Professional Documents
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ICRU REPORT 89
Volume 13 No 1–2 2013 ISSN 1473-6691 (print)
ISSN 1472-3422 (online)
ICRU REPORT 89
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Report Committee
R. Pötter (Co-Chairman), Medical University of Vienna, Vienna, Austria
C. Kirisits (Co-Chairman), Medical University of Vienna, Vienna, Austria
B. Erickson, Medical College of Wisconsin, Milwaukee, USA
C. Haie-Meder, Gustave Roussy Cancer Campus, Villejuif, France
E. Van Limbergen, University Hospital Gasthuisberg, Leuven, Belgium
J. C. Lindegaard, Aarhus University Hospital, Aarhus, Denmark
J. Rownd, Medical College of Wisconsin, Milwaukee, USA
K. Tanderup, Aarhus University Hospital, Aarhus, Denmark
B. R. Thomadsen, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA
Commission Sponsors
P. M. DeLuca, Jr., University of Wisconsin, Madison, WI, USA
A. Wambersie, Universite Catholique de Louvain, Brussels, Belgium
S. Bentzen, University of Maryland School of Medicine, Baltimore, MD, USA
R. A. Gahbauer, Ohio State University, Columbus, OH, USA
D. T. L. Jones, Cape Scientific Concepts, Cape Town, South Africa
G. F. Whitmore, Ontario Cancer Institute, Toronto, Canada
in which the development of guidance and recom- The Commission has found its relationship with
mendations can make an important contribution. all of these organizations fruitful and of substantial
benefit to the ICRU program.
ICRU’s Relationship with Other
Organizations
In addition to its close relationship with the ICRP,
Operating Funds
ICRU has developed relationships with national
and international agencies and organizations. In Financial support has been received from the fol-
these relationships, ICRU is looked to for primary lowing organizations:
guidance in matters relating to quantities, units,
and measurements for ionizing radiation, and their Accuray Incorporated
applications in the radiological sciences. In 1960, American Association of Physicists in Medicine
through a special liaison agreement, ICRU entered Belgian Nuclear Research Centre
into consultative status with the International Canadian Nuclear Safety Commission
Atomic Energy Agency (IAEA). The Commission has Federal Office Public Health, Switzerland
a formal relationship with the United Nations Helmholtz Zentrum München Hitachi, Ltd.
Scientific Committee on the Effects of Atomic International Radiation Protection Association
Radiation (UNSCEAR), whereby ICRU observers International Society of Radiology
are invited to attend annual UNSCEAR meetings. Ion Beam Applications, S.A.
The Commission and the International Organization Japanese Society of Radiological Technology
for Standardization (ISO) informally exchange notifi- MDS Nordion
cations of meetings, and ICRU is formally designated Nederlandse Vereniging voor Radiologie
for liaison with two of the ISO technical committees Philips Medical Systems, Incorporated
ICRU is a member of Consultative Committee for Radiological Society of North America
Units (CCU) – BIPM and Consultative Committee Siemens Medical Solutions
for Ionizing Radiation (CCRI(I) – BIPM and U.S. Environmental Protection Agency
Observer to CCRI(II) and CCRI (III). ICRU also U.S. Nuclear Regulatory Commission
enjoys a strong relationship with its sister organiza- Varian Medical Systems
tion, the National Council on Radiation Protection
and Measurements (NCRP). In essence, ICRU and
NCRP were founded concurrently by the same indivi- In addition to the direct monetary support pro-
duals. Presently, this long-standing relationship is vided by these organizations, many organizations
formally acknowledged by a special liaison agree- provide indirect support for the Commission’s
ment. ICRU also exchanges reports with the follow- program. This support is provided in many forms,
ing organizations: including, among others, subsidies for (1) the time of
individuals participating in ICRU activities, (2)
Bureau International des Poids et Mesures travel costs involved in ICRU meetings, and (3)
European Commission meeting facilities and services.
International Council for Science In recognition of the fact that its work is made
International Electrotechnical Commission possible by the generous support provided by all of
International Labour Office the organizations supporting its program, the
International Organization for Medical Physics Commission expresses its deep appreciation.
International Radiation Protection Association
International Union of Pure and Applied Physics Hans-Georg Menzel
United Nations Educational, Scientific and Cultural Chairman, ICRU
Organization Heidelberg, Germany
Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Abstract . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Acknowledgements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
1. Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
1.1 Developments in Epidemiology and Treatment of Cervical Cancer. . . . . . . . . . . . . . . 7
1.2 Outline of Report. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
1.2.1 Prevention, Diagnosis, Prognosis, Treatment, and Outcome . . . . . . . . . . . . . . . 8
1.2.2 Brachytherapy Techniques and Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
1.2.3 Brachytherapy Imaging for Treatment Planning . . . . . . . . . . . . . . . . . . . . . . . . . 8
1.2.4 Tumor and Target Volumes and Adaptive Radiotherapy . . . . . . . . . . . . . . . . . . 9
1.2.5 OAR- and Morbidity-Related Concepts and Volumes. . . . . . . . . . . . . . . . . . . . . . 10
1.2.6 Radiobiological Considerations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
1.2.7 Dose and Volume Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
1.2.8 Physics Aspects of Three-Dimensional Volumetric Dose Assessment . . . . . . . . 10
1.2.9 Radiographic Localization of Absorbed-Dose Points . . . . . . . . . . . . . . . . . . . . . 10
1.2.10 Sources and Dose Calculation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.2.11 Treatment Planning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.2.12 Summary of the Recommendations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.2.13 Clinical Examples. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
1.2.14 Electronic Spreadsheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
1.2.15 Report Organization: Summaries, Recommendations, and Key Messages . . 12
4.6 Radiography . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. .. .. . .. .. .. . .. .. .. . .. .. .. . .. . 41
4.7 Imaging in Treatment Planning . . . . . . . . . . . . . . .. .. .. . .. .. .. . .. .. .. . .. .. .. . .. . 43
4.7.1 Imaging in external-beam radiotherapy . .. .. .. . .. .. .. . .. .. .. . .. .. .. . .. . 43
4.7.2 Imaging in brachytherapy . . . . . . . . . . . . . .. .. .. . .. .. .. . .. .. .. . .. .. .. . .. . 43
4.8 Summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. .. .. . .. .. .. . .. .. .. . .. .. .. . .. . 45
4.9 Key Messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. .. .. . .. .. .. . .. .. .. . .. .. .. . .. . 46
5.4.5.2.1
Selection of the CTV-TIR for Various Patterns of Tumor
Response after EBRT+ + Chemotherapy . . . . . . . . . . . . . . . . . . 69
5.4.6 Uncertainties in Target Selection and Contouring . . . . . . . . . . . . . . . . . . . . . . . 70
5.5 Planning Target Volume (PTV-T) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
5.5.1 Concept of PTV-T . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
5.5.2 Geometric Uncertainties in EBRT and Brachytherapy . . . . . . . . . . . . . . . . . . . . 73
5.5.3 Geometric Uncertainties and PTV Margins in Brachytherapy . . . . . . . . . . . . . 73
5.5.4 Internal Margin and the ITV . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
5.5.4.1 External Beam Radiotherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
5.5.4.2 Brachytherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
5.5.5 Set-up Margin (External Margin) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
5.5.5.1 External Beam Radiotherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
5.5.5.2 Brachytherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
5.5.6 Preimplantation PTV. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
5.6 Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
5.7 Summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
7. Radiobiological Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
7.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
7.1.1 Dose Distributions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
7.1.2 Time – Dose Patterns. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
7.2 Time – Dose Patterns: Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
7.2.1 Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
7.2.2 Fraction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
7.2.3 Fractionated Irradiation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
7.2.4 Pulse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
7.2.5 Hypofractionation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
7.2.6 Hyperfractionation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
7.2.7 Accelerated Fractionation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
7.2.8 Fractionated HDR Irradiation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
7.2.9 PDR Irradiation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
7.2.10 Continuous LDR Irradiation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
7.2.11 Non-Continuous LDR. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
7.2.12 Overall Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
7.2.13 Mean Dose Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
7.3 Dose-Rate Effects on Recovery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
7.3.1 Low-Dose-Rate Brachytherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
7.3.2 Medium-Dose-Rate Brachytherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92
7.3.3 High-Dose-Rate Brachytherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92
7.4 Other Time-Dose Pattern-Related Radiobiological Processes. . . . . . . . . . . . . . . . . . . . 92
7.4.1 Repopulation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92
7.4.2 Reoxygenation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
7.4.3 Redistribution. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
7.5 Dose-Time Patterns and Dose Rates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
7.6 Radiobiological Consequences of Different Dose – Time Patterns . . . . . . . . . . . . . . . . 93
7.6.1 From Absorbed Dose to Biologically Equieffective Dose . . . . . . . . . . . . . . . . . . 93
7.6.2 Mathematical Modeling of the Effects of Dose Rate and Dose per Fraction,
Recovery Capacity, and Half-Time of Recovery . . . . . . . . . . . . . . . . . . . . . . . . . . 94
7.6.2.1 HDR Irradiation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 94
7.6.2.2 LDR Irradiation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95
7.6.2.3 PDR Irradiation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96
7.6.3 The Equieffective Absorbed Dose Concept, EQDX . . . . . . . . . . . . . . . . . . . . . . . . 96
7.6.4 Equieffective Dose and EQD2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99
7.6.5 Combination of EBRT and brachytherapy. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100
7.7 Recommended Common Terminology for Reporting Dose –Time Parameters of
Combined EBRT and ICBT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100
7.8 Uncertainties Related to the Dose – Time Modeling. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102
7.9 Equivalent Uniform Dose, EUD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102
7.10 Recommendations for Reporting Dose – Time Parameters . . . . . . . . . . . . . . . . . . . . . . . 103
7.11 Summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 103
Appendix A Examples
A.1 Case 1: Small Cervical Cancer Stage IB1, with Positive Nodes,Treated with 3D
Conformal EBRT and Concomitant Chemotherapy Plus Conformal Boost and
MRI-Based PDR Brachytherapy with Mould Technique . . . . . . . . . . . . . . . . . . . . . . . . 165
A.1.1 General Patient Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 165
A.1.2 Tumor Extension at Diagnosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 165
A.1.2.1 Gynecological Examination (Figure A.1.1, Table A.1.1) . . . . . . . . . . 165
A.1.2.2 MRI of the pelvic and Para-Aortic Area (Figure A.1.1, Table A.1.1) 165
A.1.2.3 Other Findings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 165
A.1.2.4 Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 165
A.1.3 Treatment Intention . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 165
A.1.4 External Beam Radotherapy. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 166
A.1.5 Brachytherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 167
A.1.5.1 Gynecological Examination at the Time of First Brachytherapy
(Figure A.1.4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 167
A.1.5.2 MRI of the Lower Pelvic Area at First Brachytherapy
(Figure A.1.4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 168
A.1.5.3 Treatment Planning Aim . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 168
A.1.5.4 Treatment Delivery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 168
A.1.5.5 Equipment Used for Brachytherapy (Figure A.1.5) . . . . . . . . . . . . . 168
A.1.6 Treatment Planning and Reporting Brachytherapy and EBRT . . . . . . . . . . . 170
A.1.6.1 Example of Dose Distribution. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 170
A.1.7 Current Patient Status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 170
A.2 Case 2: Large Cervical Cancer Stage IB2, Intracavitary, No Nodes, Treated with 3D
Conformal Box EBRT and Parametrial Boost, with Concomitant Chemotherapy,
and MRI-Based Intracavitary Tandem/Ring and Tandem/Ovoid HDR
Brachytherapy. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 171
A.2.1 General Patient Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 171
A.2.2 Tumor Extension at Diagnosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 171
A.2.2.1 Gynecological Examination (Figure A.2.1, Table A.2.1) . . . . . . . . . . 171
A.2.2.2 MRI of the Lower Pelvic Area (Figure A.2.1, Table A.2.1) . . . . . . . . 171
A.2.2.3 Other Findings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 171
A.2.2.4 Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 171
A.2.3 Treatment Intention . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 171
A.2.4 External Beam Radiotherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 171
A.2.5 Brachytherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 173
A.2.5.1 Gynecological Examination at the Time of First Brachytherapy
(Figure A.2.4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 173
A.2.5.2 MRI of the Lower Pelvic Area at First Brachytherapy
(Figure A.2.4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 174
A.2.5.3 Treatment Planning Aim . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 174
A.2.5.4 Treatment Delivery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 175
A.2.5.5 Equipment Used for Brachytherapy (Figure A.2.5) . . . . . . . . . . . . . 175
A.2.6 Treatment Planning and Reporting Brachytherapy and EBRT . . . . . . . . . . . 175
A.8 Case 8: Large Cervical Cancer Stage IIIB with No Nodes, Treated with 3D
Conformal Box with Concomitant Chemotherapy and MRI-Based Intracavitary
and Interstitial HDR Brachytherapy with Tandem/Ring Applicator and Needles . . 217
A.8.1 General Patient Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 217
A.8.2 Tumor Extension at Diagnosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 217
A.8.2.1 Gynecological Examination (Figure A.8.1, Table A.8.1) . . . . . . . . . . 217
A.8.2.2 MRI of the Pelvis (Figure A.8.1, Table A.8.1) . . . . . . . . . . . . . . . . . . . 217
A.8.2.3 Other Findings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 217
A.8.2.4 Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 217
A.8.3 Treatment Intention . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 217
A.8.4 External Beam Radiotherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 217
A.8.5 Brachytherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 220
A.8.5.1 Gynecological Examination at the Time of First Brachytherapy 220
(Figure A.8.4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
A.8.5.2 MRI of the Lower Pelvic Area at First Brachytherapy 220
(Figure A.8.4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
A.8.5.3 Treatment Planning Aim . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 220
A.8.5.4 Treatment Delivery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 220
A.8.5.5 Equipment Used for Brachytherapy (Figure A.8.5) . . . . . . . . . . . . . 221
A.8.6 Treatment Planning and Reporting Brachytherapy and EBRT . . . . . . . . . . . 222
A.8.6.1 Example of Dose Distribution. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 224
A.8.7 Current Patient Status (Figure 8.7) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 224
A.9 Case 9: Cervical Cancer Stage IIA2 Treated with 3D Conformal External-Beam
Irradiation, Concomitant Chemotherapy, and Radiograph-Based Intracavitary
Low Dose-Rate Brachytherapy with Tandem and Ovoids . . . . . . . . . . . . . . . . . . . . . . . 225
A.9.1 General Patient Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 225
A.9.2 Tumor Extension at Diagnosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 225
A.9.2.1 Gynecological Examination (Figure A.9.1, Table A.9.1) . . . . . . . . . . 225
A.9.2.2 CT of the Pelvis (Figure A.9.1, Table A.9.1) . . . . . . . . . . . . . . . . . . . . . 225
A.9.2.3 Other Findings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 225
A.9.2.4 Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 225
A.9.3 Treatment Intention . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 225
A.9.4 External Beam Radiotherapy (Figure A.9.3 and Table A.9.2) . . . . . . . . . . . . . 225
A.9.5 Brachytherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 228
A.9.5.1 Gynecological Examination at the Time of First Brachytherapy 228
(Figure A.9.4, Table A.9.1) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
A.9.5.2 Treatment Planning Aim . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 228
A.9.5.3 Treatment Delivery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 228
A.9.5.4 Equipment Used for Brachytherapy (Table A.9.4, Figure A.9.5) . . . 229
A.9.6 Treatment Planning and Reporting EBRT and Brachytherapy . . . . . . . . . . . 229
A.9.7 Current Patient Status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 229
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 234
Preface
The treatment of gynecological malignancies is one In this ICRU report, specific concepts and termin-
of the very earliest applications of radionuclides in ology are developed, comparable to the GEC ESTRO
medicine, dating from soon after Marie Curie’s discov- recommendations, for selecting and contouring the
ery and isolation of radium (226Ra). The widespread various tumor-related (adaptive) volumes, together
use of radium for the treatment of cervical malignan- with the delineation of the adjacent organs at risk
cies rapidly became common practice. Over the many (OAR). Detailed contouring of these structures and
decades since this discovery, incredible advances oc- volumes based on repetitive imaging and gynecolo-
curred in the diagnosis and treatment of such tumors. gic examination requires a comprehensive under-
These included the introduction of various radium standing of tumor spread and tumor response.
systems dealing with source application and treatment Specific dose-volume and dose-point parameters
prescription, mainly in the first half of the last century are introduced and adopted in this ICRU report for
(e.g., at Manchester and M.D. Anderson Hospital, the different tumor-related volumes and OARs,
Houston). Later, intermediate-dose rate, high-dose based on volumetric imaging as well as on tradition-
rate, and pulsed-dose rate radioactive stepping sources al radiographic imaging. This set of parameters
were developed. The latter devices employ computer- fulfill the specific needs for prescribing, recording,
controlled positioning using afterloading techniques. and reporting intracavitary and interstitial cervix
At present, fully three-dimensional treatment plan- cancer brachytherapy for the volumes of interest
ning derived from CT and MR imaging is considered located in the very inhomogeneous dose region char-
the paradigm for cervix cancer brachytherapy, re- acterized by a rapid dose fall off adjacent to the
placing the radiographic approach. These techniques radioactive sources. Essential for dose calculation,
are often combined with advanced external-beam treatment planning procedures such as applicator
therapy and concomitant cytotoxic chemotherapy reconstruction are described. This leads directly to
using three-dimensional image-guided techniques three-dimensional treatment planning with opti-
(e.g., image-guided radiotherapy and intensity- mization procedures based on the evaluation of dose-
modulated radiation therapy using a static or rotat- volume histograms (DVH) and using reference
ing gantry). These and other advances have emerged absorbed dose-points. A balanced assessment of the
since the publication of ICRU Report 38 (1985) on complex set of dose points and dose-volume para-
intracavitary therapy in gynecology. meters enables a highly individualized final dose pre-
Advances in precise, high-resolution, cost- scription for the volumes of interest. This report, as
effective volume imaging using MR and spiral CT well as clinical reports based on these parameters,
now allow accurate specification of the relationship demonstrates that these advances have helped to
between external radiation beams, brachytherapy identify and investigate correlations between dose
applicators, and the tumor and normal tissue struc- points and DVH and specific endpoints such as
tures. Brachytherapy treatment of cervix cancer is normal tissue damage and local tumor control.
most frequently used as a boost treatment toward Presently, traditional low-dose rate afterloading
the end of external beam radiation therapy (EBRT) techniques with 226Ra or 137Cs sources are being
and concomitant chemotherapy. As there is a major replaced by high-dose rate or pulsed-dose 192Ir or 60Co
tumor response during this combined treatment, sources. Computer-controlled, cable-driven afterload-
tumor volume and shape change significantly and ing devices place the sources in a variety of positions in
treatment requires an adaptive target concept. The the applicator, delivering variable doses at different
resulting high-risk clinical target volume (CTV) is locations in variable dwell times. A large variety of
defined using the residual gross tumor volume doses per fraction, dose rates, and total absorbed doses
(GTV) and the pathologically identified tissues at are prescribed and reported for the different volumes
the time of brachytherapy combined with the ana- of interest, moving away from the traditional implant
tomical topography when the applicator is in place. systems and prescription patterns. These changes and
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PRESCRIBING, RECORDING, AND REPORTING BRACHYTHERAPY FOR CANCER OF THE CERVIX
advances require the use of biophysical modeling to parameters such as: patient and tumor work up,
combine the effects of varying dose fractions, total treatment intention, EBRT and concomitant chemo-
absorbed doses and dose rates (i.e., differing from the therapy, brachytherapy, combined reporting of EBRT
conventional 2 Gy per fraction or 0.5 Gy/h) on the cor- and brachytherapy, and follow-up. This will facilitate
responding estimates of tumor and normal tissue re- the understanding of prescribing, recording, and
sponse. The report discusses such a model and the reporting across different tumor stages, EBRT and
process to estimate such response variations by means brachytherapy techniques, dose fractions, dose rates,
of the equi-effective dose concept, expressed as an total absorbed doses, in the frame of both a volumet-
EQD2 dose. This report recommends jointly reporting ric and a radiographic approach.
EQD2 results based on modeling as well as traditional Finally, the concepts and terms described in this
absorbed dose in communicating results. report follow the tradition of previous ICRU reports
This report provides comprehensive recommenda- on prescribing, recording, and reporting external
tions on prescribing, recording, and reporting brachy- beam radiotherapy (from ICRU Report 50 to 83). In
therapy focusing on volumetric imaging in cervix cancer particular, the concepts for GTV, CTV, and planning
brachytherapy. However, it is well recognized that the target volume are elaborated within the context of
majority of advanced cervix cancer patients are and cervix cancer brachytherapy, and now introduce a
will be treated in developing countries with limited new adaptive target concept. Dose-volume para-
resources. Patients in these countries are usually meters are introduced addressing the specific needs
treated with simple radiotherapy methods. This report of image-guided brachytherapy. Changes of tumor
combines prescribing, recording, and reporting for topography are integrated into these concepts and
simple methods of radiotherapy (e.g., point A prescrip- terms. What still remains to be solved is an inte-
tion) with advanced methods using dose-volume para- grated assessment of volumes and doses from EBRT
meters (e.g., D90% prescription in the adaptive target) and brachytherapy, which reflect the considerable
through an “integrated level” approach. For example, changes during the overall treatment time.
when practicing Level 2 (“advanced standard”), the The current report on prescribing, recording, and
report recommends also reporting the parameters for reporting cervix cancer brachytherapy is a joint
Level 1 (“minimum standard”). This facilitates commu- report from the ICRU and the GEC ESTRO high-
nication between centers with simple and advanced lighting the intensive and effective collaboration on
radiotherapy. cervix cancer brachytherapy during the last two
The report includes nine appendices providing a decades.
spectrum of clinical case examples to guide and
suggest various techniques for typical clinical scen- Paul M. DeLuca Jr
arios of radical cervix cancer treatment. These exam- Christian Kirisits
ples include a comprehensive set of treatment-related Richard Pötter
Abstract
This ICRU/GEC-ESTRO report starts with the essential background, including a clinical introduction, his-
torical and current techniques including the concepts of volumetric imaging for cervix cancer. One key
element is the four-dimensional adaptive target concept at certain time points during treatment by clinical
examination and imaging. For the rectum, bladder, sigmoid, adjacent bowel, and vagina in addition to con-
tours including the entire organ the report emphasizes the presence of different morbidity endpoints and
related substructures within the organ. The radiobiology chapter explains the limitations of the linear-
quadratic model, but encourages the use of the EQD2 concept as the current best option for treatment plan-
ning and overall dose reporting. A detailed concept is recommended to report dose and volume parameters
related to contours and reference points. The report includes detailed chapters on treatment planning, espe-
cially for three-dimensional volumetric approach, but also the underlying concepts of dosimetry which
remains essential for volumetric and radiography-based planning.
Acknowledgements
The Committee would like to thank the following Martine Franckena, Erasmus Medical Center,
colleagues for their essential support for some clinical Rotterdam, The Netherlands,
examples and some figures in this report: Tijana Frank, Medical University of Vienna, Vienna,
Austria,
Bethany Anderson, University of Wisconsin, Jesper F. Kallehauge, Aarhus University Hospital,
Madison Wisconsin, USA, Aarhus, Denmark,
Daniel Berger, Medical University of Vienna, Vienna, Bruce Libby, University of Virginia, Charlottesville,
Austria, VA, USA,
Marisol de Brabandere, University Hospital Nicole Nesvacil, Medical University of Vienna,
Gasthuisberg, Leuven, Belgium, Vienna, Austria, and
Isabelle Dumas, Gustave Roussy Cancer Campus, Maximilian Schmid, Medical University of Vienna,
Villejuif, France, Vienna, Austria.