NCT01367457

Brief Summary

The principal objective of the study is to evaluate the efficacy and safety of temsirolimus use in patients with Renal Cell Carcinoma and Mantle Cell Lymphoma.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
243

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2011

Longer than P75 for all trials

Geographic Reach
1 country

16 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2011

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

June 3, 2011

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 7, 2011

Completed
3.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2015

Completed
1.1 years until next milestone

Results Posted

Study results publicly available

April 27, 2016

Completed
Last Updated

April 27, 2016

Status Verified

March 1, 2016

Enrollment Period

4.2 years

First QC Date

June 3, 2011

Results QC Date

March 25, 2016

Last Update Submit

March 25, 2016

Conditions

Outcome Measures

Primary Outcomes (5)

  • Progression-free Survival (PFS)

    Progression-free survival: interval between start of treatment to first day when progressive disease (PD) was evaluated according to Response Evaluation Criteria in Solid Tumors (RECIST) for participants with RCC and Cheson criteria for participants with MCL, or death due to any cause. RECIST criteria: at least 20% increase in sum of diameters of target lesions, taking as reference the smallest sum. In addition to relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 millimeter (mm). Appearance of one or more new lesions also considered progression. Cheson criteria: appearance of any new sites of lymphoma OR at least 50% increase in product of longest perpendicular dimensions of any previously identified lymph node mass (LNM) OR at least 50% increase in longest dimension of any previously identified LNM greater than 1 cm in longest transverse dimension OR at least 50% increase in size of any previously involved site of lymphoma.

    From initiation of treatment up to disease progression (up to 80 months)

  • Percentage of Participants With Objective Response

    Objective response: percentage of participants who achieved complete remission (CR) or partial response (PR). RECIST criteria was used for participants with RCC and Cheson criteria for participants with MCL. RECIST criteria (CR: disappearance of all target lesions, any pathological lymph nodes(target or non-target) reduced in short axis to \<10 mm, PR: at least 30% decrease in sum of diameters of target lesions). Cheson criteria (CR: all lymph node masses regressed to normal size, each lymph node mass that was \>1.5 cm in longest transverse dimension regressed to \<=1.5 cm, lymph node mass that was 1.1-1.5 cm regressed to \<=1 cm, complete disappearance of all radiographic evidence of disease, PR: at least 50% decrease in sum of products of the longest perpendicular dimensions of the previously identified dominant lymph node masses, no increase in size of other lymph nodes.)

    From initiation of treatment up to disease progression (up to 80 months)

  • Duration of Response (DOR)

    Duration of response (DOR) was defined as the interval from the date the response was documented to the first date that progression of disease (PD) was observed in participants with PR or CR. RECIST criteria was used for participants with RCC and Cheson criteria for participants with MCL. PD, CR and PR are defined in primary outcome 1 and 2.

    From initiation of treatment up to disease progression (up to 80 months)

  • Overall Survival (OS)

    Overall survival (OS) was defined as the interval from the day of the start of the treatment to death, or censored to the last date when the participant was identified to be alive.

    From initiation of treatment untill death (up to 80 months)

  • Number of Participants With Treatment Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs)

    An AE was any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. An SAE was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. Treatment-emergent events were between first dose of study drug and up to 28 days after last dose that were absent before treatment or that worsened relative to pretreatment state. AEs included both SAEs and non-serious adverse events (Non-SAEs).

    Baseline to the 28 calendar days after the last administration of study drug (upto 80 months)

Study Arms (1)

Patients that received treatment with Temsirolimus

Patients with Renal Cell Carcinoma or Mantle Cell Lymphoma that have been treated with Temsirolimus as per clinical practice.

Other: Temsirolimus (Non-Interventional Study)

Interventions

There is not any intervention in this study.

Patients that received treatment with Temsirolimus

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with Renal Cell Carcinoma or Mantle Cell Lymphoma that have been treated with Temsirolimus as per clinical practice.

You may qualify if:

  • Patients with Renal Cell Carcinoma or Mantle Cell Lymphoma that have been treated with Temsirolimus as per clinical practice.

You may not qualify if:

  • Patients that do not have a minimum (pre-specified) of data in their clinical record.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (16)

Complexo Hospitalario Universitario A Coruña

A Coruña, A Coruña, 15006, Spain

Location

Hospital de La Santa Creu I Sant Pau

Barcelona, Barcelona, 08025, Spain

Location

Hospital Vall D'Hebron

Barcelona, Barcelona, 08035, Spain

Location

Hospital del Mar

Barcelona, Barcelona, 8940, Spain

Location

Hospital de Cabueñes

Cabueñes, Gijon, 33394, Spain

Location

Complexo Hospitalario Universitario A Coruña. Hospital Teresa Herrera

A Coruña, La Coruña, 15006, Spain

Location

Hospital Clinico Universitario

Santiago de Compostela, La Coruña, 15706, Spain

Location

Complejo Hospitalario Materno-Infantil Insular de Las Palmas

Las Palmas de Gran Canaria, Las Palmas, 35016, Spain

Location

Hospital General Universitario Gregorio Marañon

Madrid, Madrid, 28007, Spain

Location

Hospital Universitario La Paz

Madrid, Madrid, 28046, Spain

Location

Hospital de Madrid Norte - Sanchinarro

Madrid, Madrid, 28050, Spain

Location

Hospital de Navarra

Pamplona, Navarre, 31008, Spain

Location

Hospital Universitario Central de Asturias

Oviedo, Principality of Asturias, 33006, Spain

Location

Hospital Provincial de Castellon

Castellon, Valencia, 12002, Spain

Location

Complejo AAsistencial de Avilla

Ávila, 05004, Spain

Location

MD Anderson Cancer Center

Madrid, 28033, Spain

Location

Related Links

MeSH Terms

Conditions

Carcinoma, Renal CellLymphoma, Mantle-Cell

Interventions

temsirolimus

Condition Hierarchy (Ancestors)

AdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsKidney NeoplasmsUrologic NeoplasmsUrogenital NeoplasmsNeoplasms by SiteFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesKidney DiseasesUrologic DiseasesMale Urogenital DiseasesLymphoma, Non-HodgkinLymphomaLymphoproliferative DisordersLymphatic DiseasesHemic and Lymphatic DiseasesImmunoproliferative DisordersImmune System Diseases

Results Point of Contact

Title
Pfizer ClinicalTrials.gov Call Center
Organization
Pfizer, Inc.

Study Officials

  • Pfizer CT.gov Call Center

    Pfizer

    STUDY DIRECTOR

Publication Agreements

PI is Sponsor Employee
No
Restriction Type
OTHER
Restrictive Agreement
Yes

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 3, 2011

First Posted

June 7, 2011

Study Start

January 1, 2011

Primary Completion

April 1, 2015

Study Completion

April 1, 2015

Last Updated

April 27, 2016

Results First Posted

April 27, 2016

Record last verified: 2016-03

Locations