Page last updated: 2024-10-24

celecoxib and Carcinoma, Small Cell

celecoxib has been researched along with Carcinoma, Small Cell in 4 studies

Carcinoma, Small Cell: An anaplastic, highly malignant, and usually bronchogenic carcinoma composed of small ovoid cells with scanty neoplasm. It is characterized by a dominant, deeply basophilic nucleus, and absent or indistinct nucleoli. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1286-7)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Edelman, MJ1
Wang, X1
Hodgson, L1
Cheney, RT1
Baggstrom, MQ1
Thomas, SP1
Gajra, A1
Bertino, E1
Reckamp, KL1
Molina, J1
Schiller, JH1
Mitchell-Richards, K1
Friedman, PN1
Ritter, J1
Milne, G1
Hahn, OM1
Stinchcombe, TE1
Vokes, EE1
Natale, RB1
Blackhall, F1
Papakotoulas, PI1
Danson, S1
Thatcher, N1
Kanwar, VS1
Heath, J1
Krasner, CN1
Pearce, JM1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Randomized Phase III Double Blind Trial Evaluating Selective COX-2 Inhibition in COX-2 Expressing Advanced Non-Small Cell Lung Cancer[NCT01041781]Phase 3313 participants (Actual)Interventional2010-02-28Terminated (stopped due to DSMB recommendation)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Incidence of Toxicities as Assessed by NCI CTCAE v. 4.0

The overall toxicity rates (percentages) for grade 3 or higher adverse events considered at least possibly related to treatment (NCT01041781)
Timeframe: Up to 5 years

Interventionpercentage of patients (Number)
Arm I (Arm A: Celecoxib + Standard Chemotherapy)61.04
Arm II (Arm B: Placebo + Standard Chemotherapy)55.06

Overall Survival

Overall survival time is defined as the time from randomization to death due to any cause. The median and 95% confidence intervals are estimated using the Kaplan-Meier estimator. (NCT01041781)
Timeframe: Time between randomization and death from any cause, assessed up to 5 years

Interventionmonths (Median)
Arm I (Arm A: Celecoxib + Standard Chemotherapy)11.4
Arm II (Arm B: Placebo + Standard Chemotherapy)12.5

Prognostic Value of Urinary Prostaglandin Metabolites (PGE-M) Levels for Worse PFS for Patients Who Had Baseline Urinary PGE-M Above/Below the First Quartile (Q1)

Prognostic value of urinary prostaglandin metabolites (PGE-M) levels for worse PFS for patients who had baseline urinary PGE-M above/below the first quartile (Q1, 10.09). Progression free survival (PFS) is defined as the time from the date of randomization to the date of disease progression or death resulting from any cause, whichever comes first. Progression is defined according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. The median and 95% confidence intervals are estimated using the Kaplan-Meier estimator. (NCT01041781)
Timeframe: Up to 5 years

Interventionmonths (Median)
PGE-M < Q17.7
PGE-M >= Q14.9

Prognostic Value of Urinary Prostaglandin Metabolites (PGE-M) Levels for Worse PFS for Patients Who Had Baseline Urinary PGE-M Above/Below the Median Quartile (Q2)

prognostic value of urinary prostaglandin metabolites (PGE-M) levels for worse PFS for patients who had baseline urinary PGE-M above/below the median quartile (Q2, 15.38). Progression free survival (PFS) is defined as the time from the date of randomization to the date of disease progression or death resulting from any cause, whichever comes first. Progression is defined according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. The median and 95% confidence intervals are estimated using the Kaplan-Meier estimator. (NCT01041781)
Timeframe: Up to 5 years

Interventionmonths (Median)
PGE-M < Q26.2
PGE-M >= Q24.2

Prognostic Value of Urinary Prostaglandin Metabolites (PGE-M) Levels for Worse PFS for Patients Who Had Baseline Urinary PGE-M Above/Below the Third Quartile (Q3)

Prognostic value of urinary prostaglandin metabolites (PGE-M) levels for worse PFS for patients who had baseline urinary PGE-M above/below the median quartile (Q3, 27.86). Progression free survival (PFS) is defined as the time from the date of randomization to the date of disease progression or death resulting from any cause, whichever comes first. Progression is defined according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. The median and 95% confidence intervals are estimated using the Kaplan-Meier estimator. (NCT01041781)
Timeframe: Up to 5 years

Interventionmonths (Median)
PGE-M < Q36.0
PGE-M >= Q33.0

Progression-free Survival

Progression free survival (PFS) is defined as the time from the date of randomization to the date of disease progression or death resulting from any cause, whichever comes first. Progression is defined according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. The median and 95% confidence intervals are estimated using the Kaplan-Meier estimator. (NCT01041781)
Timeframe: Time between randomization and disease relapse or death from any cause, assessed up to 5 years

Interventionmonths (Median)
Arm I (Arm A: Celecoxib + Standard Chemotherapy)5.16
Arm II (Arm B: Placebo + Standard Chemotherapy)5.26

Response Rate

The response rate (percentage) is the percent of patients whose best response was Complete Response (CR) or Partial Response (PR) as defined by RECIST 1.1 criteria. Percentage of successes will be estimated by 100 times the number of successes divided by the total number of evaluable patients. Response rates (including complete and partial response) will be tested using Fisher's exact test (NCT01041781)
Timeframe: Up to 5 years

Interventionpercentage of patients (Number)
Arm I (Arm A: Celecoxib + Standard Chemotherapy)40
Arm II (Arm B: Placebo + Standard Chemotherapy)35

Reviews

2 reviews available for celecoxib and Carcinoma, Small Cell

ArticleYear
Irinotecan, cisplatin/carboplatin, and COX-2 inhibition in small-cell lung cancer.
    Oncology (Williston Park, N.Y.), 2003, Volume: 17, Issue:7 Suppl 7

    Topics: Antineoplastic Combined Chemotherapy Protocols; Camptothecin; Carcinoma, Small Cell; Celecoxib; Cisp

2003
Perspectives on novel therapies for bronchial carcinoma.
    Expert opinion on pharmacotherapy, 2005, Volume: 6, Issue:7

    Topics: Angiogenesis Inhibitors; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic A

2005

Trials

1 trial available for celecoxib and Carcinoma, Small Cell

ArticleYear
Phase III Randomized, Placebo-Controlled, Double-Blind Trial of Celecoxib in Addition to Standard Chemotherapy for Advanced Non-Small-Cell Lung Cancer With Cyclooxygenase-2 Overexpression: CALGB 30801 (Alliance).
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2017, Jul-01, Volume: 35, Issue:19

    Topics: Antineoplastic Combined Chemotherapy Protocols; Carboplatin; Carcinoma, Small Cell; Celecoxib; Cyclo

2017

Other Studies

1 other study available for celecoxib and Carcinoma, Small Cell

ArticleYear
Advanced small cell carcinoma of the ovary in a seventeen-year-old female, successfully treated with surgery and multi-agent chemotherapy.
    Pediatric blood & cancer, 2008, Volume: 50, Issue:5

    Topics: Adolescent; Antineoplastic Combined Chemotherapy Protocols; Benzamides; Bleomycin; Carcinoma, Small

2008