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Role of adjuvant therapy in resected periampullary adenocarcinoma: A propensity matched case-control study.
Srivastava, Anurita; Nekarakanti, Phani Kumar; Kanchodu, Sudheer; Srivastava, Siddharth; Mishra, Pramod Kumar; Saluja, Sundeep Singh.
  • Srivastava A; Department of Radiotherapy, Maulana Azad Medical College (MAMC), New Delhi, India.
  • Nekarakanti PK; Department of GI Surgery, Govind Ballabh Pant Institute of Postgraduate Medical Education & Research (GIPMER), New Delhi, India.
  • Kanchodu S; Department of GI Surgery, Govind Ballabh Pant Institute of Postgraduate Medical Education & Research (GIPMER), New Delhi, India.
  • Srivastava S; Department of Gastro Medicine, Govind Ballabh Pant Institute of Postgraduate Medical Education & Research (GIPMER), New Delhi, India.
  • Mishra PK; Department of GI Surgery, Govind Ballabh Pant Institute of Postgraduate Medical Education & Research (GIPMER), New Delhi, India.
  • Saluja SS; Department of GI Surgery, Govind Ballabh Pant Institute of Postgraduate Medical Education & Research (GIPMER), New Delhi, India.
Ann Hepatobiliary Pancreat Surg ; 28(3): 371-380, 2024 Aug 31.
Article en En | MEDLINE | ID: mdl-38600673
ABSTRACT
Backgrounds/

Aims:

The published data had contradictory information on the role of adjuvant therapy on resected periampullary carcinomas (PACA). The study was performed to evaluate the survival benefit of adjuvant treatment.

Methods:

This was a propensity score matched case-control study from a prospectively maintained database from 2004-2019. The study included patients with nonpancreatic PACA who underwent curative resection. The patients (cases) who received adjuvant chemotherapy were compared with patients (controls) who were observed alone after surgery.

Results:

Of 510 patients with PACA, 230 patients (cases = 107, controls = 123) formed the unmatched study cohort. After propensity score matching, 140 patients (cases = 70, controls = 70) formed the matched study cohort. The median overall survival (OS) was similar in cases than controls in the unmatched population but doubled non-significantly in cases after matching (unmatched population, 54 months vs. 54 months, p-value = 0.624; matched population, 71 months vs. 36 months, p-value = 0.087). However, the median recurrence-free survival (RFS) was non significantly higher in the control group (unmatched population, 59 months vs. 38 months, p-value = 0.195; matched population, 53 months vs. 40 months, p-value = 0.797). In cox regression analysis, age < 60 years, advanced T stage, and presence of perineural invasion were independent factors for worse RFS, while tumor recurrence was an independent factor for poor OS.

Conclusions:

Patients with nonpancreatic PACA may have an OS benefit from adjuvant chemotherapy, and this needs to be validated with large prospective randomized studies.
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