Survey of the use of the ICRU 38 in recording and reporting cervical cancer brachytherapy

Citation
R. Potter et al., Survey of the use of the ICRU 38 in recording and reporting cervical cancer brachytherapy, RADIOTH ONC, 58(1), 2001, pp. 11-18
Citations number
42
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
RADIOTHERAPY AND ONCOLOGY
ISSN journal
01678140 → ACNP
Volume
58
Issue
1
Year of publication
2001
Pages
11 - 18
Database
ISI
SICI code
0167-8140(200101)58:1<11:SOTUOT>2.0.ZU;2-I
Abstract
Background: A survey on the practice of reporting intracavitary cervix canc er brachytherapy (LDR and HDR) in clinical practice (CP) and in literature (LIT) was performed on the occasion of a workshop, 'ICRU 38: The Basis for a Revision', which took place at the Annual GEC ESTRO meeting in Naples in 1998. Materials and methods: The answers (n = 85) to a specific questionnaire whi ch had been sent to ail ESTRO members (n = 1600), were evaluated. Tn parall el, a systematic survey on the literature reporting cervix cancer brachythe rapy since 1985 was performed using the MEDLINE database. The main recommen dations for reporting as given in the ICRU 38 were addressed for both surve ys: technique; total reference air kerma (TRAK); dose specification to the target volume '60 Gy reference volume', to organs at risk 'ICRU rectum and bladder point' and other reference points and time-dose pattern. In additio n: some other items were investigated such as mg h, Point A, B, and in vivo dosimetry in bladder and rectum. Results: Issues related to technique (source, machine and applicator type) and to time-dose pattern are reported in the majority of patients in CP and LIT. The same applies for the following parameters: Point A is indicated i n 76% (LDR) to 89% (HDR) in CP, in 60% (LDR) to 96% (HDR) in LIT. Rectum an d bladder ICRU points are recorded in 55% (HDR) to 90% (LDR) and 58% (HDR) to 84% (LDR), respectively, in CP. On the other hand, TRAK is given in 14% (HDR) to 43% (LDR) in CP, in 0% (HDR) to 10% (LDR) in LIT. '60 Gy reference volume' is recorded in 18% (HDR) to 51% (LDR) in CP, in 0% (HDR) to 17% (L DR) in LIT. Rectum and bladder ICRU points are reported in 18% (LDR) to 28% (HDR) and 14% (HDR) to 29% (LDR), respectively, in LIT. Other reference po ints and in vivo dosimetry measurements are given in a low percentage. Dose rate and overall treatment time is reported in 100-44%. Conclusion: Recording and reporting in CP and in LIT meets the recommendati ons as given in ICRU 38 to different degrees. Specific items such as TRAK a nd the 'Reference volume' have only limited penetration into CP and LIT, wh ich applies in particular to centers using HDR brachytherapy. The discrepan cies between CP and LIT may be due to the well-known delay between change i n CP and its translation into LIT. In order to arrive at a more common lang uage for the better exchange of clinical results, it seems to be necessary to adapt some terms and recommendations. In particular, comprehensive conce pts are needed for reporting dose to points and volumes in the target and i n critical organs, according to the new potential from imaging and computer technology and from modern radiobiological insights, bridging the gap betw een LDR and HDR brachytherapy. (C) 2001 Elsevier Science Ireland Ltd. All r ights reserved.