LWBK1006-21 LWW-Govindan-Review December 12, 2011 19:6
280 DeVita, Hellman, and Rosenberg’s CANCER: Principles and Practice of Oncology Review
Question 21.3. A 55-year-old woman undergoes partial nephrectomy for clear cell car-
cinoma of the kidney, Fuhrman grade IV. The patient does well for
10 years, at which time she develops a pathologic intratrochanteric frac-
ture of her left hip. CT scanning of the chest, abdomen, pelvis, and brain
and bone scan reveals no other sites of disease. The MOST appropriate
next step is:
A. Radiation alone
B. High-dose interleukin-2 alone
C. Orthopedic resection of the tumor with reconstruction followed by
radiation
D. Temsirolimus
Questions
21.4.–21.5.
A 76-year-old man with chronic obstructive pulmonary disorder
and diabetes mellitus presents with back pain and confusion. Workup
reveals extensive metastatic disease in the lungs, bones, and liver and a
6-cm tumor in the kidney. There is no evidence of cord compression.
Laboratory studies reveal a calcium of 11.5 mg/dL and a creatinine of
2.0 mg/dL. After hydration and zoledronate, his calcium normalizes,
hemoglobin is 9.5, creatinine decreases to 1.7, and Eastern Cooperative
Oncology Group performance status is 2.
Question 21.4. The poor-risk features present in this patient include all, EXCEPT:
A. His age of>75 years
B. Hypercalcemia
C. Performance status of 2
D. Anemia
Question 21.5. The LEAST appropriate therapy in this case is:
A. Interferon-
B. Temsirolimus
C. Sunitinib
D. Sorafenib
Question 21.6. A 25-year-old Caucasian man without a medical history presents with
hematuria. Workup reveals bilateral renal cysts, at least one of them sus-
picious for malignancy. Family history is significant for a pheochromo-
cytoma in his father and a pancreatic islet cell tumor and early death
from kidney cancer in a paternal aunt. The MOST likely familial cancer
syndrome is:
A. Von Hippel-Lindau disease
B. Birt-Hogg-Dube syndrome
C. Hereditary papillary renal cancer
D. Hereditary leiomyomatosis and renal cancer