Study of Cetuximab With Radiation Followed by Consolidation Chemotherapy for NSCLC
7. december 2016 opdateret af: Ahmad Tarhini, University of Pittsburgh
A Phase II Study of Cetuximab in Combination With External Beam Radiation Followed By Consolidation Chemotherapy for Patients With Locally Advanced Non-Small Cell Lung Cancer (NSCLC)
This is an open label, phase II study in which cetuximab with concurrent thoracic radiotherapy followed by consolidation chemotherapy with paclitaxel/carboplatin/cetuximab will be administered to subjects with locally advanced NSCLC.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This is a Phase II study to determine the overall survival for patients with locally advanced NSCLC treated with cetuximab with concurrent thoracic radiotherapy followed by consolidation chemotherapy with paclitaxel/carboplatin/cetuximab.
This is a multicenter study including 36 subjects who will be males and females, both greater than 18 years of age.
All subjects will initially receive radiation and cetuximab.
Radiation will be given once a day (Monday-Friday) for approximately 6-8 weeks.
During the course of radiation, cetuximab will be given intravenously once a week.
Approximately 4-6 weeks after the last radiation dose, the subjects will be treated with chemotherapy, paclitaxel/carboplatin.
Chemotherapy will be given intravenously once every 3 weeks for 3 cycles (1 cycle=3 weeks).
Cetuximab intravenous administration will be continued throughout the entire study, once a week through week 26 including during chemotherapy.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
40
Fase
- Fase 2
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
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Florida
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Miami, Florida, Forenede Stater, 33136
- Sylvester Comprehensive Cancer Center, University of Miami
-
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Georgia
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Atlanta, Georgia, Forenede Stater, 30322
- Emory Winship Cancer Institute
-
-
Maryland
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Baltimore, Maryland, Forenede Stater, 21231
- Sidney Kimmel Comprehensive Cancer Center at John Hopkins
-
-
Ohio
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Steubenville, Ohio, Forenede Stater, 43952
- UPMC Cancer Center -Teramana Cancer Center
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Pennsylvania
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Beaver, Pennsylvania, Forenede Stater, 15009
- UPMC Cancer Center -Beaver
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Clairton, Pennsylvania, Forenede Stater, 15025
- UPMC Cancer Center - Clairton
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Greensburg, Pennsylvania, Forenede Stater, 15601
- UPMC Cancer Center - Oakbrook Commons
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Greensburg, Pennsylvania, Forenede Stater, 15601
- UPMC Cancer Center -Arnold Palmer Pavilion
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Hershey, Pennsylvania, Forenede Stater, 17033
- Penn State Cancer Institute, Penn State Milton S. Hershey Medical Center
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Indiana, Pennsylvania, Forenede Stater, 15701
- UPMC Cancer Center -Indiana
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Johnstown, Pennsylvania, Forenede Stater, 15901
- UPMC Cancer Center -John P. Murtha Pavilion
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McKeesport, Pennsylvania, Forenede Stater, 15132
- UPMC Cancer Center -McKeesport
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Monroeville, Pennsylvania, Forenede Stater, 15146
- UPMC Cancer Center -Haymaker Rd.
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Monroeville, Pennsylvania, Forenede Stater, 15146
- UPMC Cancer Center -Mosside Blvd.
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Moon Township, Pennsylvania, Forenede Stater, 15108
- UPMC Cancer Center -Sewickley Medical Center
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Mt. Pleasant, Pennsylvania, Forenede Stater, 15666
- UPMC Cancer Center -Mt. Pleasant
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New Castle, Pennsylvania, Forenede Stater, 16105
- UPMC Cancer Center -Jameson
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New Castle, Pennsylvania, Forenede Stater, 16105
- UPMC Cancer Center -New Castle
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Pittsburgh, Pennsylvania, Forenede Stater, 15213
- UPMC Presbyterian -Radiation Oncology
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Pittsburgh, Pennsylvania, Forenede Stater, 15215
- UPMC Cancer Center -Delafield Rd.
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Pittsburgh, Pennsylvania, Forenede Stater, 15215
- UPMC Cancer Center -St. Margaret
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Pittsburgh, Pennsylvania, Forenede Stater, 15232
- Universtity of Pittsburgh Cancer Institute -Hillman Cancer Center
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Pittsburgh, Pennsylvania, Forenede Stater, 15232
- UPMC Cancer Center -UPMC Shadyside
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Pittsburgh, Pennsylvania, Forenede Stater, 15237
- UPMC Cancer Center -Passavant
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Pittsburgh, Pennsylvania, Forenede Stater, 15241
- UPMC Cancer Center -Drake
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Pittsburgh, Pennsylvania, Forenede Stater, 15243
- UPMC Cancer Center -St. Clair
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Seneca, Pennsylvania, Forenede Stater, 16346
- UPMC Cancer Center -UPMC Northwest
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Uniontown, Pennsylvania, Forenede Stater, 15401
- UPMC Cancer Center -Robert Eberly Pavilion
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Uniontown, Pennsylvania, Forenede Stater, 15401
- UPMC Cancer Center -Uniontown
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Washington, Pennsylvania, Forenede Stater, 15301
- UPMC Cancer Center -Washington
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Wexford, Pennsylvania, Forenede Stater, 15090
- UPMC Cancer Center -Wexford
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Patients must have histologically or cytologically confirmed diagnosis of non-small cell lung cancer
- Patients must have surgically unresectable stage IIIA disease or stage IIIB disease without malignant pleural/pericardial effusion
- Patients must have measurable disease as per the RECIST criteria, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as >20 mm with conventional techniques or as >10 mm with spiral CT scan. See section 9.2 for the evaluation of measurable disease.
- Age >18 years. Lung cancer is extremely rare in children.
- ECOG performance status 0-1 (Karnofsky >70%; see Appendix A).
- If available, tumor tissue should be submitted for EGFR status by IHC and correlative studies.
- Patients must have normal organ and marrow function as defined below:
- leukocytes >3,000/μL
- absolute neutrophil count >1,500/μL
- platelets >100,000/μL
- total bilirubin within normal institutional limits
- AST(SGOT)/ALT(SGPT) <2.5 X institutional upper limit of normal
- creatinine within normal institutional limits OR
- creatinine clearance >60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal
- The effects of cetuximab on the developing human fetus at the recommended therapeutic dose are unknown. For this reason and because EGFR inhibitors, chemotherapeutic agents and radiation therapy, as well as other therapeutic agents used in this trial are known to be teratogenic, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
- Patients must either be not of child bearing potential or have a negative pregnancy test within 7 days of treatment. Patients are considered not of child bearing potential if they are surgically sterile (they have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or they are postmenopausal.
- Willingness to sign an approved informed consent.
Exclusion Criteria:
- Patients should not have received prior chest radiation therapy.
- Patients with a history of pulmonary fibrosis are excluded from study.
- Patients may not be receiving any other investigational agents.
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to carboplatin, paclitaxel, cetuximab or other agents used in the study.
- History of any cancer other than NSCLC (except non-melanoma skin cancer or carcinoma in situ of the cervix) within the last five years.
- Prior therapy with known specific inhibitors of the EGFR.
- History of severe allergic reaction to prior therapy with monoclonal antibodies
- Peripheral neuropathy of more than grade 1 in severity
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, significant history of uncontrolled cardiac disease ie. uncontrolled hypertension, unstable angina, recent myocardial infarction (within prior 6 months), uncontrolled congestive heart failure,and cardiomyopathy with decreased ejection fraction, or psychiatric illness/social situations that would limit compliance with study requirements.
- Pregnant women are excluded from this study because carboplatin, paclitaxel, cetuximab and radiation therapy have the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with the above agents, breastfeeding should be discontinued if the mother is treated with the agents used in this study. These potential risks may also apply to other agents used in this study.
- Patients with immune deficiency are at increased risk of lethal infections when treated with marrow-suppressive therapy. Therefore, HIV-positive patients receiving combination anti-retroviral therapy are excluded from the study because of possible pharmacokinetic interactions with carboplatin, paclitaxel and cetuximab or other agents administered during the study. Appropriate studies will be undertaken in patients receiving combination anti-retroviral therapy when indicated.
- Active hepatitis.
- History of pulmonary fibrosis.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Cetuximab
Cetuximab 400 mg/m2 IV week 0 only External beam radiation weeks 1 - 7 Cetuximab 250 mg/m2 IV weekly thereafter weeks 1 - 7 Cetuximab 250 mg/m2 IV weekly weeks 8 - 26 Carboplatin AUC = 6 IV Paclitaxel 200 mg/m2 IV Every 3 weeks x 3 Cycles |
The initial dose of cetuximab is 400 mg/m2 intravenously administered over 120 minutes, followed by weekly infusions at 250 mg/m2 IV over 60 minutes.
Subjects will receive cetuximab from week 0 through week 26.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Samlet overlevelse (OS)
Tidsramme: Op til 36 måneder
|
Op til 36 måneder
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Progression-free Survival (PFS)
Tidsramme: Up to 36 months
|
Response and progression were evaluated using the Response Evaluation Criteria in Solid Tumors (RECIST) Committee [JNCI 92(3):205-216, 2000].
Progressive Disease was defined as at least a 20% increase in the sum of the LD of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions.
|
Up to 36 months
|
|
Best Overall Response Rate (ORR) (Number of Participants)
Tidsramme: Up to 12 weeks after treatment initiation
|
The Best Overall Response is the best response (Complete Response, Partial Response, Stable Disease, Progressive Disease) recorded from the start of the study treatment until the disease progression/recurrence at end of study.
Response and progression were evaluated using the Response Evaluation Criteria in Solid Tumors (RECIST) Committee [JNCI 92(3):205-216, 2000].
Complete Response (CR) is the Disappearance of all target lesions and Partial Response (PR) is at least a 30% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD.
|
Up to 12 weeks after treatment initiation
|
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EGFR (Epidermal Growth Factor Receptor) Gene Mutation and Akt, pAkt, and MAPKinase
Tidsramme: approx. 5 years
|
EGFR (epidermal growth factor receptor) gene mutation status and Akt, pAkt, and MAPKinase in participant tumor tissue.
|
approx. 5 years
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Athanassios Argiris, MD, University of Pittsburgh
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. juni 2006
Primær færdiggørelse (Faktiske)
1. februar 2012
Studieafslutning (Faktiske)
1. februar 2012
Datoer for studieregistrering
Først indsendt
26. juni 2007
Først indsendt, der opfyldte QC-kriterier
26. juni 2007
Først opslået (Skøn)
27. juni 2007
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
1. februar 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
7. december 2016
Sidst verificeret
1. december 2016
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 05-106
- NCT00492206 (Registry Identifier: ClinicalTrials.gov)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .