Evidence map›Paper›PMID 28843653›Full record

ArticleGynecologic oncology2017

Characterization of folate receptor alpha (FRα) expression in archival tumor and biopsy samples from relapsed epithelial ovarian cancer patients: A phase I expansion study of the FRα-targeting antibody-drug conjugate mirvetuximab soravtansine.

Lainie P Martin, Jason A Konner, Kathleen N Moore, Shelly M Seward, Ursula A Matulonis, Raymond P Perez, Ying Su, Anna Berkenblit, Rodrigo Ruiz-Soto, Michael J Birrer

Open access · hybridAbstract readClinical Trial, Phase I
In one paragraph

Article in Gynecologic oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 3 pooled it
8.2field-weighted citation impact, top 2% 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

76 citing papers in PubMed, 3 syntheses or guidelines pooled it, 126 citations in OpenAlex.

  1. Morphological and molecular characterization of epithelial ovarian cancer: SEOM-SEAP consensus guidelines for biomarker integration in clinical practice.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Guideline
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  13. Clinical trial of safety and antitumor activity of farletuzumab ecteribulin in patients with platinum-resistant ovarian cancer: Phase I expansion results.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2026
    Article
  14. Folate receptor alpha in platinum-resistant ovarian cancer: prevalence in a multicenter Polish cohort and review of the evidence.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  15. Article
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  17. Management of ocular toxicity in patients with gynecologic cancer receiving novel antibody-drug conjugates: a narrative review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  18. Article
  19. Antibody-Drug Conjugates in Gynecologic Oncology: Advances, Challenges, and Future Directions.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  20. Review

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

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

10 authors at 8 institutions in 1 country.

Lainie P MartinFox Chase Cancer Center, Philadelphia, PA, United States. Electronic address: lainie.martin@fccc.edu.
Jason A KonnerMemorial Sloan Kettering Cancer Center, New York, NY, United States. Electronic address: konnerj@MSKCC.org.
Kathleen N MooreStephenson Oklahoma Cancer Center at the University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States. Electronic address: kathleen-moore@ouhsc.edu.
Shelly M SewardWayne State University - Karmanos Cancer Institute, Huntington Woods, MI, United States. Electronic address: sseward@med.wayne.edu.
Ursula A MatulonisDana Farber Cancer Institute, Boston, MA, United States. Electronic address: ursula_matulonis@dfci.harvard.edu.
Raymond P PerezUniversity of Kansas, Fairway, KS, United States. Electronic address: perezonc@gmail.com.
Ying SuImmunoGen, Inc., Waltham, MA, United States. Electronic address: ying.su@immmunogen.com.
Anna BerkenblitImmunoGen, Inc., Waltham, MA, United States. Electronic address: anna.berkenblit@immunogen.com.
Rodrigo Ruiz-SotoImmunoGen, Inc., Waltham, MA, United States. Electronic address: rodrigo.ruizsoto@gmail.com.
Michael J BirrerMassachusetts General Hospital, Boston, MA, United States. Electronic address: mbirrer@mgh.harvard.edu.
ImmunoGen (United States) · USDana-Farber Cancer Institute · USFox Chase Cancer Center · USMassachusetts General Hospital · USMemorial Sloan Kettering Cancer Center · USThe Barbara Ann Karmanos Cancer Institute · USUniversity of Kansas · USUniversity of Oklahoma Health Sciences Center · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
NCI NIH HHS P30 CA022453
6 · The paper itself

Abstract

purposeTo characterize folate receptor alpha (FRα) expression in archival and fresh biopsy tumor samples from relapsed ovarian cancer patients.

methodsPatients with ovarian tumors amenable to biopsy were eligible to enroll. Eligibility included a minimum requirement of FRα positivity in archival tumor samples (≥25% of cells with ≥2+ staining intensity). Patients received mirvetuximab soravtansine at 6mg/kg once every 3weeks. Core needle biopsies were collected before and after treatment and FRα levels assessed by immunohistochemistry. Descriptive statistics were used to summarize the association between receptor expression and response.

resultsTwenty-seven heavily pre-treated patients were enrolled. Six individuals (22%) did not have evaluable pre-treatment biopsies due to insufficient tumor cells. The concordance of FRα expression in archival and biopsy tissues was 71%, and no major shifts in receptor expression were seen in matched pre- and post-treatment biopsy samples. Adverse events were generally mild (≤grade 2) with keratopathy (48%), fatigue (44%), diarrhea, and blurred vision (each 37%) being the most common treatment-related toxicities. The confirmed objective response rate (ORR) was 22%, including two complete responses and four partial responses. Superior efficacy measures were observed in the subset of patients with the highest FRα levels (ORR, 31%; progression-free survival, 5.4months).

conclusionConcordance of FRα expression in biopsy versus archival tumor samples suggests that archival tissue can reliably identify patients with receptor-positive tumors and is appropriate for patient selection in mirvetuximab soravtansine clinical trials. Regardless of the tissue source analyzed, higher FRα expression was associated with greater antitumor activity.

Indexed as

AdultAgedAntibodies, Monoclonal, HumanizedCarcinoma, Ovarian EpithelialFemaleFolate Receptor 1HumansImmunoconjugatesMaytansineMiddle AgedMolecular Targeted TherapyNeoplasms, Glandular and EpithelialOvarian NeoplasmsAntibodies, Monoclonal, HumanizedFolate Receptor 1ImmunoconjugatesMaytansinemirvetuximab soravtansineAntibody-drug conjugateBiopsyClinical trialFolate receptor alphaOvarian cancer

Identifiers

PMID28843653
PMCPMC6893864
OpenAlexW2745539538

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.