Evidence map›Paper›PMID 27139057›Full record

Trial reportJAMA2016

Effect of Chemoradiotherapy vs Chemotherapy on Survival in Patients With Locally Advanced Pancreatic Cancer Controlled After 4 Months of Gemcitabine With or Without Erlotinib: The LAP07 Randomized Clinical Trial.

Pascal Hammel, Florence Huguet, Jean-Luc van Laethem, David Goldstein, Bengt Glimelius, Pascal Artru, Ivan Borbath, Olivier Bouché, Jenny Shannon, Thierry André and 5 more

8 registry-linked trialsAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in JAMA, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 8 registered trials, which are not on this map. Cited by 566 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
566citing papers in PubMed, 5 pooled it
52.3field-weighted citation impact, top 1% of its field
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.

NCT00634725 phase3completednot on this map

Randomized Multicenter Phase III Study in Patients With Locally Advanced Adenocarcinoma of the Pancreas: Gemcitabine With or Without Chemoradiotherapy and With or Without Erlotinib. Intergroup Study

TypeinterventionalSponsorGERCOR - Multidisciplinary Oncology Cooperative GroupRan2008 to 2014Enrolled820ConditionsPancreatic CancerArmscapecitabine, erlotinib hydrochloride, gemcitabine hydrochloride, laboratory biomarker analysis, radiation therapy
NCT04106856 phase1completednot on this mapstarted 2019, after this paper: background citation

SHAPER: A Phase 1 Study of Losartan and Hypofractionated Radiation Therapy After Induction Chemotherapy for Borderline Resectable or Locally Advanced Pancreatic Cancer

TypeinterventionalSponsorUniversity of UtahRan2019 to 2026Enrolled22ConditionsBorderline Resectable Pancreatic Adenocarcinoma, Locally Advanced Pancreatic Ductal Adenocarcinoma, Locally Advanced Unresectable Pancreatic Adenocarcinoma, Stage II Pancreatic Cancer AJCC v8ArmsHypofractionated Radiation Therapy, Losartan, Losartan Potassium
NCT04276857 narecruitingnot on this mapstarted 2025, after this paper: background citation

Systemic Therapy With a Loco-regional Treatment in Patients With Locally Advanced Pancreatic Cancer: The SMART Study

TypeinterventionalSponsorUniversity of SaskatchewanRan2025 to 2026Enrolled27ConditionsLocally Advanced Pancreatic Cancer, Irreversible ElectroporationArmsIrreversible electroporation (NanoKnife® )
NCT04570943 phase2recruitingnot on this mapstarted 2021, after this paper: background citation

Phase II Study to Assess the Interest of a Sequential Treatment With Gemcitabine/Nab-paclitaxel (GEMBRAX) and Then FOLFIRINOX Followed by Stereotactic Magnetic Resonance-guided Adaptive Radiotherapy in Patients With Locally Advanced Pancreatic Cancer

TypeinterventionalSponsorInstitut du Cancer de Montpellier - Val d'AurelleRan2021 to 2030Enrolled103ConditionsLocally Advanced Pancreatic AdenocarcinomaArmsGabrinox, MRI-GUIDED STEREOTACTIC RADIOTHERAPY
NCT04986930 phase2active not recruitingnot on this mapstarted 2021, after this paper: background citation

Randomized Phase 2 Study of mFOLFIRINOX With or Without Stereotactic Body Radiotherapy in Patients With Locally Advanced Pancreatic Adenocarcinoma

TypeinterventionalSponsorAsan Medical CenterRan2021 to 2025Enrolled92ConditionsPancreatic Adenocarcinoma, Pancreatic Cancer Non-resectableArmsSBRT+mFOLFIRINOX, mFOLFIRINOX
NCT06050317 phase2recruitingnot on this mapstarted 2023, after this paper: background citation

Sintilimab Plus Chemotherapy and Radiotherapy for Patients With Inoperable Pancreatic Cancer: a Single-arm, Exploratory, Phase II Trial

TypeinterventionalSponsorShandong Cancer Hospital and InstituteRan2023 to 2026Enrolled25ConditionsPancreas CancerArmsSintilimab Plus mFFN or NALIRIFOX and Radiation
NCT06840067 narecruitingnot on this mapstarted 2025, after this paper: background citation

Single-arm Clinical Study of Carbon Ion Radiotherapy Combined with Nituzumab and Gemcitabine for Pancreatic Cancer.

TypeinterventionalSponsorGansu Wuwei Tumor HospitalRan2025 to 2028Enrolled62ConditionsPancreatic Cancer Metastatic, Pancreatic Cancer Non-resectableArmscarbon ion radiotherapy (CIRT)
NCT07173374 phase1suspendednot on this mapstarted 2025, after this paper: background citation

Stereotactic Centralized Ablative Radiotherapy for Locally Advanced Pancreatic Cancer: A Single-Arm Phase I Safety and Feasibility Study

TypeinterventionalSponsorShandong Cancer Hospital and InstituteRan2025 to 2028Enrolled24ConditionsPancreatic Cancer, Locally Advanced Pancreatic CancerArmsSCART Dose Escalation Arm
3 · Its place in the literature

Who cites it

566 citing papers in PubMed, 5 syntheses or guidelines pooled it, 1,049 citations in OpenAlex.

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506 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 13 institutions in 4 countries.

Pascal HammelDepartment of Digestive Oncology, Beaujon Hospital (AP-HP), Clichy, France.
Florence HuguetDepartment of Radiotherapy, Tenon Hospital (AP-HP), Paris, France.
Jean-Luc van LaethemDepartment of Gastroenterology, Erasme University Hospital, Brussels, Belgium.
David GoldsteinDepartment of Medical Oncology, Prince of Wales Hospital, Sydney, Australia5Australasian Gastrointestinal Trials Group (AGITG), Camperdown, Australia6Prince of Wales Clinical School, University of New South Wales, Sydney, Australia.
Bengt GlimeliusDepartment of Radiology, Oncology, and Radiation Science, University of Uppsala, Uppsala, Sweden.
Pascal ArtruDepartment of Gastroenterology, Jean Mermoz Hospital, Lyon, France.
Ivan BorbathDepartment of Gastroenterology, Saint-Luc University Clinics, Brussels, Belgium.
Olivier BouchéDepartment of Gastroenterology, Robert Debré Hospital, Reims, France.
Jenny ShannonAustralasian Gastrointestinal Trials Group (AGITG), Camperdown, Australia6Prince of Wales Clinical School, University of New South Wales, Sydney, Australia11Department of Medical Oncology, Nepean Hospital NSW, Sydney, Australia.
Thierry AndréDepartment of Medical Oncology, Saint-Antoine Hospital (AP-HP), Paris, France.
Laurent MineurDepartment of Radiotherapy and Medical Oncology, Sainte-Catherine Institute, Avignon, France.
Benoist ChibaudelDepartment of Medical Oncology, Franco-British Hospital Institute, Levallois-Perret, France15Oncology Multidisciplinary Research Group (GERCOR), Paris, France.
Franck BonnetainDepartment of Methodology and Quality of Life in Oncology, Hospital Minjoz, Besançon, France.
Christophe LouvetDepartment of Medical Oncology, Institute Mutualiste Montsouris, Paris, France.
LAP07 Trial Group
Sorbonne Université · FRCliniques Universitaires Saint-Luc · BECooperative Trials Group for Neuro-Oncology · AUErasmus Hospital · BEGERCOR (France) · FRHôpital Beaujon · FRHôpital Privé Jean Mermo · FRHôpital Robert-Debré · FRInstitute Mutualiste Montsouris · FRInstitut Sainte Catherine · FRMethodology and Quality of Life Unit in Oncology · FRPrince of Wales Hospital · AUUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceIn locally advanced pancreatic cancer, the role of chemoradiotherapy is controversial and the efficacy of erlotinib is unknown.

objectivesTo assess whether chemoradiotherapy improves overall survival of patients with locally advanced pancreatic cancer controlled after 4 months of gemcitabine-based induction chemotherapy and to assess the effect of erlotinib on survival. DESIGN, SETTING, AND

participantsIn LAP07, an international, open-label, phase 3 randomized trial, 449 patients were enrolled between 2008 and 2011. Follow-up ended in February 2013.

interventionsIn the first randomization, 223 patients received 1000 mg/m2 weekly of gemcitabine alone and 219 patients received 1000 mg/m2 of gemcitabine plus 100 mg/d of erlotinib. In the second randomization involving patients with progression-free disease after 4 months, 136 patients received 2 months of the same chemotherapy and 133 underwent chemoradiotherapy (54 Gy plus capecitabine). MAIN OUTCOMES AND MEASURES: The primary outcome was overall survival from the date of the first randomization. Secondary outcomes were the effect of erlotinib and quality assurance of radiotherapy on overall survival, progression-free survival of gemcitabine-erlotinib and erlotinib maintenance with gemcitabine alone at the second randomization, and toxic effects.

resultsA total of 442 of the 449 patients (232 men; median age, 63.3 years) enrolled underwent the first randomization. Of these, 269 underwent the second randomization. Interim analysis was performed when 221 patients died (109 in the chemoradiotherapy group and 112 in the chemotherapy group), reaching the early stopping boundaries for futility. With a median follow-up of 36.7 months, the median overall survival from the date of the first randomization was not significantly different between chemotherapy at 16.5 months (95% CI, 14.5-18.5 months) and chemoradiotherapy at 15.2 months (95% CI, 13.9-17.3 months; hazard ratio [HR], 1.03; 95% CI, 0.79-1.34; P = .83). Median overall survival from the date of the first randomization for the 223 patients receiving gemcitabine was 13.6 months (95% CI, 12.3-15.3 months) and was 11.9 months (95% CI, 10.4-13.5 months) for the 219 patients receiving gemcitabine plus erlotinib (HR, 1.19; 95% CI, 0.97-1.45; P = .09; 188 deaths vs 191 deaths). Chemoradiotherapy was associated with decreased local progression (32% vs 46%, P = .03) and no increase in grade 3 to 4 toxicity, except for nausea. CONCLUSIONS AND RELEVANCE: In this open-label, randomized trial involving patients with locally advanced pancreatic cancer with disease controlled after 4 months of induction chemotherapy, there was no significant difference in overall survival with chemoradiotherapy compared with chemotherapy alone and there was no significant difference in overall survival with gemcitabine compared with gemcitabine plus erlotinib used as maintenance therapy.

trial registrationclinicaltrials.gov Identifier: NCT00634725.

Indexed as

ChemoradiotherapyAgedAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantDeoxycytidineDisease-Free SurvivalDisease ProgressionErlotinib HydrochlorideFemaleGemcitabineHumansMaleMiddle AgedNauseaPancreatic NeoplasmsAntineoplastic AgentsDeoxycytidineErlotinib HydrochlorideGemcitabine

Identifiers

PMID27139057
OpenAlexW2346921980

What OpenQuestion holds

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Registered trials

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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.