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Prostatic adenocarcinoma
Post-Traumatic C7 Asia B Tetraplegia Malignant Fibrous Histiocytoma Melanoma with Metastases Right Post-Traumatic Gonalgia Atrial Fibrillation Spinal Stenosis Alzheimer Disease Acute myocardial infarction Dental Case Multinodular goiter Melanoma with metastases Ovarian cancer with metastases Fistulized pilonidal cyst Cancer of Bladder Eye problem in an infant Maculopathy Peyronies disease Neuroendocrine Neoplasia Pancytopenia of uncertain pathogenesis - 2 Pancytopenia of uncertain pathogenesis Neuroroendocrine neoplasia Medulloblastoma Infiltrating basocellular carcinoma Herniated Disc of the Lumbosacral Rachis Elevation of Ca 19-9 Bronchiolitis Obliterans Organizing Pneumonia Prostate Cancer and Parkinson disease Retinitis pigmentosa Bilateral catarrhal tubotympanitis and bilateral chronic otomastoiditis Basocellular carcinoma Chronic pain of undetermined origin Malignant Tumor Complex Elbow Fracture Treating hemorrhoids - how to choose the least painful and most suitable option Obese patient with cirrhosis of the liver receives medical advice Angiosarcoma Sarcoma - a Rare Tumour of the Heart Which Treatment is Right for Your Persistant Recurrent Atrial Fibrillation? Lymph node metastases of right groin Hyper sensibility of the glans penis Autoimmune Thyroiditis and Pregnancy ALS Motor Neuron Disease Cancer of Colon Nephroblastoma Renal Cell Carcinoma Thyroid Complex Orthodontic Case Lung cancer patient seeks online medical advice when cancer reappears and spreads following surgery Online medical opinion helps confused sufferer of prostate problems Benign Prostatic Hypertrophy Bilateral Colloid Degeneration Right Microtia Carcinoma of the prostate Chromosome 22 micro-deletion syndrome Relapse of Chondrosarcoma of Cervical Spine Malignant Neoplasia of left forearm Cricotracheal resection (CTR) Spinal Disc Hernia Recurrent Abortions Endocrine Carcinoma Diabetes Retinopathy Paroxysmal Atrial Fibrillation Multiple Endocrine Neoplasia |
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| GB: 7.88 | Plts: 264 | Glu: 90 | K+: 4 | AST: 24 |
| GR: 3.85 | INR: 1.07 | Urea: 24 | Amil.: 3 | ALT: 50 |
| Hb: 11.5 | PTT: 34.5 | Creat: 0.6 | Tot. prot.: 6.9 | Tot. bili.: 0.6 |
| Hct: 34.9 | Fibr: 738 | Na+: 137 |
The expert´s opinion
Thank you for the referral and the copy of the medical records for this patient.
To summarize, the patient is a 70 year old gentleman diagnosed with colon cancer in February 2004. After undergoing a right hemicolectomy, a PET scan and CT scan revealed two hepatic lesions. He was treated with 6 cycles of FOLFOX from ____ to ____ and had a complete response. Three months later a CT of the abdomen revealed recurrent hepatic disease and celiac lymphadenopathy. He underwent directed therapy with radiofrequency ablation of the liver lesion and stereotactic radiation to the celiac lymph nodes. He then received 16 cycles of FOLFIRI from to ____ and a CT scan in _____ showed stable disease. He then received FOLFIRI + Cetuximab for 1 month and a repeat CT again showed stable disease. He then received Cetuximab alone for 1 month and a repeat CT of scan showed progressive disease in the liver and new pulmonary disease. He then received 4 cycles of FOLFOX from ____ to ____. Unfortunately a CT scan in ____ showed progression of the pulmonary disease and minimal resolution of the hepatic lesions. A PET scan on _____ revealed multiple areas of uptake in the liver and both lungs.
To summarize, the patient is a 70 year old gentleman diagnosed with colon cancer in February 2004. After undergoing a right hemicolectomy, a PET scan and CT scan revealed two hepatic lesions. He was treated with 6 cycles of FOLFOX from ____ to ____ and had a complete response. Three months later a CT of the abdomen revealed recurrent hepatic disease and celiac lymphadenopathy. He underwent directed therapy with radiofrequency ablation of the liver lesion and stereotactic radiation to the celiac lymph nodes. He then received 16 cycles of FOLFIRI from to ____ and a CT scan in _____ showed stable disease. He then received FOLFIRI + Cetuximab for 1 month and a repeat CT again showed stable disease. He then received Cetuximab alone for 1 month and a repeat CT of scan showed progressive disease in the liver and new pulmonary disease. He then received 4 cycles of FOLFOX from ____ to ____. Unfortunately a CT scan in ____ showed progression of the pulmonary disease and minimal resolution of the hepatic lesions. A PET scan on _____ revealed multiple areas of uptake in the liver and both lungs.
The patient was then seen by a surgeon for consideration of a left hepatectomy. Upon surgical exploration, his liver disease was deemed too extensive for surgical resection.
The patient is inquiring about laser resection of his metastatic lung lesions in conjunction with selective internal radiation therapy for his liver lesions. The patient should be aware that neither technique has been shown to provide “curative” treatment, and it is clear from his recent hospitalization that his liver disease is too extensive for surgical resection, the only known method of providing long-term cure. My main concern is that pursing directed treatment to either the lungs or liver or both will delay the ability to treat with systemic chemotherapy. While the patient has been heavily pretreated with chemotherapy in the past, he has not yet received Avastin (bevacizumab), one of the 5 active drugs for metastatic colon cancer, the others being 5-fluorouracil, oxaliplatin, irinotecan and cetuximab. While bevacizumab is not active as a single agent, it is active with chemotherapy. I agree with Dr.____ that the patient’s best option at the present would be to pursue additional chemotherapy with bevacizumab.
I have reviewed the manuscript by Drs._____ and ______concerning laser resection of metastatic lung lesions. While this approach looks interesting, prior patients receiving this treatment had metastatic disease to the lungs alone. I am not aware of any patients with widely metastatic disease that have been treated with this technique. As a result, I do not think it is in his best interest to pursue treatment for his pulmonary disease alone as this will likely delay further systemic treatment.
The patient was also inquiring about SIRTeX yttrium-90 microspheres. Again, this is an interesting technique however the patient must know that such therapy will only potentially treat the liver disease and will have no effect on his pulmonary disease. I have reviewed the SIRTeX web site which clearly states that capecitabine is contraindicated 2 weeks before and after SIRTeX treatment. I also reviewed the medical literature regarding SIRTeX microspheres and do not see information regarding interactions with capecitabine. It is not clear if the recommendation was made based on pre-clinical studies or simply because there are no studies using capecitabine with SIRTeX and therefore there is no toxicity related information.
Summary
With respect to clinical trials, I would recommend, prior to enrolling in any phase of clinical trial, treatment with bevacizumab plus chemotherapy. Thank you for allowing me to participate in the care of this very interesting patient. I appreciate the aggressiveness with which you and he are pursuing his care.
Sincerely,
Prof. -----















