Network


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

Hotspot


Dive into the research topics where Hsiang Chun Chen is active.

Publication


Featured researches published by Hsiang Chun Chen.


Urologic Oncology-seminars and Original Investigations | 2015

Percentage of sarcomatoid component as a prognostic indicator for survival in renal cell carcinoma with sarcomatoid dedifferentiation

Mehrad Adibi; Arun Z. Thomas; Leonardo D. Borregales; Megan M. Merrill; Rebecca S. Slack; Hsiang Chun Chen; Kanishka Sircar; Paari Murugan; Pheroze Tamboli; Eric Jonasch; Nizar M. Tannir; Surena F. Matin; Christopher G. Wood; Jose A. Karam

OBJECTIVE Renal cell carcinoma with sarcomatoid dedifferentiation (sRCC) is associated with higher stage of presentation and worse survival. The objective of this study was to examine the clinicopathologic characteristics associated with overall survival (OS), specifically examining the percentage of sarcomatoid component (PSC). METHODS We reviewed clinicopathologic data for all nephrectomized patients with confirmed sRCC. Histologic slides were rereviewed by dedicated genitourinary pathologists to ascertain PSC. Patient characteristics were tabulated overall and by disease stage. Cutpoints in the PSC providing a meaningful difference in OS were identified by recursive partitioning analysis (RPA). Factors selected included age group, gender, race, clinical stage, tumor histology, presurgical systemic therapy, lymphovascular invasion, and tumor size. The Kaplan-Meier method and log-rank test were used to assess differences in OS. RESULTS Among 186 patients with sRCC, 64 (34%) had localized, and 122 (66%) had metastatic disease at presentation. Patients had primarily clear cell histology (73%). Median follow-up was 12.1 months (range: 0.1-242.2mo). Median OS was 12.6 months (95% CI: 10.7-14.9mo). Univariate RPA identified a PSC cutpoint of 10% as prognostically significant. Patients with PSC>10% were at higher risk of death when compared with patients with PSC≤10% (45% vs. 61% 1-y OS; P = 0.04). Multivariate RPA revealed that tumor size, presence of metastatic disease, and PSC were significantly associated with OS. Among 4 identified groups, patients with localized disease and tumor size≤10cm were most likely to be alive at 1 year (89%), and patients with metastatic disease and PSC>40% were least likely to be alive at 1 year (28%; P<0.001). CONCLUSION PSC appears to be a prognostic factor in patients with sRCC, with larger percentage of involvement portending a worse survival, especially in patients with metastatic disease.


Oncology | 2016

Metastatic Gastroesophageal Adenocarcinoma Patients Treated with Systemic Therapy Followed by Consolidative Local Therapy: A Nomogram Associated with Long-Term Survivors

Hironori Shiozaki; Rebecca S. Slack; Hsiang Chun Chen; Elena Elimova; Venkatram Planjery; Nick Charalampakis; Roopma Wadhwa; Yusuke Shimodaira; Heath D. Skinner; Jeffrey H. Lee; Brian Weston; Manoop S. Bhutani; Mariela Blum-Murphy; Jane E. Rogers; Dipen M. Maru; Aurelio Matamoros; Tara Sagebiel; Jeannelyn S. Estrella; Prajnan Das; Wayne L. Hofstetter; Jeannette E. Mares; Dilsa Mizrak Kaya; Kazuto Harada; Quan Lin; Bruce D. Minsky; Brian D. Badgwell; Jaffer A. Ajani

Objective: Patients with metastatic gastroesophageal adenocarcinoma (MGEAC) have a poor but heterogeneous clinical course. Some patients have an unusually favorable outcome. We sought to identify clinical variables associated with more favorable outcomes. Methods: Of 246 patients with MGEAC, we identified 64 who received systemic therapy and eventually received local consolidation therapy. Univariate and multivariate Cox regression models were used, and a nomogram was developed. Results: Of these 64 patients, 61% had received consolidation chemoradiation (CRT) with doses of 50-55 Gy and 78% did not undergo surgery. The median follow-up time of survivors was 3.9 years, and the median overall survival (OS) from CRT start was 1.5 years (95% CI, 1.2-2.2). Surgery (as local consolidation) was an independent prognosticator for longer OS in the multivariate analysis (p = 0.02). The 5-year OS rate was 25% (SE = 6%). The contributors to the nomogram were longer duration of systemic therapy before CRT and the type of local therapy. Conclusions: Our data suggest that a subset of patients with MGEAC have an excellent prognosis (OS >5 years). However, these patients need to be identified during their clinical course so that local consolidation (CRT, surgery, or both) may be offered.


Journal of Surgical Oncology | 2016

Prognosis of gastric adenocarcinoma patients with various burdens of peritoneal metastases

Hironori Shiozaki; Elena Elimova; Rebecca S. Slack; Hsiang Chun Chen; Gregg Staerkel; Nour Sneige; Yusuke Shimodaira; Tara Sagebiel; Jeffrey H. Lee; Manoop S. Bhutani; Prajnan Das; Paul F. Mansfield; Jeannelyn S. Estrella; Brian D. Badgwell; Jaffer A. Ajani

Peritoneal metastases (PM) in patients with gastric adenocarcinoma (GAC) may be identified by diagnostic laparoscopy (DL) or imaging (I). Although prognosis is poor, some patients have excellent outcome. We compared the overall survival (OS) of patients in 3 groups: those with positive cytology (CY+) by DL (DL‐CY+), those with gross PM (GPM) by DL (DL‐GPM+) and with GPM obvious on I (I‐GPM+).


Oncologist | 2015

Hypertension and Circulating Cytokines and Angiogenic Factors in Patients With Advanced Non-Clear Cell Renal Cell Carcinoma Treated With Sunitinib: Results From a Phase II Trial

Mehmet Asim Bilen; Amado J. Zurita; Nasreen A. Ilias-Khan; Hsiang Chun Chen; Xuemei Wang; Alper Y. Kearney; Sherie Hodges; Eric Jonasch; Shixia Huang; Aarif Y. Khakoo; Nizar M. Tannir

BACKGROUND We evaluated the significance of hypertension developing during vascular endothelial growth factor (VEGF) receptor tyrosine kinase inhibitor (VEGFR-TKI) treatment and a group of cytokines and angiogenic factors (CAFs) in advanced non-clear cell renal cell carcinoma (nccRCC) patients treated with sunitinib in a phase II study. MATERIALS AND METHODS Using multiplex assays, we analyzed the levels of 38 CAFs in plasma at baseline and after 4 weeks of sunitinib therapy. Sunitinib benefit was defined as a partial response or stable disease using the Response Evaluation Criteria in Solid Tumors lasting ≥4 months. Cox proportional hazards regression models were used to assess the associations among hypertension, CAFs, and progression-free (PFS) and overall survival (OS). RESULTS Fifty-seven patients were evaluable; 53 had baseline CAF levels available. The median PFS and OS were 2.9 months (95% confidence interval [CI], 1.4-5.5) and 16.8 months (95% CI, 10.7-27.4), respectively. Sunitinib benefit was observed in 21 patients (37%). However, 33 patients (60%) developed hypertension during treatment, although no association was found with survival or response. Elevated baseline soluble tumor necrosis factor (TNF) receptor I, interleukin-8, growth-regulated oncogene, transforming growth factor-α, and VEGFR-2 levels were associated with an increased risk of death on multivariate analysis. CONCLUSION We found no association between the development of hypertension and survival or sunitinib benefit in advanced nccRCC. TNF and angiogenic/immunomodulatory mediators were identified for evaluation as markers of prognosis and VEGFR-TKI benefit in future studies.


Journal of Gastrointestinal Surgery | 2018

Central Lymph Node Metastasis in Gastric Cancer Is Predictive of Survival After Preoperative Therapy

Naruhiko Ikoma; Jeannelyn S. Estrella; Mariela A. Blum; Prajnan Das; Hsiang Chun Chen; Xuemei Wang; Keith F. Fournier; Paul F. Mansfield; Jaffer A. Ajani; Brian D. Badgwell

BackgroundIt is unclear how preoperative therapy for gastric cancer affects the metastasis rate of lymph nodes (LNs) and whether the location of positive LNs affects survival after preoperative therapy. Therefore, we determined the association between positive central lymph nodes (CnLNs) and disease stage and overall survival (OS).MethodsWe reviewed a prospectively maintained database to identify patients who had undergone resection of gastric adenocarcinoma at our institution from 2005 to 2015. CnLNs were defined as common hepatic, celiac, and proximal splenic artery LNs (stations no. 8, 9, and 11p). The frequency of CnLN metastases and risk factors affecting OS were examined.ResultsWe identified 356 patients. Preoperative therapy was administered to 66% of patients. D2 LN dissection was performed in 80% of patients, and the median number of LNs examined was 25 (IQR, 18–34). In 243 patients (68%), CnLNs had undergone separate pathologic examination; the CnLN-positive rate was 9.1% (22 of 243; station no. 8, 4.5%; no. 9, 2.1%; and no. 11p, 4.8%). CnLN metastasis was associated with shorter 3-year OS in patients with pN2/3 disease (33 vs. 62%; p = 0.004). Among patients who had undergone preoperative therapy, ypT3–4 stage (HR 2.44; p = 0.01) and positive CnLNs (HR 5.44; p < 0.001) were negatively associated with OS by multivariate analysis.ConclusionsCnLN metastases are uncommon in gastric cancer and have an adverse effect on OS in patients who have undergone preoperative therapy. Larger multi-institutional studies are needed to determine whether CnLN positivity requires a separate staging category after preoperative therapy.


BJUI | 2018

Quality of life after brachytherapy or bilateral nerve-sparing robot-assisted radical prostatectomy for prostate cancer: a prospective cohort

Pierre Blanchard; John W. Davis; Steven J. Frank; Jeri Kim; Curtis A. Pettaway; Thomas J. Pugh; Louis L. Pisters; John F. Ward; Seungtaek Choi; Brian F. Chapin; Karen E. Hoffman; Neema Navai; Mary Achim; Sean E. McGuire; Surena F. Matin; Quynh Nhu Nguyen; Usama Mahmood; William J. Graber; Hsiang Chun Chen; Xuemei Wang; Deborah A. Kuban

To provide comparative data on quality of life (QoL) after prostate cancer treatment to help patients make an informed decision regarding their choice of treatment.


BJUI | 2018

Baseline and longitudinal plasma caveolin-1 level as a biomarker in active surveillance for early-stage prostate cancer

Spyridon P. Basourakos; John W. Davis; Brian F. Chapin; John F. Ward; Curtis A. Pettaway; Louis L. Pisters; Neema Navai; Mary Achim; Xuemei Wang; Hsiang Chun Chen; Seungtaek Choi; Deborah A. Kuban; Patricia Troncoso; Sam M. Hanash; Timothy C. Thompson; Jeri Kim

To evaluate the role of caveolin‐1 (Cav‐1) as a predictor of disease reclassification (DR) in men with early prostate cancer undergoing active surveillance (AS).


Oncotarget | 2017

Patterns of relapse in patients with localized gastric adenocarcinoma who had surgery with or without adjunctive therapy: Costs and effectiveness of surveillance

Elena Elimova; Rebecca S. Slack; Hsiang Chun Chen; Venkatram Planjery; Hironori Shiozaki; Yusuke Shimodaira; Nick Charalampakis; Quan Lin; Kazuto Harada; Roopma Wadhwa; Jeannelyn S. Estrella; Dilsa Mizrak Kaya; Tara Sagebiel; Jeffrey H. Lee; Brian Weston; Manoop S. Bhutani; Mariela A. Blum Murphy; Aurelio Matamoros; Bruce D. Minsky; Prajnan Das; Paul F. Mansfield; Brian D. Badgwell; Jaffer A. Ajani

Purpose After therapy of localized gastric adenocarcinoma (GAC) patients, the costs of surveillance, relapse patterns, and possibility of salvage are unknown. Materials and Methods We identified 246 patients, who after having a negative peritoneal staging, received therapy (any therapy which included surgery) and were surveyed (every 3–6 months in the first 3 years, then yearly; ∼10 CTs and ∼7 endoscopies per patient). We used the 2016 Medicare dollars reimbursed as the “costs” for surveillance. Results Common features were: Caucasians (57%), men (60%), poorly differentiated histology (76%), preoperative chemotherapy (74%), preoperative chemoradiation (59%), and had surgery (100%). At a median follow-up of 3.7 years (range, 0.1 to 18.3), the median overall survival (OS) was 9.2 years (95% CI, 6.0 to 11.2). Tumor grade (p = 0.02), p/yp stage (p < 0.001), % residual GAC (p = 0.05), the R status (p = 0.01), total gastrectomy (p = 0.001), and relapse type (p = 0.02) were associated with OS. Relapse occurred in 79 (32%) patients (only 8% were local-regional) and 90% occurred within 36 months of surgery. P/yp stage (p < 0.001) and total gastrectomy (p = 0.01) were independent prognosticators for OS in the multivariate analysis. Only 1 relapsed patient had successful salvage therapy. The estimated reimbursement for imaging studies and endoscopies was


Oncology | 2015

Early versus Delayed Therapy of Advanced Gastric Cancer Patients - Does It Make a Difference?

Elena Elimova; Hironori Shiozaki; Rebecca S. Slack; Hsiang Chun Chen; Roopma Wadhwa; Kazuki Sudo; Nikolaos Charalampakis; Adarsh Hiremath; Jeannelyn S. Estrella; Aurelio Matamoros; Tara Sagebiel; Prajnan Das; Jane E. Rogers; Jeana L. Garris; Mariela A. Blum; Brian D. Badgwell; Jaffer A. Ajani

1,761,221.91 (marked underestimation of actual costs). Conclusions The median OS of localized GAC patients was excellent with infrequent local-regional relapses. Rigorous surveillance had a low yield and high “costs”. Our data suggest that less frequent surveillance intervals and limiting expensive investigations to symptomatic patients may be warranted.


Gastric Cancer | 2018

Preoperative chemoradiation therapy induces primary-tumor complete response more frequently than chemotherapy alone in gastric cancer: analyses of the National Cancer Database 2006–2014 using propensity score matching

Naruhiko Ikoma; Prajnan Das; Wayne L. Hofstetter; Jaffer A. Ajani; Jeannelyn S. Estrella; Hsiang Chun Chen; Xuemei Wang; Rashida A. Callender; Cong Zhu; Christina L. Roland; Keith F. Fournier; Janice N. Cormier; Paul F. Mansfield; Brian D. Badgwell

Background: Nearly 50% of gastric cancer patients are diagnosed with advanced gastric cancer (AGC). Therapy is palliative but results in ill effects. The median overall survival (OS) of AGC patients is often <12 months. It is unclear if the early initiation of therapy in all AGC patients is beneficial. Methods: A retrospective analysis of AGC patients in our database was carried out. The patients were divided into two groups: asymptomatic or symptomatic. We sought to assess whether the delay of systemic therapy was harmful in asymptomatic patients. Results: A total of 135 patients were analyzed. Most patients were symptomatic (68%), males (67%), and had low ECOG scores (0-1; 85%). In univariate analyses, ECOG performance status 0 (p = 0.005), delayed initiation of therapy (p = 0.03), and lack of symptoms (p = 0.03) were associated with a longer OS. The multivariate model for OS identified only ECOG performance status as an independent prognosticator of longer OS (p = 0.02). Asymptomatic patients who had delayed (≥4 weeks) systemic therapy had an OS rate of 77% at 1 year compared to 58% for patients treated within 4 weeks (p = 0.47). Conclusion: Symptomatic AGC patients had a poor outcome compared to asymptomatic AGC patients. Treatment delay in asymptomatic patients had no detrimental effect on OS, suggesting that the timing of therapy can be based on patient selection.

Collaboration


Dive into the Hsiang Chun Chen's collaboration.

Top Co-Authors

Avatar

Xuemei Wang

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Jaffer A. Ajani

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Prajnan Das

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Brian D. Badgwell

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Jeannelyn S. Estrella

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Usama Mahmood

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Paul F. Mansfield

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Rebecca S. Slack

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Deborah A. Kuban

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar

Elena Elimova

University of Texas MD Anderson Cancer Center

View shared research outputs
Researchain Logo
Decentralizing Knowledge