Survey
* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project
Radionuclide methods in oncology Materials for medical students Otto Lang, MD, PhD Otakar Bělohlávek, MD, CSc Dept Nucl Med Charles Univ, 3rd Med Fac Role for Nuclear Medicine Diagnosis Staging Important for proper therapy Follow-up Specific or non-specific Early detection of recurrens Treatment Specific or non-specific Tumors Metabolically active tissues – many similar properties as inflammation Increased vascularization Increased capillary permeability Newly proliferated capillaries Increased blood flow Metabolically active cells Increased energy demand Tumor cells High density of some common receptors Expression of several specific receptors Expression of some specific tumor antigenes All these properties could be used for imaging and therapy Diagnostic radiopharmaceuticals Non-specific - demonstrate tumor sites but are not specific for malignancy PET or PET-CT F-18 FDG – anaerobic metabolism Planar, SPECT or SPECT-CT Diphosphonates – bone scan Ga-67 citrate – similar to FDG – localising agent Colloids – liver-spleen scan Leukocytes – bone marrow scan MIBI – several tumors Diagnostic radiopharmaceuticals Specific – binds directly to special tumor antigens or receptors or are accumulated by special metabolic pathway PET or PET/CT - no commercially available Planar, SPECT or SPECT/CT I-123/131 MIBG for neuroendocrine tumours I-131 for differentiated thyroid carcinomas In-111 octreotide for tumours expressing somatostatin receptors. monoclonal antibodies labelled with In-111, I-123/131 or Tc-99m Therapeutic radiopharmaceuticals Non-specific Sr-89, Sm-153, Re-189 Bone pain palliation Specific I-131 Thyroid cancer, as specific diagnostic if tumor significantly accumulates Y-90 Zevalin – monoclonal antibody for B-cell lymphomas Ga-67 scan Introduced in seventies of 20th century for lymphomas (prof. Dienstbier) Mechanisms of accumulation tumour viability blood flow capillary permeability lymphatic drainage transferrin receptors on the tumour cells Ga-67 scan Procedure Patient preparation Laxatives for bowel preparation post injection, nothing else Several weeks post tumor therapy (FN) radiation therapy and chemotherapy can alter the normal pattern of gallium distribution 180 MBq is usually administered imaging follows after 48 – 72 hours WB + SPECT, middle-energy collimator Ga-67 scan Normal scan Accumulates in bone marrow and liver. Splenic uptake is variable. The kidneys are usually visualized and also lacrimal, salivary, nasopharyngeal and genital activity is often present. Female breasts can be visualized, but accumulation is physiologically symmetrical. Radioactivity is commonly seen in the colon Ga-67 scan Clinical indications lymphoma staging and monitoring effect of therapy melanoma lung cancer hepatoma Combination with other imaging modalities is necessary (SPECT/CT) Bone scan Radiopharmaceuticals Tc-99m MDP, HDP Tissue accumulation depends on blood flow capillary permeability metabolic activity of osteoblasts and osteoclasts mineral turnover 500 to 800 MBq, imaging 2 to 3 hours later – WB + SPECT Bone scan Clinical indications: Diagnosis of metastases of different tumors – staging and follow-up Positivity many months before an abnormality can be detected on X ray - method of choice to seek for bone metastases Mainly Bronchogenous carcinoma, prostate, breast, thyroid, and renal tumours Bone scan Scan pattern increased accumulation in the surrounding bone - hot lesion defect - cold lesion (some metastases –breast) - rare (very fast grow – no bone reaction) flare phenomenon – increased number of lesions in the case of effective therapy super-scan (spread malignancies) - diffusely increased uptake Liver/spleen scan Metastases of GI tumors Replaced by sono and CT Scan pattern – cold nodules, different number and size Mainly Colorectal, ovarian, breast, lung, lymphoma Always poor prognosis Thyroid scan Non-specific test with pertechnetate Mainly cold nodules – especially in children – must be biopsied!!! Bone marrow scan Colloids or leukocytes Similar as bone scan Better sensitivity FDG PET http://www.homolka.cz/nm/ For several tumors – staging and follow-up Mainly lymphomas, lung cancers, melanoma, colorectal cancers and others Not suitable for prostate cancer Patient preparation At least 1 w post chemo, 3 m radiotherapy One hour before injection physical rest Fasting, no milk, no sugar Specific methods Binding to receptors or antigens I-123 MIBG – pheochromocytoma, neuroblastoma in children In-111 Octreoscan – neuroendocrine tumors (insulinoma, vipoma, carcinoid), SCLC I-131 – thyroid cancer – follow-up and treatment Specific methods Monoclonal antibodies Anti-CEA – rather in detection of relaps In the pelvis better than CT In the liver CT better In-111 Oncoscint – colorectal, ovarian Melanoma – antibody against melanin Ga scan is better Bone scan – multiple metastases Bone scan – multiple metastases Lung cancer – cold lesion Breast cancer normal X ray with hot spot on scintigraphy Superscan – prostate cancer Bone scan - prostate cancer progression Breast cancer – FU – progr. Thyroid – folicular ca on sonography solid nodule Thyroid cancer - anaplastic Thyroid cancer Tc-99m Tc-99m post surgery I-131 Thyroid cancer –I-131 - meta Tc-99m sestamibi parathyroid adenoma early late Neuroblastoma liver and bone involvment Bone scan I-131 MIBG scan Carcinoid – liver meta Ga scan – lung cancer Ga scan - lymphomas Palpable mass on the neck lymphoma Tc-99m pertechnetate Ga-67 citrate SPECT/CT carcinoid SPECT/CT breast cancer SPECT/CT lung cancer SPECT/CT lung cancer FDG PET - normal FDG PET melanoma FDG PET Tumor of unknown origin Metastatic involvment of neck lymph nodes FDG PET Tumor of unknown origin Pharyngeal cancer FDG PET – brain tumor post th two foci on CT, only one viable tumor Staging colorectal CA Effect of therapy Lung cancer Stomach cancer PET:100 % CT: 0 % Stomach cancer PET: 80 % CT: 20 % Stomach cancer PET: 60 % CT: 40 % Stomach cancer PET: 40 % CT: 60 % Stomach cancer PET: 20 % CT: 80 % Stomach cancer PET: 0 % CT: 100 % Stomach cancer NSCLC CT: T2 N0 Mx ~ stg. IB ? NSCLC CT: T2 N0 Mx ~ stg. IB ? PET: T2 N2 M0 ~ stg. II NSCLC CT: T2 N0 Mx ~ stg. IB ? PET: T2 N2 M0 ~ stg. II PET/CT: T2 N2 M1 ~ stg. IV PET/CT is more than PET and CT