Evaluation of Clinical Outcomes of Chemotherapy or Androgen-receptor Targeting Therapy (Alone or in Combination) or Radiotherapy on the Primary Tumor in Combination With Androgen Deprivation Therapy in Metastatic Hormone-sensitive Prostate Cancer: Multicenter Observational Study of Patients Undergoing Treatment in Clinical Practice in Italian Hospitals

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Drug, Radiation
Study Type: Observational
SUMMARY

The aim of this observational study is to evaluate the clinical outcomes of treatment with docetaxel, ARTA (alone or in combination) or with radiotherapy on the primary tumor for mCSPC, in an unselected population, in clinical practice

Eligibility
Participation Requirements
Sex: Male
View:

• histologically confirmed diagnosis of adenocarcinoma of the prostate, metastatic, not undergoing previous treatment (except hormone therapy initiated no more than 4-6 months prior to docetaxel) for metastatic disease

• treatment with docetaxel, ARPI (alone or in combination) or with radiation therapy on the primary tumor in combination with ADT within normal clinical practice or expanded access programs initiated between January 2015 and December 2027.

• availability of inpatient and/or outpatient medical records for clinical data collection

Locations
Other Locations
Italy
Azienda Ospedaliera San Luigi
RECRUITING
Orbassano
Istituto Oncologico Veneto
RECRUITING
Padua
Santa Chiara Hospital
RECRUITING
Trento
Contact Information
Primary
Orazio Caffo, MD
orazio.caffo@apss.tn.it
+390461904416
Time Frame
Start Date: 2016-12-16
Estimated Completion Date: 2028-12
Participants
Target number of participants: 3000
Treatments
ADT + docetaxel
mHSPC patients treated with ADT + docetaxel
ADT + ARPI
mHSPC patients treated with ADT + ARPI
ADT + ARPI + docetaxel
mHSPC patients treated with ADT + docetaxel + ARPI
ADT + radiotherapy on primary tumor
mHSPC patients treated with ADT + radiotherapy on primary tumor
Related Therapeutic Areas
Sponsors
Leads: Santa Chiara Hospital

This content was sourced from clinicaltrials.gov

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