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Completed

NCT Number: NCT02414685

First Line TIP in Poor Prognosis TGCTs.

TIP in the 1st line treatment of GCTs patients with unfavorable decline of serum tumor markers after 1 cycle of the BEP regimen.TIP will be administered to the patient until progression, unacceptable toxicity, complete response or inability of the subject to comply with study requirements.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 2

Primary location

National Cancer Institute

Bratislava, 83310, Slovakia

About this study

Cycle 1: BEP regimen

Serum tumor markers at day 18-21:

•Patients with an unfavorable pattern of tumor marker decrease after 1 cycle of BEP will receive 4 more cycles of TIP.

TIP regimen:

  • Taxol 250 mg/ m2 iv on day 1
  • Ifosfamid 1,2 g/ m2/ day iv x 5 days
  • Cisplatin 20 mg/ m2/ day iv x 5 days One cycle of therapy consists of 22 days. Estimated duration of treatment: Until progression, unacceptable toxicity, complete response or inability of the subject to comply with study requirements.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients older than 16 years.
  • Evidence of NSGCT based on histologic examination or based on clinical evidence and high serum HCG or AFP levels (in case of clinical emergency, therapy can be started before pathologic sample is obtained if tumor markers are very elevated)
  • Testicular, retroperitoneal, or mediastinal primary site.
  • Evidence of disseminated disease (clinical stages II or III).
  • Disease classified as poor prognosis according to IGCCCG criteria:
  • Primary mediastinal NSGCT or
  • Non-pulmonary visceral metastases or
  • HCG > 50,000 UI/l, or AFP > 10,000 ng/ml, or LDH > 10 times the upper normal value.
  • No prior chemotherapy.
  • No previous carcinoma, except basal-cell carcinoma of the skin.
  • Adequate renal function: measured or calculated creatinine clearance> 60 ml/min.
  • Absolute granulocyte count >= 1,500/mm3, platelets >= 100,000 mm3, bilirubine <= 1.5 fold the upper normal value.
  • Unfavorable tumor marker decline after 1.cycle of BEP
  • Signed informed consent.

Exclusion criteria

  • Patients infected by the Human Immunodeficiency Virus (HIV).
  • Patients who do not fit inclusion criteria.

Treatment and study plan

paclitaxel

Drug

paclitaxel, ifosfamide, cisplatin until progression, unacceptable toxicity, complete response or inability of the subject to comply with study requirements

Other names: paclitaxel ebewe

ifosfamide

Drug

paclitaxel, ifosfamide, cisplatin until progression, unacceptable toxicity, complete response or inability of the subject to comply with study requirements

Other names: ifosfamide-holoxan

Cisplatin

Drug

paclitaxel, ifosfamide, cisplatin until progression, unacceptable toxicity, complete response or inability of the subject to comply with study requirements

Other names: cisplatin-hospira

Primary outcomes

  1. Complete response rate

    Time frame: 36 month

    according RECIST criteria version 1.1

Secondary outcomes

  1. Response rate

    Time frame: 36 month

    response rate after chemotherapy

  2. Progression-free survival

    Time frame: 36 month

    expressed as median and as 12-weeks post-treatment initiation continuous progression-free survival rate

  3. Number of adverse events grade III and IV

    Time frame: 36 month

  4. overall survival

    Time frame: 36 months

    Survival will be estimated from the registration date to the date of last follow-up or death. Patients will be followed at least 3 years.

Sponsors and collaborators

Lead sponsor

National Cancer Institute, Slovakia

Other Gov

Registry information

Official study title

A Treatment Strategy of the Use of 1st Line Chemotherapy in Patients With Poor-Prognosis Disseminated Non-Seminomatous Germ Cell Tumors Based on Tumor Marker Decline: A Phase II Trial of Paclitaxel, Ifosfamid and Cisplatin Regimen.

Acronym: TIP

Important dates

Study start
2015
Primary completion
2020
Study completion
2020
First posted
Apr 13, 2015
Registry last updated
Aug 7, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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