Evidence map›Paper›PMID 26961793›Full record

ArticleHormones & cancer2016

Salvage Treatment of Adrenocortical Carcinoma with Trofosfamide.

Matthias Kroiss, Timo Deutschbein, Wiebke Schlötelburg, Cristina L Ronchi, Bruno Neu, Hans-Helge Müller, Marcus Quinkler, Stefanie Hahner, Anke Heidemeier, Martin Fassnacht and 1 more

Open access · greenAbstract read
In one paragraph

Article in Hormones & cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Systemic Management of Advanced Adrenocortical Carcinoma.Current treatment options in oncology · 2024
    Review
  3. Management of adrenocortical carcinoma: are we making progress?Therapeutic advances in medical oncology · 2021
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. 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

11 authors at 2 institutions in 1 country.

Matthias KroissComprehensive Cancer Center Mainfranken, University of Würzburg, Würzburg, Germany. Kroiss_M@ukw.de.ORCID 0000-0002-7628-3161
Timo DeutschbeinDepartment of Internal Medicine I, Division of Endocrinology and Diabetology, University Hospital Würzburg, University of Würzburg, Oberdürrbacher Str. 6, 97080, Würzburg, Germany.
Wiebke SchlötelburgDepartment of Diagnostic and Interventional Radiology, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.
Cristina L RonchiDepartment of Internal Medicine I, Division of Endocrinology and Diabetology, University Hospital Würzburg, University of Würzburg, Oberdürrbacher Str. 6, 97080, Würzburg, Germany.
Bruno NeuSecond Department of Medicine, Technical University of Munich, Munich, Germany.
Hans-Helge MüllerInstitut für Medizinische Biometrie und Epidemiologie, Philipps-Universität, Marburg, Germany.
Marcus QuinklerClinical Endocrinology, Charité Campus Mitte, Charité University Medicine, Berlin, Germany.
Stefanie HahnerComprehensive Cancer Center Mainfranken, University of Würzburg, Würzburg, Germany.
Anke HeidemeierDepartment of Diagnostic and Interventional Radiology, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.
Martin FassnachtComprehensive Cancer Center Mainfranken, University of Würzburg, Würzburg, Germany.
German Adrenocortical Carcinoma Study Group
University of Würzburg · DEPhilipps University of Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adrenocortical carcinoma (ACC) has a dismal prognosis in advanced stages. Despite treatment with the adrenal toxicant mitotane and/or aggressive chemotherapy, tumor control is often short-lived. Here, we examine trofosfamide as a salvage treatment of ACC in an observational cohort study within the German ACC registry. Response defined as progression-free survival (PFS) at first tumor evaluation was assessed by RECIST 1.1 or clinically, and PFS and overall survival (OS) were estimated by the Kaplan-Meier method. Twenty-seven patients (11 males; median age 46.9 years) progressing after mitotane and three (median, range 0-5) other systemic treatments were evaluated for safety. Trofosfamide (150 mg/day) was administered as monotherapy (n = 13) or in combination with mitotane (n = 14). Overall tolerability was good with only mild adverse events. Six patients did not meet criteria for response assessment. Of the 21 patients, 8 patients had clinically progressive disease (3 deaths from ACC); among the 13 patients evaluable by RECIST 1.1, best response to treatment was stable disease (SD, n = 3) or progressive disease (n = 10). Hence, predefined response criteria were met in 3/21 patients (14 %). Median PFS was 84 days (95 % confidence interval 74-95) and median OS survival 198 days (95 % CI 89-307). One prolonged disease stabilization (best response by RECIST 1.1 -26 %) was observed for 479 days. In conclusion, trofosfamide is overall well tolerated but disease stabilization is rather rare. Accordingly, it may be used in selected cases of ACC not amenable to other treatment options such as clinical trials.

Indexed as

AdolescentAdrenal Cortex NeoplasmsAdrenocortical CarcinomaAdultAgedAntineoplastic Agents, AlkylatingCombined Modality TherapyCyclophosphamideFemaleHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasm MetastasisNeoplasm StagingRetrospective StudiesAntineoplastic Agents, AlkylatingCyclophosphamidetrofosfamide

Identifiers

PMID26961793
PMCPMC10355984
OpenAlexW2296386017

What OpenQuestion holds

Textmetadata
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.