Page last updated: 2024-10-29

ifosfamide and Lassitude

ifosfamide has been researched along with Lassitude in 7 studies

Research Excerpts

ExcerptRelevanceReference
" Measurements included carnitine plasma levels and self-reported fatigue using established child or adolescent fatigue scales and were collected during the 2nd cycle of chemotherapy, and repeated on alternating cycles up to cycle 8."7.81Fatigue and carnitine levels over multiple cycles of chemotherapy in children and adolescents. ( Hockenberry, MJ; Hooke, MC; McCarthy, K; Taylor, O, 2015)
"Ifosfamide and cisplatin cause urinary loss of carnitine, which is a fundamental molecule for energy production in mammalian cells."6.70Potential role of levocarnitine supplementation for the treatment of chemotherapy-induced fatigue in non-anaemic cancer patients. ( Baldelli, AM; Bisonni, R; Canestrari, F; Catalano, V; De Gaetano, A; Ferraro, B; Giordani, P; Graziano, F; Lai, V; Mencarini, E; Rovidati, S; Silva, R; Testa, E, 2002)
"Fatigue is the most frequent symptom experienced by children/adolescents with cancer."5.35Carnitine plasma levels and fatigue in children/adolescents receiving cisplatin, ifosfamide, or doxorubicin. ( Gregurich, M; Hockenberry, MJ; Hooke, MC; McCarthy, K, 2009)
" Measurements included carnitine plasma levels and self-reported fatigue using established child or adolescent fatigue scales and were collected during the 2nd cycle of chemotherapy, and repeated on alternating cycles up to cycle 8."3.81Fatigue and carnitine levels over multiple cycles of chemotherapy in children and adolescents. ( Hockenberry, MJ; Hooke, MC; McCarthy, K; Taylor, O, 2015)
"To examine the influence of the proposed symptom cluster of fatigue, nausea and vomiting, and sleep disturbances on clinical outcomes defined as behavior changes, depression, and performance status in children and adolescents before and after receiving cisplatin, doxorubicin, or ifosfamide chemotherapy."3.76Symptom clusters in children and adolescents receiving cisplatin, doxorubicin, or ifosfamide. ( Gregurich, M; Hockenberry, MJ; Hooke, MC; Krull, K; McCarthy, K; Sambuco, G, 2010)
"Ifosfamide is an alkylating agent used in the treatment of germ-cell tumors, sarcomas and lymphomas."3.73[Ifosfamide induced encephalopathy: 15 observations]. ( Behar, C; Dufour, C; Grill, J; Hartmann, O; Motte, J; Munzer, M; Oberlin, O; Paci, A; Sabouraud, P, 2006)
"Ifosfamide and cisplatin cause urinary loss of carnitine, which is a fundamental molecule for energy production in mammalian cells."2.70Potential role of levocarnitine supplementation for the treatment of chemotherapy-induced fatigue in non-anaemic cancer patients. ( Baldelli, AM; Bisonni, R; Canestrari, F; Catalano, V; De Gaetano, A; Ferraro, B; Giordani, P; Graziano, F; Lai, V; Mencarini, E; Rovidati, S; Silva, R; Testa, E, 2002)
"Fatigue is the most frequent symptom experienced by children/adolescents with cancer."1.35Carnitine plasma levels and fatigue in children/adolescents receiving cisplatin, ifosfamide, or doxorubicin. ( Gregurich, M; Hockenberry, MJ; Hooke, MC; McCarthy, K, 2009)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's0 (0.00)18.2507
2000's3 (42.86)29.6817
2010's3 (42.86)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Blay, JY1
Leahy, MG1
Nguyen, BB1
Patel, SR1
Hohenberger, P1
Santoro, A1
Staddon, AP1
Penel, N1
Piperno-Neumann, S1
Hendifar, A1
Lardelli, P1
Nieto, A1
Alfaro, V1
Chawla, SP1
Hooke, MC3
McCarthy, K3
Taylor, O1
Hockenberry, MJ3
Gregurich, M2
Sambuco, G1
Krull, K1
Dufour, C1
Grill, J1
Sabouraud, P1
Behar, C1
Munzer, M1
Motte, J1
Oberlin, O1
Paci, A1
Hartmann, O1
Graziano, F1
Bisonni, R1
Catalano, V1
Silva, R1
Rovidati, S1
Mencarini, E1
Ferraro, B1
Canestrari, F1
Baldelli, AM1
De Gaetano, A1
Giordani, P1
Testa, E1
Lai, V1
Yoshimoto, J1
Nasu, Y1
Akagi, T1
Obama, T1
Tsushima, T1
Ozaki, Y1
Matsumura, Y1
Ohmori, H1
Asahi, T1
Ohkita, K1

Clinical Trials (3)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Randomized, Multicenter, Phase III Trial of Trabectedin (Yondelis) Versus Doxorubicin-based Chemotherapy as First-Line Therapy in Patients With Translocation-Related Sarcomas (TRS)[NCT00796120]Phase 3121 participants (Actual)Interventional2008-11-30Completed
Sleep in Pediatric Hematopoietic Stem Cell Transplant Patients[NCT04106089]50 participants (Actual)Interventional2019-11-18Completed
A Randomised, Double Blinded Cross-over Study Comparing the Efficacy of L-carnitine Versus Placebo in the Treatment of Fatigue in Multiple Sclerosis[NCT01149525]Phase 359 participants (Actual)Interventional2010-06-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

6-month Progression - Free Survival

Percentage of participants survived for 6 months from the start of study treatment without progression of disease. Progression of the disease was associated with increasing symptoms, including pain from new or progressing lesions. Delay in disease progression generally represents a clinical benefit to the participant. (NCT00796120)
Timeframe: 6 months

Interventionpercentage of participants (Number)
Trabectedin66.7
Doxorubicin Plus Ifosfamide78.3

Duration of Response (DOR)

The DOR is defined as the time from date of first documentation of response (CR or PR, whichever comes first) to the date of documented PD or death. PR=at least 30% reduction in the sum of the longest dimensions (LD) of all target lesions in reference to the baseline sum LD, CR =Disappearance of all non-target lesions. (NCT00796120)
Timeframe: Up to 20 months

Interventiondays (Median)
TrabectedinNA
Doxorubicin Plus IfosfamideNA

Overall Survival

Overall survival defined as time from the date of randomization to the date of death. For participants who were alive at the time of analysis, overall survival was censored at the last contact date. (NCT00796120)
Timeframe: Baseline up to End of Study (an average of 4 years)

Interventionmonths (Median)
Trabectedin46.6
Doxorubicin Plus Ifosfamide33.5

Percentage of Participants With Objective Response

Tumor response was assessed according to Response Evaluation Criteria In Solid Tumors (RECIST) criteria: Partial Response (PR)=at least 30% reduction in the sum of the longest dimensions (LD) of all target lesions in reference to the baseline sum LD, Complete Response (CR) =Disappearance of all non-target lesions. Percentage of participants with objective tumor response was determined by the number of participants with PR or CR divided by the total number of response-evaluable participants. (NCT00796120)
Timeframe: Every 6 weeks during first 9 months of the study and thereafter every 9 weeks up to 20 months

Interventionpercentage of participants (Number)
Trabectedin5.9
Doxorubicin Plus Ifosfamide27.0

Progression - Free Survival (PFS)

The PFS was assessed as median number of days from the date of randomization until the first documented sign of disease progression (increase in disease; radiographic, clinical, or both) or death due to any cause, whichever occurred earlier. (NCT00796120)
Timeframe: Every 6 weeks from randomization during the first 9 months and thereafter, every 9 weeks up to 20 months

Interventionmonths (Median)
Trabectedin19.6
Doxorubicin Plus Ifosfamide8.3

Trials

2 trials available for ifosfamide and Lassitude

ArticleYear
Randomised phase III trial of trabectedin versus doxorubicin-based chemotherapy as first-line therapy in translocation-related sarcomas.
    European journal of cancer (Oxford, England : 1990), 2014, Volume: 50, Issue:6

    Topics: Adult; Aged; Anemia; Antineoplastic Combined Chemotherapy Protocols; Dioxoles; Doxorubicin; Drug Adm

2014
Potential role of levocarnitine supplementation for the treatment of chemotherapy-induced fatigue in non-anaemic cancer patients.
    British journal of cancer, 2002, Jun-17, Volume: 86, Issue:12

    Topics: Acetylcarnitine; Aged; Antineoplastic Agents; Carnitine; Cisplatin; Fatigue; Female; Humans; Ifosfam

2002

Other Studies

5 other studies available for ifosfamide and Lassitude

ArticleYear
Fatigue and carnitine levels over multiple cycles of chemotherapy in children and adolescents.
    European journal of oncology nursing : the official journal of European Oncology Nursing Society, 2015, Volume: 19, Issue:1

    Topics: Adolescent; Antineoplastic Agents; Carnitine; Child; Child, Preschool; Cisplatin; Dose-Response Rela

2015
Carnitine plasma levels and fatigue in children/adolescents receiving cisplatin, ifosfamide, or doxorubicin.
    Journal of pediatric hematology/oncology, 2009, Volume: 31, Issue:9

    Topics: Adenosine Triphosphate; Adolescent; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Prot

2009
Symptom clusters in children and adolescents receiving cisplatin, doxorubicin, or ifosfamide.
    Oncology nursing forum, 2010, Volume: 37, Issue:1

    Topics: Adolescent; Adolescent Behavior; Antineoplastic Agents; Attitude to Health; Child; Child Behavior; C

2010
[Ifosfamide induced encephalopathy: 15 observations].
    Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2006, Volume: 13, Issue:2

    Topics: Adolescent; Antineoplastic Agents, Alkylating; Child; Child, Preschool; Coma; Enzyme Inhibitors; Fat

2006
[Combination chemotherapy with cisplatin, ifosfamide and adriamycin in patients with advanced transitional cell carcinoma of the urinary tract].
    Gan to kagaku ryoho. Cancer & chemotherapy, 1985, Volume: 12, Issue:6

    Topics: Adult; Aged; Alopecia; Anorexia; Antineoplastic Combined Chemotherapy Protocols; Carcinoma, Transiti

1985