1.Doxorubicin Hydrochloride Liposome-Based CHOP Regimen in the Initial Treatment of Elderly Patients with Diffuse Large B-Cell Lymphoma: A Retrospective Study.
Xiang-Dong WANG ; Bo GUO ; Bing ZHAI ; Bo YANG ; Hui FAN ; Xue-Chun LU ; Su-Xia LI ; Hong-Li ZHU
Journal of Experimental Hematology 2021;29(4):1136-1140
OBJECTIVE:
To evaluate the efficacy and safety of CHOP regimen based on doxorubicin hydrochloride liposome in the initial treatment of elderly patients with diffuse large B-cell lymphoma (DLBCL).
METHODS:
Thirty-one patients with DLBCL treated from January 1, 2012 to December 31, 2019 were analyzed retrospectively, their median age was 83 (71-95) years old, and all of them were in Ⅲ-Ⅳ stage, including 17 cases who had international prognostic index (IPI) ≥ 3. The patients were treated with R-CHOP and CHOP regimens based on doxorubicin hydrochloride liposome. The efficacy and safety were evaluated during and after treatment.
RESULTS:
A total of 219 chemotherapy cycles and 7 median cycles were performed in 31 patients. The overall response (OR) rate and complete remission (CR) rate was 80.7% (25/31) and 61.3% (19/31), respectively, as well as 2 cases (6.5%) stable, 4 cases (12.9%) progressive. The main toxicities were as follows: the incidence of grade Ⅲ -Ⅳ neutropenia was 29% (9/31); two patients (6.5%) developed degree Ⅰ-Ⅱ cardiac events, which were characterized by new degree Ⅰ atrioventricular block; there were no cardiac events requiring emergency treatment and discontinuation of chemotherapy. The 1-year, 2-year and 3-year overall survival rate was 83.9%, 77.4% and 61.3%, respectively. The 1-year, 2-year and 3-year progression-free survival rate was 77.4%, 64.5% and 61.3%, respectively.
CONCLUSION
The chemotherapy regimen based on doxorubicin hydrochloride liposome has better efficacy and higher cardiac safety for elderly patients with DLBCL.
Aged
;
Aged, 80 and over
;
Antineoplastic Combined Chemotherapy Protocols
;
Cyclophosphamide/therapeutic use*
;
Doxorubicin/therapeutic use*
;
Humans
;
Liposomes/therapeutic use*
;
Lymphoma, Large B-Cell, Diffuse/drug therapy*
;
Prednisolone
;
Prednisone/therapeutic use*
;
Retrospective Studies
;
Rituximab/therapeutic use*
;
Vincristine/therapeutic use*
2.The Effect of Bcl-6 Expression on the Prognosis of Newly Treated Double-Expressing Lymphoma Treated with R-CHOP Regimen.
Bing-Jie FAN ; Huan CHEN ; Chen-Xing SHANGGUAN ; Xi-Yang LIU ; Yu CHANG ; Lei ZHANG
Journal of Experimental Hematology 2021;29(6):1797-1801
OBJECTIVE:
To compare the treatment outcome and prognosis of the newly-treated myc
METHODS:
152 double-expression lymphoma patients (myc
RESULTS:
The median age of 152 DEL patients was 60.5 years old (15-87 years old). 85 patients (55.9%) were Ann Arbor stage III/IV. There was no significant difference in clinical data between the patients in the two groups. Multivariate Cox regression analysis showed that bcl-6 expression, ECOG score, and stage were the independent prognostic factors for the entire group of DEL patients. There was no statistical difference in ORR between the patients in the two groups (χ2=0.749, P=0.387). Kaplan-Meier survival analysis showed that PFS and OS of the bcl-6
CONCLUSION
bcl-6
Adolescent
;
Adult
;
Aged
;
Aged, 80 and over
;
Antineoplastic Combined Chemotherapy Protocols
;
Cyclophosphamide
;
Doxorubicin
;
Humans
;
Lymphoma, Large B-Cell, Diffuse/drug therapy*
;
Middle Aged
;
Prednisolone
;
Prognosis
;
Vincristine/therapeutic use*
;
Young Adult
3.Clinical Features and Risk Factors of Systemic Lupus Erythematosus Complicated with Cytomegalovirus Infection.
Yu Ting TAN ; Xiao Chun SHI ; Xiao Qing LIU ; Xiao Feng ZENG ; Bao Tong ZHOU
Acta Academiae Medicinae Sinicae 2020;42(6):749-754
Objective To explore the clinical characteristics and risk factors of systemic lupus erythematosus(SLE)complicated with cytomegalovirus infection(CMV). Methods The medical records of patients diagnosed with SLE at discharge in the Department of Immunology at Peking Union Medical College Hospital between July 1,2017 and April 1,2019 were retrospectively reviewed,and the clinical and laboratory data related to CMV infection were analyzed. Results Of the 231 patients with SLE,115(49.8%)had CMV infection.Among them,78(67.8%)were asymptomatic CMV infection and 37(32.2%)were diagnosed with CMV disease.Univariate analysis showed the number of organs involved(
Cyclophosphamide/therapeutic use*
;
Cytomegalovirus Infections/epidemiology*
;
Humans
;
Immunosuppressive Agents/therapeutic use*
;
Lupus Erythematosus, Systemic/drug therapy*
;
Methylprednisolone/therapeutic use*
;
Prednisolone/therapeutic use*
;
Retrospective Studies
;
Risk Factors
;
Serum Albumin, Human/analysis*
4.History and Future of Treatment for Acute Stage Kawasaki Disease
Masahiro ISHII ; Takasuke EBATO ; Hirihisa KATO
Korean Circulation Journal 2020;50(2):112-119
Kawasaki disease is a form of vasculitis, mainly in small and medium arteries of unknown origin, occurring frequently in childhood. It is the leading form of childhood-onset acquired heart disease in developed countries and leads to complications of coronary artery aneurysms in approximately 25% of cases if left untreated. Although more than half a century has passed since Professor Tomisaku Kawasaki's first report in 1957, the cause is not yet clear. Currently, intravenous immunoglobulin therapy has been established as the standard treatment for Kawasaki disease. Various treatment strategies are still being studied under the slogan, “Ending powerful inflammation in the acute phase as early as possible and minimizing the incidence of coronary artery lesions,” as the goal of acute phase treatments for Kawasaki disease. Currently, in addition to immunoglobulin therapy, steroid therapy, therapy using infliximab, biological products, suppression of elastase secretion inside and outside the neutrophils, inactivated ulinastatin therapy and cyclosporine therapy, plasma exchange, etc. are performed. This chapter outlines the history and transition of the acute phase treatment for Kawasaki disease.
Aneurysm
;
Arteries
;
Biological Products
;
Coronary Vessels
;
Cyclosporine
;
Developed Countries
;
Heart Diseases
;
Immunization, Passive
;
Incidence
;
Inflammation
;
Infliximab
;
Mucocutaneous Lymph Node Syndrome
;
Neutrophils
;
Pancreatic Elastase
;
Plasma Exchange
;
Prednisolone
;
Vasculitis
5.Urrets-Zavalia Syndrome Following Trabeculectomy
Gi Seok PARK ; Yeo Kyoung WON ; Kyoung Nam KIM ; Yeon Hee LEE ; Chang sik KIM
Journal of the Korean Ophthalmological Society 2020;61(2):221-225
PURPOSE: We report a case of Urrets-Zavalia syndrome with a fixed dilated pupil after an uneventful trabeculectomy.CASE SUMMARY: Trabeculectomy was performed on a 51-year-old male who had a history of recurrent uveitis in the left eye, with uncontrolled intraocular pressure despite maximally-tolerated medial therapy. There was no unexpected event during surgery. Topical 1% atropine was used for only 2 days after surgery. In the early postoperative period, 1% prednisolone and 0.3% ofloxacin were given four times a day, then gradually reduced. One month later, only 1% prednisolone was given once a day. Intraocular pressure in his left eye was well controlled from 8–14 mmHg after surgery. One month after surgery, the pupils remained dilated. There was no reaction to topical 2% pilocarpine and no relative afferent pupillary defect or posterior synechia.CONCLUSIONS: Our case, although rare, suggests that Urrets-Zavalia syndrome should be considered in patients with well-controlled intraocular pressure after uneventful trabeculectomy.
Atropine
;
Humans
;
Intraocular Pressure
;
Male
;
Middle Aged
;
Ofloxacin
;
Pilocarpine
;
Postoperative Period
;
Prednisolone
;
Pupil
;
Pupil Disorders
;
Trabeculectomy
;
Uveitis
6.A Descriptive Review of Kerion and Non-inflammatory Tinea Capitis
Soo Min KIM ; Young Ah KIM ; Nam Joon CHO
Korean Journal of Dermatology 2019;57(4):182-190
BACKGROUND: Tinea capitis manifests either as a non-inflammatory or inflammatory type including kerion, which may cause permanent alopecia. In addition to antifungals, systemic corticosteroids (prednisolone at 1~2 mg/kg/day) have been used to reduce inflammation in patients with kerion. OBJECTIVE: We studied the clinical and laboratory features, treatments, and prognosis of tinea capitis. METHODS: We performed a retrospective review of 12 cases of kerion and 12 cases of non-inflammatory tinea capitis (median age, 8 years; range, 3 months~80 years) diagnosed using a potassium hydroxide mount at the National Health Insurance Service Ilsan Hospital between November 2011 and April 2018. RESULTS: Fungal cultures showed Microsporum species in 6 cases and Trichophyton species in 1 case. The duration of diseases and extent of lesions were greater in the kerion group than in the non-inflammatory tinea capitis group (p<0.05). Sixteen patients were treated with systemic antifungals. In the kerion group, 10 patients were treated with systemic antifungals (6 with itraconazole [median, 26 days; range, 21~58 days] and 4 with terbinafine [median, 24.5 days; range, 13~31 days]). The median intervals between the onset of treatment and scalp clearing (in 10 cases), the onset of new hair growth (in 9 cases), and complete regrowth of hair (in 7 cases) were 27 (range, 13~77), 33 (range, 19~63), and 89 (range, 42~180) days, respectively, in the kerion group. The median dosage of prednisolone used in patients with kerion was 0.26 mg/kg/day (range, 0.15~0.42) with good clinical response. CONCLUSION: The patients with kerion responded well to antifungal treatments. A lower dose of prednisolone was adequate when systemic corticosteroids were required for the treatment of kerion.
Adrenal Cortex Hormones
;
Alopecia
;
Hair
;
Humans
;
Inflammation
;
Itraconazole
;
Microsporum
;
National Health Programs
;
Potassium
;
Prednisolone
;
Prognosis
;
Retrospective Studies
;
Scalp
;
Tinea Capitis
;
Tinea
;
Trichophyton
7.Erythema Elevatum Diutinum with Various Clinicohistological Stages
Mi Yeon CHO ; Jong Hoon KIM ; You Chan KIM ; Soo Chan KIM
Korean Journal of Dermatology 2019;57(7):387-390
A 61-year-old man presented with a 3-year history of erythematous firm nodules on the hands and feet. Histopathological findings of the lesional skin revealed perivascular and diffuse neutrophilic infiltrations on the upper and mid-dermis. Increased and dilated blood vessels were observed in the upper dermis. Fibrinoid necrosis of the vessel walls was unremarkable, but endothelial swelling and scant red blood cell (RBC) extravasation were noted. Fibrosis and sclerosis of collagen fibers were noted on the deep dermis. Results of laboratory examinations, including complete blood count (CBC), routine chemistry, c-reactive protein (CRP), syphilis and human immunodeficiency virus (HIV) tests, and serum immunoglobulin electrophoresis, were all negative or within normal limit. A diagnosis of erythema elevatum diutinum was made based on the clinical and histological findings. The patient was treated with prednisolone, dapsone, colchicine, and intralesional injection of triamcinolone and showed slight improvement after treatment for 8 months.
Blood Cell Count
;
Blood Vessels
;
C-Reactive Protein
;
Chemistry
;
Colchicine
;
Collagen
;
Dapsone
;
Dermis
;
Diagnosis
;
Electrophoresis
;
Erythema
;
Erythrocytes
;
Fibrosis
;
Foot
;
Hand
;
HIV
;
Humans
;
Immunoglobulins
;
Injections, Intralesional
;
Middle Aged
;
Necrosis
;
Neutrophils
;
Prednisolone
;
Sclerosis
;
Skin
;
Syphilis
;
Triamcinolone
8.Brachial Plexus Injury after Deep Sleep
Jung Min KWAK ; Jun Ho CHOI ; Dong Yoon PARK
Clinical Pain 2019;18(1):44-47
Lying on the side while falling asleep deeply after drinking or taking a sleeping pill can cause compressive neuropathy. We report a 70-year-old male patient of medial cord of left brachial plexus injury (BPI) after deep sleep. The mechanism of the injury might be compression and stretching of brachial plexus. The electrodiagnostic study was performed and the medial cord lesion of BPI was suggested. The ultrasonography image of compression site revealed the nerve swelling of medial cord of brachial plexus and median nerve at the mid-arm level. Pharmacologic treatment including oral prednisolone and exercise training were prescribed. On 6 months after initial visit, neurologic symptom and pain were improved but mild sequelae was remained.
Accidental Falls
;
Aged
;
Brachial Plexus
;
Deception
;
Drinking
;
Electrodiagnosis
;
Humans
;
Male
;
Median Nerve
;
Neurologic Manifestations
;
Prednisolone
;
Ultrasonography
9.Tacrolimus for ulcerative colitis in children: a multicenter survey in Japan
Tadahiro YANAGI ; Kosuke USHIJIMA ; Hidenobu KOGA ; Takeshi TOMOMASA ; Hitoshi TAJIRI ; Reiko KUNISAKI ; Takashi ISIHIGE ; Hiroyuki YAMADA ; Katsuhiro ARAI ; Atsushi YODEN ; Tomoki AOMATSU ; Satoru NAGATA ; Keiichi UCHIDA ; Yoshikazu OHTSUKA ; Toshiaki SHIMIZU
Intestinal Research 2019;17(4):476-485
BACKGROUND/AIMS: Tacrolimus is effective for refractory ulcerative colitis in adults, while data for children is sparse. We aimed to evaluate the effectiveness and safety of tacrolimus for induction and maintenance therapy in Japanese children with ulcerative colitis.METHODS: We retrospectively reviewed the multicenter survey data of 67 patients with ulcerative colitis aged < 17 years treated with tacrolimus between 2000 and 2012. Patients’ characteristics, disease activity, Pediatric Ulcerative Colitis Activity Index (PUCAI) score, initial oral tacrolimus dose, short-term (2-week) and long-term (1-year) outcomes, steroid-sparing effects, and adverse events were evaluated. Clinical remission was defined as a PUCAI score < 10; treatment response was defined as a PUCAI score reduction of ≥ 20 points compared with baseline.RESULTS: Patients included 35 boys and 32 girls (median [interquartile range] at admission: 13 [11–15] years). Thirty-nine patients were steroid-dependent and 26 were steroidrefractory; 20 had severe colitis and 43 had moderate colitis. The initial tacrolimus dose was 0.09 mg/kg/day (range, 0.05–0.12 mg/kg/day). The short-term clinical remission rate was 47.8%, and the clinical response rate was 37.3%. The mean prednisolone dose was reduced from 19.2 mg/day at tacrolimus initiation to 5.7 mg/day at week 8 (P< 0.001). The adverse event rate was 53.7%; 6 patients required discontinuation of tacrolimus therapy.CONCLUSIONS: Tacrolimus was a safe and effective second-line induction therapy for steroid-dependent and steroid-refractory ulcerative colitis in Japanese children.
Adult
;
Asian Continental Ancestry Group
;
Biological Factors
;
Child
;
Colectomy
;
Colitis
;
Colitis, Ulcerative
;
Female
;
Humans
;
Immunologic Factors
;
Japan
;
Prednisolone
;
Remission Induction
;
Retrospective Studies
;
Tacrolimus
;
Ulcer
10.Clinical Manifestations of PFAPA (Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis) Syndrome from a Single Center
Minsoo SHIN ; Eun Hwa CHOI ; Mi Seon HAN
Pediatric Infection & Vaccine 2019;26(3):179-187
PURPOSE: Periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome is a leading cause of periodic fever in children. This study describes the clinical characteristics of PFAPA syndrome in patients from a single center.METHODS: Thirteen children diagnosed with PFAPA syndrome at Seoul National University Children's Hospital were included in this study. Retrospective medical chart reviews were performed.RESULTS: Among the 13 patients, 8 (61.5%) were male. The median follow-up duration was 3.3 years (range, 10 months–8.3 years). The median age of periodic fever onset was 3 years (range, 1–6 years). All patients had at least 5 episodes of periodic fever and pharyngitis, managed with oral antibiotics, before diagnosis. The median occurrence of fever was every 3.9 weeks and lasted for 4.2 days. All patients had pharyngitis and 12 (92.3%) had cervical lymphadenitis. Blood tests were performed for 12 patients, and no patients had neutropenia. Both the C-reactive protein and erythrocyte sedimentation rate were elevated at medians of 4.5 mg/dL (range, 0.4–13.2 mg/dL) and 29 mm/hr (range, 16–49 mm/hr), respectively. Throat swab cultures and rapid streptococcal antigen tests were negative. Nine (69.2%) patients received oral prednisolone at a median dose of 0.8 mg/kg, and in 6 (66.7%) patients, fever resolved within a few hours. Three (23.1%) patients received tonsillectomy and adenoidectomy.CONCLUSIONS: PFAPA syndrome should be considered when a child presents with periodic fever along with aphthous stomatitis, pharyngitis, or cervical lymphadenitis. Glucocorticoid administration is effective for fever resolution and can reduce unnecessary use of antibiotics.
Adenoidectomy
;
Anti-Bacterial Agents
;
Blood Sedimentation
;
C-Reactive Protein
;
Child
;
Diagnosis
;
Fever
;
Follow-Up Studies
;
Hematologic Tests
;
Humans
;
Lymphadenitis
;
Male
;
Neutropenia
;
Pharyngitis
;
Pharynx
;
Prednisolone
;
Retrospective Studies
;
Seoul
;
Stomatitis, Aphthous
;
Tonsillectomy
;
Yemen

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