THERApy De-escalation for TESTicular Cancer

Overview

THERATEST is looking to collect data from 30 patients actively receiving de-escalation treatments or other standard of care treatments in two UK hospitals. THERATEST is a feasibility study to determine whether patients are willing to be recruited, the impact of de-escalation treatments on patients' cancers and quality of life, whether we should proceed with these treatments in a larger study, and if so how the study should be conducted. A feasibility study prepares the ground for a larger study and improves the chances of the subsequent study producing valuable evidence, and helps to avoid wasting precious resources on larger trials that are unlikely to be informative. We hope that information from THERATEST will bridge the current knowledge gap and allow clinicians to design bigger trials to actively compare the different treatment strategies.

Detailed description

THERATEST is an observational cohort study of patients receiving SOC treatments (combination chemotherapy or radiotherapy) or de-escalated treatments (primary rRPLND or Carboplatin AUC10) treatments for stage II seminoma.

Potential patients will be identified and invited to join the THERATEST study. Patients will be allocated to the following cohorts based on whether the relevant mode of treatment is adopted as an institutional SOC in their respective institution:

A. rRPLND cohort: Patients with seminoma who are negative/low for tumour markers and unifocal ipsilateral Stage IIA or \<3cm IIB will be assessed for rRPLND. Patients who are eligible for rRPLND will undergo surgery followed by adjuvant treatment or surveillance as determined by their clinical teams based on post-operative histology as per SOC. Patients who are not deemed eligible for or decline rRPLND, will be offered either BEP/EP chemotherapy or radiotherapy with or without neoadjuvant Carboplatin AUC7 and will continue to be followed in the study.

B. Carboplatin AUC10 cohort: Patients with stage II seminoma will be offered Carboplatin AUC10. Those deemed ineligible for Carboplatin AUC10 or who decline this treatment option will be offered either BEP/EP chemotherapy or radiotherapy and will continue to be followed in the study.

Chemotherapy treatment strategies and adjuvant treatments are left to the shared decision-making between treating clinician and patient and follow institutional SOC. In both cohorts patients will be followed up for 2 years after treatment completion or until death or withdrawal of consent, whichever is the earliest. Beyond the study period, patients will be follow up as per institutional SOC protocols as part of prospective institutional audits.

Interventions

• Procedure retroperitoneal lymph node dissection
  retroperitoneal lymph node dissection
• Drug Carboplatin AUC10
  Carboplatin AUC10

Primary outcome measures

• FEASIBILITY of recruitment and retention [Time frame: through study completion, an average of 3 year]

Secondary outcome measures (5)

• QUALITY OF LIFE assessed by difference in HRQOL scores [Time frame: through study completion, an average of 3 year]
• QUALITY OF LIFE assessed by difference in differences in sexual drive, function, and overall satisfaction [Time frame: through study completion, an average of 3 year]
• Progression free SURVIVAL [Time frame: through study completion, an average of 3 year]
• OVERALL SURVIVAL [Time frame: through study completion, an average of 3 year]
• SAFETY and complication of all treatments [Time frame: through study completion, an average of 3 year]

Eligibility criteria

Inclusion criteria

Each patient must meet all of the following inclusion criteria to be enrolled in the study:

• Willing and able to provide written informed consent.
• Male.
• Age ≥ 16 years.
• Histologically confirmed seminoma (biopsy/orchidectomy)
• Clinical stage II (standard of care cross-sectional imaging).
• Ability to comply with the protocol, including but not limited to, completion of the patient-reported outcome questionnaires.

rRPLND cohort specific inclusion criteria

Participants must meet the following additional inclusion criteria to register for the rRPLND cohort:

• Stage IIA and <3cm IIB with unifocal ipsilateral lymph node within rRPLND template.
• Negative or mildly elevated serum tumour markers, defined as:

• AFP (alpha-fetoprotein) <10ng/ml and non-rising on serial testing
• BhCG (human chorionic gonadotropin) <50mg/ml
• LDH (lactate dehydrogenase) <1.5x upper limit normal
• Fit for surgery, defined as meeting all of the following criteria:

• Body mass index (BMI) <34
• Charlson comorbidity index ≤3
• ECOG Performance status 0-1
• No significant cardio-pulmonary disease, or other uncontrolled intercurrent illness that would limit fitness for surgery in the opinion of the investigator
• No previous open intra-abdominal surgery

Carboplatin AUC10 cohort specific inclusion criteria

Participants must meet the following additional inclusion criteria to register for the Carboplatin AUC10 group:

• Serum tumour markers, defined by IGCCCG "good risk" criteria:

• AFP <10ng/ml
• any BhCG
• LDH <2.5x ULN
• Glomerular filtration rate by EDTA clearance over 25 ml/min (a measured creatinine clearance using Cockcroft and Gault would be allowed if unable to perform EDTA clearance).
• ECOG Performance status 0-2.
• Patients must be sterile or agree to use adequate contraception during the period of therapy.

Exclusion criteria

• Raised AFP > 10ng/ml that does not fall to <10ng/ml following orchidectomy
• Previous chemotherapy or radiotherapy for the disease under study.
• Previous or concurrent malignancy other than testicular cancer, unless treated with curative intent and with no known active disease present for ≥2 years before enrolment and felt to be at low risk for recurrence by the treating physician (for example: non-melanoma skin cancer or lentigo maligna; breast ductal carcinoma in situ; prostatic intraepithelial neoplasia; urothelial papillary non-invasive carcinoma or urothelial carcinoma in situ).
• Any condition that, in the opinion of the investigator, would interfere with evaluation of study intervention or interpretation of patient safety or study results such as medical comorbidities impacting on QoL or medical conditions or other disorders that would affect adherence to study requirements

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model

Cohort

Study locations

United Kingdom · 1 center

• Barts and London Hospital NHS Trust — London

Identifiers

NCT: NCT06309745 · THERATEST

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗