Page last updated: 2024-11-04

temozolomide and Cells, Neoplasm Circulating

temozolomide has been researched along with Cells, Neoplasm Circulating in 2 studies

Research Excerpts

ExcerptRelevanceReference
"Differentiating treatment necrosis from tumor recurrence poses a diagnostic conundrum for many clinicians in neuro-oncology."1.62Role of circulating tumor cell detection in differentiating tumor recurrence from treatment necrosis of brain gliomas. ( Cui, Y; Gao, F; Jiang, H; Li, M; Lin, S; Ren, X; Zhao, W, 2021)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Gao, F1
Zhao, W1
Li, M1
Ren, X1
Jiang, H1
Cui, Y1
Lin, S1
Pietanza, MC1
Waqar, SN1
Krug, LM1
Dowlati, A1
Hann, CL1
Chiappori, A1
Owonikoko, TK1
Woo, KM1
Cardnell, RJ1
Fujimoto, J1
Long, L1
Diao, L1
Wang, J1
Bensman, Y1
Hurtado, B1
de Groot, P1
Sulman, EP1
Wistuba, II1
Chen, A1
Fleisher, M1
Heymach, JV1
Kris, MG1
Rudin, CM1
Byers, LA1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Multi-Center, Randomized, Double-Blind Phase II Study Comparing ABT-888, a PARP Inhibitor, Versus Placebo With Temozolomide in Patients With Relapsed Sensitive or Refractory Small Cell Lung Cancer[NCT01638546]Phase 297 participants (Actual)Interventional2012-06-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Number of Participants With Adverse Events

Tabulated According to the National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.0. Summary level. (NCT01638546)
Timeframe: From the start of treatment until 30 days from coming off treatment

InterventionParticipants (Count of Participants)
Arm I (Veliparib and Temozolomide)52
Arm II (Placebo and Temozolomide)45

Overall Response (ORR) by RECIST 1.1 Criteria

Corresponding exact two-sided 95% confidence intervals will be calculated and reported in both arms of the study. Comparisons between treatment arms will be performed using Fisher-exact test. (NCT01638546)
Timeframe: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 4 months

Interventionparticipants (Number)
Arm I (Veliparib and Temozolomide)20
Arm II (Placebo and Temozolomide)6

Overall Survival

Estimated in each treatment group using Kaplan-Meier method. Group comparisons will be performed using log-rank test. (NCT01638546)
Timeframe: From randomization to time of death

Interventionmonths (Median)
Arm I (Veliparib and Temozolomide)8.2
Arm II (Placebo and Temozolomide)7

Progression-free Survival, Calculated as the Proportion of Patients Alive and Without Evidence of Disease

Compared across the two arms using a Fisher exact test. (NCT01638546)
Timeframe: From randomization to time of progression or death, whichever occurs first, assessed at 4 months

Interventionparticipants (Number)
Arm I (Veliparib and Temozolomide)18
Arm II (Placebo and Temozolomide)11

Trials

1 trial available for temozolomide and Cells, Neoplasm Circulating

ArticleYear
Randomized, Double-Blind, Phase II Study of Temozolomide in Combination With Either Veliparib or Placebo in Patients With Relapsed-Sensitive or Refractory Small-Cell Lung Cancer.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2018, 08-10, Volume: 36, Issue:23

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents, Alkylating; Antineoplastic Combined Chemother

2018

Other Studies

1 other study available for temozolomide and Cells, Neoplasm Circulating

ArticleYear
Role of circulating tumor cell detection in differentiating tumor recurrence from treatment necrosis of brain gliomas.
    Bioscience trends, 2021, May-11, Volume: 15, Issue:2

    Topics: Adult; Brain; Brain Neoplasms; Chemoradiotherapy, Adjuvant; Diagnosis, Differential; Female; Glioma;

2021