25%
10%
0.15
5%
35%
Newer formulations have led to better tolerability of high-dose IL-2.
IL-2 has demonstrable efficacy in clear cell as well as papillary RCC.
Randomized studies have demonstrated a survival benefit associated with high-dose IL-2.
Durable complete responses are seen in a small proportion of patients receiving high-dose IL-2.
Low-dose subcutaneous and high-dose intravenous IL-2 have comparable efficacy.
Karnofsky performance score greater than 80%
Elevated calcium
Absence of prior nephrectomy
Elevated lactate dehydrogenase
Decreased hemoglobin
A 67-year-old woman with an ECOG performance status of 0, a 7-cm left renal mass, retroperitoneal adenopathy, and hepatic metastases that have doubled in size over 4 weeks
A 72-year-old man with an ECOG performance status of 2, a 5-cm right renal mass, and mild dyspnea associated with numerous pulmonary metastases
An 81-year-old man with an asymptomatic 6╯cm right renal mass and multiple hepatic metastases who has declined systemic therapy
A 50-year-old man with an Eastern Cooperative Oncology Group (ECOG) performance status of 0, a large 12-cm right renal mass, and four small pulmonary metastases
None of the above
improved tolerance to cytokine therapy.
removal of tumor burden.
removal of source of tumor-associated immunosuppressive factors.
reversal of acquired immune dysfunction.
improved T-lymphocyte function.
Lymphokine activated killer (LAK) cells augment the efficacy of both interferon-α and IL-2.
Randomized trials have demonstrated a significant survival advantage for combined IL-2 and interferon over either agent given as monotherapy.
All of the above
The combination of IL-2 and interferon leads to higher overall response rates than either agent alone.
The complete response rate with interferon-α monotherapy is 10%.
Medullary carcinoma
Papillary carcinoma
Clear cell carcinoma
Collecting duct carcinoma
Chromophobe carcinoma
IFN-α therapy
Therapy with high dose IL-2
Mediastinoscopy followed by resection of the pulmonary nodules
Observation
Biopsy of a pulmonary nodule
c-MET
PDGF
mTOR
Raf-1
VEGF
more than 70%.
15% to 20%.
less than 10%.
60% to 70%.
30% to 40%.
associated with a longer progression-free survival compared with interferon-α.
associated with a higher response rate compared with interferon-α.
associated with a better quality of life compared with interferon-α.
Bevacizumab + interferon-α
Low-dose subcutaneous IL-2
High-dose IL-2
Axitinib
Everolimus
associated with better overall survival compared with interferon-α.
Sorafenib
Sunitinib
IL-2
Temsirolimus
Interferon-α
Glut-1
TGF-á
raf-1
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