Citations

Clear

45 citation(s) found for "Goyal, Guarav".

Association between facility volume and mortality of patients with classic Hodgkin lymphoma
Goyal, Gaurav , Tella, Sri Harsha , Funni, Shealeigh A., Kommalapati, Anuhya , Inselman, Jonathan , Shah, Nilay D. , Ansell, Stephen M. , Funni, Shealeigh, Inselman, Jonathan W, Goyal, Guarav , Kommalapati, Anuhya , Go, Ronald S.

Mayo Clinic

Cancer | November 12, 2019 | Volume: 126 | Issue: 4 | Pages: 757-764

10.1002/cncr.32584 | PMID 31714588 Get It

BackgroundPrior studies in oncology have shown that a higher annual facility patient volume is associated with reduced mortality. Because classic Hodgkin lymphoma is uncommon but highly curable, this study used the National Cancer Database (2003‐2014) to analyze whether such a relationship exists for this disease.MethodsThe facilities were classified by quartiles, and random intercepts were used to account for clustering of patients within facilities. A Cox regression model was used to determine the volume‐outcome relationship.ResultsThere were 47,633 patients with classic Hodgkin lymphoma treated at 1310 facilities. The first quartile (Q1), which included 58.4% of the facilities, treated 3 or fewer patients per year, whereas the fourth quartile (Q4), which included 5.9% of the facilities, treated more than 9 patients per year. Compared with the patients treated at Q4 facilities, those treated at lower quartile facilities had a higher risk of death (hazard ratio for the third quartile [HR], 1.19; 95% confidence interval [CI], 1.1‐1.29; HR for the second quartile, 1.28; 95% CI, 1.19‐1.38; HR for Q1, 1.29; 95% CI, 1.2‐1.39) after adjustments for all other factors (P < .0001). Compared with facilities treating 10 patients per year, facilities treating 40 patients per year had approximately 27% lower overall mortality rates.ConclusionsPatients with classic Hodgkin lymphoma treated at high‐volume centers had lower overall mortality than those treated at lower volume centers. Because this is a highly curable malignancy, such differences may suggest a benefit from referral to higher volume facilities or the emulation of their care models.
Concomitant Erdheim‐Chester disease and chronic myelomonocytic leukaemia: genomic insights into a common clonal origin
Goyal, Gaurav , Liu, Yuanhang , Ravindran, Aishwarya , Al‐Kali, Aref , Patnaik, Mrinal M. , Goyal, Guarav , Ravindran, Aishwarya , Go, Ronald S. , Rech, Karen L.

Mayo Clinic

British Journal of Haematology | September 2, 2019 | Volume: 187 | Issue: 2 | Pages: No page available

10.1111/bjh.16177 | PMID 31475353 Get It

Autoimmune Encephalitis Secondary to Melanoma
Daneshmand, Ali , Goyal, Gaurav , Ζεκερίδου, Αναστασία , Hocker, Sara E. , Zekeridou, Anastasia, Goyal, Guarav , Markovic, Svetomir N. , Wijdicks, Eelco F. M.

Mayo Clinic

Annals of Internal Medicine | February 11, 2019 | Volume: 170 | Issue: 12 | Pages: 905-906

10.7326/l18-0593 | PMID 30743260 Get It

Tumor mutational burden and other predictive immunotherapy markers in histiocytic neoplasms
Goyal, Gaurav , Lau, Denise , Nagle, Alison M., Vassallo, Robert , Ryu, Jay H. , Davidge‐Pitts, Caroline , Tobin, W. Oliver , Liu, Minetta C. , Tobin, W Oliver , Goyal, Guarav , Vassallo, Robert , Ryu, Jay H , Rech, Karen L. , Koster, Matthew J. , Bennani, N. Nora , Shah, Meera , Go, Ronald S.

Mayo Clinic

Blood | January 29, 2019 | Volume: 133 | Issue: 14 | Pages: 1607-1610

10.1182/blood-2018-12-893917 | PMID 30696619 Get It

Arterial involvement in Erdheim–Chester disease
Villatoro‐Villar, Michel , Bold, Michael S., Warrington, Kenneth J. , Crowson, Cynthia S. , Goyal, Gaurav , Goyal, Guarav , Warrington, Kenneth J , Shah, Meera , Go, Ronald S. , Koster, Matthew J.

Mayo Clinic

Medicine | December 8, 2018 | Volume: 97 | Issue: 49 | Pages: e13452

10.1097/md.0000000000013452 | PMID 30544428 Get It

Abstract Erdheim-Chester disease (ECD) is a rare histiocytosis of the “L” (Langerhans) group with multisystem involvement that can affect the large and medium-sized arteries mimicking vasculitis. Aortic involvement is common but the frequency and outcome of aortic branch vessel abnormalities are less well described. Patients with ECD were retrospectively identified. Images containing information of arterial involvement within 6 months of diagnosis were considered baseline and compared to last follow-up studies. Two physicians independently reviewed the studies to evaluate for presence of abnormalities attributable to ECD. Age and sex-adjusted logistic regression models were used to examine associations between patient characteristics and vessel involvement at baseline. Among a cohort of 64 patients with ECD, 63 had baseline imaging of vascular structures. ECD involvement of at least 1 segment of the aorta was observed in 56%. Abnormalities were also observed in aortic arch branches (26%), visceral branch arteries (40%), iliofemoral arteries (31%), coronary (5%), and pulmonary (3%) arteries. Perinephric fibrosis was strongly associated with the identification of abnormalities in the thoracic aorta (OR 4.92 [1.54, 15.75]; P = .007), abdominal aorta (OR 7.57 [2.28, 25.07]; P = .001) and visceral branch arteries (OR 6.05 [1.52, 24.03]; P = .01) but not pelvic/lower extremity arteries. Complete normalization of arterial abnormalities at follow-up was only observed in 9% or less of arterial segments involved at baseline. Aortic and aortic branch vessel abnormalities are frequently observed in patients with ECD and are often asymptomatic. Partial and/or complete resolution of arterial findings is uncommon.
Predictors of survival, treatment patterns, and outcomes in histiocytic sarcoma
Kommalapati, Anuhya , Tella, Sri Harsha , Goyal, Gaurav , Goyal, Guarav , Kommalapati, Anuhya , Go, Ronald S.

Mayo Clinic

Leukemia & Lymphoma | July 22, 2018 | Volume: 60 | Issue: 2 | Pages: 553-555

10.1080/10428194.2018.1492128 | PMID 30032691 Get It

A population‐based analysis of second primary malignancies in T‐cell neoplasms
Kommalapati, Anuhya , Tella, Sri Harsha , Goyal, Gaurav , Goyal, Guarav , Kommalapati, Anuhya , Go, Ronald S. , Bennani, N. Nora

Mayo Clinic

British Journal of Haematology | July 5, 2018 | Volume: 185 | Issue: 2 | Pages: 338-342

10.1111/bjh.15451 | PMID 29974935 Get It

Florid dermatopathic lymphadenopathy—A morphological mimic of Langerhans cell histiocytosis
Ravindran, Aishwarya , Goyal, Gaurav , Failing, Jarrett, Failing, Jarrett J, Goyal, Guarav , Ravindran, Aishwarya , Go, Ronald S. , Rech, Karen L.

Mayo Clinic

Clinical Case Reports | June 22, 2018 | Volume: 6 | Issue: 8 | Pages: 1637-1638

10.1002/ccr3.1663 | PMID 30147924 Get It

Key Clinical Message The histopathology of reactive florid dermatopathic lymphadenopathy shows overlap with Langerhans cell histiocytosis ( LCH ) involving the lymph node, which may lead to misdiagnosis. These entities can be distinguished by recognition of the sinus‐based distribution of Langerhans cells in LCH , in contrast to the paracortical distribution of Langerhans cells, pigment‐laden histiocytes, and small lymphocytes in dermatopathic lymphadenopathy.
T cell/histiocyte‐rich large B cell lymphoma: incidence, demographic disparities, and long‐term outcomes
Kommalapati, Anuhya , Tella, Sri Harsha , Nowakowski, Grzegorz S. , Goyal, Gaurav , Goyal, Guarav , Kommalapati, Anuhya , Go, Ronald S.

Mayo Clinic

British Journal of Haematology | May 30, 2018 | Volume: 185 | Issue: 1 | Pages: 140-142

10.1111/bjh.15391 | PMID 29845599 Get It

Neuroradiologic manifestations of Erdheim-Chester disease
Parks, Natalie, Goyal, Gaurav , Mandrekar, Jay , Parks, Natalie E, Goyal, Guarav , Go, Ronald S. , Tobin, W. Oliver

Mayo Clinic

Neurology Clinical Practice | February 13, 2018 | Volume: 8 | Issue: 1 | Pages: 15-20

10.1212/cpj.0000000000000422 | PMID 29517068 Get It