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RRx-001 Priming of PD-1 Inhibition in the Treatment of Small Cell Carcinoma of the Vagina: A Rare Gynecological Tumor

  • Christina Brzezniak
  • , Bryan Oronsky
  • , Jane Trepel
  • , Thomas A. Summers
  • , Pedro Cabrales
  • , Min Jung Lee
  • , Regina Day
  • , Saheli Jha
  • , Scott Caroen
  • , Karen Zeman
  • , Lindsey Ferry
  • , Cindy Harmer
  • , Neil Oronsky
  • , Michelle Lybeck
  • , Harry E. Lybeck
  • , James F. Brown
  • , Tony R. Reid
  • , Corey A. Carter*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Small cell carcinoma of the vagina is rare, so rare in fact that the total number reported in English-language journals is less than 30. Due to this extremely low incidence, no specific treatment guidelines have been established, and most of what is clinically known is derived from a handful of single case reports. However, as befitting its highly aggressive histologic features, which are reminiscent of small cell lung cancer (SCLC), first-line treatment is modeled after SCLC. Herein is reported the case of a 51-year-old African-American patient with metastatic biopsy-proven small cell carcinoma of the vagina that progressed through multiple therapies: first-line cisplatin and etoposide (making it platinum-resistant) and radiotherapy, followed by the tumor macrophage-stimulating agent RRx-001 in a clinical trial called QUADRUPLE THREAT, which per protocol preceded a mandated rechallenge with cisplatin and etoposide. RECIST v.1.1 tumor progression on both RRx-001 and cisplatin/etoposide was accompanied by central necrosis in several of the enlarged lymph nodes and hepatic metastases, which may have been evidence of pseudoprogression, accounting for her ongoing longer-than-expected survival, since the necrotic tissue may have primed the activity of the PD-1 inhibitor. The lack of response to RRx-001 is hypothesized to have correlated with sparse tumor macrophage infiltration, seen on pre- and post-treatment biopsies, since the mechanism of action of RRx-001 relates to stimulation of tumor-associated macrophages.

Original languageEnglish
Pages (from-to)276-280
Number of pages5
JournalCase Reports in Oncology
Volume10
Issue number1
DOIs
StatePublished - 6 Jan 2017

Keywords

  • Chemotherapy
  • Immunotherapy
  • Pseudoprogression
  • RRx-001
  • Small cell carcinoma
  • Tumor-associated macrophage stimulation
  • Vagina

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