Biomedical subjects

D D Deshpande

Publications and source records attributed to D D Deshpande.

9 recordsLinked to original sources

PubMed2006

Peripheral dose from uniform dynamic multileaf collimation fields: implications for sliding window intensity-modulated radiotherapy.

The increase in the number of monitor units in sliding window intensity-modulated radiotherapy, compared with conventional techniques for the same target dose, may lead to an increase in peripheral dose (PD). PD from a linear accelerator was measured for 6 MV X-ray using 0.6 cm3 ionization chamber inserted at 5 cm depth into a 35 cm x 35 cm x 105 cm plastic water phantom. Measurements were made for field sizes of 6 cm x 6 cm, 10 cm x 10 cm and 14 cm x 14 cm, shaped in both static and dynamic multileaf collimation (DMLC) mode, employing strip fields of fixed width 0.5 cm, 1.0 cm, 1.5 cm, and 2.0 cm, respectively. The effect of collimator rotation and depth of measurement on peripheral dose was investigated for 10 cm x 10 cm field. Dynamic fields require 2 to 14 times the number of monitor units than does a static open field for the same dose at the isocentre, depending on strip field width and field size. Peripheral dose resulting from dynamic fields manifests two distinct regions showing a crest and trough within 30 cm from the field edge and a steady exponential fall beyond 30 cm. All dynamic fields were found to deliver a higher PD compared with the corresponding static open fields, being highest for smallest strip field width and largest field size; also, the percentage increase observed was highest at the largest out-of-field distance. For 6 cm x 6 cm field, dynamic fields with 0.5 cm and 2 cm strip field width deliver PDs 8 and 2 times higher than that of the static open field. The corresponding factors for 14 cm x 14 cm field were 15 and 6, respectively. The factors by which PD for DMLC fields increase, relative to jaws-shaped static fields for out-of-field distance beyond 30 cm, are almost the same as the corresponding increases in the number of monitor units. Reductions of 20% and 40% in PD were observed when the measurements were done at a depth of 10 cm and 15 cm, respectively. When the multileaf collimator executes in-plane (collimator 90 degrees) motion, peripheral dose decreases by as much as a factor of 3 compared with cross-plane data. The knowledge of PD from DMLC field is necessary to estimate the increase in whole-body dose and the likelihood of radiation induced secondary malignancy.

Humans↗

PubMed2001

Transperineal low-dose rate iridium-192 interstitial brachytherapy in cervical carcinoma stage IIB.

PURPOSE: To assess local control, survival and complications in patients with cervical carcinoma Stage IIB treated radically with transperineal Iridium-192 low-dose rate interstitial brachytherapy following external beam radiotherapy. PATIENTS AND METHODS: 65 women (age 25-70 years, mean 47 years) with cervical carcinoma Stage IIB were initially treated with external beam radiotherapy on a telecobalt or 6 MV linear accelerator to a dose of 50 Gy delivered in 5-6 weeks. After 2-3 weeks of completing external radiation, patients received interstitial brachytherapy with Iridium-192 (activity 0.5-1 mCi/cm) using a Syed-Neblett perineal template. The median dose delivered to the implant volume was 24 Gy (range 20-32 Gy) delivered at an average dose rate of 0.70 Gy/h (range 0.40-1.20 Gy/h). A point defined at 1.5 cm lateral to the central uterine tandem at the level of os was taken as a representative for assessing the dose to the cervix. Mean doses delivered by interstitial brachytherapy to point A, cervix, point B and rectum were 38 Gy, 34 Gy, 16 Gy and 16 Gy, respectively. RESULTS: At a median follow-up of 53 months, the actuarial disease free survival and overall survival for 65 patients at both 5 and 10 years was 64% and 44%, respectively. Response to radiotherapy was a strong predictor of local control with 82% of patients continuing to have pelvic control after initial complete response. Overall, nine (14%) patients had persistent disease, ten (15%) developed a central recurrence after initial control and three patients developed distant metastasis on follow-up. No patient had any immediate treatment-related complication. Late toxicity included grade I-II rectal reactions in five patients and grade IV bladder complication (vesico-vaginal fistula) in two patients. 5 years after treatment, one patient developed intestinal obstruction, which was relieved after conservative management. Two patients developed vaginal stenosis. The 5- and 10-year disease free survival was 48% in patients aged less than 45 years as compared to 80% in patients of more than 45 years (p = 0.009). Dose to the cervical point was a prognostic indicator with 5- and 10-year disease free survival of 47% in patients who received < 35 Gy in comparison to 80% in patients who had > 35 Gy (p = 0.03). There was no difference in local control and survival in patients with minimal and moderate parametrial involvement. Bulky disease (> 4 cm) at presentation and a longer gap between external radiation and brachytherapy showed a trend towards inferior local control. CONCLUSIONS: Interstitial brachytherapy after external beam irradiation in patients with cervical carcinoma Stage IIB results in acceptable local control, survival and complication rates. Increased dose to the cervical disease results in improved local control and survival and should therefore be considered while optimizing brachytherapy treatment plans. Comparison of the results with those of standard intracavitary therapy remains to be proven in a randomized trial.

Adenocarcinoma↗

PubMed2000

Primary carcinoma of the vagina: Tata Memorial Hospital experience.

PURPOSE: Carcinoma of the vagina is a rare gynecological malignancy comprising approximately 2% of all the gynecological malignancies. We have analyzed the treatment outcome of the patients treated at the Tata Memorial Hospital from January 1984 to December 1993. METHODS AND MATERIALS: In this 10-year period, 134 patients of primary vaginal cancers were registered at our hospital. Of these, 75 patients received complete treatment and are analyzed. RESULTS: Disease-free survival (DFS) for the whole group is 50%, and overall survival (OAS) is 60%. Most locoregional recurrences and distant failures are noted in the 2 years following treatment. DFS at 5 years is as follows: Stage I (5 patients), Stage IIA (37 patients), Stage IIB (15 patients), Stage III (14 patients), and Stage IV (4 patients); are 40%, 55%, 60%, 50%, and 25%, respectively. The DFS for patients with complete response (42 patients) to external radiation at 5 years is 68%, with partial response (25 patients) is 35%, and with poor or no response (6 patients) is 18% (p = 0.0000). We observed that brachytherapy was an important part of the treatment, and patients who received brachytherapy (59 patients), either with a vaginal intracavitary applicator (30 patients) or interstitial implant (29 patients) had a DFS of 53% and 56%, respectively, while 15 patients who received external radiation alone had a DFS of 30%. Patients receiving brachytherapy within 4 weeks of external radiation had a DFS of 60% as compared to 30% when the interval was more than 4 weeks. CONCLUSION: The factors indicating prognosis are: site and extent of involvement, presence of lymph nodes at presentation, technique of brachytherapy, and interval between external radiation and brachytherapy.

Adolescent↗

PubMed1997

Dosimetry of intracavitary applications in carcinoma of the cervix: rectal dose analysis.

The International Commission on Radiation Units and Measurements (ICRU), in its Report-38, has given certain recommendations regarding the specifications of bladder and rectal reference points in the intracavitary treatment of carcinoma of the cervix. Conforming to this report, 182 intracavitary applications performed in stage I and II cervix cases were analyzed. In 113 applications, the maximum rectal dose was found to be in a point on the anteroposterior line drawn through the centre of colpostat sources. However, for our type of applications, the point on the anteroposterior line drawn through the lower end of the uterine tube seldom gets maximum dose. In addition, it was observed that there are other dose points than the ICRU reference point receiving doses close to maximum dose. It was concluded that doses to multiple rectal reference points should be recorded, in addition to the ICRU-defined rectal reference point.

Brachytherapy↗

PubMed1996

Geometrical considerations in dose volume analysis in intracavitary treatment.

PURPOSE: The present work was aimed at to study the relationship between the volume enclosed by reference isodose surface and various geometrical parameters of the intracavitary applicator in treatment of carcinoma of cervix. MATERIAL AND METHODS: Pearshape volume of the reference isodose derived from the Total Reference Air Kerma (TRAK) and the product of its dimensions, height H, width W and thickness T which is dependent on the applicator geometry, were estimated for 100 intracavitary applications treated by Selectron LDR machine. Orthogonal radiographs taken for each patient were used for measurement of actual geometric dimensions of the applicator and carrying out the dosimetry on TP-11 treatment planning system. The dimensions H, W and T of reference isodose surface (60 Gy) were also noted. RESULTS: Ratio of the product HWT and the pearshape volume was found mainly to be a function of colpostat separation and not of other geometrical parameters like maximum vertical and anterio-posterior dimension of the applicator. The ratio remained almost constant for a particular combination of uterine tandem and colpostat. Variation in the ratios were attributed to the non-standard geometry. CONCLUSION: The ratio of the volume of reference isodose surface to the product of its dimensions in the applicator depends upon the colpostat separation.

Brachytherapy↗

PubMed1996

Design and comparison of wedge shaped midline block with rectangular block used in early stage cervical cancers.

PURPOSE: Design of an universal wedge shaped midline block for early stage cervical cancers to get uniform dose distribution around the target volume. MATERIAL AND METHODS: The method of fabrication of wedge shaped midline block is discussed for treatment of early stage cervical cancers based on the configuration of 137Cs pellets used in intracavitary applications and along with external photon beams obtained by using 60Co teletherapy machine and 6 and 10 MV linear accelerators. RESULTS: The dosimetric measurements are carried out to confirm the adequacy of thickness and shape of the block using radiation field analyzer for all the 3 energies. DISCUSSION: The dose distribution comparison has been made with wedge shaped midline block and conventional rectangular shields to show its superiority in getting homogeneous dose distribution around target volume. The shift in 184 intracavitary applications is analyzed in actual clinical applications with respect to central axis of external beams and its comparison is made with both types of blocks. With the shift of 1 cm towards lateral from midline an overdose can occur upto 12 Gy at certain points with rectangular block compared to wedge shaped midline block. CONCLUSION: Since the preparation of individual wedge shaped midline block for every application will be a difficult process for busy centers, the single wedge shaped midline block for each energy is more convenient to handle for busy centers instead of individualized compensating blocks for every intracavitary application.

Brachytherapy↗

PubMed1994

Treatment volume from total reference air kerma (TRAK) in intracavitory applications and its comparison with ICRU reference volume.

PURPOSE: A systematic dosimetry study conforming to International Commission on Radiation Units and Measurements Report Number 38, was carried out for, cancer of Cervix Stage I and II cases at Tata Memorial Hospital. METHODS AND MATERIALS: The reference Volume dimension were noted for each applicator. Also 3-D dosimetry was performed for selected cases, and actual geometric volume enclosed by various isodose surfaces were obtained. A relation was derived, which gave the volume enclosed by any isodose surface as a function of total reference air kerma of the sources in the applicator. The volume enclosed by reference isodose surface was compared with the product of its dimensions height, width, and thickness. RESULTS: The volume enclosed by any isodose surface of an intracavitary application can be easily derived from total reference air kerma of the sources within the applicator. CONCLUSION: Ratio of the volume enclosed by reference isodose surface with the product of its dimensions (HWT) could be a predictive parameter for clinical outcome, besides the reference volume specified by the report.

Brachytherapy↗

PubMed1993

CT assisted computation of collimator angle and importance of off-axis planning of inclined lesions.

In the radiation treatment of inclined lesions the longitudinal axis of beam should be always parallel to the longitudinal axis of lesion in the treatment plane. Hence the choice of correct collimator angle is of prime importance in the oblique field off-axis treatment planning of inclined lesions. In this paper a graphical method is discussed to determine the collimator angles from the CT scans taken at different off-axis planes. A phantom was constructed which can simulate conditions like inclined lesion in the patient and CT scans were taken at different levels. The collimator angles estimated from CT scans are found to match with the collimator angles obtained from simulator within +/- 1 degree for various gantry angles. The method is applied to plan a case of cancer of the oesophagus (upper third), which is a typical example of inclined lesion.

Humans↗

PubMed1992

Endobronchial brachytherapy: a preliminary experience.

Fourteen patients with malignant airway obstruction were treated with a placement of a flexible nylon catheter for low dose rate manual afterloading Iridium 192 endobronchial brachytherapy using a flexible fibreoptic bronchoscope. Eight patients had obstructive pneumonitis at initial presentation, while 6 cases were recurrences after previous external irradiation. Six evaluable patients of the former group had complete or partial reinflation of lung and were followed by external radiotherapy. Of the latter group, 3 were evaluable and had moderate to good palliation of their symptoms. No complication was observed. The technique is simple and safe with good patient compliance. Further evaluation is indicated to assess its role in the locoregional management of lung cancer.

Airway Obstruction↗