The invention provides a method for determining sensitivity of a subject to an anticancer agent, comprising measuring the level of a protein selected from the group consisting of a protein or a fragment thereof which is detected as a peak at m/z of 5,300 to 5,400, a protein or a fragment thereof which is detected as a peak at m/z of 6,130 to 6,230, a protein or a fragment thereof which is detected as a peak at m/z of 7,000 to 7,080, a protein or a fragment thereof which is detected as a peak at m/z of 7,840 to 7,920, a protein or a fragment thereof which is detected as a peak at m/z of 8,920 to 9,000, a protein or a fragment thereof which is detected as a peak at m/z of 12,440 to 12,560, a protein or a fragment thereof which is detected as a peak at m/z of 17,100 to 17,270, a protein or a fragment thereof which is detected as a peak at m/z of 18,290 to 18,470, a protein or a fragment thereof which is detected as a peak at m/z of 24,660 to 24,750, a protein or a fragment thereof which is detected as a peak at m/z of 35,980 to 36,290, a protein or a fragment thereof which is detected as a peak at m/z of 8,650 to 8,750, a protein or a fragment thereof which is detected as a peak at m/z of 9,100 to 9,200, and a protein or a fragment thereof which is detected as a peak at m/z of 11,760 to 11,890, in a specimen derived from the subject, the peaks being determined by means of a mass spectrometer.
