Arab Board Oncology Clinical flashcards
Arab Board Oncology Clinical · Build recall with a focused review session.
32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Two-hit hypothesis
- Tumor suppressor genes typically require inactivation of both alleles to promote cancer, as described by Knudson for retinoblastoma; heterozygous carriers inherit one hit and acquire the second somatically.
- Synthetic lethality
- Two gene defects are lethal only when combined; BRCA-mutant cells depend on PARP for repair, so PARP inhibition selectively kills them while sparing normal cells.
- Warburg effect
- Tumor cells preferentially use aerobic glycolysis even with oxygen present, producing lactate; this underlies FDG-PET imaging and informs metabolic targeting strategies.
- Lead-time bias
- Screening advances diagnosis without changing the time of death, artificially lengthening measured survival; mortality endpoints avoid this bias in screening trials.
- Length-time bias
- Screening preferentially detects slow-growing tumors with long preclinical phases, exaggerating apparent survival benefit; randomized mortality trials control for this.
- Positive predictive value
- Proportion of test-positives who truly have disease; unlike sensitivity and specificity, PPV rises with disease prevalence in the screened population.
- Lynch syndrome
- Hereditary mismatch repair deficiency caused by germline MMR gene mutations; confers high colorectal and endometrial cancer risk and predicts immunotherapy response in MSI-H tumors.
- TNM staging
- Anatomic classification of tumor extent (T), regional nodal involvement (N), and distant metastasis (M); stage grouping guides prognosis and treatment selection.
- Sentinel lymph node biopsy
- Identification and removal of the first draining node using dye or radiolabeled colloid; if negative, complete regional lymphadenectomy is usually unnecessary in breast cancer and melanoma.
- RECIST 1.1 progression
- Progression requires at least a 20% increase in the sum of target lesion diameters from nadir, with an absolute increase of at least 5 mm, or new lesions.
- DPYD deficiency
- Reduced dihydropyrimidine dehydrogenase activity causes severe or fatal toxicity with fluoropyrimidines; genotype-guided dose reduction is recommended before 5-FU or capecitabine.
- Immune-related adverse events
- Autoimmune toxicities from checkpoint inhibitors such as colitis, pneumonitis, thyroiditis, and hypophysitis; managed with corticosteroids and drug interruption or discontinuation by grade.
- Antibody-drug conjugate
- A monoclonal antibody linked to a cytotoxic payload that delivers chemotherapy selectively to antigen-expressing tumor cells; examples include T-DM1 and trastuzumab deruxtecan.
- Linear-quadratic model
- Radiation survival model where surviving fraction equals exp(-(alpha*d + beta*d^2)); the alpha/beta ratio predicts fractionation sensitivity of tumors versus late normal tissues.
- Biologically effective dose
- BED equals total dose times (1 + dose per fraction divided by alpha/beta); it allows comparison of different fractionation schemes in radiotherapy.
- Spinal cord tolerance
- Conventional fractionated radiotherapy limits spinal cord dose to approximately 45-50 Gy; higher cumulative doses risk radiation myelopathy, a late irreversible toxicity.
- R0 resection
- Surgical removal with microscopically negative margins; R1 indicates microscopic residual disease and R2 macroscopic residual, both associated with worse local control and survival.
- Neoadjuvant chemotherapy
- Systemic therapy given before surgery to shrink tumors, test in vivo response, and increase organ-preserving resection rates; pathologic complete response is a favorable prognostic marker.
- HIPEC
- Heated intraperitoneal chemotherapy delivered after cytoreductive surgery for selected peritoneal carcinomatosis, notably colorectal and appendiceal primaries.
- Trastuzumab deruxtecan
- A HER2-directed antibody-drug conjugate with a topoisomerase I payload; active in HER2-positive and HER2-low breast cancer and in gastric cancer.
- MGMT promoter methylation
- Epigenetic silencing of the DNA repair gene MGMT in glioblastoma; predicts benefit from temozolomide and is a favorable prognostic marker.
- MSI-H colorectal cancer
- Mismatch repair-deficient tumors with high microsatellite instability; they respond well to immune checkpoint inhibitors and have distinct prognosis.
- APL coagulopathy
- Acute promyelocytic leukemia frequently presents with disseminated intravascular coagulation; early ATRA initiation before confirmation reduces early hemorrhagic mortality.
- CML Philadelphia chromosome
- Reciprocal translocation t(9;22) creating BCR-ABL1 tyrosine kinase; targeted with imatinib or other TKIs, with deep molecular response permitting treatment discontinuation.
- Multiple myeloma CRAB criteria
- Diagnostic features: hyperCalcemia, Renal insufficiency, Anemia, and Bone lesions; plus SLiM biomarkers of malignancy such as involved/uninvolved free light chain ratio >=100.
- Febrile neutropenia
- Fever >=38.3 C once or >=38.0 C sustained with absolute neutrophil count below 500; requires empiric anti-pseudomonal beta-lactam therapy within 60 minutes.
- Tumor lysis syndrome
- Metabolic emergency with hyperkalemia, hyperphosphatemia, hyperuricemia, and hypocalcemia from rapid tumor breakdown; prevented with hydration, allopurinol, or rasburicase.
- Malignant spinal cord compression
- Back pain with progressive neurologic deficit from epidural tumor; requires immediate dexamethasone, urgent MRI, and definitive surgery or radiotherapy to preserve function.
- Hypercalcemia of malignancy
- Elevated calcium from tumor PTHrP secretion or bone destruction; managed with intravenous fluids, bisphosphonates or denosumab, and calcitonin for rapid control.
- Intention-to-treat analysis
- Analyzes all randomized participants according to assigned group regardless of adherence; preserves randomization and avoids bias from selective dropout.
- Number needed to treat
- Reciprocal of the absolute risk reduction; it estimates how many patients must be treated to prevent one additional adverse outcome.
- Phase I trial endpoint
- Primarily determines safety, maximum tolerated dose, and dose-limiting toxicity; efficacy is exploratory and response rates are typically low.