# Coexistence of Small-Cell Lung Cancer and Gastrointestinal Malignancies: A Narrative Systematic Review of Case Reports

**Authors:** Ryuichi Ohta, Natsumi Yamamoto, Kaoru Tanaka, Chiaki Sano, Hidetoshi Hayashi

PMC · DOI: 10.7759/cureus.92393 · Cureus · 2025-09-15

## TL;DR

This paper reviews rare cases where patients had both small-cell lung cancer and gastrointestinal cancers, highlighting the challenges in diagnosis and treatment.

## Contribution

The study systematically compiles and analyzes case reports to improve understanding of dual malignancies involving SCLC and GI cancers.

## Key findings

- Six cases of coexisting SCLC and GI cancers were identified, with varied treatment responses and survival outcomes.
- One GI tumor regressed after SCLC chemotherapy, suggesting shared chemosensitivity between the malignancies.
- Delayed diagnosis and disease progression were common challenges in managing these dual cancers.

## Abstract

The coexistence of small-cell lung cancer (SCLC) and primary gastrointestinal (GI) malignancies is an exceptionally rare phenomenon that complicates diagnosis and treatment. We conducted a systematic review of published case reports to better understand the clinical characteristics, therapeutic approaches, and outcomes of these patients. A comprehensive search of major databases up to April 2025 identified six eligible reports describing patients diagnosed with both SCLC and distinct GI cancers, including gastric, duodenal, rectal, and jejunal tumors, as well as one patient with multiple primary malignancies involving rectosigmoid adenocarcinoma, renal cell carcinoma, and prostate adenocarcinoma in addition to SCLC. The patients were predominantly older males with heavy smoking histories, and most cases were extensive-stage SCLC at presentation. Treatment varied widely and included platinum-based chemotherapy, immune checkpoint inhibitors, EGFR-targeted therapy, surgery, and supportive care, with clinical outcomes ranging from a few months to more than one year of survival. Several patients showed partial or complete responses to systemic therapy, and in one case, the GI malignancy regressed following chemotherapy given for SCLC, suggesting overlapping chemosensitivity. However, other patients experienced delayed diagnosis of the second malignancy or limited survival due to disease progression or comorbidities. This synthesis demonstrates that distinguishing dual primaries from metastatic disease is a critical challenge in clinical practice and highlights the need for thorough evaluation in patients with atypical or persistent symptoms. Although data remain limited, awareness of this rare coexistence may help clinicians avoid misclassification and tailor multidisciplinary treatment strategies to improve outcomes.

## Linked entities

- **Diseases:** small-cell lung cancer (MONDO:0008433), gastric cancer (MONDO:0001056), duodenal cancer (MONDO:0021335), rectal cancer (MONDO:0006519), jejunal cancer (MONDO:0006815), renal cell carcinoma (MONDO:0005086), prostate adenocarcinoma (MONDO:0005082)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** disease (MESH:D004194), renal cell carcinoma (MESH:D002292), GI cancers (MESH:D005770), prostate adenocarcinoma (MESH:D000230), primary gastrointestinal (GI) malignancies (MESH:D005767), SCLC (MESH:D055752), malignancies (MESH:D009369), gastric, duodenal, rectal, and jejunal tumors (MESH:D012004), rectosigmoid adenocarcinoma (MESH:D011350)
- **Chemicals:** platinum (MESH:D010984)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12527399/full.md

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Source: https://tomesphere.com/paper/PMC12527399