Evidence map›Paper›PMID 39754118›Full record

ArticleBMC cancer2025

Real-world clinical outcome of unresectable locally advanced & de-novo metastatic pancreatic ductal adenocarcinoma: a multicentre retrospective study.

Mohamed Aseafan, Ali H Alfakeeh, Emad Tashkandi, Mervat Mahrous, Mohammed Alghamdi, Bader Alshamsan, Marwan Al-Hajeili, Safwan Bakhsh, Kanan Alshammari, Fahad A Almugbel and 16 more

Abstract readMulticenter Study
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Mohamed AseafanSection of Medical Oncology, Department of Internal Medicine, Security Forces Hospital, Riyadh, Saudi Arabia. mjaseafan@gmail.com.
Ali H AlfakeehComprehensive Cancer Center, Medical Oncology, King Fahad Medical City, Riyadh, Saudi Arabia.
Emad TashkandiCollege of Medicine, Umm Al-Qura University, Makkah, Saudi Arabia.
Mervat MahrousDepartment of Oncology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Mohammed AlghamdiOncology Center, King Saud University Medical City, Riyadh, Saudi Arabia.
Bader AlshamsanDepartment of Medicine, College of Medicine, Qassim University, Buraydah, Saudi Arabia.
Marwan Al-HajeiliDepartment of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
Safwan BakhshDepartment of Medical Oncology, King Faisal Specialist Hospital and Research Center-Jeddah, Jeddah, Saudi Arabia.
Kanan AlshammariDepartment of Medical Oncology, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Fahad A AlmugbelDepartment of Medical Oncology, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Abdulhameed H AlfagihComprehensive Cancer Center, Medical Oncology, King Fahad Medical City, Riyadh, Saudi Arabia.
Ahmed AllehebiDepartment of Medical Oncology, King Faisal Specialist Hospital and Research Center-Jeddah, Jeddah, Saudi Arabia.
Mohamed MontaserSection of Medical Oncology, Department of Internal Medicine, Security Forces Hospital, Riyadh, Saudi Arabia.
Mohamed Hamdy ElsaftyMedical Oncology, NCI Cairo University, Cairo, Egypt.
Khaled Abd Elaziz ElnaghiOncology Centre, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Ibrahim IssaCollege of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Eesa BakshiCollege of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Sadeem AlSubaiePathology and Laboratory Medicine, Security Forces Hospital, Riyadh, Saudi Arabia.
Bandar AlMutairiDepartment of Oncology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Hoda MokhtarDepartment of Oncology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Mohamed AboelattaPrince Faisal Cancer Center, King Fahad Specialist Hospital, Qassim Health Clusster, Buraydah, Saudi Arabia.
Nedal BukhariDepartment of Oncology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Ali M AlzahraniComprehensive Cancer Center, Medical Oncology, King Fahad Medical City, Riyadh, Saudi Arabia.
Tusneem ElhassanResearch Unit, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Ali AlqahtaniDepartment of Medical Oncology, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Shouki BazarbashiDepartment of Medical Oncology, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic ductal adenocarcinoma (PDAC) remains one of the most lethal malignancies, with limited treatment options yielding poor outcomes. This study aimed to evaluate the real-world clinical characteristics, treatment patterns, and outcomes of patients with locally advanced unresectable and de-novo metastatic PDAC in Saudi Arabia, providing regional data to compare with international benchmarks.

methodsThis is a retrospective, multicentre study involving 350 patients diagnosed with unresectable locally advanced or de-novo metastatic PDAC between January 2015 and November 2023. Data were collected from 10 oncology centers across Saudi Arabia.

resultsThe median age at diagnosis was 60 years, with 63% of patients presenting with multiple metastatic sites, primarily in the liver (66.3%). FOLFIRINOX was the most common first-line treatment (55.1%), followed by gemcitabine plus nab-paclitaxel (15.1%). The median PFS for first-line treatment was 5.3 months, with FOLFIRINOX achieving the longest PFS (6.5 months). The median OS was 10.34 months for the entire cohort, with better survival outcomes observed in patients receiving FOLFIRINOX (12.3 months). Independent prognostic factors for PFS and OS included performance status, first-line regimen, and neutrophil-lymphocyte ratio (NLR). Among patients tested, 7.1% had deficient mismatch repair (d-MMR), and 5.8% harbored BRCA mutations.

conclusionsThis real-world study confirms that clinical outcomes for locally advanced unresectable and metastatic PDAC in Saudi Arabia are consistent with international data, with FOLFIRINOX showing superior outcomes over gemcitabine-based regimens. However, both treatments reflect the persistent poor prognosis of PDAC, underscoring the need for novel therapeutic strategies. Further research is warranted to optimize treatment selection and improve survival outcomes in this population.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalPancreatic NeoplasmsAdultAgedAged, 80 and overAlbuminsDeoxycytidineFemaleFluorouracilGemcitabineHumansIrinotecanLeucovorinMaleMiddle Aged130-nm albumin-bound paclitaxelAlbuminsDeoxycytidineFluorouracilfolfirinoxGemcitabineIrinotecanLeucovorinOxaliplatinPaclitaxelDe-novoDuctal adenocarcinomaLocally advancePancreatic cancerSaudi ArabiaSurvival

Identifiers

PMID39754118
PMCPMC11697791

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.