Abstract. The therapeutic effect from molecular radiation therapy (MRT), on both tumour and normal tissue, is determined by the radiation absorbed dose. Recent research indicates that as a consequence of biological variation across patients the absorbed dose can vary, for the same administered activity, by as much as two orders of magnitude. The international collaborative EURAMET-EMRP project ಯMetrology for molecular radiotherapy (MetroMRT)ರ is addressing this problem. The overall aim of the project is to develop methods of calibrating and verifying clinical dosimetry in MRT. In the present paper an overview of the metrological issues in molecular radiotherapy is provided.
Introducing the problem of molecular radiation therapyMolecular radiation therapy (MRT), also known as targeted radionuclide therapy, is a unique form of radiotherapy where a high radiation dose is delivered internally, ideally to a specific target. The therapeutic agent may be administrated in several ways: ingestion, intravenous infusion, injection to a body cavity or pathological space (locoregional therapy) or direct injection into a solid tumour.Molecular radiotherapy is routinely prescribed on the basis of administered activity of the therapeutic agent. However, uptake and retention differ from patient to patient and therefore the individual dose to the target can vary between patients given the same administered activity. Recent research indicates the range of variation can be up to two orders of magnitude, which is particularly alarming from the point of view of radiation protection [1,2]. At the low extreme, the patient might gain negligible therapeutic benefit. At the high extreme, the patient might receive more radiation than is needed to treat the tumour. Both cases technically constitute maladministrations.Recent research and new technology developments have permitted estimates of radiation dose in individual patients to target tissues and critical normal tissues at risk to be obtained. However, there has been almost no adoption of these methodologies in routine clinical MRT practice. The reasons are many, but, mainly because the methodology is difficult, there is no standardization of procedures, and there is no objective means of predicting the effect of individual patient dosimetry on treatment outcomes.In fact, when compared with conventional external beam radiotherapy, in which individual patient dosimetry is mandatory and strictly controlled according to agreed protocols, there is full traceability to primary standards, and there are even legal requirements for accuracy (within 5 % of a reference value), it is clear that MRT is urgently in need of metrological support in order to bring dosimetry practice to an acceptable and comparable standard.The new international collaborative EURAMET-EMRP project ಯMetrology for molecular radiotherapyರ (MetroMRT) is addressing this problem. The project is developing the background metrology to support routine individual MRT patient dosimetry, and together with a programme of disseminatio...