Suneil Jain | Queen's University Belfast (original) (raw)

Papers by Suneil Jain

Research paper thumbnail of Cellular signalling effects in high precision radiotherapy

Physics in medicine and biology, Jan 7, 2015

Radiotherapy is commonly planned on the basis of physical dose received by the tumour and surroun... more Radiotherapy is commonly planned on the basis of physical dose received by the tumour and surrounding normal tissue, with margins added to address the possibility of geometric miss. However, recent experimental evidence suggests that intercellular signalling results in a given cell's survival also depending on the dose received by neighbouring cells. A model of radiation-induced cell killing and signalling was used to analyse how this effect depends on dose and margin choices. Effective Uniform Doses were calculated for model tumours in both idealised cases with no delivery uncertainty and more realistic cases incorporating geometric uncertainty. In highly conformal irradiation, a lack of signalling from outside the target leads to reduced target cell killing, equivalent to under-dosing by up to 10% compared to large uniform fields. This effect is significantly reduced when higher doses per fraction are considered, both increasing the level of cell killing and reducing margin se...

Research paper thumbnail of The effect of radiation technique and bladder filling on the acute toxicity of pelvic radiotherapy for localized high risk prostate cancer

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology, 2012

The goal of this project was to see if using IMRT to deliver elective pelvic nodal irradiation (E... more The goal of this project was to see if using IMRT to deliver elective pelvic nodal irradiation (EPNI) for prostate cancer reduced acute treatment toxicity. Two hundred and thirty patients were enrolled into prospective trials delivering EPNI with a concomitant hypofractionated IMRT boost to the prostate. During accrual, the method of EPNI delivery changed as new literature emerged. Three methods were used (1) 4FB, (2) IMRT with 2cm CTV margins around the pelvic vessels as suggested by Shih et al. (2005) [7] (IMRT-Shih), and (3) IMRT with nodal volumes suggested by the RTOG (IMRT-RTOG). Initially patients were treated with an empty bladder, with the remainder treated with bladder full. Patients in the 4FB group had higher rates of grade 2 acute GI toxicities compared to the IMRT-Shih and IMRT-RTOG groups (31.9% vs 20.8% vs 7.2%, p=0.0009). Patients in the 4FB group had higher rates of grade 3 urinary frequency compared to the two IMRT groups (8.5% vs 0% vs 0%, p=0.027). However, mult...

Research paper thumbnail of Long-term follow-up of a large active surveillance cohort of patients with prostate cancer

Journal of clinical oncology : official journal of the American Society of Clinical Oncology, Jan 20, 2015

Active surveillance is increasingly accepted as a treatment option for favorable-risk prostate ca... more Active surveillance is increasingly accepted as a treatment option for favorable-risk prostate cancer. Long-term follow-up has been lacking. In this study, we report the long-term outcome of a large active surveillance protocol in men with favorable-risk prostate cancer. In a prospective single-arm cohort study carried out at a single academic health sciences center, 993 men with favorable- or intermediate-risk prostate cancer were managed with an initial expectant approach. Intervention was offered for a prostate-specific antigen (PSA) doubling time of less than 3 years, Gleason score progression, or unequivocal clinical progression. Main outcome measures were overall and disease-specific survival, rate of treatment, and PSA failure rate in the treated patients. Among the 819 survivors, the median follow-up time from the first biopsy is 6.4 years (range, 0.2 to 19.8 years). One hundred forty-nine (15%) of 993 patients died, and 844 patients are alive (censored rate, 85.0%). There w...

Research paper thumbnail of Report from the ASCO Genitourinary Cancers Symposium

Research paper thumbnail of EXPLAINING THE INCREASED USE OF FIRST-LINE CHEMOTHERAPY IN NSCLC PATIENTS IN NORTHERN IRELAND BETWEEN 2004 AND 2007

Research paper thumbnail of Comparison of acute toxicity in patients treated with a 4-field box or IMRT to deliver elective pelvic nodal irradiation for localized high-risk prostate cancer

Research paper thumbnail of PO-0685 ACUTE TOXICITY OF PELVIC AND PROSTATE RADIATION FOR HIGH RISK PROSTATE CANCER: THE IMPACT OF IMRT AND BLADDER FILLING

Research paper thumbnail of Nanoparticle technology: future opportunities in cancer treatment

Research paper thumbnail of Gleason upgrading with time in a large, active surveillance cohort with long-term follow-up

Research paper thumbnail of Gold nanoparticles cause radiosensitization in prostate cancer cell lines in hypoxic conditions

Research paper thumbnail of All that is gold does not glitter, not all those that wander are lost': the dual behaviour of gold nanoparticles in vitro

Research paper thumbnail of Biological consequences of nanoscale energy deposition near irradiated heavy atom nanoparticles

Scientific reports, 2011

Gold nanoparticles (GNPs) are being proposed as contrast agents to enhance X-ray imaging and radi... more Gold nanoparticles (GNPs) are being proposed as contrast agents to enhance X-ray imaging and radiotherapy, seeking to take advantage of the increased X-ray absorption of gold compared to soft tissue. However, there is a great discrepancy between physically predicted increases in X-ray energy deposition and experimentally observed increases in cell killing. In this work, we present the first calculations which take into account the structure of energy deposition in the nanoscale vicinity of GNPs and relate this to biological outcomes, and show for the first time good agreement with experimentally observed cell killing by the combination of X-rays and GNPs. These results are not only relevant to radiotherapy, but also have implications for applications of heavy atom nanoparticles in biological settings or where human exposure is possible because the localised energy deposition high-lighted by these results may cause complex DNA damage, leading to mutation and carcinogenesis.

Research paper thumbnail of Cell type-dependent uptake, localization, and cytotoxicity of 1.9 nm gold nanoparticles

International journal of nanomedicine, 2012

This follow-up study aims to determine the physical parameters which govern the differential radi... more This follow-up study aims to determine the physical parameters which govern the differential radiosensitization capacity of two tumor cell lines and one immortalized normal cell line to 1.9 nm gold nanoparticles. In addition to comparing the uptake potential, localization, and cytotoxicity of 1.9 nm gold nanoparticles, the current study also draws on comparisons between nanoparticle size and total nanoparticle uptake based on previously published data. We quantified gold nanoparticle uptake using atomic emission spectroscopy and imaged intracellular localization by transmission electron microscopy. Cell growth delay and clonogenic assays were used to determine cytotoxicity and radiosensitization potential, respectively. Mechanistic data were obtained by Western blot, flow cytometry, and assays for reactive oxygen species. Gold nanoparticle uptake was preferentially observed in tumor cells, resulting in an increased expression of cleaved caspase proteins and an accumulation of cells ...

Research paper thumbnail of Conventional in vivo irradiation procedures are insufficient to accurately determine tumor responses to non-uniform radiation fields

International journal of radiation biology, Jan 20, 2014

Purpose: To determine differences in overall tumor responses measured by volumetric assessment an... more Purpose: To determine differences in overall tumor responses measured by volumetric assessment and bioluminescence imaging (BLI) following exposure to uniform and non-uniform radiation fields in an ectopic prostate tumor model. Materials and methods: Bioluminescent human prostate tumor xenografts were established by subcutaneous implantation into male mice. Tumors were irradiated with uniform or non-uniform field configurations using conventional in vivo irradiation procedures performed using a 225 kVp generator with custom lead shielding. Tumor responses were measured using Vernier calipers and by BLI using an in vivo imaging system. Survival was defined as the time to quadroupling of pre-treatment tumor volume. Results: The correlation between BLI and tumor volume measurements was found to be different for un-irradiated (R = 0.61), uniformly irradiated (R = 0.34) and partially irradiated (R = 0.30) tumors. Uniformly irradiated tumors resulted in an average tumor growth delay of 60...

Research paper thumbnail of Energy Dependence of Gold Nanoparticle Radiosensitization in Plasmid DNA

The Journal of Physical Chemistry C, 2011

Research paper thumbnail of Gold nanoparticle cellular uptake, toxicity and radiosensitisation in hypoxic conditions

Radiotherapy and Oncology, 2014

Gold nanoparticles (GNPs) are novel agents that have been shown to cause radiosensitisation in vi... more Gold nanoparticles (GNPs) are novel agents that have been shown to cause radiosensitisation in vitro and in vivo. Tumour hypoxia is associated with radiation resistance and reduced survival in cancer patients. The interaction of GNPs with cells in hypoxia is explored. GNP uptake, localization, toxicity and radiosensitisation were assessed in vitro under oxic and hypoxic conditions. GNP cellular uptake was significantly lower under hypoxic than oxic conditions. A significant reduction in cell proliferation in hypoxic MDA-MB-231 breast cancer cells exposed to GNPs was observed. In these cells significant radiosensitisation occurred in normoxia and moderate hypoxia. However, in near anoxia no significant sensitisation occurred. GNP uptake occurred in hypoxic conditions, causing radiosensitisation in moderate, but not extreme hypoxia in a breast cancer cell line. These findings may be important for the development of GNPs for cancer therapy.

Research paper thumbnail of Prostate stereotactic ablative body radiotherapy using a standard linear accelerator: Toxicity, biochemical, and pathological outcomes

Radiotherapy and Oncology, 2013

Biological dose escalation through stereotactic ablative radiotherapy (SABR) holds promise of imp... more Biological dose escalation through stereotactic ablative radiotherapy (SABR) holds promise of improved patient convenience, system capacity and tumor control with decreased cost and side effects. The objectives are to report the toxicities, biochemical and pathologic outcomes of this prospective study. A phase I/II study was performed where low risk localized prostate cancer received SABR 35 Gy in 5 fractions, once weekly on standard linear accelerators. Common Terminology Criteria for Adverse Events v3.0 and Radiation Therapy Oncology Group late morbidity scores were used to assess acute and late toxicities, respectively. Biochemical control (BC) was defined by the Phoenix definition. As of May 2012, 84 patients have completed treatment with a median follow-up of 55 months (range 13-68 months). Median age was 67 years and median PSA was 5.3 ng/ml. The following toxicities were observed: acute grade 3+: 0% gastrointestinal (GI), 1% genitourinary (GU), 0% fatigue; late grade 3+: 1% GI, 1% GU. Ninety-six percent were biopsy negative post-treatment. The 5-year BC was 98%. This novel technique employing standard linear accelerators to deliver an extreme hypofractionated schedule of radiotherapy is feasible, well tolerated and shows excellent pathologic and biochemical control.

Research paper thumbnail of Radiotherapy in the presence of contrast agents: a general figure of merit and its application to gold nanoparticles

Physics in Medicine and Biology, 2008

Research paper thumbnail of Evaluation of cytotoxicity and radiation enhancement using 1.9 nm gold particles: potential application for cancer therapy

Research paper thumbnail of High dose palliative radiotherapy in NSCLC; 27Gy/6# and 39Gy/13# – is there equivalence?

Research paper thumbnail of Cellular signalling effects in high precision radiotherapy

Physics in medicine and biology, Jan 7, 2015

Radiotherapy is commonly planned on the basis of physical dose received by the tumour and surroun... more Radiotherapy is commonly planned on the basis of physical dose received by the tumour and surrounding normal tissue, with margins added to address the possibility of geometric miss. However, recent experimental evidence suggests that intercellular signalling results in a given cell's survival also depending on the dose received by neighbouring cells. A model of radiation-induced cell killing and signalling was used to analyse how this effect depends on dose and margin choices. Effective Uniform Doses were calculated for model tumours in both idealised cases with no delivery uncertainty and more realistic cases incorporating geometric uncertainty. In highly conformal irradiation, a lack of signalling from outside the target leads to reduced target cell killing, equivalent to under-dosing by up to 10% compared to large uniform fields. This effect is significantly reduced when higher doses per fraction are considered, both increasing the level of cell killing and reducing margin se...

Research paper thumbnail of The effect of radiation technique and bladder filling on the acute toxicity of pelvic radiotherapy for localized high risk prostate cancer

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology, 2012

The goal of this project was to see if using IMRT to deliver elective pelvic nodal irradiation (E... more The goal of this project was to see if using IMRT to deliver elective pelvic nodal irradiation (EPNI) for prostate cancer reduced acute treatment toxicity. Two hundred and thirty patients were enrolled into prospective trials delivering EPNI with a concomitant hypofractionated IMRT boost to the prostate. During accrual, the method of EPNI delivery changed as new literature emerged. Three methods were used (1) 4FB, (2) IMRT with 2cm CTV margins around the pelvic vessels as suggested by Shih et al. (2005) [7] (IMRT-Shih), and (3) IMRT with nodal volumes suggested by the RTOG (IMRT-RTOG). Initially patients were treated with an empty bladder, with the remainder treated with bladder full. Patients in the 4FB group had higher rates of grade 2 acute GI toxicities compared to the IMRT-Shih and IMRT-RTOG groups (31.9% vs 20.8% vs 7.2%, p=0.0009). Patients in the 4FB group had higher rates of grade 3 urinary frequency compared to the two IMRT groups (8.5% vs 0% vs 0%, p=0.027). However, mult...

Research paper thumbnail of Long-term follow-up of a large active surveillance cohort of patients with prostate cancer

Journal of clinical oncology : official journal of the American Society of Clinical Oncology, Jan 20, 2015

Active surveillance is increasingly accepted as a treatment option for favorable-risk prostate ca... more Active surveillance is increasingly accepted as a treatment option for favorable-risk prostate cancer. Long-term follow-up has been lacking. In this study, we report the long-term outcome of a large active surveillance protocol in men with favorable-risk prostate cancer. In a prospective single-arm cohort study carried out at a single academic health sciences center, 993 men with favorable- or intermediate-risk prostate cancer were managed with an initial expectant approach. Intervention was offered for a prostate-specific antigen (PSA) doubling time of less than 3 years, Gleason score progression, or unequivocal clinical progression. Main outcome measures were overall and disease-specific survival, rate of treatment, and PSA failure rate in the treated patients. Among the 819 survivors, the median follow-up time from the first biopsy is 6.4 years (range, 0.2 to 19.8 years). One hundred forty-nine (15%) of 993 patients died, and 844 patients are alive (censored rate, 85.0%). There w...

Research paper thumbnail of Report from the ASCO Genitourinary Cancers Symposium

Research paper thumbnail of EXPLAINING THE INCREASED USE OF FIRST-LINE CHEMOTHERAPY IN NSCLC PATIENTS IN NORTHERN IRELAND BETWEEN 2004 AND 2007

Research paper thumbnail of Comparison of acute toxicity in patients treated with a 4-field box or IMRT to deliver elective pelvic nodal irradiation for localized high-risk prostate cancer

Research paper thumbnail of PO-0685 ACUTE TOXICITY OF PELVIC AND PROSTATE RADIATION FOR HIGH RISK PROSTATE CANCER: THE IMPACT OF IMRT AND BLADDER FILLING

Research paper thumbnail of Nanoparticle technology: future opportunities in cancer treatment

Research paper thumbnail of Gleason upgrading with time in a large, active surveillance cohort with long-term follow-up

Research paper thumbnail of Gold nanoparticles cause radiosensitization in prostate cancer cell lines in hypoxic conditions

Research paper thumbnail of All that is gold does not glitter, not all those that wander are lost': the dual behaviour of gold nanoparticles in vitro

Research paper thumbnail of Biological consequences of nanoscale energy deposition near irradiated heavy atom nanoparticles

Scientific reports, 2011

Gold nanoparticles (GNPs) are being proposed as contrast agents to enhance X-ray imaging and radi... more Gold nanoparticles (GNPs) are being proposed as contrast agents to enhance X-ray imaging and radiotherapy, seeking to take advantage of the increased X-ray absorption of gold compared to soft tissue. However, there is a great discrepancy between physically predicted increases in X-ray energy deposition and experimentally observed increases in cell killing. In this work, we present the first calculations which take into account the structure of energy deposition in the nanoscale vicinity of GNPs and relate this to biological outcomes, and show for the first time good agreement with experimentally observed cell killing by the combination of X-rays and GNPs. These results are not only relevant to radiotherapy, but also have implications for applications of heavy atom nanoparticles in biological settings or where human exposure is possible because the localised energy deposition high-lighted by these results may cause complex DNA damage, leading to mutation and carcinogenesis.

Research paper thumbnail of Cell type-dependent uptake, localization, and cytotoxicity of 1.9 nm gold nanoparticles

International journal of nanomedicine, 2012

This follow-up study aims to determine the physical parameters which govern the differential radi... more This follow-up study aims to determine the physical parameters which govern the differential radiosensitization capacity of two tumor cell lines and one immortalized normal cell line to 1.9 nm gold nanoparticles. In addition to comparing the uptake potential, localization, and cytotoxicity of 1.9 nm gold nanoparticles, the current study also draws on comparisons between nanoparticle size and total nanoparticle uptake based on previously published data. We quantified gold nanoparticle uptake using atomic emission spectroscopy and imaged intracellular localization by transmission electron microscopy. Cell growth delay and clonogenic assays were used to determine cytotoxicity and radiosensitization potential, respectively. Mechanistic data were obtained by Western blot, flow cytometry, and assays for reactive oxygen species. Gold nanoparticle uptake was preferentially observed in tumor cells, resulting in an increased expression of cleaved caspase proteins and an accumulation of cells ...

Research paper thumbnail of Conventional in vivo irradiation procedures are insufficient to accurately determine tumor responses to non-uniform radiation fields

International journal of radiation biology, Jan 20, 2014

Purpose: To determine differences in overall tumor responses measured by volumetric assessment an... more Purpose: To determine differences in overall tumor responses measured by volumetric assessment and bioluminescence imaging (BLI) following exposure to uniform and non-uniform radiation fields in an ectopic prostate tumor model. Materials and methods: Bioluminescent human prostate tumor xenografts were established by subcutaneous implantation into male mice. Tumors were irradiated with uniform or non-uniform field configurations using conventional in vivo irradiation procedures performed using a 225 kVp generator with custom lead shielding. Tumor responses were measured using Vernier calipers and by BLI using an in vivo imaging system. Survival was defined as the time to quadroupling of pre-treatment tumor volume. Results: The correlation between BLI and tumor volume measurements was found to be different for un-irradiated (R = 0.61), uniformly irradiated (R = 0.34) and partially irradiated (R = 0.30) tumors. Uniformly irradiated tumors resulted in an average tumor growth delay of 60...

Research paper thumbnail of Energy Dependence of Gold Nanoparticle Radiosensitization in Plasmid DNA

The Journal of Physical Chemistry C, 2011

Research paper thumbnail of Gold nanoparticle cellular uptake, toxicity and radiosensitisation in hypoxic conditions

Radiotherapy and Oncology, 2014

Gold nanoparticles (GNPs) are novel agents that have been shown to cause radiosensitisation in vi... more Gold nanoparticles (GNPs) are novel agents that have been shown to cause radiosensitisation in vitro and in vivo. Tumour hypoxia is associated with radiation resistance and reduced survival in cancer patients. The interaction of GNPs with cells in hypoxia is explored. GNP uptake, localization, toxicity and radiosensitisation were assessed in vitro under oxic and hypoxic conditions. GNP cellular uptake was significantly lower under hypoxic than oxic conditions. A significant reduction in cell proliferation in hypoxic MDA-MB-231 breast cancer cells exposed to GNPs was observed. In these cells significant radiosensitisation occurred in normoxia and moderate hypoxia. However, in near anoxia no significant sensitisation occurred. GNP uptake occurred in hypoxic conditions, causing radiosensitisation in moderate, but not extreme hypoxia in a breast cancer cell line. These findings may be important for the development of GNPs for cancer therapy.

Research paper thumbnail of Prostate stereotactic ablative body radiotherapy using a standard linear accelerator: Toxicity, biochemical, and pathological outcomes

Radiotherapy and Oncology, 2013

Biological dose escalation through stereotactic ablative radiotherapy (SABR) holds promise of imp... more Biological dose escalation through stereotactic ablative radiotherapy (SABR) holds promise of improved patient convenience, system capacity and tumor control with decreased cost and side effects. The objectives are to report the toxicities, biochemical and pathologic outcomes of this prospective study. A phase I/II study was performed where low risk localized prostate cancer received SABR 35 Gy in 5 fractions, once weekly on standard linear accelerators. Common Terminology Criteria for Adverse Events v3.0 and Radiation Therapy Oncology Group late morbidity scores were used to assess acute and late toxicities, respectively. Biochemical control (BC) was defined by the Phoenix definition. As of May 2012, 84 patients have completed treatment with a median follow-up of 55 months (range 13-68 months). Median age was 67 years and median PSA was 5.3 ng/ml. The following toxicities were observed: acute grade 3+: 0% gastrointestinal (GI), 1% genitourinary (GU), 0% fatigue; late grade 3+: 1% GI, 1% GU. Ninety-six percent were biopsy negative post-treatment. The 5-year BC was 98%. This novel technique employing standard linear accelerators to deliver an extreme hypofractionated schedule of radiotherapy is feasible, well tolerated and shows excellent pathologic and biochemical control.

Research paper thumbnail of Radiotherapy in the presence of contrast agents: a general figure of merit and its application to gold nanoparticles

Physics in Medicine and Biology, 2008

Research paper thumbnail of Evaluation of cytotoxicity and radiation enhancement using 1.9 nm gold particles: potential application for cancer therapy

Research paper thumbnail of High dose palliative radiotherapy in NSCLC; 27Gy/6# and 39Gy/13# – is there equivalence?