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Morbidity, Long-term Side Effects and Quality of Life in Germ-cell Tumor Long Survivors Treated with High-dose Chemotherapy and Autologous Stem Cell Transplant

Morbidity, Long-term Side Effects and Quality of Life in Germ-cell Tumor Long Survivors Treated with High-dose Chemotherapy and Autologous Stem Cell Transplant

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05889585
Acronym
HGT-QoL
Enrollment
180
Registered
2023-06-05
Start date
2023-05-31
Completion date
2025-05-31
Last updated
2024-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Germ Cell Tumor

Brief summary

Intensified chemotherapy is an effective treatment in 30-70% of patients with refractory germ cell tumor. Since most cases are diagnosed before the age of 40, survivors can expect to live another 30 to 50 years after being successfully treated. Long-term side effects and physical and emotional consequences can therefore have a significant impact on daily life. To date, no data of this type is available in France. This study will help clinicians better understand the long-term consequences for relapsed patients receiving high-dose chemotherapy.

Interventions

OTHERquality of life questionnaire

EORTC-QLQ C-30 questionnaire The Impact of Events Scale (IES-R) Multi-Dimensional Fatigue Inventory The EORTC-QLQ C-30 Vers. 3

Sponsors

Gustave Roussy, Cancer Campus, Grand Paris
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years at diagnosis * Treated between 1990 and 2015 * Histologically confirmed diagnosis of germ cell tumor (or high level serum tumor marker-based) and: Treated for relapse with high-dose of chemotherapy (HDCT) with autologous transplant at Gustave Roussy and relapse-free. Or Treated by orchiectomy only and no evidence of relapse after a minimum of 3 years. Or Good or intermediate prognosis metastatic disease according to the IGCCCG, treated by first line cisplatin-based chemotherapy at Gustave Roussy (and surgery of residual masses if needed), with no evidence of relapse. * Ability to comply with the protocol procedures * Patient affiliated to a social security system or beneficiary of the same. 6-Who have signed a written informed consent form prior to any study specific procedure.

Exclusion criteria

* Diagnosis of second malignancy * Any other serious or unstable illness, or medical, social, or psychological condition, that could jeopardize the safety of the subject and/or his compliance with study procedures, or may interfere with the subject's participation in the study or evaluation of the study results. * Patient under guardianship or deprived of his/her liberty by a judicial or administrative decision, or incapable of giving his/her consent.

Design outcomes

Primary

MeasureTime frameDescription
Compare the quality of life between the three groups measured with the EORTC-QLQ C-30 questionnaire.Day 1To compare the quality of life in long-term survivors of germ cell cancers after high-dose chemotherapy and autologous stem cell transplant with a group of coetaneous patients treated by orchidectomy only for localized testicular tumor and a group of patients of the same age treated with first line cisplatin-based chemotherapy for good or intermediate prognosis advanced germ cell tumor.

Secondary

MeasureTime frame
Compare late side effects between the three groups.Day 1
Compare correlated morbidities between the three groups.Day 1
Compare fatigue measured by the MFI-20 scale between the three groups.Day 1
Compare symptoms of post-traumatic stress measured by the IES scale between the three groups.Day 1
Compare current social and professional situation between the three groups.Day 1

Countries

France

Contacts

Primary ContactNatacha NAOUN, MD
natacha.naoun@gustaveroussy.fr+ 33 (0)1 42 11 42 11
Backup ContactKarim Fizazi, MD, Prof.
karim.fizazi@gustaveroussy.fr+ 33 (0)1 42 11 43 17

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026