Interactive Effects of Molecular, Therapeutic, and Patient Factors on Outcome of Diffuse Low-Grade Glioma

Author:

Hervey-Jumper Shawn L.1,Zhang Yalan1,Phillips Joanna J.2,Morshed Ramin A.1,Young Jacob S.1ORCID,McCoy Lucie1ORCID,Lafontaine Marisa3ORCID,Luks Tracy3,Ammanuel Simon1,Kakaizada Sofia1,Egladyous Andrew1,Gogos Andrew1ORCID,Villanueva-Meyer Javier3ORCID,Shai Anny2,Warrier Gayathri1ORCID,Rice Terri1,Crane Jason3ORCID,Wrensch Margaret1,Wiencke John K.1,Daras Mariza14,Oberheim Bush Nancy Ann14,Taylor Jennie W.14ORCID,Butowski Nicholas1ORCID,Clarke Jennifer14,Chang Susan14,Chang Edward1ORCID,Aghi Manish1,Theodosopoulos Philip1,McDermott Michael1,Jakola Asgeir S.56ORCID,Kavouridis Vasileios K.5,Nawabi Noah7,Solheim Ole58ORCID,Smith Timothy7,Berger Mitchel S.1,Molinaro Annette M.1ORCID

Affiliation:

1. Department of Neurological Surgery, University of California, San Francisco, San Francisco, CA

2. Department of Pathology, University of California, San Francisco, San Francisco, CA

3. Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA

4. Department of Neurology, University of California, San Francisco, San Francisco, CA

5. Department of Neurological Surgery, St Olavs University Hospital, Trondheim, Norway

6. Institute of Neuroscience and Physiology, Department of Clinical Neuroscience, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden

7. Department of Neurological Surgery, Brigham and Women's Hospital, Boston, MA

8. Norwegian University of Science and Technology, Trondheim, Norway

Abstract

PURPOSE In patients with diffuse low-grade glioma (LGG), the extent of surgical tumor resection (EOR) has a controversial role, in part because a randomized clinical trial with different levels of EOR is not feasible. METHODS In a 20-year retrospective cohort of 392 patients with IDH-mutant grade 2 glioma, we analyzed the combined effects of volumetric EOR and molecular and clinical factors on overall survival (OS) and progression-free survival by recursive partitioning analysis. The OS results were validated in two external cohorts (n = 365). Propensity score analysis of the combined cohorts (n = 757) was used to mimic a randomized clinical trial with varying levels of EOR. RESULTS Recursive partitioning analysis identified three survival risk groups. Median OS was shortest in two subsets of patients with astrocytoma: those with postoperative tumor volume (TV) > 4.6 mL and those with preoperative TV > 43.1 mL and postoperative TV ≤ 4.6 mL. Intermediate OS was seen in patients with astrocytoma who had chemotherapy with preoperative TV ≤ 43.1 mL and postoperative TV ≤ 4.6 mL in addition to oligodendroglioma patients with either preoperative TV > 43.1 mL and residual TV ≤ 4.6 mL or postoperative residual volume > 4.6 mL. Longest OS was seen in astrocytoma patients with preoperative TV ≤ 43.1 mL and postoperative TV ≤ 4.6 mL who received no chemotherapy and oligodendroglioma patients with preoperative TV ≤ 43.1 mL and postoperative TV ≤ 4.6 mL. EOR ≥ 75% improved survival outcomes, as shown by propensity score analysis. CONCLUSION Across both subtypes of LGG, EOR beginning at 75% improves OS while beginning at 80% improves progression-free survival. Nonetheless, maximal resection with preservation of neurological function remains the treatment goal. Our findings have implications for surgical strategies for LGGs, particularly oligodendroglioma. [Media: see text]

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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