We sincerely appreciate your thorough review and constructive feedback on our manuscript. We are lucky to have met such a rigorous reviewer like you. We will clarify your doubts and address your concerns on each point.
## Motivation
Sorry for the earlier confusion regarding our motivation. The reason of introducing textual descriptions was to furnish the model with a general concept of each category. As established in previous work [1] [2], both definitions of organs and tumors (i.e., textual prompts) can enhance segmentation results. Therefore, it is reasonable to guide the segmentation process via the texutal prompts. However, text-guided segmentation requires effective alignment between textual and visual representations. For instance, to segment a colon tumor in T-stage 4, descriptive texts encompassing all intricate and rare cases must be provided, and the deep learning model needs to determine which situation described in the textual description corresponds to the given visual sample. In the medical domain, aligning specific details with visual information is impractical due to the presence of numerous corner cases, such as tumors with variations in shape, size, density distribution, and blurred boundaries. Furthermore, accurately determining the T-stage in the TNM staging system involves multiple modalities, including image observation (MRI, CT, PET), physical examinations, and microscopic examination of biopsy samples, necessitating more comprehensive descriptions. Unfortunately, current text encoders struggle to differentiate effectively between different cancer stages when faced with lengthy descriptions. Therefore, we utilize general knowledge to convey the concept of each tumor type instead of providing cumbersome descriptions for each T-stage. Our prompt, '**surrounding inflammation, adjacent organ invasion, or regional lymph node enlargement**,' could provide a general concept of colon tumors in different stages. To verify the effectiveness of these textual descriptions, we replaced them with short phrases (e.g., "a CT image of a colon tumor") during the inference stage. The results can be observed as follows:
| Dice(%) | Pan. | RAG. | LAG. | Eso. | Duo. | Liv. Tumor | Pan. Tumor | HV. Tumor | Colon Tumor | Colon Tumor(T4) |
| :------------------- | :---- | :---- | :---- | :---- | :---- | :--------- | :--------- | :-------- | :---------- | :-------------- |
| CAT w. short phrases | 88.87 | 72.17 | 73.12 | 74.37 | 68.99 | 70.65 | 47.80 | 68.77 | 46.31 | 54.09 |
| CAT | 89.24 | 73.69 | 74.63 | 80.10 | 73.46 | 72.73 | 49.67 | 70.11 | 48.31 | 57.37 |
The observed declines demonstrate that textual descriptions, which cover the general concept of potential cases, significantly benefit the tumor segmentation process. To provide an intuitive understanding of these results, we present the qualitative results in the **Figure** (Figure 6 of the rebuttal PDF). Additionally, we enlisted a physician to annotate the tumor regions. The figure shows that a lack of detailed knowledge leads to overlooking crucial details. Importantly, the results from CAT are more closely aligned with those delineated by the expert, who possesses professional medical knowledge. This validates our approach incorporating such textual knowledge from the medical domain.
To assess CAT’s efficacy in dealing with rare cases (i.e., the long-tailed problem), we introduce an in-house dataset where colon tumors have invaded adjacent organs. According to medical literature [3] [4], T4 colorectal tumors, which represent only about 5-8.8% of colon tumor cases, pose significant challenges in diagnosis and treatment. Our results demonstrate that CAT significantly outperforms other models in segmenting T4 colon tumors, underscoring the effectiveness of our design in handling complex medical scenarios.
[1] Clip-driven universal model for organ segmentation and tumor detection.
[2] ZePT: Zero-Shot Pan-Tumor Segmentation via Query-Disentangling and Self-Prompting
[3] Results after multi-visceral resections of locally advanced colorectal cancers: an analysis on clinical and pathological t4 tumors.
[4] Identification of risk factors for lymph node metastasis of colorectal cancer.