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1.
Asian Pac J Cancer Prev ; 20(4): 987-990, 2019 Apr 29.
Article in English | MEDLINE | ID: mdl-31030464

ABSTRACT

We present the first-ever autologous stem cell transplantation (ASCT) outcome data from a secondary-care healthcare facility. Albeit exact details of patient and disease characteristics and co-morbidity scores for all patients are not available, the engraftment and survival data is very similar to those published from large tertiary-care cancer centres, both regionally and internationally. Transplant Related Mortality (TRM) of 3.1% is within the expected range and includes a patient who died of acute drug reaction (ADR) during conditioning chemotherapy, prior to the ASCT. Furthermore, cyclophosphamide mobilization chemotherapy is given in the outpatient setting. This study is important in terms of healthcare resource optimization as well as patients' convenience and highlights that ASCT can be performed in a safe and effective manner with comparable survival rates even at a DGH, provided the centre stays abreast with the recent developments and can offer its patients with standard of care treatment of the era.


Subject(s)
Hematopoietic Stem Cell Transplantation/mortality , Hospitals, Low-Volume/statistics & numerical data , Lymphoma/mortality , Adult , Aged , Female , Follow-Up Studies , Humans , Lymphoma/classification , Lymphoma/pathology , Lymphoma/therapy , Male , Middle Aged , Prognosis , Retrospective Studies , Survival Rate , Transplantation, Autologous
3.
Ann Hematol ; 94(4): 643-9, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25345871

ABSTRACT

Treatment options are limited in myeloma relapsed or refractory to both bortezomib and lenalidomide (double-relapsed/refractory multiple myeloma; DRMM). Bendamustine is an antitumour agent that has efficacy in relapsed myeloma. We retrospectively analysed data from 30 DRMM patients who received a combination of bendamustine, thalidomide and dexamethasone (BTD) in 28-day treatment cycles. Bendamustine was administered with a cumulative dose of up to 200 mg/m(2). Thalidomide (50-150 mg) was given daily as tolerated, and dexamethasone was given at an equivalent dose of up to 160 mg per cycle. A median of 5 (2-9) treatment cycles were administered per patient. Twenty-six patients (87 %) achieved stable disease or better. At a median follow-up time of 12.1 (2.3-21.5) months, median (95 % CI) progression-free survival and overall survival were 4.0 (2.6-5.3) months and 7.2 (5.2-9.2) months, respectively. The most common grade 3-4 adverse events were haematological: anaemia (n = 8, 34.8 %), neutropenia (n = 16, 69.6 %) and thrombocytopenia (n = 10, 43.5 %). Non-haematological toxicities included pain (n = 3, 13.0 %), infection (n = 7, 30.4 %) and sensory neuropathy (n = 1, 4.3 %). We propose that BTD is a viable salvage treatment option for DRMM patients.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Boronic Acids/therapeutic use , Dexamethasone/administration & dosage , Multiple Myeloma/drug therapy , Nitrogen Mustard Compounds/administration & dosage , Pyrazines/therapeutic use , Salvage Therapy/methods , Thalidomide/analogs & derivatives , Thalidomide/administration & dosage , Aged , Aged, 80 and over , Bendamustine Hydrochloride , Bortezomib , Female , Humans , Lenalidomide , Male , Middle Aged , Multiple Myeloma/mortality , Recurrence , Retrospective Studies , Survival Analysis , Thalidomide/therapeutic use , Treatment Failure
4.
BMJ Case Rep ; 2008: bcr0620080008, 2008.
Article in English | MEDLINE | ID: mdl-21687331

ABSTRACT

A man was admitted with abdominal pain. Treatment for acute diverticulitis was instituted with intravenous antibiotics and oral limitation. Imaging demonstrated a complex inflammatory mass. Prothrombin time (PT), activated partial thromboplastin time (APTT) and fibrinogen were within normal limits. However, repeat preoperative clotting studies demonstrated a severe unexpected coagulopathy to have developed since admission that could have caused fatal intraoperative exsanguination. Direct assays showed severe, isolated deficiency of vitamin K dependent clotting factors, and mixing studies normalised both the PT and APTT, ruling out a coagulation inhibitor. The coagulopathy responded to intravenous vitamin K administration. Dietary insufficiency underlies vitamin K deficiency in the presence of normal biliary and enteral function. A significant coagulopathy can result with additional eradication of intestinal microflora. Hypoprothombinaemia is recognised as a consequence of protracted treatment with broad spectrum antibiotics, and vigilance is required for those at risk. The development of such a rapid and unexpected coagulopathy posed a complex preoperative management issue delaying operative intervention; although avoided by fortuitous preoperative screening, it could have caused significant intraoperative bleeding. The remarkably specific lack of vitamin K dependent clotting factors strongly suggested a vitamin K deficiency and administration of coumarins was ruled out.


Subject(s)
Anti-Bacterial Agents/adverse effects , Hypoprothrombinemias/chemically induced , Vitamin K Deficiency/chemically induced , Aged, 80 and over , Antifibrinolytic Agents/therapeutic use , Diverticulitis/drug therapy , Humans , Hypoprothrombinemias/drug therapy , Male , Vitamin K/therapeutic use , Vitamin K Deficiency/complications , Vitamin K Deficiency/drug therapy
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