Cancer Types A-Z

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概述

Kidney cancer, also known as Renal Cell Carcinoma (RCC), is the most common type of kidney cancer in adults, accounting for about 90% of all malignant renal tumors.
It originates from the renal tubular epithelial cells within the nephron.
The main subtypes include:

  • Clear Cell RCC (~75–80%)
  • Papillary RCC (~10–15%)
  • Chromophobe RCC (~5%)
  • Collecting duct carcinoma and Medullary carcinoma (rare, aggressive variants)

Kidney cancer typically occurs between ages 50–70 years and is more common in men.
Early-stage disease often causes few or no symptoms and is sometimes discovered incidentally on imaging.

症状

  • Hematuria (blood in urine) – most common presenting sign
  • Flank or side pain
  • Palpable mass in the abdomen or flank
  • Unexplained weight loss or fatigue
  • Fever or night sweats (paraneoplastic)
  • High blood pressure (hypertension)
  • Anemia or polycythemia (due to altered erythropoietin production)
  • Bone pain or cough in metastatic cases

(Note: The “classic triad” of hematuria, flank pain, and palpable mass occurs in <10% of modern cases.)

病因与风险因素

  • Smoking – major preventable risk factor
  • Obesity and high blood pressure
  • Chronic kidney disease or dialysis history
  • Genetic syndromes:
    • Von Hippel–Lindau (VHL) disease – associated with clear cell RCC
    • Hereditary papillary RCC (MET gene mutations)
    • Birt–Hogg–Dubé syndrome – linked to chromophobe RCC
    • Tuberous sclerosis (rare association)
  • Occupational exposure – to cadmium, trichloroethylene, or petroleum products
  • Male sex and older age

诊断方法

  • Imaging:
    • Ultrasound – initial screening tool for renal mass
    • CT or MRI of abdomen and pelvis – defines size, location, and venous invasion
    • Chest CT – checks for lung metastases
    • Bone scan / PET-CT – if symptoms suggest metastasis
  • Laboratory tests: CBC, renal and liver function, calcium, erythropoietin levels
  • Histopathology: Confirms subtype and grade via biopsy or surgical specimen
  • Staging: Based on TNM system (Tumor, Node, Metastasis)

治疗方案

  • Localized disease (Stage I–II):
    • Partial nephrectomy (nephron-sparing surgery) for small tumors (<4 cm)
    • Radical nephrectomy (removal of kidney ± adrenal gland) for larger or central tumors
  • Locally advanced or metastatic disease (Stage III–IV):
    • Targeted therapy:
      • VEGF inhibitors (sunitinib, pazopanib, axitinib)
      • mTOR inhibitors (everolimus, temsirolimus)
    • Immunotherapy:
      • Immune checkpoint inhibitors (nivolumab, pembrolizumab, ipilimumab)
    • Combination regimens: Immunotherapy + targeted therapy (current standard of care)
    • Ablation or embolization: For patients unfit for surgery
    • Radiation therapy: For palliation of metastases (e.g., bone, brain)
  • Clinical trials: Ongoing research in novel immunotherapy and personalized medicine (e.g., HIF-2α inhibitors).

预后情况

  • Localized RCC: 5-year survival rate ≈ 90–95% after surgery
  • Locally advanced (stage III): 5-year survival ≈ 60–70%
  • Metastatic (stage IV): Median survival ≈ 18–24 months with modern therapies
  • Prognostic factors: Stage, histologic subtype, performance status, and molecular features (e.g., VHL status)
  • Regular surveillance: Imaging every 6–12 months post-treatment for recurrence detection

与此类癌症共处

  • Long-term monitoring: Periodic imaging, blood work, and kidney function tests
  • Lifestyle adjustments: Quit smoking, maintain healthy weight, control blood pressure
  • Nutrition and hydration: To preserve remaining kidney function
  • Psychosocial support: Coping with anxiety, fatigue, and treatment side effects
  • Rehabilitation and survivorship programs: For recovery and quality of life
  • Fertility and sexual health counseling: If receiving targeted or immunotherapy

预防与筛查

  • Avoid smoking and reduce exposure to industrial carcinogens
  • Maintain healthy weight and blood pressure
  • Regular check-ups for individuals with family history or genetic syndromes
  • Genetic counseling and testing for VHL, Birt–Hogg–Dubé, or hereditary papillary RCC
  • Imaging surveillance for high-risk patients (e.g., VHL carriers)

FAQs

Q: Is kidney cancer always fatal?
A: No. When detected early, kidney cancer is often curable with surgery. Advanced cases can be controlled for years with modern targeted and immunotherapies.

Q: Can kidney cancer spread to other organs?
A: Yes. Common metastatic sites include the lungs, bones, liver, and brain.

Q: Is it hereditary?
A: Most cases are sporadic, but around 2–4% are hereditary.

Q: Can a person live with one kidney?
A: Yes. Most people live normal, healthy lives after removal of one kidney, provided the other is functioning well.

相关资源

  • American Cancer Society (ACS) – cancer.org
  • National Cancer Institute (NCI) – cancer.gov
  • Kidney Cancer Association (KCA) – kidneycancer.org
  • European Association of Urology (EAU) – uroweb.org
  • gov – Search “Renal Cell Carcinoma” or “Kidney Cancer”
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