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There are several ways that breast cancer can impact the skin.
- Direct extension of the cancer to the skin
- Spread of the cancer to the skin
- Side effect of chemotherapy
- Side effect of radiation
- Stress induced changes to the skin, hair and nails
The first two ways I will cover in other posts as they are important to recognize for early detection and monitoring and the last two I will discuss in separate posts to focus on practical interventions.
Chemotherapy for breast cancer can impact the skin due to the fact that it tends to target cells that are actively dividing. Radiation has a direct impact on the skin treated simply because the skin is in the direct line of treatment. Redness, erythema, ulcers, pigmentation, soreness, scarring and potentially higher risk of skin cancer have been documented.
A study in Brazil reviewed the dermatological complaints during breast cancer treatment. It found that over 94% of breast cancer patients had dermatological complaints. Hair loss topped the list followed by nail changes, then thickening of the palms and soles. Other complaints included redness, ulcers, blisters, dryness, itching, hair growth, and changes in sweating.
This study was fascinating in that it found that 22% of patients actually had skin findings at the time of diagnosis! Mammary retraction, nipple inversion, p’eau d’orange skin changes and direct extension of cancer to skin were noted.
There have been a number of therapeutic agents that have come out for breast cancer of the past few decades. They can be grouped together by class with similar mechanism of action. These classes tend to have similar effects on the skin.
It is important to note that not every breast cancer treatment caused rash requires termination of treatment. Skin manifestations of treatment are exceedingly common and difficult to avoid altogether. Approaching these rash by discussion with your oncologist and consultation with a Dermatologist can help guide management to avoid unnecessarily discontinuing effective therapeutics.
Over the years I have been accumulating a list of medications used for breast cancer. As new ones come out I will continue to update this list. I also track the literature as case reports of specific skin reactions occur to help serve as a resource for these reactions. Accurate diagnosis leads to optimal management and the best chance of maintaining effective treatment for underlying carcinomas.
Hair loss, also known as alopecia, is one of the most common side effects noted with most treatments. I will discuss in another post the types of hair loss that can occur to help address them correctly.
Drug |
Class / Mechanism of Action |
Adverse effects related to skin, hair & nails |
Abemaciclib |
Cyclin-Dependent Kinase Inhibitor |
|
Abraxane (Paclitaxel Albumin-stabilized Nanoparticle Formulation) |
Taxane |
|
Ado-Trastuzumab Emtansine |
Monoclonal HER2 Antibody |
|
Afinitor (Everolimus) |
mTOR Kinase Inhibitor |
|
Afinitor Disperz (Everolimus) |
mTOR Kinase Inhibitor |
|
Alpelisib |
Phosphatidylinositol 3- Kinase Inhibitor |
|
Anastrozole |
Aromatase Inhibitor |
**Can occur 5 days to 6 months after onset of therapy |
Aredia (Pamidronate Disodium) |
Inhibits bone resorption |
Injection site reaction |
Arimidex (Anastrozole) |
Aromatase Inhibitor |
**Can occur 5 days to 6 months after onset of therapy |
Aromasin (Exemestane) |
Aromatase Inhibitor |
**Can occur 5 days to 6 months after onset of therapy |
Capecitabine |
Antimetabolite |
|
Cyclophosphamide |
Alkylating agent |
|
Docetaxel |
Taxane |
|
Doxorubicin Hydrochloride |
Anthracycline |
|
Ellence (Epirubicin Hydrochloride) |
Anthracycline |
|
Enhertu (Fam-Trastuzumab Deruxtecan-nxki) |
Monoclonal HER2 Antibody |
|
Epirubicin Hydrochloride |
Anthracycline |
|
Eribulin Mesylate |
Microtubule inhibitor |
|
Everolimus |
mTOR Kinase Inhibitor |
|
Exemestane |
Aromatase Inhibitor |
**Can occur 5 days to 6 months after onset of therapy |
5-FU (Fluorouracil Injection) |
Antimetabolite |
|
Fam-Trastuzumab Deruxtecan-nxki |
Monoclonal HER2 Antibody |
|
Fareston (Toremifene) |
Selective estrogen receptor modulator (SERM) |
|
Faslodex (Fulvestrant) |
Estrogen Receptor Antagonist |
|
Femara (Letrozole) |
Aromatase enzyme inhibitor |
|
Fluorouracil Injection |
Antimetabolite |
|
Fulvestrant |
Estrogen receptor antagonist |
|
Gemcitabine Hydrochloride |
Nucleoside |
|
Gemzar (Gemcitabine Hydrochloride) |
Nucleoside |
|
Goserelin Acetate |
LHRH agonist (hormonal therapy) |
|
Halaven (Eribulin Mesylate) |
Microtubule inhibitor |
|
Herceptin Hylecta (Trastuzumab and Hyaluronidase-oysk) |
Monoclonal HER2 Antibody |
|
Herceptin (Trastuzumab) |
Monoclonal HER2 Antibody |
|
Ibrance (Palbociclib) |
Kinase inhibitor (Cyclin-dependent kinase 4/6 inhibitor) |
|
Infugem (Gemcitabine Hydrochloride) |
Nucleoside |
|
Ixabepilone |
Microtubule inhibitor |
|
Ixempra (Ixabepilone) |
Microtubule inhibitor |
|
Kadcyla (Ado-Trastuzumab Emtansine) |
Monoclonal HER2 Antibody |
|
Keytruda (Pembrolizumab) |
Monoclonal HER2 Antibody |
|
Kisqali (Ribociclib) |
Kinase Inhibitor |
|
Lapatinib Ditosylate |
Tyrosine Kinase Inhibitors (TKIs) |
|
Letrozole |
Aromatase Inhibitor |
**Can occur 5 days to 6 months after onset of therapy |
Lynparza (Olaparib) |
PARP inhibitor |
|
Margenza (Margetuximab-cmkb) |
Monoclonal HER2 Antibody |
|
Margetuximab-cmkb |
Monoclonal HER2 Antibody |
|
Megestrol Acetate |
Progestin |
|
Methotrexate Sodium |
Folate antagonist |
|
Neratinib Maleate |
Tyrosine Kinase Inhibitors (TKIs) |
|
Nerlynx (Neratinib Maleate) |
Tyrosine Kinase Inhibitors (TKIs) |
|
Olaparib |
PARP inhibitor |
|
Paclitaxel |
Taxane |
|
Paclitaxel Albumin-stabilized Nanoparticle Formulation |
Taxane |
|
Palbociclib |
Kinase inhibitor (Cyclin-dependent kinase 4/6 inhibitor) |
|
Pamidronate Disodium |
Inhibits bone resorption |
Injection site reaction |
Pembrolizumab |
Monoclonal HER2 Antibody |
|
Perjeta (Pertuzumab) |
Monoclonal HER2 Antibody |
|
Pertuzumab |
Monoclonal HER2 Antibody |
|
Pertuzumab, Trastuzumab, and Hyaluronidase-zzxf |
Monoclonal HER2 Antibody |
|
Phesgo (Pertuzumab, Trastuzumab, and Hyaluronidase-zzxf) |
Monoclonal HER2 Antibody |
|
Piqray (Alpelisib) |
Phosphatidylinositol 3-kinase (PI3K) inhibitor |
|
Ribociclib |
Kinase inhibitor selective cyclin-dependent |
|
Sacituzumab Govitecan-hziy |
PARP inhibitor |
|
Soltamox (Tamoxifen Citrate) |
Anti estrogen |
|
Talazoparib Tosylate |
PARP inhibitor |
|
Talzenna (Talazoparib Tosylate) |
PARP inhibitor |
|
Tamoxifen Citrate |
Anti estrogen |
|
Taxotere (Docetaxel) |
Taxane |
|
Tecentriq (Atezolizumab) |
PD-L1 monoclonal antibody |
|
Tepadina (Thiotepa) |
Nitrogen mustard type of alkylating agent |
|
Thiotepa |
Nitrogen mustard type of alkylating agent |
|
Toremifene |
Selective estrogen receptor modulator (SERM) |
|
Trastuzumab |
Monoclonal HER2 Antibody |
|
Trastuzumab and Hyaluronidase-oysk |
Monoclonal HER2 Antibody |
|
Trexall (Methotrexate Sodium) |
Folate antagonist |
|
Trodelvy (Sacituzumab Govitecan-hziy) |
PARP inhibitor |
|
Tucatinib |
Tyrosine Kinase Inhibitors (TKIs) of HER2 |
|
Tukysa (Tucatinib) |
Tyrosine Kinase Inhibitors (TKIs) of HER2 |
|
Tykerb (Lapatinib Ditosylate) |
Tyrosine Kinase Inhibitors (TKIs) |
|
Verzenio (Abemaciclib) |
Cyclin-Dependent Kinase Inhibitor |
|
Vinblastine Sulfate |
Microtubule inhibitor |
|
Xeloda (Capecitabine) |
Antimetabolite |
|
Zoladex (Goserelin Acetate) |
LHRH agonist (hormonal therapy) |
|