Evidence map›Paper›PMID 32219909›Full record

Trial reportThe oncologist2020

Renaissance of Radiotherapy in Intestinal Lymphoma? 10-Year Efficacy and Tolerance in Multimodal Treatment of 134 Patients: Follow-up of Two German Multicenter Consecutive Prospective Phase II Trials.

Gabriele Reinartz, Caroline Molavi Tabrizi, Ruediger Liersch, Hansjoerg Ullerich, Dominik Hering, Kay Willborn, Juergen Schultze, Oliver Micke, Christian Ruebe, Wolfgang Fischbach and 11 more

Open access · hybridAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in The oncologist, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 34% 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.

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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
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

21 authors at 12 institutions in 1 country.

Gabriele ReinartzDepartment of Radiation Oncology, University Hospital of Muenster, Muenster, Germany.ORCID 0000-0002-4869-5986
Caroline Molavi TabriziDepartment of Radiation Oncology, University Hospital of Muenster, Muenster, Germany.
Ruediger LierschDepartment of Medicine A (Hematology, Oncology, and Pneumology), University Hospital of Muenster, Muenster, Germany.
Hansjoerg UllerichDepartment of Medicine B (Gastroenterology and Hepatology), University Hospital of Muenster, Muenster, Germany.
Dominik HeringDepartment of Radiation Oncology, University Hospital of Muenster, Muenster, Germany.
Kay WillbornDepartment of Radiotherapy and Radiation Oncology, Pius Hospital Oldenburg, Oldenburg, Germany.
Juergen SchultzeDepartment of Radiation Oncology, University of Schleswig-Holstein, Kiel, Germany.
Oliver MickeDepartment of Radiotherapy and Radiation Oncology, Franziskus Hospital Bielefeld, Bielefeld, Germany.
Christian RuebeDepartment of Radiation Oncology, University of Saarland, Homburg, Germany.
Wolfgang FischbachDepartment of Gastroenterology and Oncology, Hospital of Aschaffenburg, Aschaffenburg, Germany.
Martin BentzDepartment of Medical Oncology, Municipal Hospital of Karlsruhe, Karlsruhe, Germany.
Severin DaumDepartment of Gastroenterology, University Charité, Berlin, Germany.
Christiane PottDepartment of Medical Oncology, University of Schleswig-Holstein, Kiel, Germany.
Markus TiemannInstitute for Hematopathology Hamburg, Hamburg, Germany.
Peter MoellerDepartment of Pathology, University of Ulm, Ulm, Germany.
Andreas NeubauerDepartment of Medical Oncology, University of Marburg, Marburg, Germany.
Martin WilhelmDepartment of Medical Oncology, Paracelsus Medical University, Klinikum Nuernberg, Germany.
Georg LenzDepartment of Medicine A (Hematology, Oncology, and Pneumology), University Hospital of Muenster, Muenster, Germany.
Wolfgang E BerdelDepartment of Medicine A (Hematology, Oncology, and Pneumology), University Hospital of Muenster, Muenster, Germany.
Normann WillichDepartment of Radiation Oncology, University Hospital of Muenster, Muenster, Germany.
Hans T EichDepartment of Radiation Oncology, University Hospital of Muenster, Muenster, Germany.
University Hospital Münster · DECharité - Universitätsmedizin Berlin · DEInstitut für Hämatopathologie Hamburg · DEKiel University · DEKlinikum Aschaffenburg · DEParacelsus Medizinische Privatuniversität · DEPhilipps University of Marburg · DEPius Hospital Oldenburg · DESaarland University · DEStädtisches Klinikum Karlsruhe · DESt. Franziskus Hospital · DEUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis article reports on the long-term impact of radiotherapy adapted to stage, histology, and previous resection in a large cohort of patients with intestinal lymphoma (iL) treated with definitive or adjuvant curative-intent radiation therapy (RT) ± chemotherapy (CHOP, MCP, or COP). PATIENTS AND

methodsIn two consecutive prospective study designs, 134 patients with indolent (stage IE-IIE) or aggressive (stage IE-IVE) iL were referred to 61 radiotherapeutic institutions between 1992 and 2003. Patients with indolent iL received extended field (EF) 30 Gy (+10 Gy boost in definitive treatment); patients with aggressive iL received involved field (IF) (EF) 40 Gy by means of stage-, histology-, and operation-adapted radiation fields.

resultsThe patients had median age 58 years and were predominantly male (2:1). Histology showed aggressive prevalence (1.6:1), stage IE-to-stage IIE ratio of iL 1.04:1, and localized stages-to-advanced stages ratio of aggressive lymphoma 23:1. Median follow-up was in total 11.7 years: 10.0 years in the first study, GIT (GastroIntestinal-Tract) 1992, and 11.8 years in the second study, GIT 1996. Lymphoma involvement was predominantly a single intestinal lesion (82.1%). Decrease of radiation field size from EF to IF in stage I aggressive iL from GIT 1992 to GIT 1996 resulted in a nonsignificant partial reduction of chronic toxicity while maintaining comparable survival rates (5-year overall survival 87.9 vs. 86.7%, 10-year overall survival 77.4 vs. 71.5%) with nonsignificant difference in event-free survival (5-year event-free survival 82.6 vs. 86.7%, 10-year event-free survival 69.7 vs. 71.5%) and lymphoma-specific survival (5-year lymphoma-specific survival 90.1 vs. 91.9%, 10-year lymphoma-specific survival 87.6% vs. 91.9%). Comparative dose calculation of two still available indolent duodenal lymphoma computed tomography scans revealed lower radiation exposure to normal tissues from applying current standard involved site RT (ISRT) 30 Gy in both cases.

conclusionRT adapted to stage, histology, and resection in multimodal treatment of iL, despite partially decreasing field size (EF to IF), achieves excellent local tumor control and survival rates. The use of modern RT technique and target volume with ISRT offers the option of further reduction of normal tissue complication probability. IMPLICATIONS FOR PRACTICE: Although patients with intestinal lymphoma (iL) are heterogeneous according to histology and subtype, they benefit from radiotherapy. Prospective study data from 134 patients with indolent iL (stage IE-IIE) or aggressive iL (stage IE-IVE) show 100% tumor control after definitive or adjuvant curative-intent radiation therapy ± chemotherapy. Radiation treatment was applied between 1992 and 2003. Median follow-up in total was 11.7 years. No radiotherapy-associated death occurred. Relapse developed in 15.7% of the entire cohort; distant failure was more frequent than local (4:1). Normal tissue complication probability can be further improved using modern involved site radiation therapy techniques.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, Non-HodgkinCombined Modality TherapyFollow-Up StudiesHumansMaleMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingProspective StudiesExtended fieldIntestinal lymphomaInvolved fieldInvolved site radiation therapyNormal tissue complication probability

Identifiers

PMID32219909
PMCPMC7216456
OpenAlexW3012984082

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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.