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Hastings, Jacquelyn

Mayo Clinic

Mayo Clinic

Citations 10

Miracle of ECMO in Stent Aspiration: A Case Report
Vasistha, Prabhav, Makey, Ian A. , Syin, D., Pang, Maoyin , Hastings, Jacquelyn, Guru, P.K., Bhattacharyya, A., Franco, Pablo Moreno , Osagiede, Osayande

B44. MITIGATING HARM: MANAGING EXPECTED AND UNEXPECTED COMPLICATIONS IN THE ICU | April 30, 2024 | Volume: No volume available | Issue: No issue available | Pages: A3621-A3621

10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a3621 Get It

Successful treatment of IgG4‐related hypertrophic pachymeningitis with induction rituximab and dexamethasone followed by maintenance rituximab
Seegobin, Karan , Moustafa, Muhamad Alhaj , Gannon, Nicole, Keller, Katelyn , Hastings, Jacquelyn, Jiang, Liuyan , Moustafa, Muhamad Alhaj , Tun, Han W. , Gupta, Vivek

Clinical Case Reports | January 27, 2021 | Volume: 9 | Issue: 3 | Pages: 1610-1614

10.1002/ccr3.3855 Get It

AbstractIgG4‐related disease (IgG4RD) with intracranial involvement is rare. We report a 56‐year‐old male who had an excellent response to rituximab and dexamethasone after going undiagnosed for 5 years. After 3 years of rituximab maintenance, he has no evidence of disease on brain MRI.
229: Tele-Monitoring Non-Critically Ill COVID-19 Patients: An Advanced Practice Provider-Led Initiative
Santos, Christan D. , Grek, Ami , Ojard, Michelle, Propst, Joshua, Hastings, Jacquelyn, Krider, Tina L., Villar, Dolores, Sanghavi, Devang , Siegel, Jason , Freeman, William D.

Critical Care Medicine | December 18, 2020 | Volume: 49 | Issue: 1 | Pages: 100-100

10.1097/01.ccm.0000726804.90208.85 Get It

Successful treatment of IgG4-related hypertrophic pachymeningitis with induction rituximab and dexamethasone followed by maintenance rituximab
Moustafa, Muhamad Alhaj , Gannon, Nicole, Keller, Katelyn , Hastings, Jacquelyn, Jiang, Liuyan , Moustafa, Muhamad Alhaj , Seegobin, Karan , Gupta, Vivek , Tun, Han W.

No container title available | September 7, 2020 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.22541/au.159946954.49575788 Get It

IgG4-related disease (IgG4RD) with intracranial involvement is rare. We report a 56-year-old male who had an excellent response to rituximab and dexamethasone after going undiagnosed for 5 years. After 3 years of rituximab maintenance, he has no evidence of disease on brain MRI.
Systemic ALK‐positive anaplastic large cell lymphoma with bilateral optic neurolymphomatosis resulting in permanent blindness
Seegobin, Karan , Moustafa, Muhamad Alhaj , Fischer, Deborah, Keller, Katelyn , Hastings, Jacquelyn, Kharfan‐Dabaja, Mohamed A. , Ayala, Ernesto , Jiang, Liuyan , Moustafa, Muhamad Alhaj , Tun, Han W. , Jiang, Liuyan , Gupta, Vivek

Clinical Case Reports | August 15, 2020 | Volume: 8 | Issue: 12 | Pages: 2629-2633

10.1002/ccr3.3231 Get It

AbstractALK‐positive ALCL can lead to rapid irreversible destruction of the optic pathway. Early treatment should be instituted in patients with CNS involvement or those at increased CNS risk.
Systemic ALK-positive anaplastic large cell lymphoma with bilateral optic neurolymphomatosis resulting in permanent blindness
Moustafa, Muhamad Alhaj , Fischer, Deborah, Keller, Katelyn , Hastings, Jacquelyn, Dabaja, Mohamed Kharfan, Ayala, Ernesto , Jiang, Liuyan , Moustafa, Muhamad Alhaj , Seegobin, Karan , Fischer, Deborah, Tun, Han W.

No container title available | July 7, 2020 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.22541/au.159414342.27789314 Get It

A 26-year-old female developed bilateral blindness after a complete remission for ALK-positive ALCL. Initial workup showed neurolymphomatosis involving the bilateral optic nerves. She underwent hematopoietic cell transplantation and she remained in complete remission after 1 year; however her vision never improved. ALCL likely led to destruction of the optic pathway.
Case report: use of Lenzilumab and Tocilizumab for the Treatment of Coronavirus Disease 2019
Melody, Megan , Nelson, Jared, Hastings, Jacquelyn, Propst, Joshua, Smerina, Michael , Mendez, Julio, Guru, Pramod

Immunotherapy | June 17, 2020 | Volume: 12 | Issue: 15 | Pages: 1121-1126

10.2217/imt-2020-0136 Get It

Primary cutaneous diffuse large B-cell lymphoma, leg-type: The Mayo Clinic experience.
Gannon, Nicole, Hastings, Jacquelyn, Menke, David M. , Kharfan‐Dabaja, Mohamed A. , Ayala, Ernesto , Jiang, Liuyan , Moustafa, Muhamad Alhaj , Parrondo, Ricardo D , Seegobin, Karan , Hoppe, Bradford S. , Tun, Han W.

Journal of Clinical Oncology | May 25, 2020 | Volume: 38 | Issue: 15_suppl | Pages: e20044-e20044

10.1200/jco.2020.38.15_suppl.e20044 Get It

e20044 Background: Primary Cutaneous Diffuse Large B-cell Lymphoma, Leg-type (PCDLBCL) is a rare lymphoma comprising 4% of all cutaneous lymphomas with an aggressive clinical course. We investigated disease characteristics and outcomes among patients PCDLBCL. Methods: Following IRB approval, we identified patients retrospectively with PCDLBCL treated at the Mayo Clinic Cancer Center 1998-2019. Results: 45 pts were identified with a median age of 71 years (Range- 48-95) and 28 (62%) were female. Disease locations were legs (62%), arms (22%), head (11%), trunk (2%) and multiple sites (2%). At diagnosis, (51%) had a single lesion, (29%) had multiple lesions in 1-2 contiguous regions, (16%) had multiple lesions in non-contiguous regions or > 2 regions and data was not available (4%). Immunohistochemistry showed positive staining for BCL-2 (92%), BCL-6 (76%), c-MYC (62%), MUM1 (95%), CD10 (11%), and cytoplasmic IgM (8/9- 89%). By Han’s criteria, (95%) had activated B cell lymphoma (ABC). Median Ki-67 was 90% (range, 50,100%). 9/12 (75%) were positive for MYD88 L265P mutation. 13/21 (62%) were double expressor and 3/22 (14%) had double hit lymphoma. 37/45 (82%) had ECOG < 2. LDH was elevated in 13/37 (35%). The median number of therapies was 1 (range; 1-11). The initial treatments were chemo-radiation (30%), chemo alone (38%), rituximab alone (11%), radiation (RT) alone (16%), rituximab-RT (2.5%), and surgical (2.5%). The median follow-up time for the whole cohort was 80 months (95% CI; 32, 169). The median progression free survival and overall survival (OS) were 20 months (95% CI; 12, 34) and 80 months (95% CI; 48, 119). 22/45 (49%) are alive. The cause of death was disease-related in 11/23 (48%). The median number of relapses was 1 (range; 0, 11) with (60%) relapsed after first line. 4/45 pts had autologous stem cell transplant after relapse. 7/45 (16%) had a systemic relapse at a median time of 35 months from diagnosis (range; 16, 112). Age above 60 years was associated with worse OS; 70 months (95% CI; 30, 99) vs NR (95% CI; 135, NR), p = 0.025. ECOG performance status < 2 was associated with better OS, NR months (95% CI; 80, NR) vs 48 months (95% CI; 3.3, 88),p = 0.0003. 1 pt received Ibrutinib on 11th relapse and had 3 years of PFS. Conclusions: PCDLBCL is predominantly ABC type, affects elderly pts and is characterized by multiple cutaneous relapses followed in some cases by systemic relapses. Increased age and poor performance status had a negative impact on OS. High incidence of MYD88 L265P mutation is observed in PCDLBCL similar to immune-privileged site lymphomas.
Hepatosplenic T-cell lymphoma: The Mayo Clinic experience.
Hastings, Jacquelyn, Gannon, Nicole, Menke, David M. , Kharfan‐Dabaja, Mohamed A. , Ayala, Ernesto , Jiang, Liuyan , Bojanini, Leyla , Moustafa, Muhamad Alhaj , Parrondo, Ricardo D , Seegobin, Karan , Hoppe, Bradford S. , Tun, Han W.

Journal of Clinical Oncology | May 25, 2020 | Volume: 38 | Issue: 15_suppl | Pages: e20036-e20036

10.1200/jco.2020.38.15_suppl.e20036 Get It

e20036 Background: Hepatosplenic T cell lymphoma (HSTL) is a rare subtype of mature T cell lymphomas accounting for less than 1 percent of non-Hodgkin lymphomas. it has been associated with poor prognosis. It typically involves sinusoids in the spleen, liver, and bone marrow. Methods: Following IRB approval, we retrospectively evaluated patients with HSTL treated at the Mayo Clinic Cancer Center 1996-2019. Kaplan-Meier survival analysis and univariate analysis to identify prognostic factors were performed. We investigated clinical characteristics and outcomes among patients with HSTL. Results: 22 patients (15 males) with median age of 45.5 years (range- 15.5-80.6) were identified. The majority of patients had B symptoms (12/22), cyotpenias (20/22), massive splenomegaly (16/22), liver involvement (13/22), and/or bone marrow involvement (14/22). Additionally, 42% tested positive for peripheral blood involvement and 8/22 (36%) were on chronic immunosuppression related to solid organ transplant (2), inflammatory bowel disease (2), and rheumatologic disorders (4). Phenotypically, the majority of patients were positive for gamma/delta (18/22), isochromosome 7q (8/13), and 4/9 (44%) tested positive for trisomy 8. Initial therapies included CHOP/CHOEP (14), ICE (2), EPOCH (1), pentostatin (1), and radiation (1). The median follow-up was 33 months (range 2,137). Progression free survival and overall survival (OS) were 9.5 months (95% CI; 1.8, 16.3) and 12 months (95% CI; 4.9, 18.5) respectively. 10/22 (45%) underwent splenectomy with one patient receiving splenectomy alone as treatment. 8/22 (36%) had stem cell transplant (SCT- 5 allogeneic and 3 autologous). Out of the 22 patients 4 (18%) were long-term survivors with 55, 74, 95, and 137 months; 3/4 had splenectomy at diagnosis and 2/4 had allogeneic SCT. The longest survivor had splenectomy only. Liver involvement was associated with worse OS; 10 months (95% CI; 1.6, 18) vs 35 months (95% CI; 4, NR), p = 0.036. Immune suppression at diagnosis was associated with worse OS; 5 months (95% CI; 1.3, 18) vs 18 months (95% CI; 9, 74), p = 0.036. A trend for better OS was seen with splenectomy and SCT. Conclusions: HSTL is a rare lymphoma with poor prognosis. Long-term survival was seen in 18% only. Liver involvement and immune suppression had a negative impact on OS. A larger cohort is needed to better evaluate the impact of different treatment options.