UP TO DATE INFORMATION AND NEWS RELATED TO CANCER RESEARCH AND TREATMENT FOR CANCER PATIENTS AND COMMUNITY.
TRANSLATE
Friday, 13 July 2018
Wednesday, 11 July 2018
Ovarian suppression imporves 8-year breast cancer survival
The addition of ovarian suppression
to tamoxifen lengthened overall survival (OS) and disease-free survival (DFS)
among premenopausal women with breast cancer, according to updated findings
from the TEXT and SOFT trials published in The New England Journal of
Medicine.
Results — which were published in
correspondence with a presentation at the ASCO Annual Meeting on freedom from
distant metastases data from the trials — also showed exemestane plus ovarian
suppression resulted in higher rates of freedom from recurrence.
The researchers performed a
prespecified updated analysis of the SOFT and TEXT trials. In the SOFT trial,
researchers randomly assigned women to receive tamoxifen alone (n = 1,021),
tamoxifen plus ovarian suppression (n = 1,024), or exemestane plus ovarian
suppression (n = 1,021). In the TEXT trial, researchers randomly assigned
patients to tamoxifen (n = 1,334) or exemestane (n = 1,338), both with ovarian
suppression. In both studies, women received treatment for 5 years.
Eight-year OS was 93.3% with
tamoxifen plus ovarian suppression group compared with 91.5% in the tamoxifen
group (HR = 0.67; 95% CI, 0.48 to 0.92). The difference with exemestane plus
ovarian suppression compared with tamoxifen alone did not reach statistical
significance (92.1%; HR = 0.85; 95% CI, 0.62-1.15).
Among women who remained
premenopausal after chemotherapy, 8-year OS was 89.4% with tamoxifen plus
ovarian suppression compared with 85.1% with tamoxifen alone (HR = 0.59; 95%
CI, 0.42 to 0.84). For exemestane plus ovarian suppression, 8-year OS was 87.2%
(HR vs. tamoxifen alone = 0.79; 95% CI, 0.57-1.09).
Among women with HER-2-negative
disease who underwent chemotherapy, 8-year OS was 85.2% among patients assigned
tamoxifen alone, 87.7% among those assigned tamoxifen plus ovarian suppression
(HR vs. tamoxifen = 0.7; 95% CI, 0.48-1.02), and 88.7% among those assigned
exemestane plus ovarian suppression (HR vs. tamoxifen = 0.71; 95% CI,
0.49-1.05).
The 8-year rate of freedom from
distant recurrence was 91.8% for exemestane plus ovarian suppression and 89.7%
for tamoxifen plus ovarian suppression (HR = 0.8; 95% CI, 0.66-0.96).
“Longer follow-up is planned for SOFT and
TEXT, data regarding survival to confirm the findings"
Monday, 9 July 2018
Cancer survivors at increased risk for endocrine diseases
Jensen MV, et al. JAMA Network Open.
2018;doi:10.1001/jamanetworkopen.2018.0349.
Marjerrison S and RD Barr. JAMA Network Open. 2018;doi:10.1001/jamanetworkopen.2018.0350.
Marjerrison S and RD Barr. JAMA Network Open. 2018;doi:10.1001/jamanetworkopen.2018.0350.
Adolescent and young adult cancer
survivors had a higher than expected rate of hospital contact for endocrine
diseases, including thyroid disease, testicular dysfunction and diabetes,
according to a Danish population-based study.
Adolescent and young adult cancer
survivors — defined as those who had a cancer diagnosis when aged 15 to 39
years — differ from younger and older patients with cancer in terms of biology,
epidemiology and clinical outcomes. This population also is at risk for
long-term morbidity associated with their cancer or cancer treatment.
Danish investigators followed 32,548
adolescent and young-adult 1-year cancer survivors (43.1% male) from the Danish
Patient Registry for a median of 10 years (range, 0-34). For a control cohort,
the investigators also assessed 188,728 cancer-free participants (43.8% male)
for a mean of 15 years (range, 0-34).
Overall, 6.5% of cancer survivors had
at least one hospital contact for an endocrine disease, whereas researchers
expected a hospitalization rate of 3.8% (rate ratio [RR] = 1.73; 95% CI,
1.65-1.81).
Male survivors appeared to be at a
higher risk for an endocrine disease than female survivors (RR = 2.41; 95% CI,
2.23-2.61 vs. RR = 1.46; 95% CI, 1.38-1.55).
Researchers observed the highest RRs
among cancer survivors for testicular hypofunction (75.12; 95% CI,
45.99-122.7), ovarian hypofunction (14.65; 95%CI, 8.29-25.86) and pituitary
hypofunction (11.14; 95% CI, 8.09-15.34).
When evaluated as the proportion of
absolute excess risks, the leading reasons for hospital contacts included
thyroid disease (38%), testicular dysfunction (17.1%) and diabetes (14.4%).
Survivors of leukemia had the highest
risk for any endocrine disease (RR = 3.97; 95% CI, 3.1-5.09), followed by
survivors of Hodgkin lymphoma (RR = 3.06; 95% CI, 2.62-3.57) and survivors of
brain cancer (RR = 3.03; 95% CI, 2.53-3.64).
Hodgkin lymphoma survivors had the
highest risk for hypothyroidism (absolute excess risk, 362 per 100,000
person-years; 95% CI, 280-443).
This knowledge can help clinicians
and patients with the highest risk to be more aware of symptoms so that
endocrine diseases can be diagnosed early. Thus, patients will receive the
right treatment earlier and hopefully prevent more severe sequelae.
https://www.healio.com/hematology-oncology/practice-management/news/in-the-journals/%7B3b51ff75-2ea4-491d-ada0-b675a5ea4bb5%7D/cancer-survivors-at-increased-risk-for-endocrine-diseases
Sunday, 8 July 2018
Metformin, a medication used to treat Diablete Mellitus type 2, inproves the response of new immunotherapies in patients with diseminated melanoma.
Friday, 6 July 2018
Brief information about a subtype of breast cancer: HER2-Positive.
Approximately 20% to 25% of breast cancer tumors over-express the HER2 protein. HER2-positive breast cancer is often more aggressive than other types of breast cancer, increasing the risk of disease progression and death. Although research has shown that trastuzumab can reduce the risk of early stage HER2-positive breast cancer returning after surgery, up to 25% of patients treated with trastuzumab experience recurrence.
What is Diffuse Intrinsic Pontine Glioma (DIPG)
Diffuse
intrinsic pontine glioma, or DIPG, is a rare, aggressive brain tumor found in
the brain stem that almost exclusively affects children. Every year in the
United States, approximately 200-400 children, ages ranging from 4 to 11, are
diagnosed with DIPG. As the tumor grows, it puts pressure on the nerves that
control essential bodily functions. Children experience symptoms including, but
not limited to: vision issues, arm and leg weakness and difficulty speaking,
breathing and heartbeat resulting in death. The median survival time is 9
months, with only 1% of all children diagnosed with DIPG surviving more than 5
years. 
Thursday, 5 July 2018
If you are a cancer survivor, please complete the following survey. It takes just 2 minutes to complete it. The information is totally anonymous and it will be used for a research purpose. Many thanks. Doctor Mendoza
https://www.surveymonkey.com/r/QJQND6M
Subscribe to:
Posts (Atom)