63 Gy)
- Long radiation fields (gt 35 cm)
- Poor radiation technique
- Neural sacrifice
- Postoperative fractures
- Wound complications
18Systemic Therapy
- Response rate gt 20
- Doxorubicin
- Dacarbazine
- Ifosfamide
19Postoperative chemotherapy
- Doxorubicin-based adjuvant chemotherapy
- 1568 patients (14 trials)
- 4 increase in OS (p0.12)
- 7 increase in OS in extremity sarcomas (p0.029)
- Tierney JF. Adjuvant chemotherapy for localised
resectable soft-tissue sarcoma of adults
meta-analysis of individual data. Sarcoma
Metaanalysis Collaboration. Lancet
199735016471654.
20Preoperative chemotherapy
- Induction chemotherapy yields complete response
in 6-9 of patients - Patients with gt 95 tumor necrosis have 11
10-year OS vs 23 - Patients with CR have 71 10-year survival rate
vs 55 with no CR - Chemotherapy does not appear to increase the rate
of limb-sparing procedures
21Surveillance strategies
- First 2 years
- HP q3months
- CXR q6months
- Imaging of tumor site q6months
- 2-5 years
- HP q6months
- CXR q12months
- Imaging of tumor site q12months
- gt 5 years
- HP and CXR q12months
22Surveillance of Abdominal Sarcomas
- First 2 years
- HP q3months
- CXR q6months
- CT of abdomen / pelvis q3months
- 2-5 years
- HP q6months
- CT of abdomen / pelvis q6months
- CXR q12months
- gt 5 years
- HP and CXR q12months
23Retroperitoneal sarcomas
- 15 of STS
- Tend to recurr locally
- Worse prognosis
- 5-year survival 40-50
- Prognostic factors
- Margin positive resection
- Large tumor at presentation
- Unresectability
- High-grade
24GIST
- Require 2-4 cm margin
- C-Kit positive (CD 117) are candidates for
Imatinib with 54 response rate in the metastatic
setting
25Recurrent sarcomas
- Local recurrence
- Aggressive resection
- Pulmonary metastasis resection
- 15-40 LT survival in completely resected tumors
- Palliative Chemotherapy
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27Puntos 0 10 20 30
40 50 60 70 80 90
100
lt 5 cm 5-10 cm
gt 10 cm
Superficial Profundo
Sup Inf Tórax Abdomen
Extremidades Tronco
Cabeza y cuello
MFH Leio Sinovio
Fibro Lipo
Otro MPNT
Edad 15 20 30 40 50
60 70 80 90
Total Puntos 0 20 40 60 80 100 120
140 160 180 200 220 240 260 280 300 320
Bajo Grado 0.04 0.06
0.1 0.15 0.2 0.3 0.4 0.5 0.6 0.7
0.8 0.88
Alto grado 0.04 0.06 .1 .15 .2
.3 .4 .5 .6 .7 .8 .88 .9
.95
Probabilidad de muerte por sarcoma a 12 años
Kattan MW, Leung DH, Brennan MF, Postoperative
nomogram for 12-year sarcoma-specific death. J
Clin Oncol. 2002 Feb 120(3)791-6
28Puntos 0 10 20 30
40 50 60 70 80 90
100
lt 5 cm 5-10 cm
gt 10 cm
Superficial Profundo
Sup Inf Tórax Abdomen
Extremidades Tronco
Cabeza y cuello
MFH Leio Sinovio
Fibro Lipo
Otro MPNT
Edad 15 20 30 40 50
60 70 80 90
Total Puntos 0 20 40 60 80 100 120
140 160 180 200 220 240 260 280 300 320
Bajo Grado 0.04 0.06
0.1 0.15 0.2 0.3 0.4 0.5 0.6 0.7
0.8 0.88
Alto grado 0.04 0.06 .1 .15 .2
.3 .4 .5 .6 .7 .8 .88 .9
.95
Probabilidad de muerte por sarcoma a 12 años
Kattan MW, Leung DH, Brennan MF, Postoperative
nomogram for 12-year sarcoma-specific death. J
Clin Oncol. 2002 Feb 120(3)791-6
29Ejemplo
- 56 años,
- Liposarcoma de extremidades inferiores,
- 6 cm, superficial,
- grado alto
30Puntos 0 10 20 30
40 50 60 70 80 90
100
lt 5 cm 5-10 cm
gt 10 cm
Superficial Profundo
Sup Inf Tórax Abdomen
Extremidades Tronco
Cabeza y cuello
MFH Leio Sinovio
Fibro Lipo
Otro MPNT
Edad 15 20 30 40 50
60 70 80 90
Total Puntos 0 20 40 60 80 100 120
140 160 180 200 220 240 260 280 300 320
Bajo Grado 12 años 0.04 0.06
0.1 0.15 0.2 0.3 0.4 0.5 0.6 0.7 0.8
0.88
Alto grado 0.04 0.06 .1 .15 .2
.3 .4 .5 .6 .7 .8 .88 .9
.95
Kattan MW, Leung DH, Brennan MF, Postoperative
nomogram for 12-year sarcoma-specific death. J
Clin Oncol. 2002 Feb 120(3)791-6
31Suma 0 7 30 3942
118
Puntos 0 10 20 30
40 50 60 70 80 90
100
lt 5 cm 5-10 cm
gt 10 cm
Superficial Profundo
Sup Inf Tórax Abdomen
Extremidades Tronco
Cabeza y cuello
MFH Leio Sinovio
Fibro Lipo
Otro MPNT
Edad 15 20 30 40 50
60 70 80 90
118
Total Puntos 0 20 40 60 80 100 120
140 160 180 200 220 240 260 280 300 320
Bajo Grado 12 años 0.04 0.06
0.1 0.15 0.2 0.3 0.4 0.5 0.6 0.7 0.8
0.88
Probabilidad de fallecer por sarcoma 23
Alto grado 0.04 0.06 .1 .15 .2
.3 .4 .5 .6 .7 .8 .88 .9
.95
Kattan MW, Leung DH, Brennan MF, Postoperative
nomogram for 12-year sarcoma-specific death. J
Clin Oncol. 2002 Feb 120(3)791-6
32- Cormier JN, Pollock RE. Soft Tissue Sarcomas. CA
Cancer J Clin 20045494109
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34- Postoperative nomogram for 12-year
sarcoma-specific death based on 2,163 patients
treated at Memorial Sloan-Kettering Cancer
Center. Abbreviations Fibro indicates
fibrosarcoma Lipo, liposarcoma
Leiomyo,leiomyosarcoma MFH, malignant fibrous
histiocytoma MPNT, malignantperipheral-nerve
tumor GR, grade SSD, sarcoma-specific death.