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Completed

NCT Number: NCT03348722

Active Surveillance or Radical Treatment for Newly Diagnosed Patients With a Localized, Low Risk, Prostate Cancer START

The purpose of the START project is to evaluate the acceptability, the safety and the cost-effectiveness of a population based program of active surveillance for patients newly diagnosed with a localized, low risk, prostate cancer.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Observational

Primary location

Oncolgy Network of Piemonte and Valle d'Aosta - Turin

Turin, 10126, Italy

About this study

Comparative effectiveness research project. All newly diagnosed prostate cancer patients fulfilling the low risk definition, resident in Piedmont or in Valle D'Aosta regions, will be invited to participate. All enrolled patients will receive full and clear information about their prognosis together with a balanced synthesis of the benefits and risks of the available treatments (active surveillance or radical treatments).

Specific objectives are:

  • To estimate, at a population level, the proportion of newly diagnosed prostate cancer at low risk, eligible for active surveillance, the proportion of those accepting to be enrolled in a cohort of active surveillance and the risk of abandoning the program during follow-up.
  • To compare the patients' and physicians' characteristics of those accepting to be managed within the active surveillance program with those preferring a radical treatment (either surgery or radiotherapy).
  • To compare, at a population level, the clinical outcomes, quality of life and costs associated to different treatment choices.

Who can participate

Healthy volunteers accepted: No

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

IInclusion Criteria:

  • Newly diagnosed low risk prostate cancer patients, defined according to the presence of all the following criteria:
  • diagnosis of adenocarcinoma of the prostate
  • prostate cancer clinical stage T1c o T2a
  • PSA <=10ng/ml at diagnosis
  • adequate biopsy sampling according to prostate volume
  • maximum of two positive cores for random sampling and of maximum two lesions for target biopsies (even if the number of positive samples if >2)
  • Gleason grade 3+3 ( in patients age>70 Gleason 3+4)
  • Residence in Piemonte or Valle D'Aosta regions;
  • Patients suitable for radical treatment (surgery or radiotherapy);
  • Age at diagnosis <= 75 years or >75 years if fragility assessment (measured with the G8 score)> = 14;
  • Patients suitability for expressing a valid consent to participate in the study.

Exclusion criteria

  • Patients previously treated for prostate cancer.
  • Patients not willing to undergo radical treatments (surgery or radiotherapy).

Treatment and study plan

Active Surveillance

Other

PSA testing (every 3 months, then every 6 after 30 months), clinical visit and DRE every 6 months, prostate biopsy after 1, 4 and 7 years

radical prostatectomy

Procedure

Radical prostatectomy (open, laparoscopic or robotic)

Radiotherapy

Radiation

External radical radiotherapy or brachitherapy

Other radical treatments

Procedure

High intensity focal ultrasound, cryotherapy, others

Primary outcomes

  1. Treatment-Free Survival (TFS)

    Time frame: Up to 24 months

    Proportion of patients in active surveillance program alive and not undergoing active treatment for prostate cancer.

Secondary outcomes

  1. Quality of Life

    Time frame: Up to 24 months

    Measured through validated questionnaire EORTC QLQ-C30 at baseline and every six months during the first 2 years.

  2. Quality of Life

    Time frame: Up to 24 months

    Measured through validated questionnaire QLQ-PR25 at baseline and every six months during the first 2 years.

  3. Quality of Life

    Time frame: Up to 24 months

    Measured through validated questionnaire IPSS at baseline and every six months during the first 2 years.

  4. Quality of Life

    Time frame: Up to 24 months

    Measured through validated questionnaire IIEF-5 at baseline and every six months during the first 2 years.

  5. Quality of Life

    Time frame: Up to 24 months

    Measured through validated questionnaire HADS at baseline and every six months during the first 2 years.

  6. Quality of Life

    Time frame: Up to 24 months

    Measured through validated questionnaire EuroQol-5D at baseline and every six months during the first 2 years.

  7. Quality of Life

    Time frame: Up to 24 months

    Measured through validated questionnaire MHLC -Form C at baseline and every six months during the first 2 years.

  8. Cost-effectiveness

    Time frame: Up to 24 months

    Incremental cost-effectiveness ratio calculated as the ratio between difference in costs and difference in QALYs (Quality Adjusted Life Years, from EQ-5D) among the treatment groups, during the first 2 years after diagnosis

Sponsors and collaborators

Lead sponsor

Rete Oncologica Piemonte, Valle d'Aosta

Other

Collaborators

  • A.O.U. Città della Salute e della Scienza
  • Compagnia di San Paolo

Registry information

Official study title

START (Active Surveillance or Radical Treatment for Newly Diagnosed Patients With a Localized, Low Risk, Prostate Cancer): an Epidemiological Study of the Oncology Network of Piemonte and Valle d'Aosta (Italy)

Acronym: START

Important dates

Study start
2015
Primary completion
2021
Study completion
2023
First posted
Nov 21, 2017
Registry last updated
Mar 31, 2023

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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