1Department of Surgery, Dr RPGMC, Tanda, Himachal Pradesh, India. 2,3Department of Surgery, Dr YSPGMC Nahan, Himachal Pradesh, India. 4Department of Surgery, SLBSGMC Nerchowk, Himachal Pradesh, India. 5Department of Surgery, IGMC Shimla, Himachal Pradesh, India
*Corresponding author: Arvind Kanwar; *Email: kanwar.ak.arvind@gmail.com
Received: 20 Dec 2023, Revised and Accepted: 24 Jan 2024
ABSTRACT
Objective: Stomach carcinoma, a complex challenge in oncology, necessitates refined staging for optimal therapeutic strategies. The comparative analysis of staging laparoscopy and contrast-enhanced computed tomography (CECT) emerges as a key exploration in this context.
Methods: Conducted at Indira Gandhi Medical College and Hospital, Shimla, this prospective study spanned one year. Biopsy-proven gastric carcinoma patients meeting inclusion criteria underwent extensive investigations, including CECT, staging laparoscopy, and diagnostic lavage. The study employed specific protocols for each procedure, ensuring comprehensive data collection.
Results: Analysis of 32 cases revealed a prevalence in the 61-70 y age group, predominantly affecting males. Diverse symptoms included pain (68.75%) and palpable mass (81.2%). Well-differentiated adenocarcinoma (43.8%) dominated, with distinct age-related patterns. The study showcased the intricate nature of gastric carcinoma, demanding tailored diagnostic approaches.
Conclusion: This study unravels the interplay between staging laparoscopy and CECT in gastric carcinoma, offering a comprehensive staging approach. The nuanced insights gained through their synergy address individual limitations, contributing to more precise evaluations and tailored interventions. The collaborative use of these modalities promises to enhance precision, ultimately improving patient outcomes in gastric carcinoma management.
Keywords: Stomach carcinoma, Staging laparoscopy, Contrast-enhanced computed tomography, Diagnostic modalities, Personalized treatment, Gastric cancer management
© 2024 The Authors. Published by Innovare Academic Sciences Pvt Ltd. This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/)
DOI: https://dx.doi.org/10.22159/ijcpr.2024v16i2.4047 Journal homepage: https://innovareacademics.in/journals/index.php/ijcpr
Stomach carcinoma, a formidable adversary in the landscape of oncology, demands a comprehensive understanding of its intricate nature to devise optimal therapeutic strategies. The quest for refining diagnostic methodologies in the face of this complex disease progression has led to an exploration of innovative staging techniques, and among these, the dynamic interplay between staging laparoscopy and Contrast-Enhanced Computed Tomography (CECT) of the abdomen emerges as a focal point for scrutiny [1]. This article endeavors to conduct a thorough comparative analysis of these staging modalities, unraveling the intricate synergy that exists between staging laparoscopy and cect abdomen in the context of carcinoma stomach [2].
The challenges inherent in managing stomach carcinoma are multifaceted, given the diversity of clinical presentations and the complex trajectory of disease progression. Accurate staging is pivotal, acting as the linchpin for determining the most appropriate and effective treatment strategy [3]. As the medical community endeavors to refine and enhance staging methodologies, the integration of innovative techniques becomes paramount. In this regard, the comparative analysis of staging laparoscopy and cect abdomen presents a compelling avenue for exploration, holding the promise of providing deeper insights into the disease and revolutionizing the approach to staging [4].
Staging laparoscopy, traditionally reserved for exploratory purposes, has evolved into an indispensable adjunctive staging method. This minimally invasive surgical procedure offers unparalleled insights into the peritoneal cavity, facilitating the identification of metastatic lesions that might elude conventional imaging [5]. The systematic inspection of the entire abdominal cavity and targeted biopsies make staging laparoscopy a valuable tool for a more personalized and targeted approach to treatment. Contrastingly, cect of the abdomen has long stood as a cornerstone in the staging process, providing detailed anatomical information through cross-sectional imaging. However, its limitations in detecting subtle peritoneal metastases and small locoregional lesions have prompted the exploration of complementary modalities [6].
This comparative analysis seeks to unravel the intricacies of the synergistic relationship between staging laparoscopy and cect abdomen. By delving into their respective strengths, limitations, and combined efficacy, the article aims to provide a nuanced understanding of how these modalities can complement each other to enhance the precision of stomach carcinoma staging. The examination of recent studies, technological advancements, and clinical outcomes will contribute to shedding light on the evolving role of staging laparoscopy when employed in conjunction with cect abdomen [7].
As we navigate through this exploration, the goal is not only to present a comparative analysis but also to contribute valuable perspectives to the ongoing discourse in oncology. By fostering a deeper understanding of the synergy between staging laparoscopy and cect abdomen, this article aspires to catalyze advancements that can translate into improved patient care and outcomes in the realm of stomach carcinoma management [8].
Study setup and design
Study Area: The study was conducted in the Department of Surgery at Indira Gandhi Medical College and Hospital, Shimla.
Study Duration: The study spanned a period of one year.
Study Description: This was a prospective study.
Study population
The study included patients with biopsy-proven gastric carcinoma in the Department of Surgery, IGMC, Shimla, who met the inclusion criteria.
Inclusion Criteria
Patients with endoscopic biopsy-proven carcinoma of the stomach deemed resectable on CECT thorax, abdomen, and pelvis.
Those who provided consent to participate in the study.
Exclusion Criteria
Patients who received neoadjuvant chemotherapy before staging laparoscopy.
Patients with proven metastasis on CECT thorax, abdomen, and pelvis.
Patients who did not provide consent.
Methodology
All eligible patients underwent a series of investigations, including haemogram, renal function tests, liver function tests, CEA, CA 19-9, chest X-ray, CECT scan, staging laparoscopy, diagnostic lavage, and histopathological examination (HPE) of biopsy specimens obtained during staging laparoscopy.
A written informed consent was obtained from all participants.
Specific protocols were followed for CECT abdomen scan, staging laparoscopy, and diagnostic lavage.
CT protocol
CECT was performed on a 64-slice MDCT (Light Speed VCT Xte: GE Healthcare).
Patients underwent an overnight fast and received approximately 1.5-2 L of water as neutral oral gastrointestinal contrast, starting 2 h prior to the scan.
Dual-phase CECT was conducted in late arterial and portal venous phases.
Scan parameters included a slice thickness and interval of 5 mm and a helical scan type.
Intravenous contrast dose was 1.5-2 ml/kg body weight administered at a rate of 3.5–4 ml/sec by an automatic pressure injector.
Staging laparoscopy protocol
Patients were placed in the supine position under general anesthesia.
A 12 mm sub/supra umbilical incision was made, and pneumoperitoneum with CO2 was established.
Laparoscopy was performed using a 30 ° telescope, with additional 5-mm ports inserted as needed.
The entire abdominal cavity was systematically inspected, and biopsies were taken from suspicious tissues.
Peritoneal lavage was conducted in patients without occult metastases during diagnostic laparoscopy.
Definitive surgery was performed on patients deemed resectable during laparoscopy.
Diagnostic lavage protocol
The peritoneal cavity was washed with 200 ml of warm normal saline solution, instilled into different abdominal regions, and aspirated under direct vision.
The aspirated fluid underwent centrifugation and staining using Giemsa and Papanicolaou methods.
Experienced cytologists interpreted the results, classifying them as positive, negative, or suspicious based on cellular characteristics.
Ethical considerations
Written informed consent was obtained from all participants.
Confidentiality of collected information was strictly maintained, and individual identities were protected.
Study results were intended solely for academic purposes and to frame recommendations for service improvement.
Table 1: Age-wise distribution of cases
Age group (Y) | No. of patients | Percentage |
41-50 | 05 | 15.6 |
51-60 | 11 | 34.4 |
61-70 | 12 | 37.5 |
71-80 | 04 | 12.5 |
Total | 32 | 100 |
Table 2: Sex-wise distribution of cases
Gender | No. of patients | Percentage |
Male | 23 | 71.8 |
Female | 9 | 28.2 |
Total | 32 | 100 |
Table 3: Distribution of patients according to signs and symptoms
Symptomatology | No. of patients | Percentage |
Symptoms | ||
Pain | 22 | 68.75 |
Anorexia | 19 | 59.37 |
Vomiting | 14 | 43.75 |
Weight loss | 18 | 56.25 |
Malena | 4 | 12.5 |
Signs | ||
Pallor | 19 | 59.3 |
Palpable mass | 26 | 81.2 |
The study analyzed 32 cases of gastric carcinoma, presenting significant findings on age, gender, symptoms, and histopathology. Table 1 revealed a predominant occurrence in the 61-70 y age group, comprising 37.5% of cases. Males exhibited a higher incidence than females, with a ratio of 2.55:1 (table 2). Symptoms were diverse, with pain (68.75%), anorexia (59.37%), and palpable mass (81.2%) being notable (table 3). Histopathological analysis (table 4) showcased well-differentiated adenocarcinoma as the most common (43.8%), predominantly affecting the 41-50 and 61-70 age groups. Moderately differentiated cases were concentrated in the 51-60 age bracket (9.3%), while poorly differentiated adenocarcinoma was prevalent in the 51-70 age group (25%). Interestingly, mucinous and neuroendocrine carcinoma each manifested in the 71-80 age group, while signet ring adenocarcinoma occurred in the 61-80 age group. These findings underscore the diverse nature of gastric carcinoma, necessitating nuanced diagnostic and therapeutic approaches tailored to age and histopathological characteristics.
Table 4: Distribution of patients according to histopathology
Histopathology | Number of patients | Percentage |
Adenocarcinoma well differentiated | 14 | 43.8 |
Adenocarcinoma moderately differentiated | 6 | 18.7 |
Adenocarcinoma poorly differentiated | 8 | 25 |
Signet ring adenocarcinoma | 2 | 6.3 |
Mucinous adenocarcinoma | 1 | 3.1 |
Neuroendocrine carcinoma | 1 | 3.1 |
The comparative analysis of staging modalities in gastric carcinoma, specifically staging laparoscopy and contrast-enhanced computed tomography (CECT) of the abdomen, reveals a nuanced synergy essential for precise disease management [9].
Stomach carcinoma poses intricate challenges due to diverse clinical presentations and complex progression trajectories. Accurate staging is pivotal for devising optimal treatment strategies, and the integration of innovative techniques becomes imperative [10, 11]. Staging laparoscopy, traditionally exploratory, has evolved into a crucial adjunctive method, offering insights into the peritoneal cavity and aiding in the identification of elusive metastatic lesions. Conversely, CECT abdomen, a cornerstone in staging, provides detailed anatomical information but faces limitations in detecting subtle peritoneal metastases [12].
This study, conducted at Indira Gandhi Medical College and Hospital, Shimla, prospectively analyzed 32 cases. The age-wise distribution highlighted a prevalence in the 61-70 y age group, with males exhibiting a higher incidence. Symptoms were diverse, emphasizing the need for comprehensive diagnostic approaches. Histopathological analysis revealed well-differentiated adenocarcinoma as the most common, predominantly affecting specific age groups [13].
The study's strength lies in its comprehensive approach, incorporating multiple diagnostic modalities. The results underscore the evolving role of staging laparoscopy when used in conjunction with CECT abdomen, offering a personalized and targeted approach.5 By unraveling the intricacies of their synergy, this research contributes valuable insights to the ongoing discourse in oncology. The aim is to catalyze advancements translating into improved patient care and outcomes in stomach carcinoma management [14].
As a prospective study with a robust methodology, including specific protocols for CECT and staging laparoscopy, this research provides a solid foundation for future investigations. Ethical considerations were meticulously adhered to, ensuring confidentiality and the well-being of participants [15].
The limitations include the single-center study setting, potentially limiting generalizability. Additionally, the sample size could be expanded for a more comprehensive understanding. Future directions could involve multi-center collaborations and exploring emerging technologies to further refine the synergy between staging laparoscopy and CECT abdomen in the context of gastric carcinoma [16].
In conclusion, our study underscores the intricate interplay between staging laparoscopy and contrast-enhanced computed tomography (CECT) in the context of gastric carcinoma. The combination of these modalities offers a comprehensive approach to staging, addressing each method's strengths and compensating for their individual limitations. The nuanced insights gained through this synergistic strategy contribute to a more accurate evaluation of disease extent, guiding tailored therapeutic interventions. As we navigate the evolving landscape of gastric carcinoma management, the collaborative use of staging laparoscopy and CECT promises to enhance precision, ultimately improving patient outcomes in this challenging oncological domain.
Nil
Declared none
Ajani JA, D’Amico TA, Almhanna K, Bentrem DJ, Chao J, Das P. Gastric cancer version 3.2016, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw. 2016;14(10):1286-312.
Japanese Gastric Cancer Association. Japanese gastric cancer treatment guidelines. 5th ed. Gastric Cancer. 2018;24(1):1-21.
Lordick F, Mariette C, Haustermans K, Obermannova R, Arnold D, ESMO Guidelines Committee. Oesophageal cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2016;27Suppl 5:v50-7. doi: 10.1093/annonc/mdw329, PMID 27664261.
Cunningham D, Allum WH, Stenning SP, Thompson JN, Van de Velde CJ, Nicolson M. Perioperative chemotherapy versus surgery alone for resectable gastroesophageal cancer. N Engl J Med. 2006;355(1):11-20. doi: 10.1056/NEJMoa055531, PMID 16822992.
Washington K. 7th edition of the AJCC cancer staging manual: stomach. 7th ed. Annals of Surgical Oncology. 2010;17(12):3077-9. doi: 10.1245/s10434-010-1362-z, PMID 20882416.
Japanese Gastric Cancer Association. English edition. Japanese classification of gastric carcinoma. Gastric Cancer. 2011;14(2):101-12.
Ychou M, Boige V, Pignon JP, Conroy T, Bouche O, Lebreton G. Perioperative chemotherapy compared with surgery alone for resectable gastroesophageal adenocarcinoma: an FNCLCC and FFCD multicenter phase III trial. J Clin Oncol. 2011;29(13):1715-21. doi: 10.1200/JCO.2010.33.0597, PMID 21444866.
Smyth EC, Verheij M, Allum W, Cunningham D, Cervantes A, Arnold D. Gastric cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2016;27Suppl 5:v38-49. doi: 10.1093/annonc/mdw350, PMID 27664260.
Hasegawa T, Kubo N, Ohira M, Sakurai K, Toyokawa T, Yamashita Y. Impact of body mass index on surgical outcomes after esophagectomy for patients with esophageal squamous cell carcinoma. J Gastrointest Surg. 2015;19(2):226-33. doi: 10.1007/s11605-014-2686-y, PMID 25398407.
Coccolini F, Cotte E, Glehen O, Lotti M, Poiasina E, Catena F. Intraperitoneal chemotherapy in advanced gastric cancer. Meta-analysis of randomized trials. Eur J Surg Oncol European Journal of Surgical Oncology. 2014;40(1):12-26. doi: 10.1016/j.ejso.2013.10.019, PMID 24290371.
Edge SB, Compton CC. The American Joint Committee on Cancer: the 7th edition of the AJCC cancer staging manual and the future of TNM. Ann Surg Oncol. 2010;17(6):1471-4. doi: 10.1245/s10434-010-0985-4, PMID 20180029.
Beom SH, Choi YY, Baek SE, Li SX, Lim JS, Son T. Multidisciplinary treatment for patients with stage IV gastric cancer: the role of conversion surgery following chemotherapy. BMC Cancer. 2018;18(1):1116. doi: 10.1186/s12885-018-4998-x, PMID 30442107.
Li Z, Shan F, Wang Y. Laparoscopic D2 lymphadenectomy plus complete mesogastrium excision (D2+CME) for gastric cancer: a single-center, high-volume experience. Ann Surg Oncol. 2021;28(1):399-407. doi: 10.1245/s10434-020-08731-y.
Al-Batran SE, Homann N, Pauligk C, Illerhaus G, Martens UM, Stoehlmacher J. Effect of neoadjuvant chemotherapy followed by surgical resection on survival in patients with limited metastatic gastric or gastroesophageal junction cancer: the AIO-FLOT3 trial. JAMA Oncol. 2017;3(9):1237-44. doi: 10.1001/jamaoncol.2017.0515, PMID 28448662.
Mezhir JJ, Shah MA, Jacks LM, Brennan MF, Coit DG, Strong VE. Positive peritoneal cytology in patients with gastric cancer: natural history and outcome of 291 patients. Ann Surg Oncol. 2010;17(12):3173-80. doi: 10.1245/s10434-010-1183-0, PMID 20585870.
Ahn HS, Lee HJ, Hahn S, Kim WH, Lee KU, Sano T. Evaluation of the seventh American Joint Committee on Cancer/International Union Against Cancer Classification of gastric adenocarcinoma in comparison with the sixth classification. Cancer. 2010;116(24):5592-8. doi: 10.1002/cncr.25550, PMID 20737569.