Outcomes of relapsed/refractory extracranial germ cell tumors treated on conventional salvage chemotherapy without stem cell rescue: Experience from a tertiary cancer center

Author:

Ramanathan Subramaniam1,Prasad Maya23ORCID,Vora Tushar4,Badira Cheriyalinkal Parambil23ORCID,Kembhavi Seema5,Ramadwar Mukta36,Khanna Nehal37,Laskar Siddhartha37ORCID,Muckaden Mary Ann38,Qureshi Sajid39ORCID,Banavali Shripad23,Chinnaswamy Girish23

Affiliation:

1. Department of Paediatric Oncology, Great North Children's Hospital Royal Victoria Infirmary Newcastle upon Tyne Tyne and Wear UK

2. Department of Paediatric Oncology Tata Memorial hospital Mumbai Maharashtra India

3. Homi Bhabha National Institute Mumbai Maharashtra India

4. Department of Paediatric Oncology SickKids Hospital Toronto Ontario Canada

5. Department of Radiology Mackay Hospital and Health Services Mackay Queensland Australia

6. Department of Pathology Tata Memorial Hospital Mumbai Maharashtra India

7. Department of Radiation Oncology Tata Memorial Hospital Mumbai Maharashtra India

8. Department of Palliative Medicine Tata Memorial Hospital Mumbai Maharashtra India

9. Department of Paediatric Surgery Tata Memorial Hospital Mumbai Maharashtra India

Abstract

AbstractBackground and aimsData on the outcome and prognostic indicators in extracranial relapsed/refractory germ cell tumors (rel/ref‐GCTs) in children are limited to a few studies. This study looks at remission rates and outcomes of rel/ref‐GCTs treated with conventional salvage chemotherapy (SC) regimens without stem cell rescue at a single center in the developing world.MethodsPatients treated at our center from January 2009 to December 2018 were included. Risk at primary presentation was stratified as all completely excised teratomas and stage I gonadal tumors being low risk (LR); stage IV ovarian, stage III–IV extragonadal GCTs as high risk (HR), and the remaining as intermediate risk (IR). SC regimens were: vinblastine–ifosfamide–cisplatin/carboplatin or paclitaxel–ifosfamide–cisplatin/carboplatin, or cisplatin/carboplatin–etoposide–bleomycin. Local therapy was either surgery and/or radiotherapy.ResultsThe analyzable cohort comprised 50 patients (44 = rel‐GCTs; 6 = ref‐GCTs) with a median age of 3.8 years and male:female ratio of 1.27:1. Primary location was ovary in 16 (32%), testicular in 10 (20%), and extragonadal in the rest (48%). Local, metastatic, and combined progression was noted in 28 (56%), 14 (28%), and eight (16%) patients, respectively, at a median time of 8.5 months. At a median follow‐up of 60 months, the 5‐year event‐free survival (EFS) and overall survival (OS) of the entire cohort (n = 50) were 42.4% and 50.0%, respectively. In patients previously exposed to platinum analogs (n = 38), 5‐year‐EFS and OS were 27.7% and 31.7%, respectively. Local relapses did better when compared to metastatic and combined relapses (5‐year EFS: 64% vs. 23% vs. 0%; p = .009). LR and IR tumors did better compared to HR (5‐year EFS: 81.5% vs. 49.3% vs. 6.5%; p = .002). Patients with normalization of tumor markers after two cycles had a superior EFS (57.6% vs. 0%; p < .001). Relapsed tumors fared better than primary refractory GCTs (5‐year EFS: 48.6% vs. 0%; p < .001).ConclusionsPrimary refractory GCTs, extragonadal rel‐GCTs, and rel/ref‐GCTs with a poor biochemical response did poorly with conventional SC and need alternative treatment strategies. The rel/ref‐testicular GCTs had the best chance of salvage despite a second recurrence (5‐year EFS and OS: 28.60% and 42.90%, respectively).

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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