Conventional cancer care is driven by evidence-based medicine. Evidence-based medicine (EBM) is the marrying of relevant research data, clinician experience, and patient preferences and values to form the best possible treatment plans for individual patients. Each of these three aspects must be taken into account when making evidence-based medical decisions.
Examples of conventional cancer care include chemotherapy, radiation therapy, surgery, targeted therapy, hormone therapy, and immunotherapy. Therapies or treatment modalities that are not currently included in conventional cancer care are often those lacking reliable evidence due to unsatisfactory performance in studies, studies of poor design/quality, or the absence of studies altogether on that topic. While this doesn't necessarily mean that a proposed therapy is ineffective or unsafe, it does mean that it doesn't qualify as evidence-based medical care until the evidence has been thoroughly established.
Everything in conventional cancer care was, at one time or another, not considered to be EBM. It wasn't until proper research data was produced that treatments like chemo or immunotherapy were introduced as a part of conventional cancer care. In time, and with sufficient research, clinical expertise, and patient input, many more treatment modalities will become standard of care in cancer treatment.
Research data can be scientifically assessed to determine its clinical relevance using a qualitative hierarchy, often referred to as an Evidence-Based Medicine (EBM) Pyramid. You can learn more about assessing the quality of research studies and the resulting evidence by visiting our Scientific Studies page.
Standard of Care (SOC) describes the protocols, guidelines, and recommendations that are in place for treating and caring for patients in a streamlined, predictable manner with a focus on the best possible outcome. SOC protocols are based on evidence-based research and real-world patient outcomes, and provide a clear path for clinicians to follow when approaching the development of an individualized treatment plan for a patient. SOC guidelines in cancer care are provided primarily by the NCCN (National Comprehensive Cancer Network) and are broken down into very specific categories and subcategories based on a patient's cancer type, stage, size/spread of cancer, specific location of cancer, inherited or acquired mutations, biomarkers, location of metastases, surgical candidacy, previous treatments, and other molecular, genetic, or biological characteristics of the cancer. The NCCN offers separate guides tailored to clinician and patient audiences, and updates are made on a regular basis. You may also see the acronym BSC, or Best Standard Care, in referring to Standard of Care.
Efficacy is the term used to describe how effective (successful, beneficial, useful, powerful) a treatment is; how well the treatment works. The higher the efficacy, the better it works.
Safety is the term used to describe the amount of risk a patient takes on while receiving a treatment with regard to side effects and overall toxicity. A treatment's "safety" describes the likelihood of effects that can have a substantial impact on a patient's life including effects like: increased chance of infection; increased chance of serious disease in other organs/organ systems; and increased chance of weakness, instability, fatigue, for example.
Side Effects, or Treatment-Related Adverse Events (TRAEs), are the off-target effects of a drug or treatment; how your body responds to exposure to or use of a treatment. These can be positive, negative, or neutral effects, though they are most often used to describe unwanted effects. The term toxicity is often used interchangeably with negative/unwanted side effects.
Tolerability refers to how well a treatment can be tolerated (dealt with, endured, accepted) and how it relates to the length of time a patient can stay on the treatment (without discontinuation) despite negative side effects or toxicity. A well-tolerated treatment is one in which most patients can complete a course of treatment with little issue. A poorly-tolerated treatment is one in which patients experience higher levels of toxicity and may need to reduce dosage or discontinue the treatment altogether because the negative effects outweigh the benefits offered.
Choosing a treatment requires the consideration of both efficacy and side effects, and determining the balance between the two for the best individual outcome.
The first-line therapy (1L) for your cancer type & stage is the first line of defense against your cancer and statistically the most likely option to be effective and/or tolerable (less toxic). The 2nd (2L) and 3rd-line (3L) options have been shown to be the next best choices if the previous line was ineffective, or if it had to be discontinued due to allergy or toxic side effects. Cancer develops resistance to treatments over time, so they don’t work as well or at all after a certain point. To combat the adaptive nature of cancer, multiple lines of therapy have been developed to attack cancer from different angles, at different times, and with different weapons. Given that each person and each cancer is unique, variations in response can occur; a patient may have a better response to a 2nd or 3rd-line than they did with the 1st, or they may not need to try a 2nd-line because the 1st was successful.
Think about this in terms of football. The team has a starting, or 1st string, quarterback and 2nd and 3rd-string backup quarterbacks. There’s nothing inherently wrong with the backups—they’ve proven themselves, just not to the same degree as our starter. Over time, we’ve learned that our 1st-string QB is more effective, more consistent with results, and has the highest chance of success. So, clearly, the 1st string is chosen to start the game because history has told us that he has the best chance of defeating our opponent. If he doesn’t perform at the expected level, then we’ll pull him out and throw our 2nd string into the game.
If you look at an FDA approved indication for a drug and it says, "for patients who have trialed/failed/progressed on A, B, or C..." then it's not indicated as 1st line treatment, but rather a 2nd or 3rd line treatment.
Cure comes from the Latin “to take care of” and palliative comes from the Latin “to cloak”
Each treatment option you encounter will either have an intent to cure or an intent to palliate. Whether a treatment is given for curative or palliative purposes will depend on the specific treatment you’re considering (have you had it before, did it work, does the data show a reliable response to this treatment for your cancer, is it for maintenance therapy or first-line treatment, etc.) and other factors including your cancer type and cancer stage. A chemotherapy drug, for example, may be given to you with curative intent, but the patient next to you may receive the same drug for palliative purposes. Many treatments for Stage IV cancers are considered palliative, not curative. Ask your oncologist if the treatments presented to you are intended to cure or control your cancer.
Clinical Significance (sometimes called clinical relevance) describes how impactful a treatment is on a patient. A treatment is considered clinically significant if it has a noticeable, measurable impact on a patient and advances their healing, recovery, functioning, or improves the management of their condition or their quality of life.
Some tests and test results are referred to as clinically relevant. This indicates whether the test, or the result of the test, has a real impact on the care and condition of the patient.
Actionable is a word used to describe what can be done clinically with a piece of information, usually a test result of some kind.. For example, if there is a therapy available that targets a specific mutation you have in your cancer, then you can consider the results of that genomic report to be actionable since there is something you can do about that mutation—you can act on it. On the other hand, if your genomic report reveals mutations for which there are no targeted therapies, then those findings are not actionable. The bottom line is if you can use the information to make a medical decision, determine a treatment plan, choose additional tests, and/or select specific therapies/interventions, then that information is considered clinically actionable. Does the information impact, inform, or influence medical decision-making? If yes, it's actionable.
A diagnosis is a determination given to patient regarding a specific condition or disease, as given by a physician or clinician, when the minimum guidelines have been met in terms of signs and symptoms, test results, physical exam, and other diagnostic measures. A diagnosis can include details about severity (stage) and other factors that may impact the treatment of the condition/disease.
A prognosis is a subjective predictive measure of the outcome of a disease based on clinician experience & expertise and retrospective patient data. In other words, the prediction is based on what a clinician has experienced with similar patients and what the data says about how patients before you have fared. A prognosis is an educated guess and can vary depending upon the clinician issuing the prognosis.
Simply put, a diagnosis is what you have and a prognosis is what that diagnosis may mean for your future.
Are clinical trials another treatment option for you? Learn the details about clinical trials in general, search for specific-to-you clinical trials that may be enrolling patients, and discover Compassionate Use
Observation of the cancer using imaging and labs, without intervention or treatment
Thomas Edison
We regularly review these resources to make sure that all links work correctly and are of value to our visitors. If you find a link that isn't working, please email coral@oncologyoffense.com. If you would like us to consider adding a resource to our list, please email us with details.
NCCN (National Comprehensive Cancer Network) Treatment Guidelines (Patient Guidelines, search by your cancer type) The NCCN Guidelines for Patients present expert recommendations in plain language to help people discuss options with their cancer care team. The NCCN Guidelines® are frequently updated by multidisciplinary panels of clinicians, researchers, and advocates. They are used by health care providers worldwide.
https://www.nccn.org/patientresources/patient-resources/guidelines-for-patients
NCCN Patient Guides for Cancer App People with cancer and caregivers can access the patient-friendly NCCN Guidelines for Patients® via the app for expert information they can use to talk to their health care team about the best treatment options.
https://www.nccn.org/guidelines/nccn-mobile-app
USPSTF The U.S. Preventive Services Task Force is an independent, volunteer panel of national experts in disease prevention and evidence-based medicine. The Task Force works to improve the health of people nationwide by making evidence-based recommendations about clinical preventive services such as screenings, counseling services, and preventive medications.
https://www.uspreventiveservicestaskforce.org/uspstf/
New approaches and procedures for cancer treatment: Current perspectives (SAGE Open Med., 2021)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366192/
Choices for Care with Advanced Cancer (When Treatment is Not an Option) (NCI)
Choices for Care with Advanced Cancer - NCI
Why Do Cancer Treatments Stop Working? Overcoming Treatment Resistance (NCI)
The Different Mechanisms of Cancer Drug Resistance: A Brief Review (Advanced Pharmaceutical Bulletin, 2017)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651054/
Multidrug Resistance in Cancer: Understanding Molecular Mechanisms, Immunoprevention and Therapeutic Approaches (Frontiers in Oncology, 2022)
https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2022.891652/full
Be the Match Patient Support Services We do more than match patients with marrow donors. We also support patients and families before, during and after a transplant through one-on-one support, financial assistance and free educational resources.
https://bethematch.org/about-us/how-we-help-patients/patient-support-services/
Overview of Second-Line Treatment for Cancer (verywellhealth) Second-line treatment is treatment for a disease or condition after the initial treatment (first-line treatment) has failed, stopped working, or has side effects that aren't tolerated. It's important to understand "lines of treatment" and how they differ from first line treatment and can play a role in clinical trials. Learn more about second line therapies and questions you should ask if your oncologist recommends this.
SHEPHERD was founded as an unapologetically human, defiantly democratic precision medicine and cancer care company leading a patient revolution around the globe. SHEPHERD dreams of a world in which every patient, from the hospitals of Brooklyn to the villages of Ethiopia, regardless of race, religion, creed, gender, socioeconomic status, or geographical location is given the optimum care most likely to afford them a fighting chance to LIVE for decades, not just days. To live is not a privilege. It's a human right. SHEPHERD's technology identifies therapies specific to your tumor’s RNA. Via mathematical analysis, it is able to identify gene expression patterns — sometimes hundreds of them — that can lead to response to specific therapies. Every patient’s data is analyzed across over 509 drugs, including FDA-approved, repurposed, and adjuvant therapies. Because it does not rely principally on mutational data, SHEPHERD has a much higher chance of finding therapeutic matches than typical DNA-based methods. This means SHEPHERD can help find drugs for even the hardest-to-treat cancers, including pediatric, metastatic, and rare.
Outcomes4Me We’re the only cancer app that integrates with the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®), from the not-for-profit alliance of 33 leading cancer centers. The NCCN Guidelines® include comprehensive guidance related to all FDA-approved treatment options. We gather cancer treatment recommendations typically meant for oncologists and use Artificial Intelligence (AI) to translate that information so you can understand it, putting you in control. With this knowledge, you can feel empowered to make the best medical decisions with your care team. Navigate your cancer care with confidence. Everyone on your team should be advocating for you, during every visit, treatment, and setback.
Deep learning in cancer diagnosis, prognosis, and treatment selection (Genome Medicine, 2021)
https://genomemedicine.biomedcentral.com/articles/10.1186/s13073-021-00968-x#Fig1
Treatment Options in Oncology (JCO Clinical Cancer Informatics, 2018)
https://ascopubs.org/doi/full/10.1200/CCI.18.00017
Leal Health Our mission is to democratize access to advanced cancer treatment. We empower patients to own their cancer journey with our AI-powered, FDA-approved decision support platform. To date we have helped make nearly 4,000,000 treatment matches for patients and have partnered with leading advocacy and patient support organizations to ensure unbiased access to cancer treatment for anyone, and everyone. Select your cancer type, complete a 2-minute questionnaire, and instantly receive a personalized list of treatments to discuss with your doctor (including standard and cutting-edge treatments and clinical trial matches).
XCures: Using AI and your medical records (including your specific mutations), XCures helps match patients with treatment options and clinical trials for free. Many patients and their loved ones will spend countless hours combing through the thousands of active clinical trials and endless anecdotal internet stories in hopes of finding relevant information and potential treatment options. The xCures platform arms cancer patients and their oncologists with the tools they need to make the most informed point-of-care decisions.
A.I. Assisted Cancer Treatment Options - xCures
My Cancer Genome is a precision cancer medicine knowledge resource for physicians, patients, caregivers and researchers that gives up-to-date information on what mutations make cancers grow and related therapeutic implications, including available clinical trials. It's a one-stop tool that matches tumor mutations to therapies, making information accessible and convenient for busy clinicians.
https://www.mycancergenome.org/
FindMeCure helps patients access the treatments of the future by supporting them in finding and applying for clinical trials. The treatments that are already available are not your only option. Inform yourself about clinical trials happening worldwide right now. We are here to provide you with free access to treatments in research and guide you along the way.
Cancer Commons: We provide patients and their caregivers with actionable information and data to make informed decisions—and minimize trial and error. Our staff scientists, in consultation with external experts, help each patient identify and access an individualized regimen of therapies that specifically target the molecular drivers of their disease. Treatment guidance is informed by the clinical experiences of previous patients.
Cancer Commons - Help for those with advanced cancer
Critical Path Institute: C-Path forms collaborative work groups comprised of diverse stakeholders to identify specific barriers to developing a safe and effective therapy for a given disease, and then creates tools and solutions that help drug developers overcome those barriers. to support drug repurposing studies in rare cancers.
Critical Path Institute (c-path.org)
Cure Match: Match Better Cancer Treatments via Genomic Biomarkers
Match Better Cancer Treatments via Genomic BioMarkers (curematch.com)
OncoExTra Test by Exact Sciences Interrogating both DNA and RNA, the OncoExTra test provides ultra-comprehensive genomic profiling that thoroughly detects clinically actionable mutations and fusions. It delivers the all-encompassing genomic insights of whole-exome (DNA) and whole-transcriptome* (RNA) sequencing, highlighting key information that is critical to personalized cancer care. High accuracy with 98.8% sensitivity and >99.9% specificity.
Travera Rapid Therapy Selection™ Test evaluates a broad range of FDA-approved drug options to assess their potential for treating your unique cancer. We Focus On Cancer Cell Weight Change. While it takes days or weeks to measure cell death, cell weight change can be measured in hours. Our Rapid Therapy Selection™ Test is available through an Early Access Program in the United States. Test ordering is for licensed physicians only. Currently, the test is not covered by insurance and must be paid for by the patient.
Xilis’ MicroOrganoSphere (MOS) powers the only assay which can provide oncologists with accurate results of drug sensitivity on a patient’s own tumor within the clinical decision-making window -- finally realizing the promise of precision medicine. Xilis is developing a panel of disease specific assays systematically testing the most important standard-of-care drugs within equipoise or difficult-decision settings to help clinicians and their patients make the most appropriate treatment decision for their unique cancer in a timely manner. The Xilis test is currently in clinical trials for assessing advanced stage colorectal and breast cancer tumors as our lead candidates. Other tumor types and drug candidates are in development.
Copyright © 2024 Oncology Offense - All Rights Reserved.
Powered by GoDaddy
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.