RecruitingNCT07161882

ALG-LungCancerRegistry (SAFRO2202)

Observational Study of the Epidemiological, Clinical, and Diagnostic Profile, Treatment Patterns, and Outcomes of Lung Cancer.


Sponsor

Société Algérienne de Formation et de Recherche en Oncologie

Enrollment

3,750 participants

Start Date

Jun 1, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

SAFRO 2202 ALG-Lung Cancer Registry is a prospective, multicenter, non-interventional observational study conducted across 21 public and university hospitals in Algeria. The objective is to characterize the epidemiological, clinical, pathological, molecular, and therapeutic features of patients diagnosed with lung cancer, including non-small cell lung cancer (NSCLC), small cell lung cancer (SCLC), and carcinoid tumors. Eligible participants are adults aged 18 years or older, diagnosed at the time of inclusion or within the previous 12 months, and fully managed in oncology or pulmonology departments. Data are collected during routine clinical care and recorded in a secure electronic case report form (eCRF). No protocol-mandated interventions or study-specific visits are required. The study plans to enroll approximately 1,500 patients per year over a 30-month period. Primary outcomes include demographic and clinical profiles, tumor histology, molecular markers, staging at diagnosis, and treatment strategies (surgery, radiotherapy, chemotherapy, targeted therapy, and immunotherapy). Secondary outcomes include treatment-related toxicities, objective response rate (ORR), progression-free survival (PFS), time to treatment discontinuation (TTD), and overall survival (OS). The findings from this registry will provide real-world evidence to support national health planning, improve lung cancer management, and guide future clinical and public health initiatives in Algeria.


Eligibility

Min Age: 18 Years

Inclusion Criteria5

  • Age ≥ 18 years
  • Histologically confirmed diagnosis of lung cancer (NSCLC, SCLC, or carcinoid tumor)
  • Diagnosed at the time of inclusion or within the 12 previous months
  • Fully managed (diagnosis, treatment, and follow-up) in an oncology or pulmonology department of one of the 21 participating public/university hospitals
  • Signed informed consent obtained

Exclusion Criteria2

  • Prior enrollment in this study
  • Participation in an interventional clinical trial

Interventions

OTHERObservational Data Collection

Collection of clinical, pathological, molecular, and treatment-related data during routine care, with no additional procedures or interventions required by the study.


Locations(21)

Centre Pierre et Marie Curie

Algiers, Algiers Province, Algeria

Chu Beni Messous - Isaad Hassani

Algiers, Algiers Province, Algeria

CHU Mohamed Lamine Debaghine - Bab-el-Oued

Algiers, Algiers Province, Algeria

Chu-Beni Messous - Isaad Hassani

Algiers, Algiers Province, Algeria

EPH Rouiba

Algiers, Algiers Province, Algeria

CLCC Annaba

Annaba, Annaba, Algeria

CLCC Batna

Batna City, Batna, Algeria

CAC-CHU Frantz Fanon

Blida, Blida Province, Algeria

CHU- Hôpital Khelil Amrane

Béjaïa, Béjaia Province, Algeria

CHU Dr Abdesselam Benbadis

Constantine, Constantine Province, Algeria

EH Didouche Mourad

Constantine, Constantine Province, Algeria

CLCC Draâ Ben Khedda

Tizi Ouzou, Draâ Ben Khedda, Algeria

CAC-Laghouat

Laghouat, Laghouat Province, Algeria

CAC Oran EL HASSI- EMIR ABDELKADER

Oran, Oran Province, Algeria

CHU Dr. Benaouda Benzerdjeb

Oran, Oran Province, Algeria

EHS 1er novembre

Oran, Oran Province, Algeria

CAC- Ouargla

Ouargla, Ouargla Province, Algeria

CAC El OUED

El Oued, Oued Souf, Algeria

CAC- Sidi Bel Abbès

Sidi Bel Abbes, Sidi Bel Abbès Province, Algeria

EPH- Sidi Ghiles

Tipasa, Sidi Ghiles, Algeria

CAC-Sétif

Sétif, Sétif Province, Algeria

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NCT07161882


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