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1.
Br J Surg ; 108(11): 1332-1340, 2021 11 11.
Article in English | MEDLINE | ID: mdl-34476473

ABSTRACT

BACKGROUND: Trials typically group cancers of the gastro-oesophageal junction (GOJ) with oesophageal or gastric cancer when studying neoadjuvant chemoradiation and perioperative chemotherapy, so the results may not be fully applicable to GOJ cancer. Because optimal neoadjuvant treatment for GOJ cancer remains controversial, outcomes with neoadjuvant chemoradiation versus chemotherapy for locally advanced GOJ adenocarcinoma were compared retrospectively. METHODS: Data were collected from all patients who underwent neoadjuvant treatment followed by surgery for adenocarcinoma located at the GOJ at a single high-volume institution between 2002 and 2017. Postoperative major complications and mortality were compared between groups using Fisher's exact test. Overall survival (OS) and disease-free survival (DFS) were assessed by log rank test and multivariable Cox regression analyses. Cumulative incidence functions were used to estimate recurrence, and groups were compared using Gray's test. RESULTS: Of 775 patients, 650 had neoadjuvant chemoradiation and 125 had chemotherapy. These groups were comparable in terms of clinical tumour and lymph node categories, although the chemoradiation group had greater proportions of white men, complete pathological response to chemotherapy, and smaller proportions of diffuse cancer, poor differentiation, and neurovascular invasion. Postoperative major complications (20.0 versus 17.6 per cent) and 30-day mortality (1.7 versus 1.6 per cent) were not significantly different between the chemoradiation and chemotherapy groups. After adjustment, type of therapy (chemoradiation versus chemotherapy) was not significantly associated with OS (hazard ratio (HR) 1.26, 95 per cent c.i. 0.96 to 1.67) or DFS (HR 1.27, 0.98 to 1.64). Type of recurrence (local, regional, or distant) did not differ after neoadjuvant chemoradiation versus chemotherapy. CONCLUSION: In patients undergoing surgical resection for locally advanced adenocarcinoma of the GOJ, OS and DFS did not differ significantly between patients who had neoadjuvant chemoradiation compared with chemotherapy.


Treating advanced cancer of the gastro-oesophageal junction (GOJ) poses a challenge given its location in the distal oesophagus and proximal stomach, and whether it should be treated as oesophageal or gastric cancer. Given the indistinct location, it is unclear whether GOJ cancer should be treated with neoadjuvant chemoradiation, which is the treatment of choice for advanced oesophageal cancers, or perioperative chemotherapy, which is the treatment of choice for advanced gastric cancers. Few studies have addressed treatment options specifically for GOJ cancers. This study investigated whether there was a difference in survival between patients with GOJ cancer who were treated with chemoradiation versus chemotherapy.


Subject(s)
Adenocarcinoma/therapy , Antineoplastic Agents/therapeutic use , Esophageal Neoplasms/therapy , Esophagectomy/adverse effects , Esophagogastric Junction , Neoplasm Staging , Adenocarcinoma/diagnosis , Adenocarcinoma/mortality , Aged , Chemoradiotherapy, Adjuvant , Esophageal Neoplasms/diagnosis , Esophageal Neoplasms/mortality , Female , Follow-Up Studies , Humans , Incidence , Male , Middle Aged , New York/epidemiology , Postoperative Complications/epidemiology , Prognosis , Retrospective Studies , Survival Rate/trends
2.
Clin Exp Dermatol ; 42(8): 881-886, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28748571

ABSTRACT

Porokeratosis, a disorder of keratinisation, is clinically characterized by the presence of annular plaques with a surrounding keratotic ridge. Clinical variants include linear, disseminated superficial actinic, verrucous/hypertrophic, disseminated eruptive, palmoplantar and porokeratosis of Mibelli (one or two typical plaques with atrophic centre and guttered keratotic rim). All of these subtypes share the histological feature of a cornoid lamella, characterized by a column of 'stacked' parakeratosis with focal absence of the granular layer, and dysmaturation (prematurely keratinised cells in the upper spinous layer). In recent years, a proposed new subtype, follicular porokeratosis (FP_, has been described, in which the cornoid lamella are exclusively located in the follicular ostia. We present four new cases that showed typical histological features of FP.


Subject(s)
Hair Follicle/pathology , Porokeratosis/pathology , Skin/pathology , Aged , Aged, 80 and over , Female , Humans , Lentigo/complications , Lentigo/pathology , Male , Middle Aged , Porokeratosis/classification , Porokeratosis/complications
10.
Clin Exp Dermatol ; 36(1): 42-5, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20497187

ABSTRACT

Toxic epidermal necrolysis (TEN) is a life-threatening, immune-mediated reaction, characterized by severe cutaneous and mucosal blisters and erosions. It often presents with flu-like symptoms, followed by a maculopapular, urticarial, purpuric or erythema multiforme-like eruption, which then evolves into blisters and sheet-like erosions. Presentation with pustules, however, is not well described in the English literature, and may lead to delayed diagnosis. We present two unusual cases of TEN that initially presented with pustular lesions.


Subject(s)
Erythema Multiforme/pathology , Stevens-Johnson Syndrome/pathology , Biopsy , Diagnosis, Differential , Erythema Multiforme/immunology , Female , Humans , Male , Middle Aged , Severity of Illness Index , Stevens-Johnson Syndrome/immunology , Young Adult
11.
Science ; 181(4102): 843-4, 1973 Aug 31.
Article in English | MEDLINE | ID: mdl-17816237

ABSTRACT

New data support the contention that the mercury content of Greenland glacial ices has not increased dramatically in recent years but rather is distributed nonhomogeneously through the ice sheet.

14.
Clin Exp Dermatol ; 34(8): 895-7, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19508573

ABSTRACT

We report a case of eruptive disseminated superficial porokeratosis occurring in a 63-year-old man with no history of excessive sun exposure. Unlike disseminated superficial actinic porokeratosis, this condition resolved rapidly with minimal topical treatment. This is most likely to have represented a drug-induced phenomenon, which is very rarely reported in the dermatological literature.


Subject(s)
Anti-Bacterial Agents/adverse effects , Drug Eruptions , Leg Dermatoses/chemically induced , Porokeratosis/chemically induced , Drug Eruptions/pathology , Humans , Leg Dermatoses/pathology , Male , Middle Aged , Porokeratosis/pathology , Treatment Outcome
18.
Am J Surg ; 213(3): 494-497, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28129918

ABSTRACT

BACKGROUND: Patients with intraductal papillary mucinous neoplasm (IPMN) are at risk for invasive pancreatic cancer. We aim to characterize the impact of smoking on IPMN malignant progression. METHODS: Patients undergoing pancreatic resection for IPMN (1991-2015) were retrospectively reviewed using a prospectively collected database. RESULTS: Of 422 patients identified, 324 had complete data for analysis; 55% were smokers. Smoking status did not impact IPMN malignant progression (smokers/non-smokers: 22%/18% invasive grade; p = 0.5). Smokers were younger than non-smokers at the time of IPMN diagnosis (63 versus 68 years; p = 0.001). This association also held in the invasive IPMN subgroup (65 versus 72 years, p = 0.01). Despite this observation, rate of symptoms at diagnosis, cancer stage, and median survival were the same between smokers and non-smokers. CONCLUSION: Although smoking is not associated with IPMN malignant progression, invasive IPMN is diagnosed at a younger age in smokers. These data suggest tobacco exposure may accelerate IPMN malignant progression.


Subject(s)
Adenocarcinoma, Mucinous/pathology , Carcinoma, Pancreatic Ductal/pathology , Disease Progression , Pancreatic Neoplasms/pathology , Smoking , Adenocarcinoma, Mucinous/surgery , Adult , Age Factors , Aged , Aged, 80 and over , Carcinoma, Pancreatic Ductal/surgery , Humans , Male , Middle Aged , Pancreatic Neoplasms/surgery , Retrospective Studies
19.
Eur J Cancer ; 42(4): 467-72, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16406507

ABSTRACT

We performed a phase I study with the thrombospondin-1-mimetic angiogenesis inhibitor ABT-510 combined with 5-fluorouracil and leucovorin (5-FU/LV) to determine safety profile and assess pharmacokinetic interactions. Patients with advanced solid malignancies received LV 20 mg/m(2) followed by 5-FU 425 mg/m(2) both administered intravenously in 15 min daily for 5 days every 4 weeks. ABT-510 was administered subcutaneously twice daily continuously from day 2 onwards. Blood and urine samples for pharmacokinetic analyses were collected at days 1, 5 and 22. Twelve patients received a total of 45 cycles of 5-FU/LV combined with ABT-510. ABT-510 dose levels studied were 50 and 100 mg. The combination was well tolerated, with a toxicity profile comparable to that of 5-FU/LV alone. At the dose levels studied no significant pharmacokinetic interactions were observed. These data indicate that ABT-510 administered twice daily subcutaneously can be safely combined with 5-FU/LV administered daily for 5 days, every 4 weeks.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Thrombospondin 1/antagonists & inhibitors , Aged , Angiogenesis Inhibitors/administration & dosage , Angiogenesis Inhibitors/adverse effects , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Antineoplastic Combined Chemotherapy Protocols/pharmacokinetics , Female , Fluorouracil/administration & dosage , Fluorouracil/adverse effects , Fluorouracil/pharmacokinetics , Humans , Infusions, Intravenous , Leucovorin/administration & dosage , Leucovorin/adverse effects , Leucovorin/pharmacokinetics , Male , Middle Aged , Oligopeptides/administration & dosage , Oligopeptides/adverse effects , Oligopeptides/pharmacokinetics , Treatment Outcome
20.
J Clin Pathol ; 59(8): 884-6, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16873568

ABSTRACT

A successful move towards subspecialised reporting in cellular pathology in the setting of a small to medium-sized district general hospital staffed by five consultant pathologists is described. This move has been facilitated by implementation of a prospective workload allocation system. Perceived benefits in service delivery and career progression are highlighted.


Subject(s)
Hospitals, District/organization & administration , Hospitals, General/organization & administration , Pathology Department, Hospital/organization & administration , Pathology, Clinical/organization & administration , Cytodiagnosis/methods , England , Humans , Medical Staff, Hospital/organization & administration , Medicine , Personnel Staffing and Scheduling/organization & administration , Specialization , Workload
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