# Phase II study of ipilimumab and nivolumab in leptomeningeal carcinomatosis

**Authors:** Priscilla K. Brastianos, Matthew R. Strickland, Eudocia Quant Lee, Nancy Wang, Justine V. Cohen, Ugonma Chukwueke, Deborah Anne Forst, April Eichler, Beth Overmoyer, Nancy U. Lin, Wendy Y. Chen, Aditya Bardia, Dejan Juric, Ibiayi Dagogo-Jack, Michael D. White, Jorg Dietrich, Naema Nayyar, Albert E. Kim, Christopher Alvarez-Breckenridge, Maura Mahar, Joana L. Mora, Brian V. Nahed, Pamela S. Jones, Helen A. Shih, Elizabeth R. Gerstner, Anita Giobbie-Hurder, Scott L. Carter, Kevin Oh, Daniel P. Cahill, Ryan J. Sullivan

PMC · DOI: 10.1038/s41467-021-25859-y · Nature Communications · 2021-10-12

## TL;DR

This study shows that combining two immunotherapy drugs can improve survival in patients with a rare and severe brain cancer complication.

## Contribution

The study is the first to demonstrate promising survival outcomes and safety of combined ipilimumab and nivolumab in leptomeningeal carcinomatosis.

## Key findings

- Eight out of 18 patients were alive at three months, meeting the primary endpoint of improved survival.
- One-third of patients experienced significant adverse events, but the treatment was generally well-tolerated.
- The results suggest the need for larger trials to confirm the efficacy of this treatment combination.

## Abstract

Leptomeningeal disease (LMD) is a common complication from solid tumor malignancies with a poor prognosis and limited treatment options. We present a single arm Phase II study of 18 patients with LMD receiving combined ipilimumab and nivolumab until progression or unacceptable toxicity (NCT02939300). The primary end point is overall survival at 3 months (OS3). Secondary end points include toxicity, cumulative time-to-progression at 3 months, and progression-free survival. A Simon two-stage design is used to compare a null hypothesis OS3 of 18% against an alternative of 44%. Median follow up based on patients still alive is 8.0 months (range: 0.5 to 15.9 months). The study has met its primary endpoint as 8 of 18 (OS3 0.44; 90% CI: 0.24 to 0.66) patients are alive at three months. One third of patients have experienced one (or more) grade-3 or higher adverse events. Two patients have discontinued protocol treatment due to unacceptable toxicity (hepatitis and colitis, respectively). The most frequent adverse events include fatigue (N = 7), nausea (N = 6), fever (N = 6), anorexia (N = 6) and rash (N = 6). Combined ipilimumab and nivolumab has an acceptable safety profile and demonstrates promising activity in LMD patients. Larger, multicenter clinical trials are needed to validate these results.

Leptomeningeal metastases from solid tumors are a rare complication with a very poor prognosis. Here the authors report the efficacy and safety of combined ipilimumab and nivolumab in patients with leptomeningeal carcinomatosis.

## Linked entities

- **Diseases:** leptomeningeal carcinomatosis (MONDO:0700219)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, Pdcd1 (programmed cell death 1) [NCBI Gene 18566] {aka Ly101, PD-1, Pdc1}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, Ctla4 (cytotoxic T-lymphocyte-associated protein 4) [NCBI Gene 12477] {aka Cd152, Ctla-4, Ly-56}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** neuro-endocrine carcinoid tumor (MESH:D002276), headache (MESH:D006261), Abdominal pain or discomfort (MESH:D015746), Ovarian 1 (MESH:D010051), colitis (MESH:D003092), Brain metastases (MESH:D001932), Aspiration pneumonia (MESH:D011015), leukoencephalopathy (MESH:D056784), neurological or autoimmune toxicity (MESH:D020274), Fever (MESH:D005334), immunodeficiency (MESH:D007153), Melanoma 2 (MESH:D008545), aseptic meningitis (MESH:D008582), Small cell lung carcinoma 1 (MESH:D055752), infectious meningitis (MESH:D003141), bladder cancer (MESH:D001749), gait instability (MESH:D043171), Esophageal adenocarcinoma 1 (MESH:D000230), lung nodule (MESH:D003074), Constitutional Fatigue (MESH:D005221), Leptomeningeal metastases (MESH:D009362), Anorexia (MESH:D000855), Nausea (MESH:D009325), autoimmune disease (MESH:D001327), Extracranial disease (MESH:D004194), Glioblastoma 1 (MESH:D005909), CNS disease (MESH:D002493), Diarrhea (MESH:D003967), Gastrointestinal disorders (MESH:D005767), brain (MESH:D001927), nevus (MESH:D009506), lung cancer (MESH:D008175), rash (MESH:D005076), Vomiting (MESH:D014839), Musculoskeletal Back pain (MESH:D059352), Lymph nodes (MESH:D000072717), Hodgkin's lymphoma (MESH:D006689), Stable disease (MESH:D060050), Anaplastic astrocytoma 1 (MESH:D001254), LMD (MESH:D008577), melanocytic dysplasia (MESH:D009508), pneumonitis (MESH:D011014), malignancies (MESH:D009369), neurological toxicities (MESH:D020258), disorders Pruritus 4 (22%) - -   Rash 6 (33%) - -   Vascular disorders Hypotension (MESH:D007022), neurological deficits (MESH:D009461), NSCLC (MESH:D002289), esophageal carcinoma (MESH:D004938), hematological malignancies (MESH:D019337), cerebellar syndrome (MESH:D002526), Sepsis (MESH:D018805), Toxicities (MESH:D064420), immune-related adverse events (MESH:D002318), HCC (MESH:D006528), Breast Cancer 8 (MESH:D001943), deaths (MESH:D003643), Unknown (MESH:D009382), carcinomatosis meningitis (MESH:D055756), Renal Acute kidney injury (MESH:D058186), Weight loss (MESH:D015431)
- **Chemicals:** nivolumab (MESH:D000077594), ipilimumab (MESH:D000074324), aImmune (-), dexamethasone (MESH:D003907), glucose (MESH:D005947)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC8511104/full.md

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Source: https://tomesphere.com/paper/PMC8511104