Throid carcinoma 231
47. Thyroid Carcinoma
47.1 General considerations
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Stage grouping (AJCC/ UICC) |
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Papillary or follicular carcinomas |
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Stage age < 45 years age > 45 years |
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I any T any N M0 T1 N0 M0 |
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II any T any N M1 T2,3 N0 M0 |
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III T4 N0 M0 anyT N1 M0 |
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IV anyT anyN M1 |
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Undifferentiated carcinoma |
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IV anyT any N any M (all cases are stage IV) |
Well – differentiated (papillary and follicular) thyroid carcinoma is well treatable with a good prognosis, Current therapeutic protocots include surgery (predominantly total thyroidectomy), followed, if necessary by complementary radioiodine (131 I) and/ or external beam radiation. The administration of thyroxin is another measure to reduce the proliferation of residual thyroid tissue or metastases and additionally it is given for hormonal substitution. For patients not or no longer treatable by surgery or radiotherapy palliative chemotherapy is indicated .
About 30 % of the tumors dedifferentiate and may finally develop into highly malignant anaplastic thyroid carcinoma. These are inaccessible to conventional therapy, but aggressive multimodality treatment regimens which combine surgery, chemotherapy and radiotherapy have shown some promise in disase control.
Medullary thyroid carcinomas (see Neuro-endocrine Malignancies) are also highly aggressive tumors. Multimodality treatment with surgery and/or external beam radiotherapy and chemotherapy can result in local control of disease and enhanced survival.
Literature: for review e.g.
AIN. Baillieres Best Pract. Res. Clin. Endocrinol. Metab. 14 (2000): 615 –
629 (management of undifferentiated thyroid cancer)
GIMM, Cancer Lett. 26 (2001): 143-156
GIUFFRIDA and GHARIB, Ann. Ocnol. 11(2000): 1083-1089 (diagnosis and treatment of anaplastic thyroid carcinoma)
HAUGEN, Rev. Endocr. Metab. Disord. 1 (2000): 147 – 154 (initial treatment of differentiated thyroid carcinoma)
HURLEY, Endocr. Pract. 6(2000): 401- 406
ORLANDI et al, Endocr. Relat. Cancer 8 (2001) : 135 – 147 (medullary
thyroid carcinoma)
SCHLUMBERGER and TORLANTANO, Baillieres Best Pract. Res.
Clin.
Endocrinol. Metab. 14 (2000): 601 – 613 (papillary and follicular thyroid
carcinoma)
SCHMUTZLER and KOEHRLE, Eur. J. Endocrinol. 143 (2000): 15 – 24
(innovative treatment strategies)
SHERMAN, Rev. Endocr. Metab Disord. 1 (2000): 165-171 (management of metastatic differentiated thyroid carcinoma)
Van TOL et al, Crit. Rev. Oncol. Hematol. 38 (2001): 79 – 91 (differentiated thyroid carcinoma in the elderly )
232 Thyroid Carcinoma
47.2 Radioiodine
Literature: e.g.
De KEIZER et al, Eur. J. Nucl. Med. 28 (2001): 198 – 202
MAXON, Q. J. Nucl. Med. 43 (1999): 313- 323
PETRICH et al, Eur. J. Nucl. Med. 28 (2001): 203-208
REINERS and FARAHATI, Q. J. Nucl. Med. 43 (1999): 324-335
ROOS and SMITH, Int. J. Radiat. Oncol. Biol. Phys. 44(1999):493-495
47.3 Single agent chemotherapy
Treatment may be attempted with doxorubicin or cisplatin. paclitaxel appears to have some activity against anaplastic thyroid carcinoma.
47.3.1 Doxorubicin
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Coxorubicin 75 mg/m2 i.v. (bolus) d 1 |
To be repeted every 3 weeks
Literature:
GOTTLIEB and STRATTON HILL, Cancer Chemother. Rep. 6 ( 1975):
283- 296
47.3.2. Paclitaxel
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Paclitaxel 140 mg/m2 i.v. (96 h inf) d 1-4* or 225 mg/m2 i.v. ( 1 h inf) weekly |
*To be repeted every 3 weeks
Literature:
AIN. et , al , Thyroid 10 (2000): 587-594
47.4 Combination chemotherapy
Coxorubicin + cisplatin
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Coxorubicin 60 mg/m2 i.v. (bolus) d 1 |
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Cisplatin 40 mg/m2 i.v. (30 min inf) d 1 |
To be repeted every 3(-4) weeks
Literature:
SHIMAOKA et al, Cancer 56 (1985): 2155-2160