Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Jay P. Reddy is active.

Publication


Featured researches published by Jay P. Reddy.


International Journal of Radiation Oncology Biology Physics | 2015

Predictors of Radiation Pneumonitis in Patients Receiving Intensity-Modulated Radiation Therapy for Hodgkin and Non-Hodgkin Lymphoma

Chelsea C. Pinnix; Grace L. Smith; S.A. Milgrom; Eleanor M. Osborne; Jay P. Reddy; Mani Akhtari; Valerie Klairisa Reed; I. Arzu; Pamela K. Allen; Christine F. Wogan; Michele A. Fanale; Yasuhiro Oki; Francesco Turturro; Jorge Romaguera; Luis Fayad; Nathan Fowler; Jason R. Westin; Loretta J. Nastoupil; Fredrick B. Hagemeister; M. Alma Rodriguez; Sairah Ahmed; Yago Nieto; Bouthaina S. Dabaja

PURPOSE Few studies to date have evaluated factors associated with the development of radiation pneumonitis (RP) in patients with Hodgkin lymphoma (HL) and non-Hodgkin lymphoma (NHL), especially in patients treated with contemporary radiation techniques. These patients represent a unique group owing to the often large radiation target volumes within the mediastinum and to the potential to receive several lines of chemotherapy that add to pulmonary toxicity for relapsed or refractory disease. Our objective was to determine the incidence and clinical and dosimetric risk factors associated with RP in lymphoma patients treated with intensity modulated radiation therapy (IMRT) at a single institution. METHODS AND MATERIALS We retrospectively reviewed clinical charts and radiation records of 150 consecutive patients who received mediastinal IMRT for HL and NHL from 2009 through 2013. Clinical and dosimetric predictors associated with RP according to Radiation Therapy Oncology Group (RTOG) acute toxicity criteria were identified in univariate analysis using the Pearson χ(2) test and logistic multivariate regression. RESULTS Mediastinal radiation was administered as consolidation therapy in 110 patients with newly diagnosed HL or NHL and in 40 patients with relapsed or refractory disease. The overall incidence of RP (RTOG grades 1-3) was 14% in the entire cohort. Risk of RP was increased for patients who received radiation for relapsed or refractory disease (25%) versus those who received consolidation therapy (10%, P=.019). Several dosimetric parameters predicted RP, including mean lung dose of >13.5 Gy, V20 of >30%, V15 of >35%, V10 of >40%, and V5 of >55%. The likelihood ratio χ(2) value was highest for V5 >55% (χ(2) = 19.37). CONCLUSIONS In using IMRT to treat mediastinal lymphoma, all dosimetric parameters predicted RP, although small doses to large volumes of lung had the greatest influence. Patients with relapsed or refractory lymphoma who received salvage chemotherapy and hematopoietic stem cell transplantation were at higher risk for symptomatic RP.


Stem Cells Translational Medicine | 2014

Simvastatin Radiosensitizes Differentiated and Stem-Like Breast Cancer Cell Lines and Is Associated With Improved Local Control in Inflammatory Breast Cancer Patients Treated With Postmastectomy Radiation

Lara Lacerda; Jay P. Reddy; Diane Liu; Richard A. Larson; Li Li; Hiroko Masuda; Takae Brewer; Bisrat G. Debeb; Wei Xu; Gabriel N. Hortobagyi; Thomas A. Buchholz; Naoto Ueno; Wendy A. Woodward

Reported rates of local failure after adjuvant radiation for women with inflammatory breast cancer (IBC) and triple‐negative non‐IBC are higher than those of women with receptor‐expressing non‐IBC. These high rates of locoregional recurrence are potentially influenced by the contribution of radioresistant cancer stem cells to these cancers. Statins have been shown to target stem cells and improve disease‐free survival among IBC patients. We examined simvastatin radiosensitization of multiple subtypes of breast cancer cell lines in vitro in monolayer and mammosphere‐based clonogenic assays and examined the therapeutic benefit of statin use on local control after postmastectomy radiation (PMRT) among IBC patients. We found that simvastatin radiosensitizes mammosphere‐initiating cells (MICs) of IBC cell lines (MDA‐IBC3, SUM149, SUM190) and of the metaplastic, non‐IBC triple‐negative receptor cell line (SUM159). However, simvastatin radioprotects MICs of non‐IBC cell lines MCF‐7 and SKBR3. In a retrospective clinical study of 519 IBC patients treated with PMRT, 53 patients used a statin. On univariate analysis, actuarial 3‐year local recurrence‐free survival (LRFS) was higher among statin users, and on multivariate analysis, triple negative breast cancer, absence of lymphatic invasion, neoadjuvant pathological tumor response to preoperative chemotherapy, and statin use were independently associated with higher LRFS. In conclusion, patients with IBC and triple‐negative non‐IBC breast cancer have the highest rates of local failure, and there are no available known radiosensitizers. We report significant improvement in local control after PMRT among statin users with IBC and significant radiosensitization across triple‐negative and IBC cell lines of multiple subtypes using simvastatin. These data suggest that simvastatin should be justified as a radiosensitizing agent by a prospective clinical trial.


Leukemia & Lymphoma | 2016

Primary cutaneous B-cell lymphoma (non-leg type) has excellent outcomes even after very low dose radiation as single-modality therapy.

Mani Akhtari; Jay P. Reddy; Chelsea C. Pinnix; Pamela K. Allen; Eleanor M. Osborne; Jillian R. Gunther; S.A. Milgrom; Grace L. Smith; Christine F. Wogan; Nathan Fowler; Maria Alma Rodriguez; Bouthaina S. Dabaja

Primary cutaneous B cell lymphomas (PCBCL) are rare; although data on outcomes and treatment are limited, traditionally they have been treated with radiation doses in excess of 24 Gy. We retrospectively identified and reviewed all cases of PCBCL treated at our institution from 2002–2014. Thirty-nine patients with PCBCL (42 lesions) were identified. Radiation was the only treatment for most patients. All lesions had a complete response and none had in-field failures; seven patients had out-of-field relapses, three of which were salvaged with radiation therapy. No differences in PFS or OS were found for patients given low-dose (≤ 12 Gy) versus high-dose (> 12 Gy) radiation. PCBCL is an indolent entity with a long clinical course and excellent response to radiation therapy and successful salvage of recurrent disease, even when doses are as low as 4 Gy. Given the above findings, we recommend the initial use of low-dose irradiation for PCBCL.


Leukemia & Lymphoma | 2017

Radiation therapy improves survival in patients with testicular diffuse large B-cell lymphoma*

Jennifer C. Ho; Bouthaina S. Dabaja; Sarah A. Milgrom; Grace L. Smith; Jay P. Reddy; Ali Mazloom; Ken H. Young; Lijuan Deng; L. Jeffrey Medeiros; Wenli Dong; Pamela K. Allen; T.Y. Andraos; Nathan Fowler; Loretta J. Nastoupil; Yasuhiro Oki; Luis Fayad; Francesco Turturro; Sattva S. Neelapu; Jason R. Westin; Fredrick B. Hagemeister; Maria Alma Rodriguez; Chelsea C. Pinnix

Abstract In 120 Stage I–IV testicular diffuse large B-cell lymphoma (DLBCL) patients treated from 1964 to 2015, we assessed the benefits of prophylactic contralateral testicular radiation (RT) and prophylactic central nervous system (CNS) therapy on overall, progression free, testicular relapse free, and CNS relapse free survival (OS, PFS, TRFS, and CRFS, respectively). Seventy percent of patients received RT, 53% received anthracyclines and rituximab (modern therapy), and 61% received CNS prophylaxis. On univariate analysis RT was associated with improved TRFS, PFS, and trended toward improved OS. On multivariate analysis (MVA), RT was significantly associated with improved OS and PFS; the PFS benefit persisted among patients receiving modern therapy. CNS prophylaxis was associated with improved OS, PFS, and TRFS, but not CRFS on univariate analysis, and was not significant on MVA. RT is associated with improved survival, and should be considered for all testicular DLBCL patients, but additional strategies are needed to prevent CNS relapse.


Clinical Lung Cancer | 2017

Influence of Surveillance PET/CT on Detection of Early Recurrence After Definitive Radiation in Stage III Non–small-cell Lung Cancer

Jay P. Reddy; Chad Tang; Tina Shih; Bumyang Kim; Charissa Kim; Quynh Nhu Nguyen; James W. Welsh; Marcelo F. Benveniste; Jianjun Zhang; Zhongxing Liao; Daniel R. Gomez

Background There are few data to support the use of varying imaging modalities in evaluating recurrence in non–small‐cell lung cancer (NSCLC). We compared the efficacy of surveillance positron emission tomography (PET)/computed tomography (CT) versus CT scans of the chest in detecting recurrences after definitive radiation for NSCLC. Materials and Methods We retrospectively analyzed 200 patients treated between 2000 and 2011 who met the inclusion criteria of stage III NSCLC, completion of definitive radiation treatment, and absence of recurrence within the initial 6 months. These patients were then grouped on the basis of the use of PET/CT imaging during postradiation surveillance. Patients who received ≥ 1 PET/CT scans within 6 months of the end of radiation treatment were placed in the PET group whereas all others were placed in the CT group. We compared survival times from the end of treatment to the date of death or last follow‐up using log rank tests. Multivariate analysis was conducted to identify factors associated with decreased survival. Results In the entire cohort, median event‐free survival (EFS) was 26.7 months, and median overall survival (OS) was 41.2 months. The CT group had a median EFS of 21.4 months versus 29.4 months for the PET group (P = .59). There was no difference in OS between the CT and PET groups (median OS of 41.2 and 41.3 months, respectively; P = .59). There was also no difference in local recurrence‐free survival or distant metastases‐free survival between the CT‐only and PET/CT groups (P = .92 and P = .30, respectively). Similarly, in multivariate analysis, stratification into the PET group was not associated with improved EFS (hazard ratio [HR], 0.90; 95% confidence interval [CI], 0.61‐1.34; P = .60) or OS (HR, 1.2; 95% CI, 0.83‐1.7; P = .34). Conclusions In stage III NSCLC patients treated with definitive radiation and without early recurrence, PET/CT scan surveillance did not result in decreased time to detection of locoregional or distant recurrence or improved survival. Micro‐Abstract To determine the optimal surveillance approach in the setting of locally‐advanced non–small‐cell lung cancer (NSCLC) treated with definitive radiation, we compared 2 commonly used strategies, positron emission tomography (PET)/computed tomography (CT)‐based and CT‐based. There were no differences in baseline clinical or treatment characteristics or any of the survival outcomes examined between the 2 groups. These results suggest that routine PET/CT imaging after definitive radiation treatment for locally‐advanced NSCLC confers no benefit in early detection of recurrence.


Radiotherapy and Oncology | 2015

Antiepileptic drug use improves overall survival in breast cancer patients with brain metastases in the setting of whole brain radiotherapy

Jay P. Reddy; Shaheenah Dawood; Melissa Mitchell; Bisrat G. Debeb; Elizabeth S. Bloom; Ana M. Gonzalez-Angulo; Erik P. Sulman; Thomas A. Buchholz; Wendy A. Woodward

BACKGROUND AND PURPOSE There is mounting evidence that histone deacetylase (HDAC) inhibitors, e.g. valproic acid (VPA), synergize with radiation to improve outcomes in several cancers. This study was conducted to ascertain whether VPA affected outcomes in breast cancer patients with brain metastases treated with whole brain radiotherapy (WBRT). MATERIALS AND METHODS Records from 253 breast cancer patients with brain metastases treated with WBRT were reviewed. Data regarding use of all antiepileptic drugs (AEDs) were extracted. Kaplan-Meier survival times were calculated using the date of brain involvement as time zero. Cox proportional hazard models were used to determine the association between patient and tumor characteristics and overall survival (OS). RESULTS Median OS for the entire patient cohort was 6 months. Patients receiving VPA (n=20) had a median OS of 11 months versus 5 months for those not receiving VPA (p=0.028). Median OS was 9 months for patients taking any AED (n=101) versus 4 months for those not taking AEDs (p=0.0003). On multivariate analysis both VPA and AED use were associated with improved OS (HR 0.61, p=0.0419; HR 0.59, p=0.0002, respectively). CONCLUSIONS This study suggests the use of AEDs, including VPA, is associated with improved OS in breast cancer patients with brain metastases following WBRT.


British Journal of Haematology | 2018

Pre-treatment neutrophil/lymphocyte ratio and platelet/lymphocyte ratio are prognostic of progression in early stage classical Hodgkin lymphoma

Jay P. Reddy; Mike Hernandez; Jillian R. Gunther; Bouthaina S. Dabaja; Geoffrey V. Martin; Wen Jiang; Mani Akhtari; Pamela K. Allen; Bradley J. Atkinson; Grace L. Smith; Chelsea C. Pinnix; Sarah A. Milgrom; Zeinab Abou Yehia; Eleanor M. Osborne; Yasuhiro Oki; Hun Lee; Fredrick B. Hagemeister; Michelle A. Fanale

To determine whether pre‐treatment neutrophil/lymphocyte (NLR) or platelet/lymphocyte ratios (PLR) are predictive for progression in early‐stage classical Hodgkin lymphoma (cHL), we derived NLR and PLR values for 338 stage I/II cHL patients and appropriate cut‐off point values to define progression. Two‐year freedom from progression (FFP) for patients with NLR ≥6·4 was 82·2% vs. 95·7% with NLR <6·4 (P < 0·001). Similarly, 2‐year FFP was 84·3% for patients with PLR ≥266·2 vs. 96·1% with PLR <266·2 (P = 0·003). On univariate analysis, both NLR and PLR were significantly associated with worse FFP (P = 0·001). On multivariate analysis, PLR remained a significant, independent prognostic factor (P < 0·001).


British Journal of Haematology | 2017

Early-stage Hodgkin lymphoma outcomes after combined modality therapy according to the post-chemotherapy 5-point score: can residual pet-positive disease be cured with radiotherapy alone?

Sarah A. Milgrom; Chelsea C. Pinnix; Hubert H. Chuang; Yasuhiro Oki; Mani Akhtari; Osama Mawlawi; Naveen Garg; Jillian R. Gunther; Jay P. Reddy; Grace L. Smith; Eric Rohren; Frederick B. Hagemeister; Hun J. Lee; Luis Fayad; Wenli Dong; Eleanor M. Osborne; Zeinab Abou Yehia; Michelle A. Fanale; Bouthaina S. Dabaja

Early‐stage classical Hodgkin lymphoma (HL) patients are evaluated by an end‐of‐chemotherapy positron emission tomography‐computed tomography (eoc‐PET‐CT) after doxorubicin, bleomycin, vinblastine and dacarbazine (ABVD) and before radiation therapy (RT). We determined freedom from progression (FFP) in patients treated with ABVD and RT according to the eoc‐PET‐CT 5‐point score (5PS). Secondarily, we assessed whether patients with a positive eoc‐PET‐CT (5PS of 4–5) can be cured with RT alone. The cohort comprised 174 patients treated for stage I‐II HL with ABVD and RT alone. ABVD was given with a median of four cycles and RT with a median dose of 30·6 Gy. Five‐year FFP was 97%. Five‐year FFP was 100% (0 relapses/98 patients) for patients with a 5PS of 1–2, 97% (2/65) for a 5PS of 3, 83% (1/8) for a 5PS of 4, and 67% (1/3) for a 5PS of 5 (P < 0·001). Patients with positive eoc‐PET‐CT scans who were selected for salvage RT alone had experienced a very good partial response to ABVD. Risk factors for recurrence in this subgroup included a small reduction in tumour size and a ‘bounce’ in ≥1 PET‐CT parameter (reduction then rise from interim to final scan). Thus, a positive eoc‐PET‐CT is associated with inferior FFP; however, appropriately selected patients can be cured with RT alone.


Blood | 2017

Reclassifying patients with early-stage Hodgkin lymphoma based on functional radiographic markers at presentation

Mani Akhtari; Sarah A. Milgrom; Chelsea C. Pinnix; Jay P. Reddy; Wenli Dong; Grace L. Smith; Osama Mawlawi; Zeinab Abou Yehia; Jillian R. Gunther; Eleanor M. Osborne; T.Y. Andraos; Christine F. Wogan; Eric Rohren; Naveen Garg; Hubert H. Chuang; Joseph D. Khoury; Yasuhiro Oki; Michelle A. Fanale; Bouthaina S. Dabaja

The presence of bulky disease in Hodgkin lymphoma (HL), traditionally defined with a 1-dimensional measurement, can change a patients risk grouping and thus the treatment approach. We hypothesized that 3-dimensional measurements of disease burden obtained from baseline 18F-fluorodeoxyglucose positron emission tomography-computed tomography (PET-CT) scans, such as metabolic tumor volume (MTV) and total lesion glycolysis (TLG), would more accurately risk-stratify patients. To test this hypothesis, we reviewed pretreatment PET-CT scans of patients with stage I-II HL treated at our institution between 2003 and 2013. Disease was delineated on prechemotherapy PET-CT scans by 2 methods: (1) manual contouring and (2) subthresholding of these contours to give the tumor volume with standardized uptake value ≥2.5. MTV and TLG were extracted from the threshold volumes (MTVt, TLGt) and from the manually contoured soft-tissue volumes. At a median follow-up of 4.96 years for the 267 patients evaluated, 27 patients were diagnosed with relapsed or refractory disease and 12 died. Both MTVt and TLGt were highly correlated with freedom from progression and were dichotomized with 80th percentile cutoff values of 268 and 1703, respectively. Consideration of MTV and TLG enabled restratification of early unfavorable HL patients as having low- and high-risk disease. We conclude that MTV and TLG provide a potential measure of tumor burden to aid in risk stratification of early unfavorable HL patients.


Journal of Cancer | 2017

Impact of statin use on outcomes in triple negative breast cancer

Simona F. Shaitelman; Michael C. Stauder; Pamela K. Allen; Sangeetha M. Reddy; Susan Lakoski; Bradley J. Atkinson; Jay P. Reddy; Diana Amaya; William Guerra; Naoto Ueno; Abigail S. Caudle; Welela Tereffe; Wendy A. Woodward

Purpose: We sought to investigate if the use of HMG Co-A reductase inhibitors (statins) has an impact on outcomes among patients with triple negative breast cancer (TNBC). Methods: We reviewed the cases of women with invasive, non-metastatic TNBC, diagnosed 1997-2012. Clinical outcomes were compared based on statin use (defined as ever use during treatment vs. never use). We identified a subset of women for whom a 5-value lipid panel (5VLP) was available, including total cholesterol, low density lipoprotein, high density lipoprotein, very low density lipoprotein, and triglycerides. The Kaplan-Meier method was used to estimate median overall survival (OS), distant metastases-free survival (DMFS), and local-regional recurrence-free survival (LRRFS). A Cox proportional hazards regression model was used to test the statistical significance of prognostic factors. Results: 869 women were identified who met inclusion criteria, with a median follow-up time of 75.1 months (range 2.4-228.9 months). 293 (33.7%) patients used statins and 368 (42.3%) had a 5VLP. OS, DMFS, and LRRFS were not significant based on statin use or type. Controlling for the 5VLP values, on multivariable analysis, statin use was significantly associated with OS (HR 0.10, 95% CI 0.01-0.76), but not with DMFS (HR 0.14, 95% CI 0.01-1.40) nor LRRFS (HR 0.10 95% CI 0.00-3.51). Conclusions: Statin use among patients with TNBC is not associated with improved OS, although it may have a benefit for a subset of patients. Prospective assessment would be valuable to better assess the potential complex correlation between clinical outcome, lipid levels, and statin use.

Collaboration


Dive into the Jay P. Reddy's collaboration.

Top Co-Authors

Avatar

Bouthaina S. Dabaja

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Chelsea C. Pinnix

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Grace L. Smith

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Mani Akhtari

University of Texas Medical Branch

View shared research outputs
Top Co-Authors

Avatar

S.A. Milgrom

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Eleanor M. Osborne

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Jillian R. Gunther

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Michelle A. Fanale

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Pamela K. Allen

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Wendy A. Woodward

University of Texas MD Anderson Cancer Center

View shared research outputs
Researchain Logo
Decentralizing Knowledge