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Featured researches published by Wenli Dong.


Bone Marrow Transplantation | 2015

Low-, medium- and high-dose steroids with or without aminocaproic acid in adult hematopoietic SCT patients with diffuse alveolar hemorrhage

Nisha Rathi; Anne Rain Tanner; Andrew Dinh; Wenli Dong; Lei Feng; Joe Ensor; Suzy Wallace; Sajid A. Haque; Gabriela Rondon; Kristen J. Price; Uday Popat; Joseph L. Nates

Diffuse alveolar hemorrhage (DAH) is a poorly understood complication of transplantation carrying a high mortality. Patients commonly deteriorate and require intensive care unit (ICU) admission. Treatment with high-dose steroids and aminocaproic acid (ACA) has been suggested. The current study examined 119 critically ill adult hematopoietic transplant patients treated for DAH. Patients were subdivided into low-, medium- and high-dose steroid groups with or without ACA. All groups had similar baseline characteristics and severity of illness scores. Primary objectives were 30, 60, 100 day, ICU and hospital mortality. Overall mortality (n=119) on day 100 was high at 85%. In the steroids and ACA cohort (n=82), there were no significant differences in 30, 60, 100, day, ICU and hospital mortality between the dosing groups. In the steroids only cohort (n=37), the low-dose steroid group had a lower ICU and hospital mortality (P=0.02). Adjunctive treatment with ACA did not produce differences in outcomes. In the multivariate analysis, medium- and high-dose steroids were associated with a higher ICU mortality (P=0.01) as compared with the low-dose group. Our data suggest that treatment strategies may need to be reanalyzed to avoid potentially unnecessary and potentially harmful therapies.


Clinical Lymphoma, Myeloma & Leukemia | 2013

Zoledronic acid for prevention of bone loss in patients receiving primary therapy for lymphomas: A prospective, randomized controlled phase III trial

Jason R. Westin; Michael A. Thompson; Vince D. Cataldo; Luis Fayad; Nathan Fowler; Michelle A. Fanale; Saatva Neelapu; Felipe Samaniego; Jorge Romaguera; Jatin J. Shah; Peter McLaughlin; Barbara Pro; Larry W. Kwak; Perpetua Sanjorjo; William A. Murphy; Camillo Jimenez; Bela B. Toth; Wenli Dong; Fredrick B. Hagemeister

UNLABELLEDnIn patients with newly diagnosed lymphoma, low bone mineral density (BMD) is common at diagnosis and worsens with therapy. Our randomized phase III trial demonstrates that 2 doses of zoledronic acid (ZA) and supplementation with calcium and vitamin D effectively prevent further bone loss.nnnBACKGROUNDnPatients with lymphoma are at risk of development of bone mineral density (BMD) loss from therapy with high-dose corticosteroids and alkylating agents. Zoledronic acid (ZA), a bisphosphonate, may prevent this complication of therapy. We evaluated the effect of ZA on the change in BMD and surrogate biomarkers in patients with lymphoma receiving initial chemotherapy.nnnPATIENTS AND METHODSnOur phase III trial randomized 74 patients with newly diagnosed lymphoma and a baseline BMD of ≥ -2.0 to receive oral calcium and vitamin D daily with or without ZA at enrollment and at 6 months after enrollment. BMD was evaluated at baseline and 1 year after enrollment. Secondary biomarker endpoints were collected at baseline and at 3, 6, 9, and 12 months after enrollment.nnnRESULTSnForty-three percent of patients had baseline osteopenia. Fifty-three patients were evaluable for response: 24 received ZA and had stable BMD during the observation period, whereas 29 patients in the control group had decreased BMD (P < .05 at lumbar spine and bilateral femoral neck). Twenty-one randomized patients were not evaluable for response because of lymphoma progression or death, withdrawn consent/incomplete testing, or ineligibility. Bone biomarkers were higher in the control group at all intervals after treatment (P < .001). No fractures or intervention-related toxicities were observed during this trial.nnnCONCLUSIONSnNewly diagnosed patients with lymphoma are at risk of low BMD, which may worsen with therapy. Treatment with ZA effectively stabilizes BMD and prevents bone loss. Our data suggest that BMD testing and prophylaxis should be considered as an early intervention for a preventable problem.


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.


International Journal of Radiation Oncology Biology Physics | 2017

Chemotherapy Response Assessment by FDG-PET-CT in Early-stage Classical Hodgkin Lymphoma: Moving Beyond the Five-Point Deauville Score

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

PURPOSEnIn early-stage classical Hodgkin lymphoma, fluorodeoxyglucose positron emission tomography (PET)-computed tomography (CT) scans are performed routinely after chemotherapy, and the 5-point Deauville score is used to report the disease response. We hypothesized that other PET-CT parameters, considered in combination with Deauville score, would improve risk stratification.nnnMETHODS AND MATERIALSnPatients treated for stage I to II Hodgkin lymphoma from 2003 to 2013, who were aged ≥18xa0years and had analyzable PET-CT scans performed before and after chemotherapy, were eligible. The soft tissue volume (STV), maximum standardized uptake value, metabolic tumor volume, and total lesion glycolysis were recorded from the PET-CT scans before and after chemotherapy. Reductions were defined as 1xa0-xa0(final PET-CT value)/(corresponding initial PET-CT value). The primary endpoint was freedom from progression (FFP).nnnRESULTSnFor 202 patients treated with chemotherapy with or without radiation therapy, the 5-year FFP was 89% (95% confidence interval 85%-93%). All PET-CT parameters were strongly associated with the Deauville score (P<.001) and FFP (P<.0001) on univariate analysis. The Deauville score was highly predictive of FFP (C-index 0.89) but was less discriminating in the Deauville 1 to 4 subset (C-index 0.67). Therefore, we aimed to identify PET-CT parameters that would improve risk stratification for this subgroup (n=187). STV reduction was predictive of outcomexa0(C-index 0.71) and was dichotomized with an optimal cutoff of 0.65 (65% reduction in STV). A model incorporating the Deauville score and STV reduction predicted FFP more accurately than either measurement alone in the Deauville 1 to 4 subset (C-index 0.83). The improvement in predictive accuracy of this composite measure compared with the Deauville score alone met statistical significance (P=.045).nnnCONCLUSIONSnThe relative reduction in tumor size is an independent predictor of outcome. Combined with the Deauville score, it might improve risk stratification and contribute to response-adapted individualization of therapy.


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.


Practical radiation oncology | 2017

Craniospinal irradiation prior to stem cell transplant for hematologic malignancies with CNS involvement: Effectiveness and toxicity after photon or proton treatment ☆

Jillian R. Gunther; Ahmad R. Rahman; Wenli Dong; Zeinab Abou Yehia; Partow Kebriaei; Gabriela Rondon; Chelsea C. Pinnix; S.A. Milgrom; Pamela K. Allen; Bouthaina S. Dabaja; Grace L. Smith

PURPOSE/OBJECTIVE(S)nCraniospinal irradiation (CSI) improves local control of leukemia/lymphoma with central nervous system (CNS) involvement; however, for adult patients anticipating stem cell transplant (SCT), cumulative treatment toxicity is a major concern. We evaluated toxicities and outcomes for patients receiving proton or photon CSI before SCT.nnnMETHODS AND MATERIALSnWe identified 37 consecutive leukemia/lymphoma patients with CNS involvement who received CSI before SCT at our institution. Photon versus proton toxicities during CSI, transplant, and through 100 days posttransplant were compared using Fisher exact and Wilcoxon rank sum tests. Long-term neurotoxicity, disease response, and overall survival were analyzed.nnnRESULTSnThirty-seven patients (23 photon, 14 proton) underwent CSI for CNS involvement of acute lymphoblastic leukemia (49%), acute myeloblastic leukemia (22%), chronic lymphocytic leukemia (3%), chronic myelocytic leukemia (14%), lymphoma (11%), and myeloma (3%). CSI was used for consolidation (30 patients, 81%) and gross disease treatment (7 patients, 19%). Median radiation dose (interquartile range) was 24 Gy (23.4-24) for photons and 21.8 Gy (21.3-23.6) for protons (P = .03). Proton CSI was associated with lower rates of Radiation Therapy Oncology Group grade 1-3 mucositis during CSI (7% vs 44%, P = .03): 1 grade 3 with protons versus 5 grade 1, 3 grade 2, and 2 grade 3 with photons. During CSI, other toxicities (infection, gastrointestinal symptoms) did not differ. Allogeneic stem cell transplant (SCT) was used in 95% of patients, with 53% of patients in remission before SCT. Myeloablative conditioning was used for 76%. During SCT admission and 100 days post-SCT, toxicities did not differ by CSI technique. Successful engraftment occurred in 95% of patients (P = .67). Progression or death occurred for 47% of patients, with only 1 CNS relapse.nnnCONCLUSIONnIn our cohort, CSI offered excellent local control for CNS-involved hematologic malignancies in the pre-SCT setting. Acute mucositis occurred less frequently with proton CSI with comparable peritransplant/long-term toxicity profile, suggesting the need to further explore the benefit/toxicity profile of this technique.


International Journal of Radiation Oncology Biology Physics | 2016

Prognostic Significance of the Postchemotherapy Positron Emission Tomography (PET)/Computed Tomography in Early-Stage Hodgkin Lymphoma: Can PET-Positive Patients Be Cured With Radiation Alone?

S.A. Milgrom; Grace L. Smith; Chelsea C. Pinnix; Wenli Dong; Mani Akhtari; Osama Mawlawi; Eric Rohren; Naveen Garg; Hubert H. Chuang; Jay P. Reddy; Jillian R. Gunther; Eleanor M. Osborne; Z. Abou Yehia; Yasuhiro Oki; Michelle A. Fanale; Bouthaina S. Dabaja


International Journal of Radiation Oncology Biology Physics | 2016

Postchemotherapy Positron Emission Tomography/Computed Tomography Scans in Early-Stage Hodgkin Lymphoma: Moving Beyond the Deauville 5-Point Scale

S.A. Milgrom; Wenli Dong; Mani Akhtari; Grace L. Smith; Chelsea C. Pinnix; Osama Mawlawi; Eric Rohren; Naveen Garg; Hubert H. Chuang; Z. Abou Yehia; Jay P. Reddy; Jillian R. Gunther; Eleanor M. Osborne; Yasuhiro Oki; Michelle A. Fanale; Bouthaina S. Dabaja


International Journal of Radiation Oncology Biology Physics | 2016

Restratifying Early-Stage Hodgkin Lymphoma Patients Using Novel Functional Imaging Parameters

Mani Akhtari; Jay P. Reddy; Wenli Dong; S.A. Milgrom; Grace L. Smith; Chelsea C. Pinnix; Z. Abou Yehia; Jillian R. Gunther; Eleanor M. Osborne; Osama Mawlawi; Eric Rohren; Hubert H. Chuang; Naveen Garg; Michelle A. Fanale; Bouthaina S. Dabaja

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Bouthaina S. Dabaja

University of Texas MD Anderson Cancer Center

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Chelsea C. Pinnix

University of Texas MD Anderson Cancer Center

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Grace L. Smith

University of Texas MD Anderson Cancer Center

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Jay P. Reddy

University of Texas MD Anderson Cancer Center

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Jillian R. Gunther

University of Texas MD Anderson Cancer Center

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Michelle A. Fanale

University of Texas MD Anderson Cancer Center

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S.A. Milgrom

University of Texas MD Anderson Cancer Center

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Eleanor M. Osborne

University of Texas MD Anderson Cancer Center

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Eric Rohren

Baylor College of Medicine

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Hubert H. Chuang

University of Texas MD Anderson Cancer Center

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