Search results for "protocols"

showing 10 items of 782 documents

The natural history of breast carcinoma in patients withor = 10 metastatic axillary lymph nodes before and after the advent of adjuvant therapy: a mu…

2005

BACKGROUND The majority of patients with breast carcinoma with ≥ 10 metastatic axillary lymph nodes (ALNs) develop recurrent disease within 5 years from diagnosis. The purpose of the current study, performed retrospectively, was to characterize the natural history of this subset of patients, both before and after the advent of adjuvant anthracycline-based chemotherapy and tamoxifen. METHODS Retrospectively, patients with primary breast carcinoma (N = 882) with ≥ 10 metastatic ALNs, treated between 1954 and 1998, were selected from 3 institutions: The University of Texas M. D. Anderson Cancer Center (Houston, TX); the Institut Gustave Roussy (Villejuif, France); and Hospital Clinico Universi…

OncologyCancer Researchmedicine.medical_specialtyAxillary lymph nodesAnthracyclineBreast NeoplasmsDisease-Free SurvivalMetastasisInstitut Gustave RoussyInternal medicineAntineoplastic Combined Chemotherapy ProtocolsmedicineAdjuvant therapyHumansAnthracyclinesRetrospective Studiesbusiness.industryCarcinomaCancerMiddle Agedmedicine.diseasePrognosisCombined Modality TherapySurgerySurvival RateTamoxifenmedicine.anatomical_structureOncologyChemotherapy AdjuvantLymphatic MetastasisAxillaHormonal therapyFemalebusinessBreast carcinomaFollow-Up StudiesCancer
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Society for Immunotherapy of Cancer (SITC) clinical practice guideline on immunotherapy for the treatment of hepatocellular carcinoma.

2021

Patients with advanced hepatocellular carcinoma (HCC) have historically had few options and faced extremely poor prognoses if their disease progressed after standard-of-care tyrosine kinase inhibitors (TKIs). Recently, the standard of care for HCC has been transformed as a combination of the immune checkpoint inhibitor (ICI) atezolizumab plus the anti-vascular endothelial growth factor (VEGF) antibody bevacizumab was shown to offer improved overall survival in the first-line setting. Immunotherapy has demonstrated safety and efficacy in later lines of therapy as well, and ongoing trials are investigating novel combinations of ICIs and TKIs, in addition to interventions earlier in the course…

OncologyCancer Researchmedicine.medical_specialtyCarcinoma Hepatocellularantineoplastic protocols; guidelines as topic; immunotherapy; liver neoplasmsBevacizumabmedicine.medical_treatmentImmunologyGuidelines as TopicDiseaseQuality of life (healthcare)AtezolizumabInternal medicineliver neoplasmmedicineImmunology and AllergyHumansRadiation treatment planningRC254-282Pharmacologybusiness.industryLiver Neoplasmsantineoplastic protocolsCancerNeoplasms. Tumors. Oncology. Including cancer and carcinogensGuidelineImmunotherapymedicine.diseaseantineoplastic protocolOncologyMolecular MedicineImmunotherapybusinessHumanmedicine.drugJournal for immunotherapy of cancer
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Interferon-alpha combined with cytarabine in chronic myelogenous leukemia - clinical benefits.

2001

During the last decade, several studies have evaluated the treatment of chronic phase chronic myeloid leukemia (CML) with a combination of interferon (IFN)-alpha and low- dose cytarabine (Ara-C). This combination therapy has been shown to be superior compared to monotherapy with IFN-alpha in randomized studies with regard to hematologic and cytogenetic remissions. However, the survival benefit is small, and the toxicity of the combination therapy is high. This paper reviews the published studies on IFN-alpha/low-dose Ara-C for the treatment of chronic phase CML and discusses the value of the combination therapy.

OncologyCancer Researchmedicine.medical_specialtyCombination therapyAlpha interferonInterferonhemic and lymphatic diseasesInternal medicineLeukemia Myelogenous Chronic BCR-ABL PositiveAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansChronic phase CMLClinical Trials as Topicbusiness.industryCytarabineInterferon-alphaHematologymedicine.diseaseSurvival benefitOncologyToxicityCytarabinebusinessChronic myelogenous leukemiamedicine.drugLeukemialymphoma
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Role of gemcitabine-based combination therapy in the management of advanced pancreatic cancer: a meta-analysis of randomised trials.

2013

Background: Pancreatic cancer is the fourth leading cause of cancer-related death worldwide. Gemcitabine is the mainstay treatment for advanced disease. However, almost all up-to-date trials, that evaluated the benefit of gemcitabine-combination schedules, failed to demonstrate an improvement in overall survival (OS). In this study, we performed a systematic review and a meta-analysis of randomised clinical trials (RCTs) to investigate the efficacy and safety of gemcitabine-based combination regimens as compared to gemcitabine alone in the management of pancreatic cancer. Methods: Clinical trials were collected by searching different databases (PubMed, Embase and the Central Registry of Con…

OncologyCancer Researchmedicine.medical_specialtyCombination therapyCochrane LibraryDeoxycytidinePancreatic cancerInternal medicineAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansCombination therapyAdvanced pancreatic cancerRandomized Controlled Trials as Topicbusiness.industryHazard ratioCancerCombination chemotherapymedicine.diseaseGemcitabineGemcitabineSurgeryClinical trialPancreatic NeoplasmsMeta-analysisOncologybusinessmedicine.drugEuropean journal of cancer (Oxford, England : 1990)
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Feasibility and tolerability of sequential doxorubicin/paclitaxel followed by cyclophosphamide, methotrexate, and fluorouracil and its effects on tum…

2005

Abstract Purpose: The European Cooperative Trial in Operable breast cancer (ECTO) randomly tested whether efficacy of adjuvant doxorubicin followed by i.v. cyclophosphamide, methotrexate, and fluorouracil (CMF; doxorubicin → CMF, arm A) could be improved by adding paclitaxel (doxorubicin/paclitaxel → CMF) as adjuvant (arm B) or primary systemic therapy (PST, arm C). We report here feasibility, tolerability, locoregional antitumor activity, and breast conservation rate. Methods: A total of 1,355 women entered the study. Feasibility and safety were compared in arm A versus arms B plus C. Surgical findings were compared in arms A plus B versus arm C. Results: Grade 3 or 4 National Cancer Insti…

OncologyCancer Researchmedicine.medical_specialtyCyclophosphamidePaclitaxelmedicine.drug_classBreast NeoplasmsPharmacologyAntimetabolitechemistry.chemical_compoundBreast cancerInternal medicineAntineoplastic Combined Chemotherapy ProtocolsPreoperative CaremedicineHumansDoxorubicinCyclophosphamideAgedAged 80 and overbusiness.industryMiddle Agedmedicine.diseaseCombined Modality TherapyMethotrexateTreatment OutcomeOncologyTolerabilityPaclitaxelchemistryFluorouracilDoxorubicinMultivariate AnalysisMethotrexateFemaleFluorouracilbusinessmedicine.drugClinical cancer research : an official journal of the American Association for Cancer Research
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Metronomic Chemotherapy for Metastatic Breast Cancer.

2021

<b><i>Background:</i></b> As disease control and quality of life play a leading role in metastatic breast cancer (MBC), metronomic chemotherapy (MCT) is gaining popularity alongside conventional chemotherapy (CCT) and targeted therapies. <b><i>Summary:</i></b> MCT, defined as continuous administration of low-dose chemotherapeutic agents, is accepted as a therapy that exerts its effects via immunomodulation, anti-angiogenesis and direct cytotoxic effects. Oral administration of MCT is safe, easy to handle, and allows for flexible drug dosing. Dose accumulations associated with non-tolerable side effects are rare, so the medication can be admini…

OncologyCancer Researchmedicine.medical_specialtyCyclophosphamideReceptor ErbB-2Antineoplastic AgentsBreast NeoplasmsVinorelbinelaw.inventionCapecitabineRandomized controlled triallawOral administrationInternal medicineAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansCyclophosphamideCapecitabinebusiness.industryHematologymedicine.diseaseMetastatic breast cancerMetronomic ChemotherapyOncologyQuality of LifeMethotrexateFemalebusinessmedicine.drugOncology research and treatment
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“Dose-Dense Primary Chemotherapy, as Part of Multidisciplinary Treatment, for Inoperable Stage III B Breast Cancer - Long-Term Results of a Phase II …

2007

<i>Background:</i> Primary chemotherapy as part of multidisciplinary approach is the established treatment for inoperable stage III B breast cancer. The primary endpoints were conversion to operable disease and feasibility of conservative surgery (breast-conserving therapy: BCT); secondary were clinical and pathological complete response rate, local and distant control and safety of the primary regimen. <i>Methods:</i> Between 1998 and 2001, 40 inoperable breast cancer patients ≤60 years, 72% T4abc and 28% T4d, received 6 cycles of primary PEV dose-dense regimen: cisplatin 50 mg/m<sup>2</sup>, epirubicin 100 mg/m<sup>2</sup> and vinorelbine 25…

OncologyCancer Researchmedicine.medical_specialtyDose-dense chemotherapymedicine.medical_treatmentBreast NeoplasmsMastectomy SegmentalBreast cancerInternal medicineAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansStage (cooking)EtoposideMastectomyEpirubicinEtoposideChemotherapybusiness.industryCancerGeneral MedicineMiddle Agedmedicine.diseaseCombined Modality TherapySurgeryTreatment OutcomeOncologyFemaleCisplatinbusinessMastectomymedicine.drugEpirubicinFollow-Up Studies
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Phase II Trial of Preoperative Irinotecan–Cisplatin Followed by Concurrent Irinotecan–Cisplatin and Radiotherapy for Resectable Locally Advanced Gast…

2009

Purpose To determine in a Phase II trial whether preoperative irinotecan–cisplatin (IC) followed by concurrent IC therapy and radiotherapy (IC/RT) improved outcome in patients with resectable, locally advanced gastric adenocarcinoma (GC) or esophagogastric junction cancer (EGJC). Patients and Methods Patients with resectable Stage II–IV, M0 GC or EGJC made up the study population. The primary endpoint was pathologic complete response (pCR). Two courses of IC (irinotecan, 65mg/m 2 ; cisplatin, 30mg/m 2 on Days 1 and 8 every 21 days) were given. Patients without progression then received IC/RT, consisting of daily radiotherapy (45Gy) with concurrent IC (irinotecan, 65mg/m 2 ; cisplatin, 30mg/…

OncologyCancer Researchmedicine.medical_specialtyEsophageal Neoplasmsmedicine.medical_treatmentAdenocarcinomaNeutropeniaIrinotecanGastroenterologyDrug Administration ScheduleStomach NeoplasmsInternal medicineAntineoplastic Combined Chemotherapy ProtocolsHumansMedicineRadiology Nuclear Medicine and imagingProspective StudiesProspective cohort studySurvival rateCisplatinChemotherapyRadiationbusiness.industryRemission Inductionmedicine.diseaseCombined Modality TherapySurvival RateRadiation therapyIrinotecanOncologySpainPreoperative PeriodAdenocarcinomaCamptothecinEsophagogastric JunctionCisplatinbusinessAlgorithmsmedicine.drugInternational Journal of Radiation Oncology*Biology*Physics
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Third-line therapy for advanced non-small-cell lung cancer patients: a feasible therapeutic option?

2010

Two decades ago best supportive care was considered a valid therapeutic option for advanced non-small cell lung cancer (NSCLC) patients until the evidence derived from meta-analysis showed symptom improvement and a survival advantage from systemic chemotherapy. A further advantage was reported when docetaxel and pemetrexed were used as second-line treatment after failure of first-line platinum-based chemotherapy. Furthermore, the biologic therapies targeting the epidermal growth factor receptor – erlotinib and gefitinib – have modified the therapeutic approach to second- and third-line treatment of NSCLC patients. In fact, to date, erlotinib is the only drug to be licensed for third-line th…

OncologyCancer Researchmedicine.medical_specialtyLung NeoplasmsTherapeutic approachGefitinibInternal medicineCarcinoma Non-Small-Cell LungAntineoplastic Combined Chemotherapy ProtocolsmedicineBiomarkers TumorHumansEpidermal growth factor receptorLung cancerneoplasmsClinical Trials as Topicbiologybusiness.industryCancerGeneral Medicinemedicine.diseasePrognosisrespiratory tract diseasesSurgeryPemetrexedOncologyDocetaxelbiology.proteinErlotinibbusinessmedicine.drugOncology
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Gemcitabine-based doublets versus single-agent therapy for elderly patients with advanced nonsmall cell lung cancer: a Literature-based Meta-analysis.

2009

BACKGROUND: Although platinum-based combinations are considered the best option of care for patients with advanced nonsmall cell lung cancer (NSCLC), single-agent therapy is the preferred treatment for older patients. Since the late 1990s, various combinations of third-generation agents (gemcitabine [G], vinorelbine, docetaxel, and paclitaxel) have been tested, yielding contradictory results. The authors of this report performed a literature-based meta-analysis to assess the efficacy and tolerability of G-based doublets compared with single-agent chemotherapy for elderly patients with NSCLC. METHODS: Data from all published, randomized, phase 3 trials that compared a G-based doublet with a …

OncologyCancer Researchmedicine.medical_specialtyLung Neoplasmsmedicine.medical_treatmentVinorelbineVinblastineDeoxycytidineInternal medicineCarcinoma Non-Small-Cell LungAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansLung cancerSurvival rateAgedRandomized Controlled Trials as TopicChemotherapybusiness.industryCancerVinorelbinemedicine.diseaseGemcitabineGemcitabineSurgeryGemcitabinecancerOncologyDocetaxelTolerabilityClinical Trials Phase III as TopicTaxoidsbusinessmedicine.drugCancer
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