Docetaxel and Cyclophosphamide Chemotherapy Guide

Total Page:16

File Type:pdf, Size:1020Kb

Docetaxel and Cyclophosphamide Chemotherapy Guide Docetaxel and cyclophosphamide chemotherapy guide For patients with breast cancer 1 Table of Contents What is chemotherapy? ..................................... 4 What should I discuss with my doctor before starting chemotherapy ....................................... 5 What are docetaxel and cyclophosphamide? ..... 9 How should I prepare for treatment? .................. 9 What can I expect during my treatment? .......... 10 What are the common side effects of docetaxel and cyclophosphamide treatment? .................. 12 How do I manage common side effects? ......... 13 Where can I get support? ................................. 32 2 Your health care team Oncologist: _______________________________ Pharmacist: _______________________________ Nurse: _______________________________ Dietitian: _______________________________ Social worker: ___________________________________ Medical Day Care: 416-864-5222 2 Donnelly Nursing Unit: 416-864-5099 3 What is chemotherapy? Chemotherapy is a type of treatment for cancer. Chemotherapy can be a single drug or it can be a few types of drugs at the same time. When used alone or along with surgery or radiation therapy, chemotherapy can often shrink a tumour or prevent its spread. How does it work? Chemotherapy kills cells that grow quickly. This is why it kills cancer cells. But it also affects healthy cells that grow fast. This includes cells in the mouth and stomach lining, bone marrow, skin and hair. This is why patients having chemotherapy treatment get side effects such as hair loss, nausea and low blood cell counts. As a rule, chemotherapy is given in cycles of treatment. There is a time of no treatment between cycles. This lets normal cells recover before the next cycle begins. 4 What should I discuss with my doctor before starting chemotherapy? Your health history • Tell your oncologist about any other health problems you have or had. Some health problems may affect the outcomes with this treatment. • Tell other healthcare professionals you are seeing about the type of chemotherapy you are having. Vaccines, surgery and dental work • You should have all your dental work done before you start your treatment. • Check with your oncologist before you have any vaccines, surgery or dental treatment. 5 Other medicines, herbs and supplements • Tell your oncologist, chemotherapy nurse, dietitian and pharmacist about any over the counter, herbal or doctor-prescribed medicines or vitamins you are taking. • Check with your oncologist, chemotherapy nurse, dietitian or pharmacist before you start taking any new drugs, including vitamins and herbal or alternative treatments. • Tell your oncologist if you are taking ASA (Aspirin®), ibuprofen (Advil® or Motrin®), acetaminophen (Tylenol®), naproxen (Aleve®) or blood thinners. 6 Your menstrual cycles (periods) • Your periods may become heavier or lighter. This change could be permanent. • You may develop symptoms of menopause such as hot flashes, vaginal dryness, mood swings and changes in sexual desire. Talk to your doctor about these symptoms if they bother you. Birth Control • Women who have not yet reached menopause should take steps to avoid getting pregnant while being treated. Chemotherapy may harm your baby. • Talk to your oncologist about what kind of birth control you can use to make sure you do not become pregnant. 7 Pregnancy and fertility • If you want to have children, speak to your oncologist before starting your first treatment. Chemotherapy may affect your chances of having a baby in the future. • Tell your oncologist as soon as possible if you become pregnant. Breastfeeding • If you have a baby, do not breastfeed while being treated with chemotherapy. Ask your oncologist how long you should wait to breastfeed after your final chemotherapy treatment. Ask your chemotherapy nurse, pharmacist or oncologist if you have any questions. 8 What are docetaxel and cyclophosphamide? Docetaxel and cyclophosphamide are the names of chemotherapy drugs, used together, to treat breast cancer. They are both liquids and are given through a needle in your arm. One cycle of docetaxel and cyclophosphamide is 3 weeks (21 days). You will be considered for treatment once every 3 weeks for 4 cycles. How should I prepare for treatment? Before starting each docetaxel and cyclophosphamide treatment, your doctor will give you a prescription for dexamethasone tablets to help prevent some of the side effects. Start taking your dexamethasone tablets the morning and night before your chemotherapy treatments. Follow your doctor’s instructions on how to take these medicines. While being treated, do not eat grapefruit, starfruit or seville orange and the juices and products made from them. They may increase your side effects. Otherwise, most patients can eat and drink as normal before treatments. Your oncologist will tell you if you need to change what you eat. 9 What can I expect during my treatment? On the day of your treatments you will come to the Medical Day Care Unit: 1. You will have a blood test before each treatment to check your blood counts. Low blood counts can mean your body will not be able to handle another dose of chemotherapy and your treatment may be delayed. 2. In the Medical Day Care Unit a chemotherapy nurse will give you docetaxel and cyclophosphamide through a needle into your arm. 3. Tell your chemotherapy nurse right away if you feel any burning or pain around the needle site when having your chemotherapy. Docetaxel can cause damage to tissue around the needle if it leaks out. 4. Tell your chemotherapy nurse if, during your treatment, you: Feel short of breath Have pains in your chest Notice itching, swelling or severe rash These can be signs that you might be allergic to docetaxel. Go to the emergency room right 10 away if you have these symptoms after you leave the Medical Day Care Unit. 5. Once your treatment is done you can go home. 11 What are the common side effects of docetaxel and cyclophosphamide treatment? Side effects of chemotherapy depend on the types of drugs used and how your body reacts to those drugs. Nausea (sickness in stomach) and vomiting Hair thinning Numbness or tingling in the hands or feet Fatigue (tiredness and weakness) Pain in the muscles or joints Diarrhea Mild swelling in arms and legs (puffiness) Sores in your mouth Infection (fever, chills, cough, sore throat) Unusual bleeding or bruising Heartburn Watery eyes Nail changes Dry itchy skin Pain with urination 12 How do I manage common side effects? Nausea and vomiting Nausea and vomiting is common with the docetaxel and cyclophosphamide treatment. It is usually the worst during the first 12 to 48 hours after treatment and often gets better in 3 to 7 days. You may be given a prescription for medicine to take before your chemotherapy treatment to prevent nausea and vomiting. You may also get a prescription for medicine to take if you have nausea or vomiting even though you already took the prevention medicine. This is called rescue medicine. Your pharmacist will explain these medicines to you. What you can do • Try to take your rescue medicine for nausea and vomiting as soon as you start to feel nauseated or 30 minutes before a certain time you think you will have nausea and vomiting (for example before dinner time). • If you vomit within 30 minutes of taking your anti-nausea pills or see a pill come up, you can take another pill. • Drink lots of liquids. 13 • Get fresh air and plenty of rest. • Eat small meals often and limit spicy, strong smelling foods. When to get help If you vomit for more than 24 hours or feel nausea longer than 48 hours, even though you are taking your nausea medicine, contact your doctor or nurse. 14 Hair thinning Hair thinning usually starts 2 to 3 weeks after your first treatment. Your scalp may feel tingly as your hair is falling out. What you can do • Use a gentle shampoo and a soft hair brush. • Avoid using dyes, perms, bleaches and hair sprays until 6 months after your last chemotherapy treatment. • Protect your scalp from sun exposure and cold weather. • Consider cutting your hair short before it falls out. • Ask your chemotherapy nurse for information about wigs and head coverings. 15 Numbness and tingling in hands and feet Numbness and tingling is caused by the effects of docetaxel on your nerves. Your feeling may slowly return to normal after treatment ends. Contact your doctor if you • Have trouble doing up buttons, writing or picking up small objects • Have pain or difficulty moving your hands and feet 16 Tiredness and weakness Feeling tired and weak is most common after the first 7 days of each cycle. You may feel more and more tired with each treatment. It takes a few months for the tiredness to go away even after your treatment has ended. Your energy level will improve over time. A low red blood cell level can also make you tired. When your oncologist does blood work they will monitor your red blood cells. What you can do Eat well-balanced meals. Do mild exercise such as walking. Be sure to rest well when you need to. Call your doctor or nurse if you Have shortness of breath Fall and hurt yourself Feel dizzy when walking or when getting up out of bed 17 Muscle and joint pain You may have muscle and joint pain for a few days after each treatment. What you can do • Take any medicines your doctor prescribed you for pain. Follow your doctor or pharmacist’s instructions. • If your pain becomes unbearable, ask your oncologist or clinic pharmacist if you can take acetaminophen (Tylenol®) or ibuprofen (Advil® or Motrin®). Your oncologist may prescribe a medicine for your pain instead. • Rest when you need to and try doing light exercise. 18 Diarrhea (loose watery stools) What you can do • To treat diarrhea you may use loperamide (Imodium®) or a stronger anti-diarrhea medicine called Lomotil®.
Recommended publications
  • Combination of Cabazitaxel and Plicamycin Induces Cell Death in Drug Resistant B-Cell Acute Lymphoblastic Leukemia
    Clinical and Translational Science Institute Centers 9-1-2018 Combination of cabazitaxel and plicamycin induces cell death in drug resistant B-cell acute lymphoblastic leukemia Rajesh R. Nair West Virginia University Debbie Piktel West Virginia University Werner J. Geldenhuys West Virginia University Laura F. Gibson West Virginia University Follow this and additional works at: https://researchrepository.wvu.edu/ctsi Part of the Medicine and Health Sciences Commons Digital Commons Citation Nair, Rajesh R.; Piktel, Debbie; Geldenhuys, Werner J.; and Gibson, Laura F., "Combination of cabazitaxel and plicamycin induces cell death in drug resistant B-cell acute lymphoblastic leukemia" (2018). Clinical and Translational Science Institute. 34. https://researchrepository.wvu.edu/ctsi/34 This Article is brought to you for free and open access by the Centers at The Research Repository @ WVU. It has been accepted for inclusion in Clinical and Translational Science Institute by an authorized administrator of The Research Repository @ WVU. For more information, please contact [email protected]. HHS Public Access Author manuscript Author ManuscriptAuthor Manuscript Author Leuk Res Manuscript Author . Author manuscript; Manuscript Author available in PMC 2019 September 01. Published in final edited form as: Leuk Res. 2018 September ; 72: 59–66. doi:10.1016/j.leukres.2018.08.002. Combination of cabazitaxel and plicamycin induces cell death in drug resistant B-cell acute lymphoblastic leukemia Rajesh R. Naira, Debbie Piktelb, Werner J. Geldenhuysc,
    [Show full text]
  • Cyclophosphamide-Etoposide PO Ver
    Chemotherapy Protocol LYMPHOMA CYCLOPHOSPHAMIDE-ETOPOSIDE ORAL Regimen Lymphoma – Cyclophosphamide-Etoposide PO Indication Palliative treatment of malignant lymphoma Toxicity Drug Adverse Effect Cyclophosphamide Dysuria, haemorrragic cystitis (rare), taste disturbances Etoposide Alopecia, hyperbilirubinaemia The adverse effects listed are not exhaustive. Please refer to the relevant Summary of Product Characteristics for full details. Patients diagnosed with Hodgkin’s Lymphoma carry a lifelong risk of transfusion associated graft versus host disease (TA-GVHD). Where blood products are required these patients must receive only irradiated blood products for life. Local blood transfusion departments must be notified as soon as a diagnosis is made and the patient must be issued with an alert card to carry with them at all times. Monitoring Drugs FBC, LFTs and U&Es prior to day one of treatment Albumin prior to each cycle Dose Modifications The dose modifications listed are for haematological, liver and renal function and drug specific toxicities only. Dose adjustments may be necessary for other toxicities as well. In principle all dose reductions due to adverse drug reactions should not be re-escalated in subsequent cycles without consultant approval. It is also a general rule for chemotherapy that if a third dose reduction is necessary treatment should be stopped. Please discuss all dose reductions / delays with the relevant consultant before prescribing, if appropriate. The approach may be different depending on the clinical circumstances. Version 1.1 (Jan 2015) Page 1 of 6 Lymphoma- Cyclophosphamide-Etoposide PO Haematological Dose modifications for haematological toxicity in the table below are for general guidance only. Always refer to the responsible consultant as any dose reductions or delays will be dependent on clinical circumstances and treatment intent.
    [Show full text]
  • PEMD-91-12BR Off-Label Drugs: Initial Results of a National Survey
    11 1; -- __...._-----. ^.-- ______ -..._._ _.__ - _........ - t Ji Jo United States General Accounting Office Washington, D.C. 20648 Program Evaluation and Methodology Division B-242851 February 25,199l The Honorable Edward M. Kennedy Chairman, Committee on Labor and Human Resources United States Senate Dear Mr. Chairman: In September 1989, you asked us to conduct a study on reimbursement denials by health insurers for off-label drug use. As you know, the Food and Drug Administration designates the specific clinical indications for which a drug has been proven effective on a label insert for each approved drug, “Off-label” drug use occurs when physicians prescribe a drug for clinical indications other than those listed on the label. In response to your request, we surveyed a nationally representative sample of oncologists to determine: . the prevalence of off-label use of anticancer drugs by oncologists and how use varies by clinical, demographic, and geographic factors; l the extent to which third-party payers (for example, Medicare intermediaries, private health insurers) are denying payment for such use; and l whether the policies of third-party payers are influencing the treatment of cancer patients. We randomly selected 1,470 members of the American Society of Clinical Oncologists and sent them our survey in March 1990. The sam- pling was structured to ensure that our results would be generalizable both to the nation and to the 11 states with the largest number of oncologists. Our response rate was 56 percent, and a comparison of respondents to nonrespondents shows no noteworthy differences between the two groups.
    [Show full text]
  • Consumer Medicine Information
    DBL™ Docetaxel Concentrated Injection docetaxel Consumer Medicine Information What is in this leaflet It works by stopping cells from • wheezing or difficulty breathing growing and multiplying. or a tight feeling in your chest This leaflet answers some common Ask your doctor if you have any • swelling of the face, lips, tongue questions about DBL Docetaxel, questions about why this medicine or other parts of the body Concentrated Injection. has been prescribed for you. • rash, itching, hives or flushed, red It does not contain all the available Your doctor may have prescribed it skin information. It does not take the for another reason. • dizziness or light-headedness place of talking to your doctor or This medicine is not addictive. • back pain pharmacist. This medicine is available only with Do not use DBL Docetaxel, All medicines have risks and a doctor’s prescription. benefits. Your doctor has weighed Concentrated Injection if you have, You may have taken another the risks of you taking DBL or have had, any of the following Docetaxel, Concentrated Injection medicine to treat your breast, non medical conditions: small cell lung cancer, ovarian, against the benefits they expect it • severe liver problems prostate or head and neck cancer. will have for you. • blood disorder with a reduced However, your doctor has now number of white blood cells If you have any concerns about decided to treat you with docetaxel. taking this medicine, ask your There is not enough information to Do not use this medicine if you are doctor or pharmacist. recommend the use of this medicine pregnant or intend to become Keep this leaflet with the medicine.
    [Show full text]
  • Inhibition of Cyclophosphamide and Mitomycin C-Induced Sister Chromatid Exchanges in Mice by Vitamin C
    ICANCERRESEARCH46,2670-2674, June 19861 Inhibition of Cyclophosphamide and Mitomycin C-induced Sister Chromatid Exchanges in Mice by Vitamin C G. Krishna,' J. Nath, and T. Ong Natio,wilnstitutefor OccupationaiSafety and Health, Division ofRespiratory Disease Studies, Morgansown, West Virginia 26505-2888 fG. K., T. 0.], andDivision of PlantandSoil Sciences,West VirginiaUniversity,Morgantown,West Visijnia 265O6fJ.N.J ABSTRACF The research reported here was performed to determine the effect of ascorbic acid on SCEs induced by CPA and MMC in Ascorbic acid (vitamin C) is known to act as an antimutagen and in vivo and in vivo/in vitro conditions in bone marrow and anticarcinogen in several test systems. However, there is no report of its spleen cells of mice. Analysis of SCEs is a sensitive cytogenetic effect on carcinogen-induced chromosomal damage in vii'o in animals. technique for detecting cellular chromosomal damage (11). The present study was performed to determine whether or not ascorbic SCEs are visualized as reciprocal exchangesof staining inten acid affects sister ébromatidexchanges (SCEs) induced by cyclophos sities between sister chromatid arms in metaphase cells that phamide (CPA) and mitomycin C (MMC) in bone marrow and spleen cells in mice. The results indicate that ascorbic acid per se did not cause have replicated twice in the presenceof BrdUrd. a significantincreaseinSCEsin mice.However,increasingconcentra tions of ascorbic acid caused decreasing levels of CPA- and MMC induced SCEs in both cell types in rho. At the highest concentration of MATERIALS AND METHODS ascorbic acid, 6.68 gfkg, approximately 75 and 40% SCE inhibition in Animals. Male CD-I mice were purchased from Charles River Breed both cell types was noted for CPA and MMC, respectively.
    [Show full text]
  • Chemotherapy Protocol
    Chemotherapy Protocol BREAST CANCER CYCLOPHOSPHAMIDE-EPIRUBICIN-PACLITAXEL (7 day) Regimen • Breast Cancer – Cyclophosphamide-Epirubicin-Paclitaxel (7 day) Indication • Neoadjuvant / adjuvant therapy of early breast cancer • WHO Performance status 0, 1 Toxicity Drug Adverse Effect Cyclophosphamide Dysuria, haemorrhagic cystitis, taste disturbances Epirubicin Cardio-toxicity, urinary discolouration (red) Hypersensitivity, hypotension, bradycardia, peripheral Paclitaxel neuropathy, myalgia and back pain on administration The adverse effects listed are not exhaustive. Please refer to the relevant Summary of Product Characteristics for full details. Monitoring Regimen • FBC, U&Es and LFTs prior to each cycle. • Ensure adequate cardiac function before starting treatment with epirubicin. Baseline LVEF should be measured, particularly in patients with a history of cardiac problems or in the elderly. Dose Modifications The dose modifications listed are for haematological, liver and renal function only. Dose adjustments may be necessary for other toxicities as well. In principle all dose reductions due to adverse drug reactions should not be re- escalated in subsequent cycles without consultant approval. It is also a general rule for chemotherapy that if a third dose reduction is necessary treatment should be stopped. Please discuss all dose reductions / delays with the relevant consultant before prescribing if appropriate. The approach may be different depending on the clinical circumstances. The following is a general guide only. Version 1.2 (November 2020) Page 1 of 7 Breast – Cyclophosphamide-Epirubicin-Paclitaxel (7 day) Haematological Prior to prescribing the following treatment criteria must be met on day one of treatment. Criteria Eligible Level Neutrophils equal to or more than 1x10 9/L Platelets equal to or more than 100x10 9/L Consider blood transfusion if patient symptomatic of anaemia or has a haemoglobin of less than 8g/dL If counts on day one are below these criteria for neutrophils and platelets then delay treatment for seven days.
    [Show full text]
  • 5-Fluorouracil + Adriamycin + Cyclophosphamide) Combination in Differentiated H9c2 Cells
    Article Doxorubicin Is Key for the Cardiotoxicity of FAC (5-Fluorouracil + Adriamycin + Cyclophosphamide) Combination in Differentiated H9c2 Cells Maria Pereira-Oliveira, Ana Reis-Mendes, Félix Carvalho, Fernando Remião, Maria de Lourdes Bastos and Vera Marisa Costa * UCIBIO, REQUIMTE, Laboratory of Toxicology, Faculty of Pharmacy, University of Porto, Rua de Jorge Viterbo Ferreira, 228, 4050-313 Porto, Portugal; [email protected] (M.P.-O.); [email protected] (A.R.-M.); [email protected] (F.C.); [email protected] (F.R.); [email protected] (M.L.B.) * Correspondence: [email protected] Received: 4 October 2018; Accepted: 3 January 2019; Published: 10 January 2019 Abstract: Currently, a common therapeutic approach in cancer treatment encompasses a drug combination to attain an overall better efficacy. Unfortunately, it leads to a higher incidence of severe side effects, namely cardiotoxicity. This work aimed to assess the cytotoxicity of doxorubicin (DOX, also known as Adriamycin), 5-fluorouracil (5-FU), cyclophosphamide (CYA), and their combination (5-Fluorouracil + Adriamycin + Cyclophosphamide, FAC) in H9c2 cardiac cells, for a better understanding of the contribution of each drug to FAC-induced cardiotoxicity. Differentiated H9c2 cells were exposed to pharmacological relevant concentrations of DOX (0.13–5 μM), 5-FU (0.13–5 μM), CYA (0.13–5 μM) for 24 or 48 h. Cells were also exposed to FAC mixtures (0.2, 1 or 5 μM of each drug and 50 μM 5-FU + 1 μM DOX + 50 μM CYA). DOX was the most cytotoxic drug, followed by 5-FU and lastly CYA in both cytotoxicity assays (reduction of 3-(4,5-dimethylthiazol-2- yl)-2,5-diphenyl tetrazolium bromide (MTT) and neutral red (NR) uptake).
    [Show full text]
  • Cyclophosphamide-Doxorubicin Ver
    Chemotherapy Protocol BREAST CANCER CYCLOPHOSPHAMIDE-DOXORUBICIN Regimen Breast Cancer – Cyclophosphamide-Doxorubicin Indication Primary systemic (neoadjuvant) therapy of breast cancer Adjuvant therapy of high risk (greater than 5%) node negative breast cancer WHO Performance status 0, 1, 2 Toxicity Drug Adverse Effect Cyclophosphamide Dysuria, haemorrhagic cystitis, taste disturbances Doxorubicin Cardio toxicity, urinary discolourisation (red) The adverse effects listed are not exhaustive. Please refer to the relevant Summary of Product Characteristics for full details. Monitoring Regimen FBC, U&E’s and LFT’s prior to each cycle. Ensure adequate cardiac function before starting treatment with doxorubicin. Baseline LVEF should be measured, particularly in patients with a history of cardiac problems or in the elderly. Dose Modifications The dose modifications listed are for haematological, liver and renal function only. Dose adjustments may be necessary for other toxicities as well. In principle all dose reductions due to adverse drug reactions should not be re- escalated in subsequent cycles without consultant approval. It is also a general rule for chemotherapy that if a third dose reduction is necessary treatment should be stopped. Version 1.1 (Aug 2014) Page 1 of 6 Breast – Cyclophosphamide-Doxorubicin Please discuss all dose reductions / delays with the relevant consultant before prescribing if appropriate. The approach may be different depending on the clinical circumstances. The following is a general guide only. Haematological Prior to prescribing the following treatment criteria must be met on day 1 of treatment. Criteria Eligible Level Neutrophil equal to or more than 1x109/L Platelets equal to or more than 100x109/L Consider blood transfusion if patient symptomatic of anaemia or has a haemoglobin of less than 8g/dL If counts on day one are below these criteria for neutrophil and/or platelets then delay treatment for seven days.
    [Show full text]
  • Identification of Inhibitors of Ovarian Cancer Stem-Like Cells by High-Throughput Screening Roman Mezencev, Lijuan Wang and John F Mcdonald*
    Mezencev et al. Journal of Ovarian Research 2012, 5:30 http://www.ovarianresearch.com/content/5/1/30 RESEARCH Open Access Identification of inhibitors of ovarian cancer stem-like cells by high-throughput screening Roman Mezencev, Lijuan Wang and John F McDonald* Abstract Background: Ovarian cancer stem cells are characterized by self-renewal capacity, ability to differentiate into distinct lineages, as well as higher invasiveness and resistance to many anticancer agents. Since they may be responsible for the recurrence of ovarian cancer after initial response to chemotherapy, development of new therapies targeting this special cellular subpopulation embedded within bulk ovarian cancers is warranted. Methods: A high-throughput screening (HTS) campaign was performed with 825 compounds from the Mechanistic Set chemical library [Developmental Therapeutics Program (DTP)/National Cancer Institute (NCI)] against ovarian cancer stem-like cells (CSC) using a resazurin-based cell cytotoxicity assay. Identified sets of active compounds were projected onto self-organizing maps to identify their putative cellular response groups. Results: From 793 screening compounds with evaluable data, 158 were found to have significant inhibitory effects on ovarian CSC. Computational analysis indicates that the majority of these compounds are associated with mitotic cellular responses. Conclusions: Our HTS has uncovered a number of candidate compounds that may, after further testing, prove effective in targeting both ovarian CSC and their more differentiated progeny. Keywords: High-throughput screening, Ovarian cancer, Cancer stem cells Background alternative strategies. One approach has been to evaluate Ovarian cancer is the most lethal of gynecological can- molecules known to be inhibitory against pathways cers [1] despite its typically high initial response rate to believed to be deregulated in CSC (e.g., the Hedgehog, chemotherapy [2].
    [Show full text]
  • Prevalence and Safety of Off-Label Use of Chemotherapeutic Agents in Older Patients with Breast Cancer: Estimates from SEER-Medicare Data
    Supplemental online content for: Prevalence and Safety of Off-Label Use of Chemotherapeutic Agents in Older Patients With Breast Cancer: Estimates From SEER-Medicare Data Anne A. Eaton, MS; Camelia S. Sima, MD, MS; and Katherine S. Panageas, DrPH J Natl Compr Canc Netw 2016;14(1):57–65 • eAppendix 1: J-Codes Representing Intravenous Chemotherapy • eAppendix 2: Established Sequential Adjuvant Chemotherapy Regimens for Breast Cancer • eTable 1: Patient Characteristics © JNCCN—Journal of the National Comprehensive Cancer Network | Volume 14 Number 1 | January 2016 Eaton et al - 1 eAppendix 1: J-Codes Representing Intravenous Chemotherapy J-Code Agent J-Code Agent J9000 Injection, doxorubicin HCl, 10 mg J9165 Injection, diethylstilbestrol diphosphate, 250 J9001 Injection, doxorubicin HCl, all lipid mg formulations, 10 mg J9170 Injection, docetaxel, 20 mg J9010 Injection, alemtuzumab, 10 mg J9171 Injection, docetaxel, 1 mg J9015 Injection, aldesleukin, per single use vial J9175 Injection, Elliotts’ B solution, 1 ml J9017 Injection, arsenic trioxide, 1 mg J9178 Injection, epirubicin HCl, 2 mg J9020 Injection, asparaginase, 10,000 units J9179 Injection, eribulin mesylate, 0.1 mg J9025 Injection, azacitidine, 1 mg J9180 Epirubicin HCl, 50 mg J9027 Injection, clofarabine, 1 mg J9181 Injection, etoposide, 10 mg J9031 BCG (intravesical) per instillation J9182 Etoposide, 100 mg J9033 Injection, bendamustine HCl, 1 mg J9185 Injection, fludarabine phosphate, 50 mg J9035 Injection, bevacizumab, 10 mg J9190 Injection, fluorouracil, 500 mg J9040 Injection,
    [Show full text]
  • Chemotherapy and Polyneuropathies Grisold W, Oberndorfer S Windebank AJ European Association of Neurooncology Magazine 2012; 2 (1) 25-36
    Volume 2 (2012) // Issue 1 // e-ISSN 2224-3453 Neurology · Neurosurgery · Medical Oncology · Radiotherapy · Paediatric Neuro- oncology · Neuropathology · Neuroradiology · Neuroimaging · Nursing · Patient Issues Chemotherapy and Polyneuropathies Grisold W, Oberndorfer S Windebank AJ European Association of NeuroOncology Magazine 2012; 2 (1) 25-36 Homepage: www.kup.at/ journals/eano/index.html OnlineOnline DatabaseDatabase FeaturingFeaturing Author,Author, KeyKey WordWord andand Full-TextFull-Text SearchSearch THE EUROPEAN ASSOCIATION OF NEUROONCOLOGY Member of the Chemotherapy and Polyneuropathies Chemotherapy and Polyneuropathies Wolfgang Grisold1, Stefan Oberndorfer2, Anthony J Windebank3 Abstract: Peripheral neuropathies induced by taxanes) immediate effects can appear, caused to be caused by chemotherapy or other mecha- chemotherapy (CIPN) are an increasingly frequent by different mechanisms. The substances that nisms, whether treatment needs to be modified problem. Contrary to haematologic side effects, most frequently cause CIPN are vinca alkaloids, or stopped due to CIPN, and what symptomatic which can be treated with haematopoetic taxanes, platin derivates, bortezomib, and tha- treatment should be recommended. growth factors, neither prophylaxis nor specific lidomide. Little is known about synergistic neu- Possible new approaches for the management treatment is available, and only symptomatic rotoxicity caused by previously given chemo- of CIPN could be genetic susceptibility, as there treatment can be offered. therapies, or concomitant chemotherapies. The are some promising advances with vinca alka- CIPN are predominantly sensory, duration-of- role of pre-existent neuropathies on the develop- loids and taxanes. Eur Assoc Neurooncol Mag treatment-dependent neuropathies, which de- ment of a CIPN is generally assumed, but not 2012; 2 (1): 25–36. velop after a typical cumulative dose. Rarely mo- clear.
    [Show full text]
  • Chemotherapy Protocol
    Chemotherapy Protocol BREAST CANCER CYCLOPHOSPHAMIDE-DOCETAXEL-DOXORUBICIN (TAC) Regimen Breast Cancer – Cyclophosphamide-Docetaxel-Doxorubicin (TAC) Indication Adjuvant therapy for node positive early breast cancer WHO Performance status 0, 1, 2 Toxicity Drug Adverse Effect Cyclophosphamide Dysuria, haemorrhagic cystitis, taste disturbances Hypersensitivity, fluid retention, neuropathy, joint pains, nail Docetaxel changes, fatigue Doxorubicin Cardio toxicity, urinary discolourisation (red) The adverse effects listed are not exhaustive. Please refer to the relevant Summary of Product Characteristics for full details. Monitoring Regimen FBC, U&E’s and LFT’s prior to each cycle. Ensure adequate cardiac function before starting treatment. Baseline LVEF should be measured, particularly in patients with a history of cardiac problems or in the elderly. Dose Modifications The dose modifications listed are for haematological, liver and renal function only. Dose adjustments may be necessary for other toxicities as well. In principle all dose reductions due to adverse drug reactions should not be re- escalated in subsequent cycles without consultant approval. It is also a general rule for chemotherapy that if a third dose reduction is necessary treatment should be stopped. Version 1.1 (Aug 2014) Page 1 of 8 Breast – Cyclophosphamide-Docetaxel-Doxorubicin (TAC) Please discuss all dose reductions / delays with the relevant consultant before prescribing if appropriate. The approach may be different depending on the clinical circumstances. The following is a general guide only. Haematological Prior to prescribing the following treatment criteria must be met on day one of treatment. Criteria Eligible Level Neutrophil equal to or more than 1x109/L Platelets equal to or more than 100x109/L Consider blood transfusion if patient symptomatic of anaemia or has a haemoglobin of less than 8g/dL If counts on day one are below these criteria for neutrophils and/or platelets then delay treatment for seven days.
    [Show full text]