Monday was Gyn Cancer Poster day at #ASCO24.
Here are a few posters along with their study conclusions that I found most interesting this year.
Tumor-informed ctDNA as an objective marker for postoperative residual disease in epithelial ovarian cancer. #5544
"The present tumor-informed dPCR SV fingerprint ctDNA approach
demonstrated feasibility with remarkably high detection rates pre- and
postoperatively. Postoperative ctDNA levels differed substantially based
on postoperative tumor residuals. These findings suggest that this
personalized approach could be used to develop a dPCR SV detection assay
and may have clinical utility for postoperative MRD evaluation in
patients with primary advanced HGSOC."
Through the years there has been a lot of talk regarding detecting circulating tumor DNA in the blood of patients. This study showed ctDNA could be used as a marker in ovarian cancer .
Differences in physical
and emotional distress amongst patients undergoing neoadjuvant
chemotherapy versus surgery for advanced ovarian cancer:
Patient-reported outcomes at diagnosis. #5546
"Advanced OC patients have high psychosocial needs, with NACT patients
reporting severe perceived symptoms on PRO measures. The PSS-10 may be a
valuable screening tool for patients undergoing NACT to prioritize
supportive care services."
Use of cell-free DNA
from ascites to identify variants and tumour evolution in a cohort of
patients with advanced ovarian cancer. #5547
This work "demonstrated the reliability of using cfDNA from ascites for
molecular profiling, allowing a liquid biopsy of ovarian cancer when
tumor tissue access may be restricted. This approach improves
accessibility of tumour material, allowing capture of clinically
actionable mutations prior to surgery or upon recurrence, following
tumour evolution."
There is a difference between cfDNA and ctDNA- "The ctDNA is the fraction of cfDNA that originates from tumor cells,
which comes from three sources: apoptosis, necrosis, and active
secretion. While ctDNA can come from apoptosis with fragment lengths
similar to healthy patients, ctDNA is more fragmented or shorter than
cfDNA [20,32,33]. " Source : NIH
Gemcitabine plus cisplatin in recurrent ovarian, fallopian tube, and primary peritoneal cancer. #5548
"Cisplatin in combination with gemcitabine demonstrates activity
regardless of platinum sensitivity status in patients with recurrent
ovarian cancer. However, longer platinum-free interval is associated
with improved response to this therapy".
Evaluation of a novel extracellular vesicle (EV) based ovarian cancer (OC) screening test in asymptomatic postmenopausal women. #5553
"The OC Test is capable of highly sensitive and specific detection of
HGSC in asymptomatic postmenopausal women one year prior to Dx and can
detect HGSC up to three years prior to Dx with superior sensitivity and
specificity compared to CA125."
Finding a screening test for ovarian cancer is important. This is a different approach looking at extracellular vesicles. " Extracellular vesicles (EVs) are generated
and released by cells as part of various physiological and pathological
processes, including the progression of ovarian cancer. "Source Science Direct
The BEV1L study: Do
real-world outcomes associated with the addition of bevacizumab to
first-line chemotherapy in patients with ovarian cancer reinforce
clinical trial findings? #5563
"This real world study provides support for findings from ICON7 and GOG-0218,
suggesting that the benefit of adding bev to first line chemotherapy may be limited to patients
with high-risk clinical factors ( Stage IV disease or stage III disease with visible residual disease or no evidence of surgery). "
Association of physical activity with self-reported quality of life after primary chemotherapy for ovarian cancer. #5574
"We observed positive associations between health tracker physical
activity data and pt-reported QOL. Stronger associations were observed
in younger pts. Interventions aimed at increasing physical activity may
have broader quality of life benefits for individuals with ovarian
cancer."
When I was first diagnosed I was told to rest during chemotherapy treatment. When I recurred a few years later I was told to try to walk each day. I'm glad that theren is now data saying that exercise has QOL benefits.
Artificial intelligence to
predict homologous recombination deficiency in ovarian cancer from
whole-slide histopathological images. #5578
"By harnessing the power of deep neural networks (DNN), we provide a
rapid and scalable solution for HRD prediction, circumventing the
limitations of traditional molecular assays. Successful integration of
this deep learning model into routine pathology workflows could
significantly enhance diagnostic efficiency, reduce the turnaround time
and financial cost compared with molecular assay. "
There were a number of talks at ASCO related to the use of AI. HRD is a marker used to manage ovarian cancer patient treatments.
Germline genetic profiles of women with ovarian malignancies: A Myriad Collaborative Research Registry study #5585
"Based on this large registry, our data showed that over 15% of patients
with ovarian malignancies have mutations in BRCA (12.5%) or Lynch genes
(2.6%) with varying prevalence by race, age, and tumor site. Noted
disparities indicate the importance of universal testing in patients
with epithelial ovarian malignancies."
I knew that Lynch syndrome was associated with endometrial cancer but I did not associate ovarian cancer with Lynch sydrome.
Which posters caught your eye? Share them in a comment below.
Tomorrow, I will post about a equity symposium I attended as well as the connections and reconnections I made at the annual meeting.
Dee
Every Day is a Blessing!
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