Hematologic Toxicity and Bone Marrow-Sparing Strategies in Chemoradiation for Locally Advanced Cervical Cancer: A Systematic Review

Author:

Konnerth Dinah1,Gaasch Aurelie1ORCID,Zinn Annemarie1,Rogowski Paul1ORCID,Rottler Maya1,Walter Franziska1,Knoth Johannes2ORCID,Sturdza Alina2,Oelmann Jan3,Grawe Freba45,Bodensohn Raphael6ORCID,Belka Claus1,Corradini Stefanie1ORCID

Affiliation:

1. Department of Radiation Oncology, University Hospital, LMU Munich, 81377 Munich, Germany

2. Department of Radiation Oncology, Comprehensive Cancer Center, Medical University of Vienna, 1090 Vienna, Austria

3. Department of Radiation Oncology, Göttingen University Hospital, 37075 Göttingen, Germany

4. DKFZ Hector Cancer Institute at the University Medical Center Mannheim, 69120 Heidelberg, Germany

5. Department of Clinical Radiology and Nuclear Medicine, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University Mannheim, 68167 Mannheim, Germany

6. Department of Radiation Oncology, University Hospital Tübingen, 72076 Tübingen, Germany

Abstract

The standard treatment for locally advanced cervical cancer typically includes concomitant chemoradiation, a regimen known to induce severe hematologic toxicity (HT). Particularly, pelvic bone marrow dose exposure has been identified as a contributing factor to this hematologic toxicity. Chemotherapy further increases bone marrow suppression, often necessitating treatment interruptions or dose reductions. A systematic search for original articles published between 1 January 2006 and 7 January 2024 that reported on chemoradiotherapy for locally advanced cervical cancer and hematologic toxicities was conducted. Twenty-four articles comprising 1539 patients were included in the final analysis. HT of grade 2 and higher was observed across all studies and frequently exceeded 50%. When correlating active pelvic bone marrow and HT, significant correlations were found for volumes between 10 and 45 Gy and HT of grade 3 and higher. Several dose recommendations for pelvic bone and pelvic bone marrow sparing to reduce HT were established, including V10 < 90–95%, V20 < 65–86.6% and V40 < 22.8–40%. Applying dose constraints to the pelvic bone/bone marrow is a promising approach for reducing HT, and thus reliable implementation of therapy. However, prospective randomized controlled trials are needed to define precise dose constraints and optimize clinical strategies.

Publisher

MDPI AG

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