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1.
Cancers (Basel) ; 15(7)2023 Mar 27.
Article in English | MEDLINE | ID: mdl-37046656

ABSTRACT

BACKGROUND: Breast cancer is rare in men. This population-based study aimed to determine outcomes of male breast cancer in relation to residence and other variables. METHODS: In this retrospective cohort study, men diagnosed with breast cancer in Saskatchewan during 2000-2019 were evaluated. Cox proportional multivariable regression analyses were performed to determine the correlation between survival and clinicopathological and contextual factors. RESULTS: One hundred-eight eligible patients with a median age of 69 years were identified. Of them, 16% had WHO performance status ≥ 2 and 61% were rural residents. The stage at diagnosis was as follows: stage 0, 7%; I, 31%; II, 42%; III, 11%; IV, 8%. Ninety-eight percent had hormone receptor-positive breast cancer. The median disease-free survival of urban patients was 97 (95% CI: 50-143) vs. 64 (46-82) months of rural patients (p = 0.29). The median OS of urban patients was 127 (94-159) vs. 93 (32-153) months for rural patients (p = 0.27). On multivariable analysis, performance status ≥ 2, hazard ratio (HR) 2.82 (1.14-6.94), lack of adjuvant systemic therapy, HR 2.47 (1.03-5.92), and node-positive disease, HR 2.32 (1.22-4.40) were significantly correlated with inferior disease-free survival in early-stage invasive breast cancer. Whereas stage IV disease, HR 7.8 (3.1-19.5), performance status ≥ 2, HR 3.25 (1.57-6.71), and age ≥ 65 years, HR 2.37 (1.13-5.0) were correlated with inferior overall survival in all stages. CONCLUSIONS: Although residence was not significantly correlated with outcomes, rural men had numerically inferior survival. Poor performance status, node-positive disease, and lack of adjuvant systemic therapy were correlated with inferior disease-free survival.

2.
Curr Oncol ; 29(7): 4748-4767, 2022 07 07.
Article in English | MEDLINE | ID: mdl-35877237

ABSTRACT

Triple-negative breast cancer (TNBC) has a worse prognosis and remains the most challenging breast cancer subtype to treat. This is largely related to the heterogeneity of this disease and the lack of reliable oncological targets. In this review, we discuss the current standard-of-care treatment options for metastatic TNBC, including recent advances with the use of immunotherapy, PARP inhibitors and antibody-drug conjugates. This review also explores new agents and novel combinations arising in the field for the treatment of advanced TNBC.


Subject(s)
Triple Negative Breast Neoplasms , Humans , Immunotherapy , Prognosis , TOR Serine-Threonine Kinases/therapeutic use , Triple Negative Breast Neoplasms/drug therapy , Triple Negative Breast Neoplasms/pathology
3.
Curr Oncol ; 29(7): 5139-5149, 2022 07 20.
Article in English | MEDLINE | ID: mdl-35877267

ABSTRACT

Breast cancer (BC) is the most common malignancy among women in Canada. Adjuvant treatment in early BC can reduce the risk of BC recurrence. Historically, the decision for adjuvant chemotherapy for early BC was made only based on clinical and tumour characteristics. In recent years, there has been an effort toward developing genomic assays as a predictive and prognostic tool to improve precision in estimating disease recurrence, sensitivity to systemic treatment and ultimately with clinical utility for guidance regarding adjuvant systemic treatment(s). There are various commercial genomic tests available for early-stage ER+/HER-2 negative BC. This paper will review the Oncotype DX 21-gene Recurrence Score (RS), MammaPrint, EndoPredict, Prosigna®, and Breast Cancer Index (BCI) genomic assays. We will also focus on these genomic assays' clinical application and utility in node-positive early-stage BC based on the most recent evidence and guidance recommendations.


Subject(s)
Breast Neoplasms , Breast Neoplasms/pathology , Chemotherapy, Adjuvant , Female , Gene Expression Profiling , Genomics , Humans , Neoplasm Recurrence, Local/drug therapy
4.
Sci Rep ; 12(1): 1068, 2022 01 20.
Article in English | MEDLINE | ID: mdl-35058536

ABSTRACT

Adjuvant trastuzumab has been associated with superior survival in women with ≥ T1c or node-positive HER2-positive early-stage breast cancer; however, there is a lack of phase III trials in women with T1a/bN0 disease. Our study aimed to assess the outcomes of women with HER2-positive T1a/bN0 breast cancer who received adjuvant trastuzumab in Saskatchewan, Canada. We evaluated all women diagnosed with HER2-positive T1a/bN0 breast cancer in Saskatchewan between 2008 and 2017. We performed Cox proportional multivariable analysis to determine factors correlated with survival. In addition, inverse probability treatment weighting (IPTW) using propensity score was performed to assess benefit of adjuvant trastuzumab. Ninety-one eligible women with a median age of 61 years (range 30-89) were identified. Thirty-nine (43%) women received adjuvant trastuzumab. Women who received trastuzumab were younger and had a higher rate of T1b disease. Overall, 3% of women who received trastuzumab compared to 12% of women who did not receive trastuzumab developed breast cancer recurrence (p = 0.23). Five-year disease-free survival (DFS) of women who received adjuvant trastuzumab was 94.8% compared to 82.7% of women who did not receive trastuzumab (p = 0.22). Five-year overall survival was 100% of women who received trastuzumab compared to 90.4% of women who did not receive adjuvant trastuzumab (p = 0.038). In the multivariable analysis, grade III tumors were correlated with inferior DFS (hazard ratio [HR] 5.5, 95% CI [1.7-17.7]). The propensity score using the inverse probability of treatment weighting showed that lack of adjuvant trastuzumab was correlated inferior DFS, with an HR of 4 (95% CI 1.05-15.5). Women with HER2-positive T1a/bN0 breast cancer had overall low recurrence of breast cancer. However, the results of this exploratory analysis indicate that women who received adjuvant trastuzumab had better survival.


Subject(s)
Breast Neoplasms/drug therapy , Trastuzumab/therapeutic use , Adult , Aged , Aged, 80 and over , Antibodies, Monoclonal, Humanized/therapeutic use , Breast Neoplasms/pathology , Canada/epidemiology , Chemotherapy, Adjuvant/methods , Cohort Studies , Disease-Free Survival , Female , Humans , Middle Aged , Neoplasm Recurrence, Local/drug therapy , Proportional Hazards Models , Receptor, ErbB-2/genetics , Receptor, ErbB-2/metabolism
5.
Crit Rev Oncol Hematol ; 169: 103540, 2022 Jan.
Article in English | MEDLINE | ID: mdl-34808376

ABSTRACT

AIM: Conduct a systematic review of the effectiveness of systemic therapies for adult recurrent glioblastoma (rGBM). METHODS: We electronically searched for randomized controlled trials from three major databases and four conferences from 2009-Dec 2020. Two independent reviewers conducted screening, data extraction, and quality assessment. RESULTS: 48 randomized trials were identified. Outcome reporting was inconsistent: overall survival (OS) in 46 studies, progression free survival in 37 studies, 6-month PFS in 30 studies, objective response rate in 28 studies, and 6-month OS in 7 studies. Network meta-analysis was not feasible due to heterogeneity in outcome reporting and single-study linkages. Most studies compared lomustine (8 studies), bevacizumab (18), or temozolomide (8) with other treatments. The median OS across all studies ranged from 3 to 17.6 months. CONCLUSIONS: Based on level one evidence, there is no superior systemic regimen for rGBM. rGBM is a heterogeneous population with no single regimen demonstrating OS benefit. Registration number: CRD42020148512.


Subject(s)
Brain Neoplasms , Glioblastoma , Adult , Bevacizumab , Brain Neoplasms/drug therapy , Glioblastoma/drug therapy , Humans , Neoplasm Recurrence, Local/drug therapy , Progression-Free Survival , Randomized Controlled Trials as Topic , Temozolomide
6.
Curr Oncol ; 28(3): 1803-1822, 2021 05 11.
Article in English | MEDLINE | ID: mdl-34064867

ABSTRACT

Background: Hormone receptor-positive and HER2-negative breast cancer (HR + BC) is the most prevalent breast cancer. Endocrine therapy is the mainstay of treatment, however, due to the heterogeneous nature of the disease, resistance to endocrine therapy is not uncommon. Over the past decades, the emergence of novel targeted therapy in combination with endocrine therapy has shown improvement in outcomes of HR + BC. This paper reviews available data of targeted therapy and the results of pivotal clinical trials in the management of HR + BC. Methods: A literature search in PubMed and Google Scholar was performed using keywords related to HR + BC and targeted therapy. Major relevant studies that were presented in international cancer research conferences were also included. Results: Endocrine therapy with tamoxifen and aromatase inhibitors are backbone treatments for women with early-stage HR + BC leading to a significant reduction in mortality. They can also be used for primary prevention in women with a high risk of breast cancer. Preliminary data has shown the efficacy of adjuvant cyclin-dependent kinase (CDK) 4/6 inhibitor, abemaciclib, in high-risk disease in combination with aromatase inhibitors. For most women with advanced HR + BC, endocrine therapy is the primary treatment. Recent evidence has shown that the use of CKD 4/6 inhibitors, mTOR inhibitors, and PI3K inhibitors in combination with endocrine therapy has been associated with better outcomes and delays initiation of chemotherapy. Several novel agents are under study for HR + BC. Discussion: Targeted treatment options for HR + BC have evolved. The future of overcoming resistance to targeted therapy, novel compounds, and predictive markers are key to improving HR + BC outcomes.


Subject(s)
Breast Neoplasms , Aromatase Inhibitors/therapeutic use , Breast Neoplasms/drug therapy , Female , Hormones , Humans , Phosphatidylinositol 3-Kinases , Receptors, Estrogen
7.
BMJ Case Rep ; 14(1)2021 Jan 28.
Article in English | MEDLINE | ID: mdl-33509862

ABSTRACT

Small cell lung cancer (SCLC) is a deadly and rapidly progressive disease that can present with various paraneoplastic syndromes on initial workup. Acquired factor VIII (FVIII) deficiency, also known as acquired haemophilia A (AHA), has been identified as a rare paraneoplastic syndrome in SCLC. Here, we present a 61-year-old woman with a massive gastrointestinal bleed and prolonged activated partial thromboplastin time (PTT) in the emergency department. She was diagnosed with rare paraneoplastic AHA secondary to extensive-stage SCLC (ES-SCLC). She was treated with high-dose steroids and factor bypassing agents, which led to the resolution of bleeding and undetectable FVIII inhibitor levels. She was subsequently treated for ES-SCLC with carboplatin, etoposide and atezolizumab. This case report highlights a rare clinical presentation of paraneoplastic AHA that necessitates prompt recognition in patients with SCLC with ongoing bleeding and elevated PTT.


Subject(s)
Adrenal Gland Neoplasms/diagnosis , Gastrointestinal Hemorrhage/diagnosis , Hemophilia A/diagnosis , Lung Neoplasms/diagnosis , Paraneoplastic Syndromes/diagnosis , Small Cell Lung Carcinoma/diagnosis , Abdomen , Adrenal Gland Neoplasms/complications , Adrenal Gland Neoplasms/drug therapy , Adrenal Gland Neoplasms/secondary , Anemia/diagnosis , Anemia/etiology , Antineoplastic Agents/therapeutic use , Autoantibodies/immunology , Coagulants/therapeutic use , Erythrocyte Transfusion , Factor VIII/immunology , Factor VIII/therapeutic use , Factor VIIa/therapeutic use , Female , Gastrointestinal Hemorrhage/etiology , Hemophilia A/etiology , Hemophilia A/immunology , Hemophilia A/therapy , Humans , Immunosuppressive Agents/therapeutic use , Lung Neoplasms/complications , Lung Neoplasms/pathology , Lymphadenopathy , Mediastinum , Middle Aged , Paraneoplastic Syndromes/etiology , Paraneoplastic Syndromes/immunology , Paraneoplastic Syndromes/therapy , Small Cell Lung Carcinoma/complications , Small Cell Lung Carcinoma/drug therapy , Small Cell Lung Carcinoma/secondary
8.
J Can Assoc Gastroenterol ; 2(4): 153-160, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31616856

ABSTRACT

BACKGROUND AND AIMS: Maintaining disease remission improves outcomes for pregnant women with Crohn's disease (CD). As symptoms may correlate poorly with disease activity in the gravid state, we investigated the utility of bowel sonography during pregnancy to assess disease activity. METHODS: We conducted a prospective observational cohort study of pregnant women with CD undergoing bowel sonography between July 1, 2012, and December 1, 2016. Clinically active disease was defined using standardized clinical indices (Harvey Bradshaw Index >4 for active disease). Sonographic findings were graded as inactive (normal, mild) or active (moderate, severe) by expert radiologists. RESULTS: There were 91 pregnancies in 82 CD patients. Symptoms were present in 12 pregnancies; however, eight (67%) had sonographic findings of inactive disease, and escalation of therapy was not initiated. Conversely, sonographically active disease in seven asymptomatic pregnancies resulted in four women escalating therapy. The remaining three women declined escalation of therapy, one had a miscarriage, and the other two women had persistently active disease on sonography and endoscopy at one-year postpartum. CONCLUSIONS: Bowel ultrasound may detect subclinical inflammation in asymptomatic pregnant women with CD and stratify CD activity in symptomatic patients. Therefore, bowel sonography should be considered as a useful adjunct for the assessment of the pregnant woman with Crohn's disease.

9.
BMJ Case Rep ; 12(1)2019 Jan 10.
Article in English | MEDLINE | ID: mdl-30635302

ABSTRACT

The clinical scenario of a female patient with a pelvic mass, elevated CA125 tumour marker, pleural effusion and ascites is often associated with malignancy. However, not all cases are malignant. Non-malignant diseases, such as Meigs syndrome and pseudo-Meigs syndrome, must be part of your differential. We present a 56-year-old woman with dyspnoea secondary to a right pleural effusion. After further investigations, a serum cancer antigen-125 was found to be elevated at 437.3 U/mL. CT of her abdomen and pelvis showed a large heterogeneous mass in the pelvis measuring 13.2×9.7×15.1 cm with mild ascites. She was initially thought to have ovarian carcinoma and underwent total abdominal hysterectomy and bilateral salpingo-oophorectomy with omental biopsy. Pathology from the surgical specimen revealed a hydropic leiomyoma and after removal of pelvic mass her pleural effusion and ascites completely resolved. She was ultimately diagnosed with the rare pseudo-Meigs syndrome.


Subject(s)
Leiomyoma/pathology , Meigs Syndrome/pathology , Ovarian Neoplasms/pathology , Ascites/complications , Ascites/diagnosis , CA-125 Antigen/blood , Diagnosis, Differential , Dyspnea/diagnosis , Dyspnea/etiology , Female , Humans , Hysterectomy/methods , Leiomyoma/diagnosis , Meigs Syndrome/diagnostic imaging , Meigs Syndrome/surgery , Middle Aged , Ovarian Neoplasms/surgery , Pleural Effusion/complications , Pleural Effusion/diagnosis , Rare Diseases , Salpingo-oophorectomy/methods , Tomography, X-Ray Computed/methods , Treatment Outcome
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