Interstitial brachytherapy is a cancer treatment in which radioactive material is placed closely to the target tissue of the affected site using an afterloader (HDR-brachytherapy) or manually (LDR- and PDR-brachytherapy). For HDR-brachytherapy, the accuracy of this placement is calibrated using an external reference system that locates the radioactive material according to the radiation levels measured at locations around the source. At each of these locations, a scintillator produces light when irradiated by the radioactive material. This light is proportional to the level of radiation at each location. The light produced by each scintillator is converted to an electrical signal that is proportional to the light and the radiation level at each location. The radioactive material is located according to the plurality of electrical signals.

Interstitial brachytherapy is a cancer treatment in which radioactive material is placed directly in the target tissue of the affected site using an afterloader. The accuracy of radiation placement is monitored during the cancer treatment. The location plan for the radioactive material may be adjusted during the cancer treatment based on real-time analysis of the location and dosage of radiation measured in, at and around the target tissue of the affected site.

An apparatus and method for using rotating shield brachytherapy (RSBT). In an aspect, the RSBT system and method can be used to maintain or increase tumor dose relative to conventional techniques with a dramatic reduction in radiation dose to the urethra, rectum, and bladder in the treatment of prostate cancer through placing partially shielded radiation sources away from sensitive tissues. In an aspect, the invention is an apparatus and method for the precise angular and linear positioning of multiple partially-shielded radiation sources in interstitial needles. In a further aspect, the invention comprises a monitoring and control apparatus for the precise and simultaneous angular positioning of multiple shield-containing catheters in the RBST system by measuring and correcting deviations between actual and desired catheter angular positions and depth in real time before and during treatment delivery.

The invention relates to a device for supporting the testing of a brachytherapy applicator prior to the use of the brachytherapy applicator in brachytherapy radiation treatments.

The invention also relates to a method for testing of a brachytherapy applicator prior to the use of the brachytherapy applicator in brachytherapy radiation treatments.

The present disclosure lies in the field of medical radiotherapy and relates to an applicator for a medical radiotherapy device, an applicator system for a medical radiotherapy device and a method for using an applicator or an applicator system. The applicator includes an applicator head and an applicator body. The applicator head and the applicator body are embodied such that the applicator head can be assembled on, and disassembled from, the applicator body, in each case without damage.

An intervention system employs an interventional device (10), and a sensor wire (20) manually translatable within a lumen (11). The intervention system further employs a reconstruction controller (44) for reconstructing a shape of the interventional tool (10) responsive to a sensing of a manual translation of the sensor wire (20) within the lumen (11) (e.g., a EM sensor being attached to/embedded within a guide wire), and for determining a reconstruction accuracy of a translation velocity of the sensor wire (20) within the lumen (11) to thereby facilitate an accurate reconstruction of the shape of the interventional tool (10). The reconstruction accuracy may be determined by the reconstruction controller (44) as an acceptable translation velocity being less than an acceptable threshold, an unacceptable translation velocity being greater than an unacceptable threshold, and/or a borderline translation velocity being greater than the acceptable threshold and less than the unacceptable threshold. The reconstruction controller (44) generates an acceptability indicator that may be visualizing or audibly communicated via a user interface (48).

The present invention relates to a body insertable device having an outer body being bent; and an inner body positioned inside the outer body, having an accommodation space in which the resource soured is accommodated, and being capable of rotating inside the outer body, wherein a radiation emission direction is continuously adjusted by rotation of the inner body.

Methods and devices for minimally-invasive delivery of radiation to the eye (such as the posterior portion of the eye) including cannula systems with multiple treatment positions and/or multiple channels in the distal tip of the cannula systems. The channels can accommodate emanating sources and exposing a target at various treatment positions. The emanating sources may be annulus-shaped.

A catheter apparatus (10) includes a tubular member (11); multiple fluid-flow pipe members (13), each having a proximal end (19) and a distal end (18), and being disposed along a first axial direction of the tubular member; multiple node members (15) disposed along a first axial direction of the tubular member, wherein two adjacent node members (15) form a segment (1a); and a periphery member (14), wherein the periphery member (14) wraps the multiple node members (15) to form a space (1b) with the segment (1a) formed between the two adjacent node members (15). The catheter apparatus (10) can irradiate the entire diffuse tumor during one brachytherapy process without repeated placement of the catheter. Meanwhile, it can be smoothly inserted into the patient's narrow body cavity because there are no external balloons. A brachytherapy system adopts the catheter apparatus (10).

The invention relates to a system and a method for assisting in planning a radiation therapy treatment, the treatment being delivered on the basis of a treatment plan including error-prone parameter values of first treatment parameters. In the system, a robustness evaluation unit (10) obtains planned parameter values of the first treatment parameters, generates perturbed parameter configurations including perturbed values of the first treatment parameters, the perturbed parameter values deviating from the planned parameter values by possible error values of the first treatment parameters occurring during the treatment, and estimates for each perturbed parameter configuration a radiation dose distribution resulting from a treatment delivered on the basis of the perturbed parameter configuration and/or determines the treatment plan on the basis of the perturbed parameter configurations.