Learn about conventional, complementary, and integrative therapies.
Dealing with treatment side effects? Learn about evidence-based therapies to alleviate your symptoms.
Click the orange button to the right to learn more.
Women suffer chemo side effects more, according to the study linked below. That’s the bad news. The good news is that women, on average, live longer and suffer fewer relapses than men do.
In my experience as a long-term cancer survivor, oncologists don’t study or talk about short-term and long-term side effects of the therapies that they prescribe. I’m not trying to be critical. I’m simply saying that oncology focuses on treating the newly diagnosed cancer patient.
But I have researched therapies to reduce possible side effects. These therapies break into two groups. The first is to prepare your body for the toxicity it will be dealing with during therapy and the second type of therapy are those that you can do during and after therapy.
Remember that each side effect is linked to a page on PeopleBeatingCancer.org that is about that specific side effect.
I believe that if a newly diagnosed cancer patient understood what treatment was going to do to them, they would work harder to prevent side effects. If you have not begun therapy, please prepare your body for treatment. If you have already begun treatment, scroll down the page to learn more about evidence-based therapies shown to reduce side effects.
Scroll down the page and post a question or a comment if there’s anything you’d like to know about breast cancer.
Good luck,
Fatigue is the most frequently reported side effect of cancer treatment.
Symptoms
It can occur with chemotherapy, radiation, immunotherapy, and hormone therapy.
Research
https://pubmed.ncbi.nlm.nih.gov/31124358/
Chemotherapy-induced nausea and vomiting (CINV) remains one of the most common treatment toxicities.
High-risk drugs
Modern anti-nausea medications have improved control, but symptoms still affect many patients.
Research
https://pubmed.ncbi.nlm.nih.gov/31568169/
Hair loss is extremely common with chemotherapy and certain targeted drugs.
Features
Hair usually regrows after therapy but may have changes in texture or color.
Research
https://pubmed.ncbi.nlm.nih.gov/31999363/
Cancer therapy often suppresses bone marrow, leading to reduced red blood cells.
Symptoms
Anemia is especially common during chemotherapy.
Research
https://pubmed.ncbi.nlm.nih.gov/33544943/
Pain may result from:
Pain management is a major component of oncology care.
Research
https://pubmed.ncbi.nlm.nih.gov/31522570/
Certain chemotherapy drugs damage nerves.
Symptoms
Drugs commonly responsible include taxanes and platinum chemotherapy.
Research
https://pubmed.ncbi.nlm.nih.gov/30993793/
Many cancer patients develop insomnia during treatment.
Causes include:
Research
https://pubmed.ncbi.nlm.nih.gov/29554424/
Cancer therapy often alters appetite.
Women may experience:
Research
https://pubmed.ncbi.nlm.nih.gov/30883368/
Women treated with hormone-blocking therapies often develop menopausal symptoms.
Common examples:
These are especially common in breast cancer survivors receiving endocrine therapy.
Research
https://pubmed.ncbi.nlm.nih.gov/29691516/
Many women report cognitive difficulties during and after treatment.
Symptoms include:
This effect can persist months or years after therapy.
Research
https://pubmed.ncbi.nlm.nih.gov/30741680/
Abstract
Background
Sex is a recognised modifier of physiology, immunity, and social exposures, yet its
independent association with survival and adverse event (AE) prognosis in contemporary
anticancer therapy remains poorly defined. The aim of the present study was to assess the
participant data (IPD) meta-analysis.
Methods
IPD supporting FDA approval of anticancer medicines for solid tumours between 2011 and
2021 were accessed via the Vivli and YODA data sharing platforms. A two-stage random-
effects meta-analysis approach was employed, using Cox proportional hazards regression to
estimate sex-based prognostic differences in overall survival (OS), progression-free survival
(PFS), and grade ≥3 AEs. Analyses were adjusted for key baseline covariates.
Results
In a pooled cohort of 20,806 participants from 39 phase II–III trials supporting US FDA
approvals of anticancer medicines for advanced solid tumours, across 12 tumour types,
female sex was associated with significantly improved OS (HR 0.79, 95% CI 0.73-0.85;
P<0.001) and PFS (HR 0.84, 95% CI 0.79-0.89; P<0.001). Conversely, females experienced
a higher risk of grade ≥3 AEs (HR 1.12, 95% CI 1.07-1.18; P<0.001).
Conclusions
In the largest analysis of IPD from trials supporting FDA drug approvals, we found that females
had a 21% lower risk of death and a 16% lower risk of progression, but a 12% higher risk of
severe adverse events. These findings highlight the value of the IPD sharing and the
importance of sex-stratified evidence for risk stratification, dose optimisation and patient
counselling.
In conclusion, this pooled IPD meta-analysis of oncology trials supporting recent anticancer
drug approvals found that female sex was associated with a 21% lower risk of death, a 16%
lower risk of disease progression and a 12% higher risk of grade ≥3 AEs. These associations
were largely consistent across 12 advanced solid tumour types and evaluated subgroups
Women suffer chemo side effects more Women suffer chemo side effects more Women suffer chemo side effects more