Literature DB >> 36187518

Post-treatment Residual Clinicopathological Outcomes in Testicular Germ Cell Tumours.

Ranjitha Vodigenahalli Nagaraj1, B Vishal Rao1, Jayakarthik Yoganarsimha2, Daphne Fonseca1, Suseela Kodandapani1, Ashwin Giridhar2, Rakesh Sharma2, Senthil Rajappa3, Thammineedi Subramanyeshwar Rao2, Challa Sundaram1.   

Abstract

Surgical resection is a generally accepted treatment for residual masses after chemotherapy for metastatic testicular germ cell tumour (GCT). About half the patients have necrosis in post-chemotherapy residual masses, whereas rest have viable tumour and teratoma. The likelihood of leaving behind teratoma with its subsequent complications such as growing teratoma syndrome necessitates resection outweighing its surgical complications. Ours is a retrospective observational study and aims at assessing post-chemotherapy residual masses in testicular GCTs and to predict importance of teratomatous and non-seminomatous components. A total of 62 cases of testicular GCTs resected after chemotherapy between January 2012 and June 2019 were included. Demographic, clinical, biochemical and imageological findings were noted and categorised according to WHO classification (2016). They were divided into two groups - those who underwent retroperitoneal lymph node dissection (RPLND) post-high inguinal orchidectomy (HIO) and chemotherapy (CT) as group 1 (n = 40) and those who underwent HIO and/or RPLND post-chemotherapy as group 2 (n = 22). The gross and microscopic examination was carried out to assess response to chemotherapy in terms of residual viable tumour, necrosis and teratoma. Viable tumour, necrosis and teratoma were 10%, 62.5% and 35% respectively in group 1 and in group 2, the same were 15%, 70% and 25% respectively in HIO specimen and 7%, 50% and 21% respectively in RPLND specimen. All the cases with viable tumour were proven to be yolk sac tumours (YST) based on morphology and immunohistochemistry (IHC).Twenty cases had teratoma in the post-CT residual masses out of which 11 cases had teratoma despite reduction in size. At a median follow-up of 47.85 months, 5 cases in group 1 and 2 cases in group 2 showed relapse and it was observed that group 1 had a prolonged relapse-free survival over group 2. Our study re-emphasises the importance of performing resection of residual mass post-CT irrespective of the size, imageological or biochemical evidence of tumour regression. There does not appear to be reliable predictors of post-chemotherapy histology of residual masses indicating the continued need for surgical resection in specialised centres. © Indian Association of Surgical Oncology 2021.

Entities:  

Keywords:  Post-chemotherapy; Residual; Testicular germ cell tumours

Year:  2022        PMID: 36187518      PMCID: PMC9515290          DOI: 10.1007/s13193-021-01491-6

Source DB:  PubMed          Journal:  Indian J Surg Oncol        ISSN: 0975-7651


  17 in total

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Journal:  J Clin Oncol       Date:  2000-01       Impact factor: 44.544

2.  Post-chemotherapy residual mass in non-seminomatous testicular cancer. The role of retroperitoneal lymph node dissection.

Authors:  Salwa El Sayed; João P S Grando; Silvio H M Almeida; Nicola Mortati Neto; Horácio A Moreira
Journal:  Int Braz J Urol       Date:  2004 Sep-Oct       Impact factor: 1.541

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Authors:  Sung Bin Park; Won Chan Lee; Jeong Kon Kim; Seong Hoon Choi; Byeong Seong Kang; Kyung Hyun Moon; Young Min Kim; Yoong Ki Jeong
Journal:  Eur Radiol       Date:  2011-05-29       Impact factor: 5.315

4.  Equivalence of three or four cycles of bleomycin, etoposide, and cisplatin chemotherapy and of a 3- or 5-day schedule in good-prognosis germ cell cancer: a randomized study of the European Organization for Research and Treatment of Cancer Genitourinary Tract Cancer Cooperative Group and the Medical Research Council.

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Journal:  J Clin Oncol       Date:  2001-03-15       Impact factor: 44.544

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Journal:  Ann Oncol       Date:  2018-08-01       Impact factor: 32.976

6.  Retroperitoneal lymph node dissection for residual masses after chemotherapy in nonseminomatous germ cell testicular tumor.

Authors:  Murilo A Luz; Ahmed F Kotb; Saad Aldousari; Fadi Brimo; Simon Tanguay; Wassim Kassouf; Armen G Aprikian
Journal:  World J Surg Oncol       Date:  2010-11-09       Impact factor: 2.754

7.  A 5-year followup study of asymptomatic men with testicular microlithiasis.

Authors:  Brian J DeCastro; Andrew C Peterson; Raymond A Costabile
Journal:  J Urol       Date:  2008-03-04       Impact factor: 7.450

8.  Autopsy findings in 154 patients with germ cell tumors of the testis.

Authors:  J J Bredael; D Vugrin; W F Whitmore
Journal:  Cancer       Date:  1982-08-01       Impact factor: 6.860

9.  Teratoma in the orchiectomy specimen and volume of metastasis are predictors of retroperitoneal teratoma in post-chemotherapy nonseminomatous testis cancer.

Authors:  Stephen D W Beck; Richard S Foster; Richard Bihrle; Thomas Ulbright; Michael O Koch; Gregory R Wahle; Lawrence H Einhorn; John P Donohue
Journal:  J Urol       Date:  2002-10       Impact factor: 7.450

10.  Postchemotherapy residual masses in germ cell tumor patients: content, clinical features, and prognosis. Medical Research Council Testicular Tumour Working Party.

Authors:  S P Stenning; M C Parkinson; C Fisher; G M Mead; P A Cook; S D Fossa; A Horwich; W G Jones; E S Newlands; R T Oliver; A E Stenwig; P M Wilkinson
Journal:  Cancer       Date:  1998-10-01       Impact factor: 6.860

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