Hematologic Toxicity and Bone Marrow-Sparing Strategies in Chemoradiation for Locally Advanced Cervical Cancer: A Systematic Review.
Dinah KonnerthAurélie GaaschAnnemarie ZinnPaul RogowskiMaya RottlerFranziska WalterJohannes KnothAlina SturdzaJan OelmannFreba GraweRaphael BodensohnClaus BelkaStefanie CorradiniPublished in: Cancers (2024)
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.
Keyphrases
- bone marrow
- rectal cancer
- locally advanced
- mesenchymal stem cells
- oxidative stress
- randomized controlled trial
- primary care
- healthcare
- newly diagnosed
- bone mineral density
- ejection fraction
- robot assisted
- stem cells
- systematic review
- prognostic factors
- soft tissue
- clinical trial
- early onset
- minimally invasive
- bone regeneration
- oxide nanoparticles
- postmenopausal women