
NEW YORK (Reuters Health), Aug 2 - Patients with rare but aggressive anaplastic thyroid carcinomas responded extremely well to radiation and concomitant docetaxel in a small case series from Austria.
Four of the six patients had complete remissions, and the other two had partial responses. At a median follow-up of 21.5 months, only one patient has died, according to senior author Dr. Markus Raderer of the Medical University of Vienna and colleagues.
Median survival with these tumors is usually in the range of three months, the authors say.
In a June 30 online article in the Journal of Clinical Endocrinology & Metabolism, the research team reports that all six received standard external-beam radiation along with docetaxel at a flat dose of 100 mg every three weeks. A complete course of treatment consisted of six cycles, or 60 Gy, but three patients stopped at 40, 44, and 50 Gy because of side effects.
Three patients had tumor debulking surgery before treatment began, but none had complete resections. Two patients had lung metastases.
All patients had severe side effects from therapy, nearly always as a result of the radiation. All had to be hospitalized for parenteral nutrition and fluid replacement.
So far, individual survival durations from the start of therapy are 3.5, 12, 18, 21, 32, and 40 months. Only one patient -- the one who survived 40 months -- has died. This patient relapsed with lung metastases.
Thus, despite the severe toxicities, the researchers conclude that the approach is effective and "larger trials are warranted."
Source: http://link.reuters.com/kev52n
J Clin Endocrinol Metab 2010.
Last Updated: 2010-07-30 13:56:24 -0400 (Reuters Health)
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![Examples of ultrasound findings and techniques. (A) Images in a 39-year-old male patient with a mass in the left thigh. The mass is heterogeneous on the B-mode US image (compared with the patient in D) and showed increased microvascularity (superb microvascular imaging [SMI]) and shear-wave elastography (SWE) values. Undifferentiated pleomorphic sarcoma was diagnosed at biopsy (with pleomorphic rhabdomyosarcoma in surgical specimen). (B) Images in an 18-year-old male patient with a mass in the left leg. The mass is hypoechoic on the B-mode image, with no other findings suggestive of malignancy. The lesion is in contact with the cortex of the tibia, which is slightly irregular. CT revealed a doubtful anteromedial tibial erosion. The microvascular study demonstrated high vascularization, suggestive of malignancy. Periosteal Ewing sarcoma was diagnosed with both histologic and immunohistochemical confirmation. (C) Images in a 69-year-old female patient with a lump growing on the outside of the left leg. Multiple SWE examinations were performed (please note the high values obtained in the measurements, whereas the color map highlights the stiffness relative to adjacent tissues). SMI showed areas of increased vascularization to target for sampling. Undifferentiated spindle cell sarcoma was diagnosed at biopsy, with residual leiomyosarcoma in the surgical specimen after neoadjuvant therapy. (D) Images in a 56-year-old female patient with a mass in the right thigh. The mass is heterogeneous at both B-mode ultrasound (similar to patient A) and MRI (coronal T2-weighted spectral attenuated inversion recovery [SPAIR]; T1-weighted pre-contrast and postcontrast imaging), which even shows uptake after the administration of paramagnetic contrast material, which is traditionally suggestive of malignancy. Low values at SMI and elastography are suggestive of benignity. Spindle cell lipoma was diagnosed at biopsy, with atypical spindle cell lipomatous tumor in the surgical specimen.](https://img.auntminnieeurope.com/mindful/smg/workspaces/default/uploads/2026/08/images-radiol250278fig2.APCFLSvX6p.jpg?auto=format%2Ccompress&fit=crop&h=112&q=70&w=112)









