Method for monitoring the irradiation control unit of an ion-beam therapy system

• US 6,614,038 B1
• Filed: 12/05/2001
• Issued: 09/02/2003
• Est. Priority Date: 02/19/1999
• Status: Expired due to Term

• Current Assignee: Gessellschaft Fur Schwerionenforschung MbH
• Original Assignee: Gessellschaft Fur Schwerionenforschung MbH
• Inventors: Voss, Bernd, Poppensieker, Klaus, Haberer, Thomas, Schardt, Dieter, Brand, Holger
• Primary Examiner(s): Lee, John R.
• Assistant Examiner(s): Hashmi, Zia R.
• Application Number:
  US09/913,741
• Time in Patent Office: 636 Days
• Field of Search: 250/492.3, 250/398, 250/496.1, 250/396.HL, 250/306, 250/307, 250/251, 328/235, 328/233, 328/234
• US Class Current: 250/492.3
• CPC Class Codes: A61N 2005/1074 Details of the control system, e.g. user interfaces
• CPC Class Codes: A61N 2005/1087 Ions; Protons
• CPC Class Codes: A61N 5/1043 Scanning the radiation beam, e.g. spot scanning or raster scanning
• CPC Class Codes: A61N 5/1048 Monitoring, verifying, controlling systems and methods
• CPC Class Codes: G21K 5/04 with beam-forming means

Abstract

The invention relates to a method of checking the calculated [sic] irradiation control unit of an ion beam therapy system which comprises a raster scanning device arranged in a beam guidance system and having vertical deflection means and horizontal deflection means for the vertical and horizontal deflection of a treatment beam at right angles to its beam direction, so that the treatment beam is deflected by the raster scanning device onto an isocenter of the irradiation station and scans a specific area surrounding the isocenter, data sets and permanently stored data of a control computer, parameters of measuring sensors and desired current values of scanner magnets being checked.

Claims

1. A method of checking the irradiation control unit of a heavy ion beam therapy system, the heavy ion beam therapy system comprising

at least one ion source (1),

an accelerator device (2, 5) for accelerating the ions from the ion source (1) in the form of a treatment beam (11),

a beam guidance system (6, 8) in order to feed the treatment beam (11) from the accelerator device (2, 5) to at least one irradiation station for treating a patient, the beam guidance system (6, 8) comprising at least one beam guidance line (6), and

a raster scanning device arranged in the beam guidance system (6, 8) and having vertical deflection means (13) and horizontal deflection means (14) for the vertical and horizontal deflection of the treatment beam (11) at right angles to its beam direction, so that the treatment beam (11) is deflected by the raster scanning device onto an isocenter (10) of the irradiation station and scans a specific area surrounding the isocenter (10), and data sets and permanently stored data of a control computer, parameters of measuring sensors, desired current values of scanner magnets, and and [sic] desired currents of scanner magnet currents being compared with actual magnet current values, characterized in that the permanent storage of permanently stored data is checked and calibration tests of measuring sensors are carried out, and in that the data sets and programs to be loaded into front end processors from the central control computer are read back after being loaded and are compared with the output data, all the data paths through which the data pass as they are loaded being checked when the data are read back, and specific programs writing the programs and data sets in server computers of a monitoring system into front end memories and reading said data back and comparing them automatically with programs and data in the dedicated memory before each irradiation and, only after it has been ensured by checking that all the programs and data sets which have to be loaded into front end computers of a monitoring system and executed from there correspond exactly to those on data memories of the monitoring system, safe operation being assumed.

2. The method as claimed in claim 1, characterized in that all the input data which are required for a patient irradiation are loaded into the sequence control of the central control computer.

3. The method as claimed in claim 1, characterized in that an alarm message is displayed by a therapy operating computer if deviations occur between data read back and output data.

4. The method as claimed in claim 3, characterized in that the central control computer and a monitoring computer are informed about the alarm.

5. The method as claimed in claim 3, characterized in that in the event of an alarm, an interlock unit is not released by the therapy operating computer, nor is a patient operation released.

6. The method as claimed in claim 1, characterized in that each deviation between the data read back and an original data set triggers an alarm.

7. The method as claimed in claim 1, characterized in that a last irradiation point in the event of a power failure is available as permanently stored data.

8. The method as claimed in claim 7, characterized in that the number of the irradiation point when a shutdown condition occurs is saved and stored as permanently stored data, in spite of power failure.

9. The method as claimed in claim 1, characterized in that in order to check the permanent storage of data, a monitoring system of the central control computer is loaded with an irradiation plan,

this plan is carried out without an active beam,

artificial switching from one irradiation site to the next is carried out,

the voltage supply of a motherboard for processor cards is switched off at a well-defined treatment site and

after the system has been restarted, the last irradiation site is read out and compared with the well-defined irradiation site.

10. The method as claimed in claim 1, characterized in that the checking of the permanent storage is carried out before each treatment block.

11. The method as claimed in claim 7, characterized in that in the event of deviations between the values read after the power failure and the values last present before the power failure, the therapy system is not released for patient treatment.

12. The method as claimed in claim 1, characterized in that the desired current values of scanner magnet currents are compared with the actual values in terms of value and time, the actual values being permitted to exceed neither value nor time tolerance limits.

13. The method as claimed in claim 12, characterized in that the maximum setting time for a current step of 2 A is checked for dt_x≦

175 μ

s and for dt_y≦

325 μ

s.

14. The method as claimed in claim 12, characterized in that an absolute current accuracy of dI=0.3 A is required.

15. The method as claimed in claim 1, characterized in that a calibration check and monitoring of the temperature and pressure of the counting gas of an ionization chamber is carried out.

16. The method as claimed in claim 1, characterized in that pressure and temperature of the counting gas are measured with electronic sensors.

17. The method as claimed in claim 16, characterized in that the measured values are registered by a monitoring system and converted into absolute units with calibration factors input there.

18. The method as claimed in claim 16, characterized in that the calibration of the sensors is carried out with the aid of reference measuring instruments.

19. The method as claimed in claim 16, characterized in that the counting gas pressure and the temperature are registered and logged digitally.

20. The method as claimed in claim 16, characterized in that the external air pressure and the room temperature at the location of the monitoring system are measured with absolutely calibrated instruments.

21. The method as claimed in claim 16, characterized in that the absolute values for air pressure and room temperature are measured daily directly on the reference instruments, compared with the values displayed by the monitoring system and logged.

22. The method as claimed in claim 16, characterized in that the values for counting gas pressure and counting gas temperature are registered once per minute, and a time profile of the values is displayed graphically.

23. The method as claimed in claim 16, characterized in that an alarm is output if deviations of more than 20 hPA/5C (sic) are determined in the course of one day.